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首页> 外文期刊>The pharmacogenomics journal >Synapsin II gene expression in the dorsolateral prefrontal cortex of brain specimens from patients with schizophrenia and bipolar disorder: Effect of lifetime intake of antipsychotic drugs
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Synapsin II gene expression in the dorsolateral prefrontal cortex of brain specimens from patients with schizophrenia and bipolar disorder: Effect of lifetime intake of antipsychotic drugs

机译:精神分裂症和双相情感障碍患者脑标本的背外侧前额叶皮层突触素II基因表达:终生服用抗精神病药物的影响

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摘要

Synapsins are neuronal phosphoproteins crucial to regulating the processes required for normal neurotransmitter release. Synapsin II, in particular, has been implied as a candidate gene for schizophrenia. This study investigated synapsin II mRNA expression, using real-time reverse transcriptase-PCR, in coded dorsolateral prefrontal cortical samples provided by the Stanley Foundation Neuropathology Consortium. Synapsin IIa was decreased in patients with schizophrenia when compared with both healthy subjects and patients with bipolar disorder, whereas synapsin IIb was only significantly reduced in patients with schizophrenia when compared with healthy subjects but not in patients with bipolar disorder. Furthermore, lifetime antipsychotic drug use was positively associated with synapsin IIa expression in patients with schizophrenia. Results suggest that impairment of synaptic transmission by synapsin II reduction may contribute to dysregulated convergent molecular mechanisms, which result in aberrant neural circuits that characterize schizophrenia, while implicating involvement of synapsin II in therapeutic mechanisms of currently prescribed antipsychotic drugs.
机译:突触蛋白是神经元磷酸化蛋白,对调节正常神经递质释放所需的过程至关重要。特别地,突触蛋白II被暗示为精神分裂症的候选基因。这项研究使用实时逆转录酶PCR技术研究了由Stanley Foundation Neuropathology Consortium提供的编码背外侧前额叶皮层样品中突触蛋白II mRNA的表达。与健康受试者和双相情感障碍患者相比,精神分裂症患者的突触蛋白IIa降低,而与健康受试者相比,精神分裂症患者中突触蛋白IIb仅显着降低,而双相情感障碍患者则没有。此外,精神分裂症患者终生使用抗精神病药物与突触蛋白IIa表达呈正相关。结果表明,突触素II减少对突触传递的损害可能导致失调的收敛分子机制,从而导致表征精神分裂症的异常神经回路,同时牵涉突触素II参与目前处方的抗精神病药物的治疗机制。

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