Department of Pharmacy and Biomedical Sciences, La Trobe Institute for Molecular Science, La Trobe University, Bendigo, VIC 3550, Australia.
Drug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, Kuala Lumpur 50300, Malaysia.
Int J Mol Sci. 2021 Nov 2;22(21):11910. doi: 10.3390/ijms222111910.
5-hydroxytryptamine type 3 (5-HT) receptors are ligand gated ion channels, which clearly distinguish their mode of action from the other G-protein coupled 5-HT or serotonin receptors. 5-HT receptors are well established targets for emesis and gastrointestinal mobility and are used as adjunct targets in treating schizophrenia. However, the distribution of these receptors is wider than the nervous system and there is potential that these additional sites can be targeted to modulate inflammatory and/or metabolic conditions. Recent progress in structural biology and pharmacology of 5-HT receptors have provided profound insights into mechanisms of their action. These advances, combined with insights into clinical relevance of mutations in genes encoding 5-HT subunits and increasing understanding of their implications in patient's predisposition to diseases and response to the treatment, open new avenues for personalized precision medicine. In this review, we recap on the current status of 5-HT receptor-based therapies using a biochemical and physiological perspective. We assess the potential for targeting 5-HT receptors in conditions involving metabolic or inflammatory disorders based on recent findings, underscoring the challenges and limitations of this approach.
5-羟色胺 3 型(5-HT)受体是配体门控离子通道,其作用方式明显有别于其他 G 蛋白偶联的 5-HT 或血清素受体。5-HT 受体是止吐和胃肠道动力的既定靶点,也被用作治疗精神分裂症的辅助靶点。然而,这些受体的分布范围比神经系统更广,因此有可能针对这些额外的靶点来调节炎症和/或代谢状况。5-HT 受体的结构生物学和药理学的最新进展为其作用机制提供了深刻的见解。这些进展,加上对编码 5-HT 亚基的基因突变的临床相关性的了解,以及对其在患者易患疾病和对治疗反应中的影响的理解不断加深,为个性化精准医学开辟了新途径。在这篇综述中,我们从生化和生理学的角度回顾了基于 5-HT 受体的治疗方法的现状。我们根据最近的发现评估了在涉及代谢或炎症性疾病的情况下靶向 5-HT 受体的潜力,强调了这种方法的挑战和局限性。