首页> 外文会议>Proceedings of the 2010 Biomedical Sciences and Engineering Conference >5.7: Presentation session: Neuroscience informatics: “Pathway-assisted investigation of atypical antipsychotic drugs and serotonin receptors in schizophrenia”
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5.7: Presentation session: Neuroscience informatics: “Pathway-assisted investigation of atypical antipsychotic drugs and serotonin receptors in schizophrenia”

机译:5.7:演讲:神经科学信息学:“在精神分裂症中非典型抗精神病药和血清素受体的途径辅助研究”

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Clozapine and its four related drugs (olanzapine, quetiapine, risperidone and ziprasidone) are the most frequently used treatments for schizophrenia in the world. The underlying mechanisms are not well understood. In this study, we investigated the features of these five drugs through their related genes at the pathway level. For each drug, we first identified the pathways that the drugs might be involved in. We found that these five drugs are all significantly involved in five pathways, i.e., G-protein coupled receptor signaling, cAMP-mediated signaling, serotonin receptor (5-HT) signaling, AMPK signaling, and cardiac hypertrophy signaling. Among these pathways, the serotonin receptor (5-HTR) pathway is an important neurotransmitter-related pathway in psychiatric disorders. Therefore, we further investigated the functional relationship between the five drugs and serotonin receptors based on the experimental data of activation, chemical-protein interaction, expression, inhabitation, and regulation of binding. We constructed a drug-5HTR network including these five drugs, serotonin receptors, and their relationships and found that clozapine has more interactors and more complicated connections with serotonin receptors than the other four drugs. Additionally, clozapine has two unique relationships with HTR2A, one of the most susceptible candidate genes for schizophrenia. These results indicated that clozapine might have a different action during the treatment process of schizophrenia from the other four drugs
机译:氯氮平及其四种相关药物(奥氮平,喹硫平,利培酮和齐拉西酮)是世界上最常用的精神分裂症治疗药物。潜在的机制还没有被很好地理解。在这项研究中,我们通过途径水平上的相关基因研究了这五种药物的特征。对于每种药物,我们首先确定了这些药物可能参与的途径。我们发现这五种药物都显着参与了五种途径,即G蛋白偶联受体信号传导,cAMP介导的信号传导,血清素受体(5- HT)信号,AMPK信号和心脏肥大信号。在这些途径中,5-羟色胺受体(5-HTR)途径是精神疾病中重要的神经递质相关途径。因此,我们根据激活,化学-蛋白质相互作用,表达,居住和结合调节的实验数据,进一步研究了五种药物与5-羟色胺受体之间的功能关系。我们构建了包括这五种药物,5-羟色胺受体及其关系的5HTR药物网络,发现氯氮平比其他四种药物具有更多的相互作用剂和与5-羟色胺受体的更复杂的连接。此外,氯氮平与HTR2A有两种独特的关系,HTR2A是精神分裂症最易感的候选基因之一。这些结果表明氯氮平在精神分裂症的治疗过程中可能与其他四种药物具有不同的作用

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