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药物逆向工程:以氯卡色林为例。

Reverse Engineering Drugs: Lorcaserin as an Example.

作者信息

Schwasinger-Schmidt Tiffany, Preskorn Sheldon H

机构信息

Department of Internal Medicine, University of Kansas School of Medicine-Wichita, Wichita, KS, USA.

Department of Psychiatry and Behavioral Science, University of Kansas School of Medicine-Wichita, Wichita, KS, USA.

出版信息

Adv Neurobiol. 2023;30:195-206. doi: 10.1007/978-3-031-21054-9_8.

Abstract

Novel central nervous system (CNS)-based therapies have been difficult to produce due to the complexity of the brain, limited knowledge of CNS-based disease development and associated pathways, difficulty in penetrating the blood brain barrier, and a lack of reliable biomarkers of disease. Reverse engineering in drug development allows the utilization of new knowledge of disease pathways and the use of innovative technology to develop medications with enhanced efficacy and reduced toxicities. Lorcaserin was developed as a specific 5HT serotonin receptor agonist for the treatment of obesity with limited off-target effects at the 5HT and 5HT receptors. This receptor specificity limited the hallucinogenic and cardiovascular side effects noted with other serotonin receptor agonists. Reverse engineering approaches to drug development reduce the cost of producing new medications, identify specific populations of patients that will derive the most benefit from therapy, and produce novel therapies with greater efficacy and limited toxicity.

摘要

由于大脑的复杂性、对中枢神经系统疾病发展及相关途径的了解有限、难以穿透血脑屏障以及缺乏可靠的疾病生物标志物,基于中枢神经系统的新型疗法一直难以研发出来。药物研发中的逆向工程允许利用疾病途径的新知识,并运用创新技术来开发疗效增强且毒性降低的药物。洛卡塞林被开发为一种特异性5-羟色胺(5HT)血清素受体激动剂,用于治疗肥胖症,对5HT和5HT受体的脱靶效应有限。这种受体特异性限制了其他血清素受体激动剂所具有的致幻和心血管副作用。药物研发中的逆向工程方法降低了生产新药的成本,确定了将从治疗中获得最大益处的特定患者群体,并产生了疗效更高且毒性有限的新型疗法。

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