1. Herrera B, Murillo MM, Alvarez-Barrientos A, Beltrn J, Fernndez M, Fabregat I. Source of early reactive oxygen species in the apoptosis induced by transforming growth factor-(beta) in fetal rat hepatocytes. Free Rad Biol Med 2004; 36:16-26.
2. Circu ML, Aw TY Reactive oxygen species, cellular redox systems, and apoptosis. Free Rad Biol Med 2008; 48:749-762.
3. Conklin KA. Chemotherapy-associated oxidative stress: impact on chemotherapeutic effectiveness. Integr Cancer Ther 2004; 3:294-300.
4. Hosseinzadeh L, Behravan J, Mosaffa F, Bahrami G, Bahrami A, Karimi G. Curcumin potentiates doxorubicin-induced apoptosis in H9c2 cardiac muscle cells through generation of reactive oxygen species. Food Chem Toxicol 2011; 49:1102–1109.
5. Lopes AM, Meisel A, Dirnagl U, Carvalho FD, Bastos Mde L. Doxorubicin induces biphasic neurotoxicity to rat cortical neurons. Neurotoxicology 2008; 29:286-293.
6. Tangpogon J, Miriyala S, Noel T, Sinthupibulyakit C, Jungsuwadee P, St Clair DK. Doxorubicin induced central nevous system toxicity and protection by xanthone derivatives of Garcinia mangostana. Neuroscience 2011; 175:292–299.
7. Cardoso S, Santos RX, Carvalho C, Correia S, Pereira G, Pereira S, Oliveira P, Santos MS, Proença T. Doxorubicin increases the susceptibility of brain mitochondria to Ca2+-induced permeability transition and oxidative damage. Free Radic Biol Med 2008; 45:1395–1402.
8. Karlsson M, Kurz T, Brunk UT, Nilsson SE, Frennesson CI. “What does the commonly used DCF test for oxidative stress really show?” Biochem J 2010; 428:183–190.
9. Janelsins MC, Roscoe JA, Berg MJ, Thompson BD, Gallagher MJ, Morrow GR, et al. IGF-1 partially restores chemotherapy-induced reductions in neural cell proliferation in adult C57BL/6 mice. Cancer Invest 2010; 28:544–553.
10. Kesler s, Janelsins M, Koovakkattu D, Palesh O, Mustian K, Morrow G, et al. Reduced hippocampal volume and verbal memory performance associated with interleukin-6 and tumor necrosis factor-alpha levels in chemotherapy-treated breast cancer survivors. Brain Behav Immun 2013; 30:S109–S116.
11. Mozaffarian V. A Dictionary of Iranian Plant Names. Tehran: Farhang Moaser Publishers; 1978.
12. Nematollahi F, Rustaiyan A, Larijani K, Nadimi M. Essential oil composition of Artemisia biennis Willd and Pulicariaundulata (L.) C.A. Mey., two Compositae herbs growing wild in Iran. J Essent Oil Res 2006; 18:339–341.
13. Lopes-Lutz D, Alviano DS, Alviano CS, Kolodziejczyk PP. Screening of chemical composition, antimicrobial and antioxidant activities of Artemisia essential oils. Phytochemistry 2008; 69:1732-1738.
14. Emami A, Zamani Taghizadeh Rabe SH, Ahi A, Mahmoudi M. Study on toxic effects of Artemisia spp. fractions from Iran on human cancer cell lines. J Zanjan Univ Med Sci 2010; 18:58-67.
15. Mojarrab M, Naderi R, Heshmati Afshar F. Screening of different extracts from Artemisia species for their potential antimalarial activity. Iran J Pharm Res 2015: 14:603-608.
16. Emami A, Zamani Taghizadeh Rabe SH, Ahi A, Mahmoudi M. Inhibitory activity of eleven Artemisia species from Iran against Leishmania major parasites. Iran J Basic Med Sci 2012; 15: 807-811.
17. Iranshahi M, Emami SA, Mahmoud-Soltani M. Detection of sesquiterpene lactones in ten Artemisia species population of Khorasan provinces. Iran J Basic Med Sci 2007; 10:183-188.
18. Singh KN, Lal B. Ethnomedicines used against four common ailments by the tribal communities of Lahaul-Spiti in Western Himalaya. J Ethnopharmacol 2008; 4; 115:147-159.
19. Hatami T, Emami SA, Miraghaee SS, Mojarrab M. Total phenolic contents and antioxidant activities of different extracts and fractions from the aerial parts of Artemisia biennis Willd. Iran J Pharm Res 2014; 13:551–559.
20. Hatanaka H. Nerve growth factor-mediated stimulation of tyrosine hydroxylase activity in a clonal rat pheochromocytoma cell line. Brain Res 1981; 222:225–233.
21. Rebois RV, Reynolds E, Toll L, Howard BD. Storage of dopamine and acetylcholine in granules of PC12, a clonal pheochromocytoma cell line. Biochemistry 1980; 19:1240–1248.
22. Klaassen CD. Casarett & Doull’s Toxicology. 7 th ed. McGraw Hill; 2007.p.30- 31.
23. Malstorm B, Andreasson L, Reinhammer B. The enzymeas. Boyer; 1975.p.533.
24. Hosseinzadeh L, Khorand A, Aliabadi A. Discovery of 2- Phenyl –N-(5-(trifluoromethyl) – 1, 3, 4- thiadiazol-2-yl) acetamid derivatives as apoptosis inducer via caspase pathway whit potential anticancer activity. Arch Pharm Chem Life 2013; 346:812–818.
25. Shokoohinia Y, Hosseinzadeh L, Alipour M, Mostafaie A, Mohammadi-Motlagh HR. Comparative evaluation of cytotoxic and apoptogenic effects of several coumarins on human cancer cell lines: osthole induces apoptosis in p53-deficient H1299 cells. Adv Pharmacol Sci 2014; 2014:847574.
26. Shokoohinia Y, Hosseinzadeh L, Moieni-Arya M, Mostafaie A, Mohammadi-Motlagh HR. Osthole attenuates doxorubicin-Induced apoptosis in PC12 cells through inhibition of mitochondrial dysfunction and ROS production. Biomed Res Int 2014; 2014:156848.
27. Pal S, Ahir M, Sil PC. Doxorubicin-induced neurotoxicity is attenuated by a 43-kD protein from the leaves of Cajanus indicus L. via NF-κB and mitochondria dependent pathways. Free Radic Res 2012; 46:785-798.
28. Oz E, Ilhan. Effects of melatonin in reducing the toxic effects of doxorubicin. Mol Cell Biochem 2006; 286:11-15.
29. Zhang ZC, Su G, Li J, Wu H, Xie XD. Two new neuroprotective phenolic compounds from Gastrodiaelata. J Asian Nat Prod Res 2013; 15:619-623.
30. Choi RC, Zhu JT, Yung AW, Lee PS, Xu SL, Guo AJ, et al. Synergistic action of flavonoids, baicalein, and daidzein in estrogenic and neuroprotective effectspp A development of potential health products and therapeutic drugs against alzheimer's disease. Evid Based Complementary Altern Med 2013; 63:56-94.
31. Shi J, Li CJ, Yang JZ, Yuan YH, Chen NH, Zhang DM. Coumarin glycosides and iridoid glucosides with neuroprotective effects from Hydrangea paniculata. Planta Med 2012; 78:1844-1850.