Document Type : Original Article
1 Laboratory of Molecular Neuroscience, Kerman Neuroscience Research Center (KNRC), Kerman University of Medical Sciences, Kerman, Iran 2 Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran
2 Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran
Diabetes mellitus is a major health concern for human and according to the reports published by World Health Organization (WHO), the prevalence of diabetes for all age-groups worldwide is estimated to be 4.4% in 2030 (1). Diabetic neuropathies are heterogeneous groups of disorders which present a wide range of abnormalities. Such disorders are among the most common long-term complications of diabetes and are important sources of morbidity and mortality (2).
Almost 50% of the diabetic patients develop neuropathy with symptoms including spontaneous pain, hypoesthesia, allodynia and hyperalgesia (3). Despite significant progress in the treatment of pain, a variety of pathological pains, particularly diabetic neuropathic pain, cannot still be alleviated and they are refractory to the currently available analgesics. Therefore, biomedical investigations are performed
to reveal cellular and molecular factors that are affected in the central nervous system during chronic pain to introduce potential targets for new drugs.
Although hyperglycemia is considered to be a major pathogenic factor in the development of diabetic neuropathy, the mechanisms associated with this disease have not yet been fully understood (4).
It has been demonstrated that changes in the extracellular GABA levels and impaired GABAA receptor-mediated inhibition are occurred in neuropathic situations (5, 6). Spinal delivery of bicuculline, a GABAA receptor antagonist reduced formalin-evoked flinching and tactile allodynia in diabetic rats (7). Furthermore, GABAA receptor-mediated depression of the spinal Hoffmann's reflex (a reflectory reaction of muscles after electrical stimulation of sensory fibers) was also absent in the spinal cord of diabetic rats (7). It has been reported
that GABA content as well as GABA receptor binding sites significantly decreased in the brain stem of pancreatectomised hyperglycemic rats (8).
Neurosteroids are synthesized in oligodendro-cytes, astrocytes, schwann cells and some neurons, such as purkinje, retinal amacrine and ganglion cells and hippocampal neurons (9). Recent experimental findings bring new insights into the decline of neurosteroid synthesis in the CNS during aging and also in various neurodegenerative diseases (10).
Synthesis of neurosteroids declines during stressful conditions and in chronic inflammatory and neurodegenerative diseases. However, recent bio-chemical reports indicate that spinal neurosteroids are important factors for the control of pain (11) and also they show the potential applications of neurosteroids in the therapeutic management of painful neuropathic conditions (12, 13). It has been shown that some neurosteroids produce neuroprote-ctive effects against streptozotocin (STZ)-induced diabetic neuropathy at the neurophysiological, neur-opathological, biochemical and functional levels (14).
Since neurosteroids had shown protective effects in numerous cellular models of neurodegenerative diseases (9, 10) and elicited antinociception in neuropathic situations (11), the present study was designed to evaluate the preventive effects of neurosteroid allopregnanolone in animal models of diabetic neuropathic pain by evaluating its possible effect on the predicted diabetes-induced spinal GABAA down-regulation.
Materials and Methods
The experiments were carried out on male Wistar rats that were housed in a room with 12 hr light/dark cycle with controlled temperature (22 ± 1°C). Food and water were available ad libitum. Animals (weighing 220-250 g) were handled daily (between 9:00-11:00 AM) 5 days before the experiment in order to adapt them to the experiment procedure and minimize nonspecific stress responses. Rats were randomly divided into several experimental groups, each containing 6-8 animals. The experiments followed the guidelines on ethics standard for investigation of experimental pain in animals (15) and approved by the Animal Experimentation Ethics Committee of Kerman Neuroscience Research Center (EC/KNRC/90).
In vivo experimental protocol
Diabetes was induced by a single intraperitoneal injection of 55 mg/kg (IP) streptozotocin (STZ) freshly dissolved in 0.1 mol/l citrate buffer. Rats receiving an injection of citrate buffer were used as control. One week later, diabetes was confirmed in STZ -injected rats by measuring serum glucose concentrations (16). The glucose concentration was assayed enzymatically using a glucose oxidase peroxidase (GOD-POD) kit (Pars Azmon Co, Iran). The rats with blood glucose ≥ 350 mg/dl were considered to have diabetes. One week after the STZ injection, the diabetic rats were given allopregnanolone (5 and 20 mg/kg/day for 6 weeks, orally). Seven weeks after the STZ administration, the animals were decapitated under CO2 anesthesia. Control rats were killed in the same way 7 weeks after receiving vehicle injection.
Nociceptive threshold was assessed by tail-flick test (17). The intensity of the beam was adjusted to produce a mean control reaction time between 4 and 6 sec. The cut-off time was fixed at 15 sec in order to avoid any damage to the tail. In this manner, we were able to reveal potential, subtle alternations that may occur in basal thermal nociception (18, 19). The tail-flick latency for each rat was determined three times and the mean was designated as the baseline latency value. Experimentally-induced decreases in control tail-flick latency provide an indication of hyperalgesia as a marker of neuropathy.
Tissue extraction and preparation
Rats were anesthetized (using CO2) and decapitated. The spinal column was cut through the pelvic girdle and a hydraulic extrusion was performed by inserting a 16 gauge needle into the sacral vertebral canal and expelling with ice-cold saline. The tissues were placed on ice in a glass petri dish, and the dorsal half of the lumbar spinal cord was dissected. Tissue samples were weighed and immediately frozen in liquid nitrogen and stored at -70°C until assay.
Rota-rod treadmill test was performed to evaluate motor coordination of the animals (20). Briefly, the rats were placed individually on the rotating rod apparatus for two trials; on day zero and in the fourth week of the test. The rats were initially trained to maintain themselves on the rotating rod for more than 3 min. The rats were scored for their latency to fall (in seconds) in each trial.
RT-PCR analysis of GABAA receptor
Total cellular RNAs was isolated from the dorsal half of the lumbar spinal cord by a modification of the guanidine isothiocyanate-phenol-chloroform method using RNX+ reagent and a semiquantitative RT-PCR method was used (21). Briefly, the RT-PCR reaction was performed using Oligo-dT primer and M-MuLV reverse transcriptase, based on the manufacturer protocol (Fermentas GMBH, Germany). The reactions were incubated at 42°C for 60 min and then inactivated at 70°C for 10 min. Three separate PCR reactions were used for studying the gene expression in the samples obtained from each rat.
Table 1. Effect of allopregnanolone (ALLO) on serum glucose levels and body weight of diabetic animals. Values represent mean ± SEM (n=6-8)
Each PCR reaction was carried out using selective forward and reverse primers for β-actin (as an internal standard) and γ2 subunit of GABAA receptor. The primers of γ2 subunit were designed using online NCBI’s facility and cDNA sequences of the gene taken from
The sequence of primers used was:
γ2 forward: 5'- AGC CCG GAA GTC TCT GCC CAA -3', γ2 reverse: 5'- CCT CCC GTG TCT CCA GGC TCC -3', β-actin forward: 5'-CCC AGA GCA AGA GAG GCA TC-3', β-actin reverse: 5'-CTC AGG AGG AGC AAT GAT CT-3'.
Taq DNA polymerase (Roche, Germany) was used for DNA amplification and reactions were set up according to the manufacturer protocol. The PCR reactions were incubated for 5 min at 94°C, followed by 25 cycles of thermal cycling (45 sec at 94°C, 45 sec at 55°C and 45 sec at 72°C). The final cycle was followed by a 5 min extension step at 72°C. The reaction parameters were adjusted to obtain a condition with a linear relation between the number of PCR cycles and PCR products and with linear relation between the initial amount of cDNA template and PCR product. According to the results obtained from these tests, 25 cycles of amplification were used for analyzing all samples. Then, PCR products were subsequently analyzed on 1.5% agarose LMMP (Roche, Germany) gel and bands were quantified by densitometry using Lab Works analyzing software (UVP, UK). The possibility of the presence of contaminating genomic DNA was ruled out by using the yield of reverse transcriptase-minus (RT−) reaction, instead of cDNA template which caused no DNA amplification (data not shown). Finally, a semiquantitative PCR technique was used to estimate the levels of γ2 subunit of GABAA receptor mRNA in tissue samples, normalized to an internal standard (β-actin).
The results are expressed as mean ± SEM. The differences in the mean of data between groups were determined by one-way ANOVA, followed by the Newman–Keuls test. P<0.05 was considered significant.
The effect of allopregnanolone (ALLO) on serum glucose levels and body weight in diabetic animals
Diabetic rats developed hyperglycemia within one week after streptozotocin injection and serum glucose concentrations were significantly increased in diabetic animals compared with control animals (P<0.001). The levels of glucose remained at high levels 7 week after STZ injection. The data showed a significant change (increase) in the weight of control rats during the time curse of the study. At the end of the study (week 7), the weights of diabetic group were significantly lower than those at the start of study (Table 1). Treatment with ALLO (5 and 20 mg/kg/day for 7 weeks) had no attenuating effect on the serum glucose of the diabetic animals (Table 1). The weights of diabetic rats that received 5 and 20 mg/kg ALLO did not significantly decrease during the time course of the study and were higher than those in diabetic non-treated and vehicle-treated animals.
The effect of ALLO on nociceptive threshold in diabetic animals
As shown in Figure 1A, diabetic animals showed a significant decrease in the nociceptive threshold (hyperalgesic response). The hyperalgesia appeared 2 weeks after STZ injection and persisted almost unchanged for up to the end of study (week 7). However, 5 and 20 mg/kg ALLO attenuated diabetes-induced hyperalgesia (Figure 1A).
At the end of the study, the tail flick latency was significantly (P<0.001) lower in diabetic rats (5.54±0.13) as compared to the control animals (2.69±0.19). However, administration of ALLO at doses of 5 and 20 mg/kg significantly prevented the induction of diabetes-induced thermal hyperalgesia in the 7th week of the test (Figure 1B).
The effect of ALLO on diabetes induced motor deficit
Rota-rod test has been conducted to assess motor coordination of rats (20). Diabetic rats showed significant reduction in their motor coordination and their ability to maintain themselves over the rota rod apparatus was significantly decreased (P<0.001) as compared to the control non-diabetic animals. Treatment of diabetic animals with 5 and 20 mg/kg of ALLO increased retention time to 85.5 and 76.3 % of the control value, respectively (Figure 2).
The effect of ALLO on γ2 mRNA in diabetic animals
Ethidium bromide staining of PCR products showed a single band of the expected size for β-actin (830 bp) and forγ2 subunit (337 bp). Diabetic animals showed a significant decrease in γ2 mRNA
Figure 1. Effect of allopregnanolone (ALLO, 5 and 20 mg/kg) on the development of diabetes-induced thermal hyperalgesia during the time course of the study (A) and comparison of nociceptive threshold at the end (week 7) of the study (B) in rats. Values are expressed as the mean ± SEM (n=6–8). ***P<0.001 versus control (Cont) group. +++P<0.001 versus the diabetic group
Figure 2. Effect of allopregnanolone (ALLO) on the Rotarod treadmill performance of diabetic rats. Values are expressed as the mean ± SEM (n=6–8). ** P<0.01, *** P<0.001 compared to control. +P<0.05, ++P<0.01 compared to diabetic group
level. Allopregnanolone at the dose of 5 mg/kg could prevent γ2 down-regulation in diabetic animals. Furthermore, treatment with 20 mg/kg ALLO [T1] significantly attenuated diabetes-induced down-regulation of γ2 subunit (Figure 3).
Diabetic neuropathy is one of the most common complications affecting more than 50-60% of diabetic patients. The pathology of diabetic neuropathy involves oxidative stress, advanced glycation end, polyol pathway flux and protein kinase C activation (3). Here, the STZ-induced diabetic rats were used as an in vivo model for the study of diabetic neuropathic pain. This study shows that the neurosteroid allopregnanolone has a pro-tective effect against diabetes-induced hyperalgesia.
Figure 3. The level of γ2 mRNA in dorsal portion of lumbar spinal cord in control, diabetic (Diab) and allopregnanolone-treated diabetic rats (Diab+ALLO). Each value in the graph represents the mean ± SEM band density ratio for each group (n=5). β-actin was used as an internal control. **P<0.01, ***P <0.001 versus control animals. ++P < 0.01, +++P<0.001 versus diabetic group
Hyperglycemia induces oxidative stress in diabetic neurons and then mitochondrial damage occurs due to excess formation of reactive oxygen species (ROS) and reactive nitrogen species (RNS) (22). Therefore, it seems that compounds with antioxidant property might exert neuroprotective effects and may be promising in practice. It has been reported that ALLO markedly induces a protective effect on sleep deprivation-induced anxiety-like behavior and oxidative damage in mice (23). Furthermore, ALLO has a beneficial effect in the treatment of Niemann-Pick C disease due to its ability to restore the intracellular antioxidant defense (24). The protective effects of neurosteroids against oxidative stress could be through both genomic and non-genomic pathways (25). Not surprisingly, the mentioned neurosteroid with antioxidant activity could be protective in this in vivo model of diabetic neuropathy.
An impaired spinal GABAergic inhibitory function is known to have a critical role in neuropathic pain conditions (5, 6). However, it is unknown whether the severity of neuropathic pain is determined by the degree of these GABAergic impairments. Our data suggest that dysfunctional GABAA receptor production is coincident with the induction of pain behavior in STZ-induced diabetic rats. ALLO could significantly prevent diabetes-induced spinal GABAA receptor down-regulation.
Impairment of GABAergic transmission is developed in different models of neuropathic pain (5, 6) as well as in diabetic rats (7). It has been reported that the expression of the genes encoding the α1, α2, β2 and β3 GABAA channel subunits is down-regulated in pancreatic islets of type 2 diabetic individuals (26). In addition, GABA content as well as GABA receptor binding sites was significantly decreased in the brain stem of diabetic rats (8).
It seems that impairment in GABA signaling is involved in the induction of painful diabetic neuropathy. Surprisingly, the use of neural cell lines that are able to deliver GABA, as inhibitory neurotransmitters, in a model of chronic pain offers a novel approach to pain management. Transplants of neuronal cells bioengineered to synthesize GABA near the spinal dorsal horn, can reverse the development of chronic neuropathic pain and inhibit allodynia, tactile and thermal hyperalgesia following peripheral nerve injury (27). In addition, intra-spinal transplantation of GABAergic neural progenitor cells reduces neuropathic pain and suppresses the exaggerated dorsal horn neuronal firing by restoring dorsal horn inhibition in rats with unilateral chronic constriction injury of the sciatic nerve (28).
It has been documented that spinal GABAA agonists may provide a specific therapy for neuropathic pain. It was reported that isoguvacine, a selective GABAA receptor agonist prevents tactile allodynia and thermal hyperalgesia produced by spinal nerve ligation model of neuropathic pain (29). HZ166, a novel GABAA receptor subtype-selective benzodiazepine site ligand has antihyperalgesic property in mouse models of inflammatory and neuropathic pain (30).
Therefore, based on our results it seems that the inhibition of diabetes-induced spinal GABAA receptor down-regulation by neurosteroid ALLO could be accompanied in anti-hyperalgesic effect of this drug. Hormones play an important role in modulating the overall excitability of neurons. GABAA receptors contain γ subunits that mediate tonic inhibition in the central nervous system. The most potent endogenous modulators of GABAA receptors are neurosteroids that act as positive allosteric modulators (31). However, the exact mechanism(s) underlying the regulation of GABA subunit gene expression by neurosteroids has not been fully clarified and needs to be studied in future investigation.
Taken together, the results suggest that ALLO prevents diabetic neuropathic pain. The mechanisms underlying such effects may be, at least in part, due to resduction of diabetes-induced GABA receptor down-regulation. Our findings propose therapeutic potential of neurosteroids in the attenuation of diabetes consequences such as neuropathy.
This work was financially supported by Kerman Neuroscience Research Center (KNRC/90), Kerman, Iran. The results described in this paper were part of a student thesis (S Afrazi).