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首页> 外文期刊>Journal of affective disorders >Chronic clomipramine treatment restores hippocampal expression of glial cell line-derived neurotrophic factor in a rat model of depression
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Chronic clomipramine treatment restores hippocampal expression of glial cell line-derived neurotrophic factor in a rat model of depression

机译:慢性氯米帕明治疗可在抑郁症大鼠模型中恢复胶质细胞源性神经营养因子的海马表达

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摘要

Background: Because there is evidence that certain neurotrophic factors are involved in depression and the mechanism of antidepressant treatment, it is hypothesized that neurotrophic factors may also play a functional role in the etiology of depression and treatment. Glial cell line-derived neurotrophic factor (GDNF) is a member of the transforming growth factor (TGF-β)-super- family. We performed a study to assess the impact of chronic unpredictable stress (CUS) and clomipramine treatment on GDNF expression in the rat hippocampus. Method: Using a rat model of CUS-induced depression, we administered clomipramine, one of the typical antidepressants, every day for 3 weeks starting 2 weeks after the beginning of the experiment. GDNF level in the hippocampus was detected by immunohistochemsitry, Western blot analysis, and reverse transcription-polymerase chain reaction (RT-PCR). Behavioral changes were measured by forced swimming test (FST) and open field test (OFT). Results: Animals exposed to CUS showed depression-like behavior and exhibited a significant decrease in GDNF expression in the hippocampus. Chronic clomipramine treatment reversed the behavioral deficits and the decrease in GDNF levels induced by CUS. Limitation: The relatively small number of the depression-model rats may cause some bias of behavioral tests. Conclusion: In our study, chronic clomipramine treatment restored GDNF expression in the hippocampus of CUS-induced depression rats, suggesting that GDNF is involved in the behavioral responses to antidepressants. The beneficial effects of clomipramine suggest that GDNF may be a viable target for new antidepressant drug development.
机译:背景:由于有证据表明某些神经营养因子参与了抑郁症和抗抑郁药的治疗机制,因此推测神经营养因子在抑郁症和治疗的病因中也可能起一定作用。胶质细胞系衍生的神经营养因子(GDNF)是转化生长因子(TGF-β)超家族的成员。我们进行了一项研究,以评估慢性不可预测的压力(CUS)和氯米帕明治疗对大鼠海马中GDNF表达的影响。方法:使用大鼠CUS诱发的抑郁症模型,我们从实验开始后的2周开始,连续3周每天服用氯米帕明(一种典型的抗抑郁药)。通过免疫组织化学,Western印迹分析和逆转录聚合酶链反应(RT-PCR)检测海马中GDNF的水平。行为变化通过强迫游泳测试(FST)和野外测试(OFT)进行测量。结果:暴露于CUS的动物表现出抑郁样行为,并且海马中GDNF表达显着降低。慢性氯米帕明治疗可逆转行为缺陷和CUS诱导的GDNF水平下降。局限性:抑郁模型大鼠的数量相对较少,可能会导致行为测试有些偏差。结论:在我们的研究中,慢性氯米帕明治疗可恢复CUS诱发的抑郁症大鼠海马中GDNF的表达,表明GDNF参与了抗抑郁药的行为反应。氯米帕明的有益作用表明,GDNF可能是新的抗抑郁药开发的可行目标。

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