Molecular Modeling and Drug Discovery Core for District of Columbia Developmental Center for AIDS Research (DCD-CFAR), Washington DC 20059, USA.
Curr Top Med Chem. 2013;13(11):1353-62. doi: 10.2174/15680266113139990039.
Serotonin (5-hydroxytryptamine, 5-HT) receptors are neuromodulator neurotransmitter receptors which when activated trigger a signal transduction cascade within cells resulting in cell-cell communication. 5-hydroxytryptamine receptor 2B (5-HT2B) is a subtype of the seven members of 5-hydroxytrytamine receptors family which is the largest member of the super family of 7-transmembrane G-protein coupled receptors (GPCRs). Not only do 5-HT receptors play physiological roles in the cardiovascular system, gastrointestinal and endocrine function as well as the central nervous system, but they also play a role in behavioral functions. In particular 5-HT2B receptor is widely spread with regards to its distribution throughout bodily tissues and is expressed at high levels in the lungs, peripheral tissues, liver, kidneys and prostate, just to name a few. Hence 5-HT2B participates in multiple biological functions including CNS regulation, regulation of gastrointestinal motality, cardiovascular regulation and 5-HT transport system regulation. While 5-HT2B is a viable drug target and has therapeutic indications for treating obesity, psychosis, Parkinson's disease etc. there is a growing concern regarding adverse drug reactions, specifically valvulopathy associated with 5-HT2B agonists. Due to the sequence homology experienced by 5-HT2 subtypes there is also a concern regarding the off-target effects of 5-HT2A and 5-HT2C agonists. The concepts of sensitivity and subtype selectivity are of paramount importance and now can be tackled with the aid of in silico studies, especially cheminformatics, to develop models to predict valvulopathy associated toxicity of drug candidates prior to clinical trials. This review has highlighted three in silico approaches thus far that have been successful in either predicting 5-HT2B toxicity of molecules or identifying important interactions between 5-HT2B and drug molecules that bring about valvulopathy related toxicities.
血清素(5-羟色胺,5-HT)受体是神经调质神经递质受体,当被激活时,会在细胞内引发信号转导级联反应,从而导致细胞间通讯。5-羟色胺受体 2B(5-HT2B)是 5-羟色胺受体家族七个成员中的一种亚型,是 7-跨膜 G 蛋白偶联受体(GPCR)超家族中最大的成员。5-HT 受体不仅在心血管系统、胃肠道和内分泌功能以及中枢神经系统中发挥生理作用,而且在行为功能中也发挥作用。特别是 5-HT2B 受体在其在全身组织中的分布方面广泛分布,并且在肺部、外周组织、肝脏、肾脏和前列腺等组织中表达水平较高。因此,5-HT2B 参与多种生物学功能,包括中枢神经系统调节、胃肠道动力调节、心血管调节和 5-HT 转运系统调节。虽然 5-HT2B 是一个可行的药物靶点,并且具有治疗肥胖症、精神病、帕金森病等疾病的治疗指征,但人们越来越关注药物的不良反应,特别是与 5-HT2B 激动剂相关的瓣膜病。由于 5-HT2 亚型经历了序列同源性,因此也存在 5-HT2A 和 5-HT2C 激动剂的脱靶效应的担忧。敏感性和亚型选择性的概念至关重要,现在可以借助计算机辅助药物设计研究,特别是化学信息学,来开发模型,以在临床试验之前预测候选药物与瓣膜病相关的毒性。这篇综述强调了迄今为止已经成功的三种计算方法,这些方法要么成功预测了分子的 5-HT2B 毒性,要么确定了 5-HT2B 与引起瓣膜病相关毒性的药物分子之间的重要相互作用。