<?xml version="1.0" encoding="utf-8"?>
			<journal>
			<title>Iranian Journal of Basic Medical Sciences</title>
			<title_fa></title_fa>
			<short_title></short_title>
			<subject>Medical Sciences</subject>
			<web_url>https://ijbms.mums.ac.ir/</web_url>
			<journal_hbi_system_id>0</journal_hbi_system_id>
			<journal_hbi_system_user></journal_hbi_system_user>
			<journal_id_issn>2008-3866</journal_id_issn>
			<journal_id_issn_online>2008-3874</journal_id_issn_online>
			<journal_id_pii></journal_id_pii>
			<journal_id_doi></journal_id_doi>
			<journal_id_iranmedex></journal_id_iranmedex>
			<journal_id_magiran></journal_id_magiran>
			<journal_id_sid></journal_id_sid>
			<journal_id_nlai></journal_id_nlai>
			<journal_id_science></journal_id_science>
			<language>en</language>
			<pubdate>
				<type>jalali</type>
				<year>2026</year>
				<month>9</month>
				<day>1</day>
			</pubdate>
			<pubdate>
				<type>gregorian</type>
				<year>2026</year>
				<month>9</month>
				<day>1</day>
			</pubdate>
			<volume>29</volume>
			<number>9</number>
			<publish_type>online</publish_type>
			<publish_edition>1</publish_edition>
			<article_type>fulltext</article_type>
			<articleset><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Localized chemotherapy through nanofiber scaffolds: Progress, challenges, and future directions</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Review Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Nanofiber-based localized chemotherapy has attracted growing attention as an effective approach to address the shortcomings of conventional systemic cancer therapies by enabling site-specific, sustained, and controlled drug delivery. This review focuses on the emerging role of implantable nanofibrous drug delivery systems in improving cancer treatment outcomes by reducing systemic side effects, enhancing therapeutic efficacy, and improving local tumor management. Special emphasis is placed on electrospinning, a widely used and flexible fabrication method for producing nanofibrous scaffolds, and on the development of chitosan-based nanocomposites and other functional polymer systems that offer high drug-loading capacity and adjustable release behavior. In addition, tumor-targeted drug delivery strategies, including surface modification and ligand–receptor-mediated targeting, are discussed for their potential to improve treatment selectivity and address multidrug resistance. Key challenges related to clinical translation, safety considerations, large-scale fabrication, and long-term performance are also critically analyzed. Finally, the review outlines future research directions aimed at advancing nanofiber-based localized chemotherapy toward practical clinical applications.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Cancer Treatment, Drug Delivery, Electrospun nanofibers, Localized chemotherapy, Nanomedicine</keyword>
				<start_page>1296</start_page>
				<end_page>1312</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28090.html</web_url>
			<author_list><author>
				<first_name>Akram</first_name>
				<middle_name></middle_name>
				<last_name>Firouzi-Amandi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>akramfirouziamandi@gmail.com</email>
				<code>123475</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran|Department of Pharmaceutical Engineering, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Seyed Abbas</first_name>
				<middle_name></middle_name>
				<last_name>Shahrtash</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>seyedabbassh@gmail.com</email>
				<code>123476</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Pharmaceutical Engineering, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Samaneh</first_name>
				<middle_name></middle_name>
				<last_name>Moradi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>samanehmoradi@gmail.com</email>
				<code>123477</code>
				<coreauthor>No</coreauthor>
				<affiliation>Departments of Internal Medical, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mehdi</first_name>
				<middle_name></middle_name>
				<last_name>Dadashpour</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>dadashpourmehdi1400@gmail.com</email>
				<code>123474</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran|Cancer Research Center, Semnan University of Medical Sciences, Semnan, Iran|Department of Medical Biotechnology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Tohid</first_name>
				<middle_name></middle_name>
				<last_name>Kazemi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>tohdikazemi@gmail.com</email>
				<code>123478</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran|Immunology Research Center, Tabriz University of Medical Sciences, Semnan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Inflammasome-associated pyroptosis and tumor angiogenesis in prostate cancer</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Review Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Tumor angiogenesis in prostate cancer is increasingly recognized as a dynamic process shaped by inflammatory signaling, endothelial adaptation, and microenvironmental stress. However, the mechanistic contribution of inflammasome-associated pyroptosis to vascular remodeling remains insufficiently integrated, particularly in relation to functional vascular endpoints such as perfusion, permeability, and therapeutic delivery. This review critically evaluates current evidence linking inflammasome activation and pyroptotic signaling to angiogenic remodeling within prostate tumor microenvironments. Current mechanistic and translational studies addressing inflammasome signaling, gasdermin-associated membrane permeabilization, endothelial activation, cytokine amplification, and vascular remodeling were synthesized with emphasis on spatial heterogeneity, hypoxia-associated stress, and methodological limitations. Available evidence suggests that inflammasome-associated pathways may influence angiogenic remodeling through interleukin-1-mediated endothelial activation, myeloid-cell inflammatory amplification, extracellular signaling, and context-dependent pyroptotic responses. Emerging findings further indicate that vascular consequences vary according to metabolic stress, compartment-specific signaling, and local inflammatory states. However, interpretation remains limited by reliance on static tissue measurements, bulk inflammatory analyses, and indirect vascular readouts that insufficiently distinguish inflammasome priming from terminal pyroptotic execution. Inflammasome-associated pyroptotic signaling may contribute to vascular remodeling in prostate cancer under defined biological conditions, although substantial mechanistic and translational uncertainties remain. Improved integration of spatial inflammatory profiling and functional vascular assessment may support more precise therapeutic targeting and clinically relevant vascular interpretation in heterogeneous prostate tumor microenvironments.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Angiogenesis, Endothelium, Gasdermin D, Inflammasomes, Interleukin-1beta, Prostatic, Neoplasms Pyroptosis, Tumor Microenvironment</keyword>
				<start_page>1313</start_page>
				<end_page>1336</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28116.html</web_url>
			<author_list><author>
				<first_name>Hamzeh</first_name>
				<middle_name>J.</middle_name>
				<last_name>Alameer</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>hamzehj.alameer3000@gmail.com</email>
				<code>123603</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Faculty of Allied Medical Sciences, Hourani Center for Applied Scientific Research, Al-Ahliyya Amman University, Amman, Jordan</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Rafid</first_name>
				<middle_name>Kamal</middle_name>
				<last_name>Jameel</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>rafid.kamal@alnoor.edu.iq</email>
				<code>123604</code>
				<coreauthor>No</coreauthor>
				<affiliation>College of Pharmacy, Alnoor University, Mosul, Iraq</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mahzuna</first_name>
				<middle_name></middle_name>
				<last_name>Nasretdinova</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>luna_1088@mail.ru</email>
				<code>123605</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Otorhinolaryngology, Samarkand State Medical University, Samarkand, Uzbekistan</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Ravshan</first_name>
				<middle_name></middle_name>
				<last_name>Sultanov</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>ravshansultanov.4846@gmail.com</email>
				<code>123606</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Fundamental Sciences, Termez University of Economics and Service, Termez, Uzbekistan</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Djamila</first_name>
				<middle_name></middle_name>
				<last_name>Polatova</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>laylo.djuraeva.88@bk.ru</email>
				<code>123607</code>
				<coreauthor>No</coreauthor>
				<affiliation>Scientific-Practical Medical Center for Pediatric Oncology, Hematology and Immunology, Tashkent, Uzbekistan</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohammed</first_name>
				<middle_name>Abdul</middle_name>
				<last_name>Alaal</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mohammed.abdul.alaal@iunajaf.edu.iq</email>
				<code>123608</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Pharmacy, College of Pharmacy, The Islamic University, Najaf, Iraq</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Navin</first_name>
				<middle_name>Kumar</middle_name>
				<last_name>Tailor</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>navin_kumar_tailor@outlook.com</email>
				<code>123609</code>
				<coreauthor>No</coreauthor>
				<affiliation>University Institute of Pharma Sciences, Chandigarh University, Mohali, Punjab, India</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Ritesh</first_name>
				<middle_name></middle_name>
				<last_name>Singh</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>drritesh7211@yahoo.com</email>
				<code>123610</code>
				<coreauthor>No</coreauthor>
				<affiliation>Center for Research Impact &amp; Outcome, Chitkara University Institute of Engineering and Technology, Chitkara University, Rajpura, 140401, Punjab, India</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Principles and regulatory pathways of exosome-based products in wound healing: Insights from the Iranian Food and Drug Organization Guideline</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Review Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Wound healing is a critical clinical challenge, particularly for chronic and refractory wounds complicated by infection, necrosis, amputation, and death. Recently, cell derivatives, particularly extracellular vesicles (EVs) from mesenchymal stem cells, have emerged as promising cell-free therapeutic agents in regenerative medicine. The review aims to introduce small extracellular vesicles (sEVs) as a next-generation therapeutic strategy and to describe different EV types according to the Global Regulatory Framework (GRF). We also compare techniques for isolating, purifying, and characterizing sEVs and evaluate sEV-based therapies in tissue engineering, focusing on their scope and limitations.A narrative review of the literature was conducted, focusing on preclinical and clinical studies investigating EV-based therapies in wound healing, along with an investigation of the GRF, particularly the Iranian Food and Drug Administration (IFDA) guideline on EVs. The IFDA has recently established a framework for categorizing extracellular particles and highlighting the structural complexity and functional diversity of EVs. sEVs demonstrate significant therapeutic potential for wound repair by promoting angiogenesis, enhancing epithelialization, modulating inflammation, and accelerating tissue remodeling. To enhance the stability and therapeutic lifespan of sEVs, advanced delivery systems, including hydrogels, nanofibers, and biomatrices, are used to preserve structural integrity, physicochemical stability, biological functionality, and morphological characteristics, and to control their release at the injury site. EV-based therapies represent a promising and versatile approach in regenerative medicine for wound healing. Despite challenges in isolation, characterization, scalable manufacturing, and regulatory approval, sEV-based therapeutics offer a biocompatible, cost-effective, and versatile platform that bridges nanotechnology and regenerative medicine.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Biological Products, Drug approval, Exosomes, Extracellular vesicles, Government regulation, Nanomedicine, Regenerative medicine, Wound healing</keyword>
				<start_page>1337</start_page>
				<end_page>1354</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28145.html</web_url>
			<author_list><author>
				<first_name>Delnavaz</first_name>
				<middle_name></middle_name>
				<last_name>Nazari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>delnavaznazari@gmail.com</email>
				<code>123731</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Veterinary Basic Sciences, SR.C., Islamic Azad University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Banafsheh</first_name>
				<middle_name></middle_name>
				<last_name>Heidari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>ban_heidari@yahoo.com</email>
				<code>123732</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Regenerative Medicine in Wound Healing, Medical Laser Research Center, Yara Institute, ACECR, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Nazanin</first_name>
				<middle_name></middle_name>
				<last_name>Akbari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>nazaninakbarii000@gmail.com</email>
				<code>123733</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Biology, Shahid Beheshti University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Zahra</first_name>
				<middle_name></middle_name>
				<last_name>Soleymani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>zahra.solymani@yahoo.com</email>
				<code>123734</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Veterinary Basic Sciences, SR.C., Islamic Azad University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Potential role of ferroptosis in sterile acute lung injury induced by a non-hypoxic ischemia-reperfusion insult</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Ferroptosis, a regulated form of necrotic cell death, is implicated in the pathogenesis of hypoxic lung ischemia-reperfusion injury (LIRI). However, its role in non-hypoxic LIRI, which occurs in common clinical conditions such as trauma and pulmonary embolism, remains unclear. Given that ferroptosis has been implicated in sterile inflammation and lipid peroxidation is a hallmark of this process, this study aimed to investigate the potential role of ferroptosis in inflammatory responses during non-hypoxic LIRI.Materials and Methods: Non-hypoxic LIRI was induced in C57BL/6 mice by occluding the left pulmonary artery for 1 hr, followed by 30 min of reperfusion. The treatment group received liproxstatin-1 (Lip-1; 10 mg/kg, IP) 1 hr before surgery. IL-6 levels in plasma and lung tissue were measured by ELISA. For the in vitro model, normal human bronchial epithelial (NHBE) cells were exposed to nutritional ischemia for 1 hr and then reperfused for 2 hr. Cells were pretreated with Lip-1 (200 nM) 12 hr before ischemia. CXCL1 release was measured by ELISA, and lipid reactive oxygen species (ROS) accumulation was assessed by BODIPY 581/591 C11 fluorescence.Results: Non-hypoxic LIRI markedly increased IL-6 levels in plasma and lung tissue, as well as CXCL1 levels and lipid ROS accumulation in NHBE cells. Pretreatment with Lip-1 significantly reduced these inflammatory responses and lipid ROS accumulation compared with untreated LIRI.Conclusion: Our findings suggest that ferroptosis-associated lipid peroxidation is associated with sterile inflammatory responses during non-hypoxic LIRI in both systemic and epithelial compartments. Lip-1 attenuated these responses, highlighting a potential strategy for non-hypoxic LIRI.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Chemokine CXCL1, Inflammation, Interleukin-6, Lipid Peroxidation, Reperfusion injury</keyword>
				<start_page>1355</start_page>
				<end_page>1360</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28089.html</web_url>
			<author_list><author>
				<first_name>Farzaneh</first_name>
				<middle_name></middle_name>
				<last_name>Kianian</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>kianian.f1989@gmail.com</email>
				<code>123470</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Anesthesia and Perioperative Care, University of California, San Francisco, and San Francisco General Hospital, San Francisco, CA, USA|Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Xiaoli</first_name>
				<middle_name></middle_name>
				<last_name>Tian</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>xiaoli.tian@ucsf.edu</email>
				<code>123471</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anesthesia and Perioperative Care, University of California, San Francisco, and San Francisco General Hospital, San Francisco, CA, USA</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Daisuke</first_name>
				<middle_name></middle_name>
				<last_name>Maruyama</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>daisuke.maruyama@ucsf.edu</email>
				<code>123472</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anesthesia and Perioperative Care, University of California, San Francisco, and San Francisco General Hospital, San Francisco, CA, USA</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Arun</first_name>
				<middle_name></middle_name>
				<last_name>Prakash</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>arun.prakash@ucsf.edu</email>
				<code>123473</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anesthesia and Perioperative Care, University of California, San Francisco, and San Francisco General Hospital, San Francisco, CA, USA</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Quercetin attenuates ferroptosis-associated myocardial injury in rats after coronary microembolization by activating the Nrf2/HO-1 signaling pathway</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Coronary microembolization (CME) significantly contributes to the progression of heart failure and is strongly associated with adverse clinical outcomes in patients. Ferroptosis has been implicated in CME-induced myocardial injury. Quercetin has well-documented anti-inflammatory and antioxidant properties and shows therapeutic potential in coronary artery disease. However, its precise mechanism for regulating ferroptosis during CME-mediated myocardial injury remains unclear. This study aims to elucidate the therapeutic effects of quercetin and its underlying molecular mechanisms that regulate ferroptosis in cardiomyocytes following CME.Materials and Methods: The Sprague-Dawley(SD) rats were randomly divided into four groups (n=7 each): Sham, CME, CME+Quercetin (Que), and CME+Quercetin+ML385 (Que+ML385). The CME model was produced by injecting microspheres into the left ventricles. We administered pharmacological treatments as follows: The Que and Que+ML385 groups received daily oral quercetin (250 mg/kg) starting 7 days before model induction until the procedure day. Additionally, we pretreated the Que+ML385 group with intraperitoneal injection of ML385 (30 mg/kg) 2 hr before CME induction. The comprehensive evaluations include cardiac function assessment, quantification of serum biomarkers of myocardial injury, cardiac tissue histology, and analysis of ferroptosis-related molecular markers to evaluate quercetin’s therapeutic effects.Results: Quercetin pretreatment significantly improved cardiac function, reduced serum markers of myocardial injury, and decreased microinfarction size. At the molecular level, quercetin up-regulated Nrf2 and HO-1 expression and attenuated biochemical markers of cardiomyocyte ferroptosis. However, ML385 co-treatment attenuated this protective effect.Conclusion: Quercetin may inhibit ferroptosis in cardiomyocytes by activating the Nrf2/HO-1 signaling pathway, thereby improving CME-related cardiac dysfunction and reducing myocardial injury.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Coronary-microembolization, Ferroptosis, Nrf2/HO-1, Oxidative stress, Quercetin</keyword>
				<start_page>1361</start_page>
				<end_page>1368</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28126.html</web_url>
			<author_list><author>
				<first_name>Junwen</first_name>
				<middle_name></middle_name>
				<last_name>Huang</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>1763435278@qq.com</email>
				<code>123654</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Guangxi Cardiovascular Institute, Nanning 530021, Guangxi, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Zhiqi</first_name>
				<middle_name></middle_name>
				<last_name>Tang</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>476003466@qq.com</email>
				<code>123655</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Guangxi Cardiovascular Institute, Nanning 530021, Guangxi, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Jiacong</first_name>
				<middle_name></middle_name>
				<last_name>Nong</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>njc_1996@163.com</email>
				<code>123656</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Guangxi Cardiovascular Institute, Nanning 530021, Guangxi, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Guangpeng</first_name>
				<middle_name></middle_name>
				<last_name>Tu</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>doctortgp@163.com</email>
				<code>123657</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Guangxi Cardiovascular Institute, Nanning 530021, Guangxi, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Xueyi</first_name>
				<middle_name></middle_name>
				<last_name>Feng</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>770462414@qq.com</email>
				<code>123658</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Guangxi Cardiovascular Institute, Nanning 530021, Guangxi, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Lang</first_name>
				<middle_name></middle_name>
				<last_name>Li</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>drlilang@gxmu.edu.cn</email>
				<code>123653</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Guangxi Cardiovascular Institute, Nanning 530021, Guangxi, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Carvacrol attenuated acute renal injury induced by unilateral ureteral obstruction in male rats</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Three-day unilateral ureteral obstruction (UUO) leads to acute renal injury. Carvacrol regulates inflammatory factors and reduces oxidative stress and apoptosis. Therefore, we are assessing the renoprotective effect of carvacrol against 3-day UUO in rats.Materials and Methods: Thirty-six male rats were randomized into six groups (n=6): control, carvacrol (100 mg/kg, IP), UUO, and UUO+carvacrol (25, 50, or 100 mg/kg). UUO was induced by ligating the left ureter for 3 days. Carvacrol was administered intraperitoneally once daily for three consecutive days, starting one hour after UUO induction. After treatment, hemodynamic parameters including mean arterial pressure (MAP), renal perfusion pressure (RPP), renal blood flow (RBF), and renal vascular resistance (RVR) were measured. Kidney function markers such as blood urea nitrogen (BUN) and serum creatinine were assessed. Oxidative stress and anti-oxidant status were evaluated by measuring malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), and total anti-oxidant capacity (TAC) in kidney tissue. Western blot analysis determined expression levels of Bax, Bcl-2, cleaved caspase-3, tumor necrosis factor alpha (TNF-α), and nuclear transcription factor p65 (NF-κB p65). Renal damage score (RDS) was surveyed by the hematoxylin and eosin method.Results: UUO significantly raised RVR, RDS, and MDA, serum creatinine, cleaved caspase-3, BUN, NF-κB p65, Bax, TNF-α protein levels (P&lt;0.05), and also reduced RBF, TAC, GPx, SOD, and Bcl-2 protein expression (P&lt;0.05) in left renal tissue, and carvacrol (100 mg/kg) could significantly mitigate the changes affected by UUO.Conclusion: Our study revealed that carvacrol protects against UUO-induced renal injury through its potent anti-oxidant, anti-inflammatory, and anti-apoptotic properties.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Apoptosis, Carvacrol, Inflammation, Oxidative stress, Unilateral ureteral obstruction</keyword>
				<start_page>1369</start_page>
				<end_page>1376</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28127.html</web_url>
			<author_list><author>
				<first_name>Ayat</first_name>
				<middle_name></middle_name>
				<last_name>Kaeidi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>a.kayedi@gmail.com</email>
				<code>123659</code>
				<coreauthor>No</coreauthor>
				<affiliation>Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran|Department of Physiology and Pharmacology, Rafsanjan University of Medical Sciences, Rafsanjan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Elham</first_name>
				<middle_name></middle_name>
				<last_name>Hakimizadeh</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>hakimizadeh_elham@yahoo.com</email>
				<code>123660</code>
				<coreauthor>No</coreauthor>
				<affiliation>3 Immunology of Infectious Diseases Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, afsanjan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Seyed Hadi</first_name>
				<middle_name></middle_name>
				<last_name>Jafari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>hadijafari669@gmail.com</email>
				<code>123661</code>
				<coreauthor>No</coreauthor>
				<affiliation>1 Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Jalal</first_name>
				<middle_name></middle_name>
				<last_name>Hassanshahi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>hasanshahij@gmail.com</email>
				<code>123662</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran|Department of Physiology and Pharmacology, Rafsanjan University of Medical Sciences, Rafsanjan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Modular 3D culture platform combining methylcellulose, testicular ECM, and Sertoli cells for in vitro spermatogenesis</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): We aimed to develop and characterize a 3D culture platform combining methylcellulose (MC) with decellularized testicular extracellular matrix (ECM) and Sertoli cell co-culture to support human spermatogonial stem cell (SSC) survival and differentiation.Materials and Methods: Human testicular cells were isolated and characterized by immunofluorescence and flow cytometry. Sheep testicular tissue was decellularized using detergents and characterized by several histology techniques. ECM was solubilized and mixed with MC at various ratios to make hybrid hydrogels. Hydrogels were characterized for pore size, porosity, mechanical properties, gelation kinetics, and degradation kinetics using scanning electron microscopy, rheological analysis, turbidity analysis, and mass loss assays. Human SSCs and Sertoli cells were cultured in 3D hydrogels for four weeks under differentiation conditions. Cell viability was assessed using the MTT assay, and gene expression of SSC, meiotic, post-meiotic, and apoptotic markers was evaluated by RT-PCR.Results: After four weeks of proliferation, PLZF-positive cells increased from 19% to 73%. Decellularization reduced DNA content by 96% while preserving key matrix components. Hybrid hydrogels displayed interconnected porous structures with pore sizes of about 65–181 µm. All functional hydrogels supported cell viability; however, ECM-rich hydrogels significantly up-regulated PRM2 compared to 2D controls, indicating enhanced post-meiotic differentiation. MC-only scaffolds displayed elevated pro-apoptotic BAX expression compared to ECM-rich matrices, suggesting that bioactive ECM ligands confer cytoprotection.Conclusion: The modular MC/ECM hybrid hydrogel provides a tunable, physiologically relevant 3D culture system that is superior to conventional approaches in supporting SSC maintenance and differentiation, offering promise for fertility preservation strategies.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Cell differentiation, Decellularized extracellular matrix, Hydrogels, Methylcellulose, Sertoli cells, Germline adult stem cells</keyword>
				<start_page>1377</start_page>
				<end_page>1389</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28087.html</web_url>
			<author_list><author>
				<first_name>Narjes</first_name>
				<middle_name></middle_name>
				<last_name>Feizollahi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>n.feizollahi@yahoo.com</email>
				<code>123455</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Ehsan</first_name>
				<middle_name></middle_name>
				<last_name>Heidarian</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>ehsan666hd@gmail.com</email>
				<code>123456</code>
				<coreauthor>No</coreauthor>
				<affiliation>Urology and Nephrology Research Center, Research Institute for Urology and Nephrology, Shahid Beheshti University of Medical Sciences,Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mehdi</first_name>
				<middle_name></middle_name>
				<last_name>Forouzesh</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>forouzeshiran@gmail.com</email>
				<code>123457</code>
				<coreauthor>No</coreauthor>
				<affiliation>Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Maryam</first_name>
				<middle_name></middle_name>
				<last_name>Salem</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>maryamsalem1111@gmail.com</email>
				<code>123458</code>
				<coreauthor>No</coreauthor>
				<affiliation>Research Laboratory for Embryology and Stem Cells, Department of Anatomical Sciences, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran|Infertility Department, Alavi Hospital, Ardabil University of Medical Science, Ardabil, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Soheil</first_name>
				<middle_name></middle_name>
				<last_name>Kianirad</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>soheilkid@gmail.com</email>
				<code>123459</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Chemical and Petroleum Engineering, Sharif University of Technology, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Nasrin</first_name>
				<middle_name>Ghanami</middle_name>
				<last_name>Gashti</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>nasrin.ghanamigashti@ul.ie</email>
				<code>123460</code>
				<coreauthor>No</coreauthor>
				<affiliation>Bernal Institute and School of Engineering, University of Limerick, Limerick, Ireland</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Masoome</first_name>
				<middle_name></middle_name>
				<last_name>Jabarpour</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>masoomejabarpour@yahoo.com</email>
				<code>123461</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Infertility, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Rasool</first_name>
				<middle_name></middle_name>
				<last_name>Setareyi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>rasoolstar.76@gmail.com</email>
				<code>123462</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Life Science Engineering, Faculty of New Science and Technology, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Ayob</first_name>
				<middle_name></middle_name>
				<last_name>Jabari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>jabariayob@yahoo.com</email>
				<code>123463</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Obstetrics and Gynecology, Molud Infertility Treatment Center, Zahedan University of Medical Sciences, Zahedan, Iran|Clinical Immunology Research Center, Zahedan University of Medical Sciences, Zahedan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Farnaz</first_name>
				<middle_name></middle_name>
				<last_name>Khadivi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>farnazkhadivi031@gmail.com</email>
				<code>123464</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anatomy, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran|Medical Plants Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Morteza</first_name>
				<middle_name></middle_name>
				<last_name>Koruji</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>koruji1@gmail.com</email>
				<code>123465</code>
				<coreauthor>No</coreauthor>
				<affiliation>Stem Cell and Regenerative Medicine Research Center, Iran University of Medical Sciences, Tehran, Iran|Department of Anatomy, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohammad</first_name>
				<middle_name></middle_name>
				<last_name>Naji</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>naji_m_f@yahoo.com</email>
				<code>123466</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Urology and Nephrology Research Center, Research Institute for Urology and Nephrology, Shahid Beheshti University of Medical Sciences,Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mehdi</first_name>
				<middle_name></middle_name>
				<last_name>Abbasi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>abbasima@tums.ac.ir</email>
				<code>123467</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Down-regulation of AGXT2L1 promotes the development of nonalcoholic fatty liver disease</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): To investigate the role of alanine-glyoxylate aminotransferase 2-like1 (AGXT2L1) in Nonalcoholic fatty liver disease (NAFLD) and its underlying mechanisms.Materials and Methods: Changes in AGXT2L1 expression during NASH progression were analyzed using tissue samples, cell experiments, and animal models. RNA sequencing was performed on experimental mice to explore potential mechanisms by assessing inflammatory factors, cell apoptosis, and endoplasmic reticulum stress.Results: Compared with normal tissues, AGXT2L1 expression was reduced in multiple liver diseases. Both in vitro and in vivo experiments confirmed that down-regulation of AGXT2L1 exacerbated NASH severity. RNA sequencing initially indicated that abnormal AGXT2L1 expression primarily affects phospholipid metabolism. Additionally, animal experiments showed that AGXT2L1 deficiency increased the number of apoptotic hepatocytes and elevated the expression of endoplasmic reticulum stress markers.Conclusion: Decreased AGXT2L1 expression is an evident alteration in liver injury. It has been indicated that down-regulation of AGXT2L1 promotes NAFLD development, possibly through three pathways: activation of inflammatory responses, promotion of hepatocyte apoptosis, and enhancement of endoplasmic reticulum stress.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Alanine-glyoxylate-aminotransferase 2-like1- (AGXT2L1), Apoptosis, ER stress, Inflammation, Nonalcoholic fatty liver disease (NAFLD), Phospholipid metabolism</keyword>
				<start_page>1390</start_page>
				<end_page>1397</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28088.html</web_url>
			<author_list><author>
				<first_name>Yue</first_name>
				<middle_name></middle_name>
				<last_name>Yu</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>1479727708@qq.com</email>
				<code>123469</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Radiation Oncology, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Lu</first_name>
				<middle_name></middle_name>
				<last_name>Wu</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>melody80017@163.com</email>
				<code>123468</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Radiation Oncology, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Berberine protects against behavioral deficits, memory dysfunction, and callosal demyelination in cuprizone-intoxicated C57BL/6 mice</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Multiple sclerosis (MS) is a neurological disorder marked by progressive demyelination and neuroinflammation. Berberine, a plant-derived isoquinoline alkaloid found in Berberis species, has notable anti-inflammatory and antioxidant properties. This study aimed to evaluate berberine’s protective effects against cuprizone intoxication in C57BL/6 mice.Materials and Methods: C57BL/6 mice received a cuprizone-containing diet (0.2% w/w) for five weeks and were concurrently treated with berberine (5 or 10 mg/kg). Body weight, motor coordination, exploratory and locomotor activity, memory function, oxidative stress biomarkers, and inflammatory cytokines were assessed. Histopathological evaluation of myelination was performed using Luxol Fast Blue staining.Results: Berberine treatment improved exploratory behavior, locomotor activity, and memory function compared with cuprizone-only mice. Oxidative stress analysis showed that berberine significantly reduced malondialdehyde (MDA) levels and increased total thiol content. Berberine also attenuated cuprizone-induced increases in interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α). Histological findings indicated that berberine preserved myelin integrity, prevented myelin degradation, and reduced the severity of demyelination in the corpus callosum.Conclusion: These findings indicate that berberine confers protective effects against cuprizone-induced behavioral deficits, memory dysfunction, and callosal demyelination in C57BL/6 mice. The neuroprotective actions of berberine appear to be mediated by suppression of oxidative stress and inflammatory cytokines.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Berberine, Cuprizone, Demyelination, Multiple Sclerosis, Oxidative stress</keyword>
				<start_page>1398</start_page>
				<end_page>1405</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28117.html</web_url>
			<author_list><author>
				<first_name>Mohaddeseh Sadat</first_name>
				<middle_name></middle_name>
				<last_name>Alavi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>alavimhd@mums.ac.ir</email>
				<code>123611</code>
				<coreauthor>No</coreauthor>
				<affiliation>Pharmacological Research Center of Medicinal Plants, Basic Sciences Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran|Department of Pharmacology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Seyede Faeze</first_name>
				<middle_name></middle_name>
				<last_name>Hosseini</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>hosseinifaeze@alumni.um.ac.ir</email>
				<code>123612</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Amir</first_name>
				<middle_name></middle_name>
				<last_name>Afkhami-Goli</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>amirgoli@cc.iut.ac.ir</email>
				<code>123613</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mahsa</first_name>
				<middle_name></middle_name>
				<last_name>Aminizade</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mah.aminizadeh@gmail.com</email>
				<code>123614</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Pharmacology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Emad</first_name>
				<middle_name></middle_name>
				<last_name>Mokarramdust</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>blackrider865@yahoo.com</email>
				<code>123615</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Pharmacology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Naghmeh</first_name>
				<middle_name></middle_name>
				<last_name>Layegh Khavidaki</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>naghmehlayegh@gmail.com</email>
				<code>123616</code>
				<coreauthor>No</coreauthor>
				<affiliation>Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Fatemeh</first_name>
				<middle_name></middle_name>
				<last_name>Forouzanfar</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>forouzanfarf@mums.ac.ir</email>
				<code>123617</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Neuroscience, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Hamid Reza</first_name>
				<middle_name></middle_name>
				<last_name>Sadeghnia</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>sadeghniahr@mums.ac.ir</email>
				<code>123618</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Pharmacological Research Center of Medicinal Plants, Basic Sciences Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran|Department of Pharmacology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Liquiritin ameliorates atherosclerosis in ApoE-/- mice by modulating SIRT1 and lipid metabolism</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Atherosclerosis (AS) and dyslipidemia are major contributors to cardiovascular disease; however, safe and effective therapeutic strategies remain limited. Liquiritin, a natural flavonoid, exhibits potential metabolic and cardiovascular benefits in human beings. This study investigated the effects of liquiritin on AS, lipid metabolism, and hepatic steatosis in high-fat diet (HFD)-induced ApoE-/- mice.Materials and Methods: Mice were intraperitoneally administered liquiritin (20 mg/kg/day) for 12 weeks. Histological and biochemical analyses revealed that chronic liquiritin treatment did not induce hepatotoxicity, nephrotoxicity, or growth impairment, as evidenced by preserved liver and kidney architecture, unchanged serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine, and blood urea nitrogen (BUN) levels, and stable body weight.Results: Liquiritin markedly attenuated aortic root plaque formation, lipid deposition, and fibrotic areas (P&lt;0.001) in ApoE-/- mice. Furthermore, liquiritin significantly improved serum and hepatic lipid profiles by reducing triglyceride, total cholesterol, and LDL-C levels (P&lt;0.001) and alleviating hepatic steatosis (P&lt;0.001), as confirmed by histological analyses. Mechanistic studies demonstrated that liquiritin restored hepatic SIRT1 expression, down-regulated PPARγ and LXRα, and up-regulated ABCA1 (P&lt;0.001), suggesting the modulation of key lipid metabolism pathways.Conclusion: These findings demonstrate that liquiritin protects against AS and hepatic lipid accumulation by modulating SIRT1-mediated lipid metabolism (P&lt;0.001), emphasizing its potential as a treatment option for metabolic and cardiovascular disorders.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Atherosclerosis, Dyslipidemia, Hepatic steatosis, Lipid metabolism, Liquiritin, SIRT1</keyword>
				<start_page>1406</start_page>
				<end_page>1412</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28124.html</web_url>
			<author_list><author>
				<first_name>Kang</first_name>
				<middle_name></middle_name>
				<last_name>Ye</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>1329627285@qq.com</email>
				<code>123637</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Internal Medicine-Cardiovascular, Guangming Traditional Chinese Medicine Hospital of Pudong New Area, Shanghai 201321, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Jing</first_name>
				<middle_name></middle_name>
				<last_name>Shi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>20136135@qq.com</email>
				<code>123638</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Internal Medicine-Cardiovascular, Guangming Traditional Chinese Medicine Hospital of Pudong New Area, Shanghai 201321, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Ping</first_name>
				<middle_name></middle_name>
				<last_name>Gong</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>chengeziyu@163.com</email>
				<code>123639</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Internal Medicine-Cardiovascular, Guangming Traditional Chinese Medicine Hospital of Pudong New Area, Shanghai 201321, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Zhongsheng</first_name>
				<middle_name></middle_name>
				<last_name>Zhu</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>drzzs66@163.com</email>
				<code>123640</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Internal Medicine-Cardiovascular, Guangming Traditional Chinese Medicine Hospital of Pudong New Area, Shanghai 201321, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Intranasal administration of spike-specific mRNA-LNP confers more protection than the intramuscular route against SARS-CoV-2</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Intranasal vaccination mimics natural infection and induces mucosal immunity against respiratory viruses. This study compared the immunogenicity and protective efficacy of a nucleoside-modified messenger RNA (mRNA) encoding the SARS-CoV-2 spike protein, encapsulated in lipid nanoparticles (LNPs), administered via intranasal (I.N) versus intramuscular (I.M) routes.Materials and Methods: BALB/c mice received mRNA-LNP vaccines at 1, 5, or 10 µg doses intramuscularly. Antibody responses (Immunoglobulin G/IgA [IgG/IgA]), neutralization titers (conventional virus neutralization test [cVNT]), and interferon-gamma (IFN-γ) responses were assessed to select the optimal dose. The selected 5 µg dose was then administered to mice and Syrian hamsters via I.N or I.M routes. Post-challenge, lung viral loads (50% Tissue Culture Infectious Dose [TCID₅₀]/ml) and weight changes were evaluated.Results: The 5 µg dose induced robust humoral and cellular immunity (cVNT &gt;5 log₂). Intranasal delivery elicited strong spike-specific IgA in nasal washes. Although I.M vaccination produced higher serum neutralizing titers (51.2 vs. 22.0), I.N vaccination conferred superior protection with a 4-log reduction in lung viral load (~10¹ TCID₅₀/ml) versus I.M and controls (~10² TCID₅₀/ml). I.N-vaccinated hamsters were completely protected from weight loss, whereas I.M-vaccinated animals showed mild weight reduction (~1%).Conclusion: Intranasal mRNA-LNP administration elicits potent mucosal and systemic immunity and provides superior protection against SARS-CoV-2 challenge compared to I.M vaccination, underscoring its promise as a transformative strategy for respiratory virus vaccines.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>COVID-19 vaccines, Intranasal Administration, Lipid nanoparticles, mRNA vaccines, Mucosal immunity, SARS-CoV-2</keyword>
				<start_page>1413</start_page>
				<end_page>1423</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28148.html</web_url>
			<author_list><author>
				<first_name>Mohsen</first_name>
				<middle_name></middle_name>
				<last_name>Abdoli</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mohsen.abdoli20@gmail.com</email>
				<code>123755</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Hoorieh</first_name>
				<middle_name></middle_name>
				<last_name>Soleimanjahi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>soleimanjahihorie@gmail.com</email>
				<code>123756</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Sara</first_name>
				<middle_name></middle_name>
				<last_name>Soudi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>soudi@modares.ac.ir</email>
				<code>123757</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Asghar</first_name>
				<middle_name></middle_name>
				<last_name>Abdoli</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>asghar.abdoli7@gmail.com</email>
				<code>123758</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Electroacupuncture ameliorates diabetic renal injury by regulating the AMPK-autophagy signaling pathway</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Diabetic nephropathy (DN) is a common complication of diabetes mellitus (DM) and the leading cause of end-stage renal disease worldwide. Despite evidence supporting the renoprotective effects of electroacupuncture (EA), the underpinning molecular mechanisms require further investigation. This study was designed to evaluate the therapeutic efficacy of EA in mice with DN and to elucidate its potential mechanisms of action.Materials and Methods: A DN model was established in male C57BL/6 mice by streptozotocin (STZ) injection and validated. Mice were randomly allocated into four groups: control, normal+electroacupuncture (EA), DN, and DN+EA. EA was applied at Yanglingquan and Zusanli acupoints in the treatment groups. Renal histology and ultrastructure were examined. AMPK and downstream autophagy-related molecule expression were analyzed by qRT-PCR and Western blot.Results: Renal tissues from DN mice exhibited suppressed autophagy, marked by decreased microtubule-associated protein 1 light chain 3-II (LC3-II) and increased Sequestosome-1 (p62) expression, along with reduced phosphorylation of AMP-activated protein kinase (AMPK) and Unc-51 Like Autophagy Activating Kinase 1(ULK1) and increased Phosphorylated mammalian target of rapamycin (p-mTOR) levels after 8 weeks, indicating impaired autophagy and renal injury. EA treatment reversed these alterations by enhancing AMPK and ULK1 phosphorylation, restoring autophagy, and mitigating renal damage.Conclusion: The AMPK signaling pathway represents a novel therapeutic target for DN. Our data indicate that EA facilitates renal protection by activating AMPK/ULK1-mediated autophagy, implicating EA as a viable strategy for targeting this pathway.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>AMP-activated protein- kinase, Autophagy, Diabetic nephropathy, Electroacupuncture, ULK1</keyword>
				<start_page>1424</start_page>
				<end_page>1432</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28150.html</web_url>
			<author_list><author>
				<first_name>Zehao</first_name>
				<middle_name></middle_name>
				<last_name>Zhang</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>3640753930@qq.com</email>
				<code>123766</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Nephrology, Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People’s Hospital, Lishui, Zhejiang 323000, China|The Nephrology Department of Xijing Hospital, The Fourth Military Medical University, Xi’an, Shaanxi 710032, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Meijuan</first_name>
				<middle_name></middle_name>
				<last_name>Xiang</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>626297276@qq.com</email>
				<code>123767</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Nephrology, Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People’s Hospital, Lishui, Zhejiang 323000, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Lejian</first_name>
				<middle_name></middle_name>
				<last_name>Lan</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>8753530@qq.com</email>
				<code>123768</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Nephrology, Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People’s Hospital, Lishui, Zhejiang 323000, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Duo</first_name>
				<middle_name></middle_name>
				<last_name>Peng</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>pengduo11@126.com</email>
				<code>123769</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Nephrology, Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People’s Hospital, Lishui, Zhejiang 323000, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Lixia</first_name>
				<middle_name></middle_name>
				<last_name>You</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>1187801941@qq.com</email>
				<code>123770</code>
				<coreauthor>No</coreauthor>
				<affiliation>The Nephrology Department of Xijing Hospital, The Fourth Military Medical University, Xi’an, Shaanxi 710032, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mengmeng</first_name>
				<middle_name></middle_name>
				<last_name>Jia</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>877983143@qq.com</email>
				<code>123771</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Nephrology, Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People’s Hospital, Lishui, Zhejiang 323000, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Jianyun</first_name>
				<middle_name></middle_name>
				<last_name>Peng</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>pengjianyun1@163.com</email>
				<code>123765</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Nephrology, Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People’s Hospital, Lishui, Zhejiang 323000, China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>High-intensity interval training attenuates neuroinflammation and seizure activity via miR-146a/NF-κB signaling in chronic mesial temporal lobe epilepsy</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Regular exercise training has emerged as a non-pharmacological approach that can beneficially impact disease progression in epileptic patients, but the underlying molecular pathways remain unclear. In this study, we investigated the effects of eight weeks of high-intensity interval training (HIIT), recognized as a time-efficient form of aerobic exercise, on hippocampal neuroinflammation and seizure activity in a kainic acid rat model of chronic Mesial temporal lobe epilepsy (MTLE).Materials and Methods: After induction of epilepsy via intrahippocampal injection of kainic acid, rats were randomly divided into 4 groups: Control, Sham, Epilepsy, and Epilepsy+HIIT. After an acclimatization period, rats in the exercise group performed 8 weeks of HIIT. The HIIT protocol consisted of running at 90% of Vmax, with active rest periods at 30% of Vmax. At the end of week 8, rats were sacrificed, and hippocampal tissue was extracted for Western blotting and real-time qPCR.Results: After 8 weeks of HIIT, our data showed that IL-1β (P&lt;0.0001), IRAK1 (P&lt;0.0001), NF-κB (P&lt;0.0001), and p-NMDA (P&lt;0.0001) levels were significantly lower than in the epileptic group. Additionally, miR-146a levels were significantly lower than in the epileptic group (P&lt;0.001). Seizure intensity also decreased in parallel with the reduction in inflammation.Conclusion: Our results indicate that HIIT could serve as a potent anti-inflammatory and neuroprotective tool in chronic MTLE through regulating the miR-146a/NF-κB/pNMDA pathway, highlighting that regular chronic exercise training could be a complementary therapeutic option for drug-resistant epilepsy.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Convulsion, Epilepsy, Exercise training, Hippocampus, Inflammation</keyword>
				<start_page>1433</start_page>
				<end_page>1439</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28149.html</web_url>
			<author_list><author>
				<first_name>Leila</first_name>
				<middle_name></middle_name>
				<last_name>Saremi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>leila.saremi@ut.ac.ir</email>
				<code>123759</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Exercise Physiology, Faculty of Sport Sciences and Health, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohamadreza</first_name>
				<middle_name></middle_name>
				<last_name>Kordi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mrkordi@ut.ac.ir</email>
				<code>123760</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Exercise Physiology, Faculty of Sport Sciences and Health, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Amir Hossein</first_name>
				<middle_name></middle_name>
				<last_name>Saffar Kohneh Quchan</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>amirsaffar@ut.ac.ir</email>
				<code>123761</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Exercise Physiology, Faculty of Sport Sciences and Health, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Younes</first_name>
				<middle_name></middle_name>
				<last_name>Sarkabood</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>younessarkabood@ut.ac.ir</email>
				<code>123763</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Exercise Physiology, Faculty of Sport Sciences and Health, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Siroos</first_name>
				<middle_name></middle_name>
				<last_name>Choobineh</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>choobineh@ut.ac.ir</email>
				<code>123762</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Exercise Physiology, Faculty of Sport Sciences and Health, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Zahra</first_name>
				<middle_name></middle_name>
				<last_name>Javaheri</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>javaheri.z1256@ut.ac.ir</email>
				<code>123764</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Exercise Physiology, Faculty of Sport Sciences and Health, University of Tehran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Neuroprotective effect of selenium in rats subjected to chronic intermittent cold and immobilization stress: The role of phosphorylated tau</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): The current study aimed to investigate the potential neuroprotective effect of selenium against cognitive dysfunction in rats subjected to chronic intermittent stress. Materials and Methods: Ninety adult male Wistar rats were randomly assigned into five groups (n=18): (1) N: non-stressed group; (2) CS: cold-stressed non-treated group; (3) IS: immobilized-stressed non-treated group; (4) CS/Se: cold-stressed/ selenium-treated group; and (5) IS/Se: immobilized-stressed/selenium-treated group. Memory and learning were assessed using the Morris Water Maze, novel object recognition, and Y-maze tests. After completion of neurobehavioral tests, fasting retro-orbital blood samples were collected from all rats. Stress hormones, serum sodium and potassium, oxidative stress markers (malondialdehyde (MDA), total antioxidant capacity (TAC), glutathione peroxidase (GPx), and thioredoxin reductase (TrxR)), and the proinflammatory markers (tumor necrosis factor-alpha (TNF-α), intercellular adhesion molecule-1 (ICAM-1)) were measured. Histopathological examination of the hippocampus and immunohistochemistry of p-tau were performed. Results: The results indicated that memory and learning were impaired by chronic intermittent stress. This was associated with histopathological changes of the hippocampus and increased the expression of p-tau. Selenium administration improved the cognitive dysfunction as indicated by behavioral tests. Also, it reduced the levels of stress hormones, sodium, MDA, and the proinflammatory markers. It significantly enhanced the antioxidant enzyme activities and increased the potassium level. In addition, it improved the histopathological changes of the hippocampus and decreased the expression of p-tau.Conclusion: Coadministration of selenium to rats subjected to chronic stress improved cognitive dysfunction by its antioxidant and anti-inflammatory effects, as well as via downr-egulation of p-tau in the hippocampus.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Chronic stress, Cognitive impairment, Hippocampus, Neuroinflammation, Oxidative stress, p-tau, Rat, Selenium</keyword>
				<start_page>1440</start_page>
				<end_page>1447</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28125.html</web_url>
			<author_list><author>
				<first_name>Mohamed</first_name>
				<middle_name>A.</middle_name>
				<last_name>Abdallah</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mwmdy@yahoo.com</email>
				<code>123646</code>
				<coreauthor>No</coreauthor>
				<affiliation>Medical Physiology Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt|Medical Physiology Department, Faculty of Medicine, Menoufia National University, Menoufia, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Hesahm</first_name>
				<middle_name>A.D.</middle_name>
				<last_name>Abdel-Razek</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>h_abdelrazek@hotmail.com</email>
				<code>123647</code>
				<coreauthor>No</coreauthor>
				<affiliation>Medical Physiology Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Sohair</first_name>
				<middle_name>A.</middle_name>
				<last_name>Saleh</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>dr_sohairasaleh@hotmail.com</email>
				<code>123648</code>
				<coreauthor>No</coreauthor>
				<affiliation>Medical Physiology Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Rasha</first_name>
				<middle_name>S.A.</middle_name>
				<last_name>Elseadawy</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>dr.rashaneuro@yahoo.com</email>
				<code>123649</code>
				<coreauthor>No</coreauthor>
				<affiliation>Neuropsychiatry Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mona</first_name>
				<middle_name>A.</middle_name>
				<last_name>Kora</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>monakora1987@gmail.com</email>
				<code>123650</code>
				<coreauthor>No</coreauthor>
				<affiliation>Pathology Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Amal</first_name>
				<middle_name>Gamal</middle_name>
				<last_name>Younis</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>amal.mousa@med.menofia.edu.eg</email>
				<code>123651</code>
				<coreauthor>No</coreauthor>
				<affiliation>Medical Physiology Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt|Medical Physiology Department, Faculty of Medicine, Menoufia National University, Menoufia, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Heba</first_name>
				<middle_name>Rady</middle_name>
				<last_name>Salem</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>heba.salem.12@med.menofia.edu.eg</email>
				<code>123652</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Medical Physiology Department, Faculty of Medicine, Menoufia University, Shebin-Elkom, Egypt|Medical Physiology Department, Faculty of Medicine, Menoufia National University, Menoufia, Egypt</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>MiR-124 alleviates cerebral ischemia-reperfusion injury by targeting SLC1A5 to inhibit neuronal ferroptosis</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Original Article</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): This study aimed to investigate whether miR-124 alleviates neurological injury in cerebral ischemia-reperfusion injury (CIRI) mice by targeting Solute Carrier Family 1 Member 5 (SLC1A5) to regulate ferroptosis. Materials and Methods: One hundred twenty male C57BL/6 mice were randomly assigned to Sham, CIRI model, miR-124 mimic, miR-124 inhibitor, miR-124 vector, and Ferrostatin-1 (Fer-1) groups. One week before modeling, the viral groups received 2.0 μl of the corresponding viral vector via right lateral ventricle injection. Additionally, the Fer-1 group received intraperitoneal injections of ferrostatin-1 (5.0 mg/kg). Following the establishment of the MCAO model by the wire occlusion method. At different time points, the Longa method was employed to assess the degree of neurological deficit. TTC staining was used to detect cerebral infarction volume. ELISA was applied to measure changes in SOD, MDA, GSH, and Fe²⁺. qRT-PCR was utilized to detect the expression levels of miR-124, SLC1A5, and GPX4, and Immunohistochemistry was detected SLC1A5-positive cells. Finally, the miR-124/SLC1A5 interaction was predicted by bioinformatics and validated by a dual-luciferase assay and western blot.Results: Compared with the sham group, the CIRI group showed reduced neurological scores, elevated MDA/Fe²⁺, and decreased SOD/GSH/GPX4. miR-124 mimic treatment significantly improved these parameters, similar to Fer-1, whereas miR-124 inhibition exacerbated injury and increased SLC1A5 expression. Dual-luciferase assay confirmed SLC1A5 as a direct target of miR-124.Conclusion: Collectively, these data indicate that MiR-124 attenuates CIRI-induced neurological damage, potentially by targeting SLC1A5 to inhibit ferroptosis, as evidenced by up-regulation of GPX4 and GSH.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Cerebral ischemia, Ferroptosis, MiR-124, Neuroprotection, Reperfusion injury, Solute carrier family 1 member 5</keyword>
				<start_page>1448</start_page>
				<end_page>1455</end_page>
				<web_url>https://ijbms.mums.ac.ir/article_28146.html</web_url>
			<author_list><author>
				<first_name>Zhu</first_name>
				<middle_name></middle_name>
				<last_name>Yizhen</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>yzzhu2005@126.com</email>
				<code>123735</code>
				<coreauthor>No</coreauthor>
				<affiliation>Class 5, Grade 2023, Clinical Medicine, Guizhou Medical University, Gui’an New District, Guizhou 561113, People’s Republic of China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Jiang</first_name>
				<middle_name></middle_name>
				<last_name>Qian</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>1849697109@qq.com</email>
				<code>123738</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anatomy and Neurobiology, Guizhou Medical University School of Basic Medicine, Gui’an New District, Guizhou 561113, People’s Republic of China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Long</first_name>
				<middle_name></middle_name>
				<last_name>Tingting</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>786664953@qq.com</email>
				<code>123736</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anatomy and Neurobiology, Guizhou Medical University School of Basic Medicine, Gui’an New District, Guizhou 561113, People’s Republic of China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Huang</first_name>
				<middle_name></middle_name>
				<last_name>Tao</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>1742739402@qq.com</email>
				<code>123739</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Anatomy and Neurobiology, Guizhou Medical University School of Basic Medicine, Gui’an New District, Guizhou 561113, People’s Republic of China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Zhu</first_name>
				<middle_name></middle_name>
				<last_name>Junde</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>jdzhu73@126.com</email>
				<code>123737</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Anatomy and Neurobiology, Guizhou Medical University School of Basic Medicine, Gui’an New District, Guizhou 561113, People’s Republic of China</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article>
			</articleset>
			</journal>