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Differential expression of synaptic vesicle proteins after repeated electroconvulsive seizures in rat frontal cortex and hippocampus

机译:大鼠额叶皮质和海马反复电惊厥发作后突触小泡蛋白的差异表达

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Electroconvulsive therapy (ECT) remains the treatment of choice for patients with severe or drug-resistant depressive disorders, yet the mechanism behind its efficacy and the effect on neurotransmission is essentially unknown. As synaptic vesicle proteins (SVPs) are required for vesicle fusion and neurotransmitter release, we have examined the effect of single and repeated electroconvulsive seizures (ECS), an animal model of ECT, on the expression of 14 SVPs in the rat frontal cortex and the hippocampus using quantitative real-time polymerase chain reaction (real-time qPCR). Only in the frontal cortex, the mRNA level of synapsin 11 was significantly upregulated after repeated ECS. In contrast, the mRNA levels of 6 of the 14 SVPs were significantly regulated in the hippocampus after ECS. We found that SNAP29 was upregulated and synaptotagmin III was downregulated after one single ECS in the hippocampus. Furthermore, SNAP29, synapsin I, synapsin III, VAMP2, and VAMP5 were significantly upregulated, whereas synaptotagmin III was significantly downregulated after repeated ECS in the hippocampus. We suggest that these genes are highly important in the long-term therapeutic effect of ECS, and thus it can be hypothesized that the SVPs are involved in the pathophysiology of depression.
机译:电痉挛疗法(ECT)仍然是患有严重或耐药性抑郁症的患者的首选治疗方法,但其功效和对神经传递的作用背后的机制基本上是未知的。由于突触囊泡蛋白(SVPs)是囊泡融合和神经递质释放所必需的,我们已经检查了一次和多次电惊厥性癫痫发作(ECS)(一种ECT的动物模型)对14种SVPs在大鼠额叶皮层和皮层中表达的影响。海马使用定量实时聚合酶链反应(实时qPCR)。重复ECS后,仅在额叶皮质中突触蛋白11的mRNA水平显着上调。相比之下,ECS后海马中14个SVP中的6个的mRNA水平受到显着调节。我们发现海马中只有一个ECS后,SNAP29上调,突触标签蛋白III下调。此外,在海马反复进行ECS后,SNAP29,突触素I,突触素III,VAMP2和VAMP5显着上调,而突触标记素III则显着下调。我们建议这些基因在ECS的长期治疗效果中非常重要,因此可以假设SVP参与了抑郁症的病理生理。

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