Kumar Bhupinder, Gupta Vivek Prakash, Kumar Vinod
Laboratory of Organic and Medicinal Chemistry, Centre for Pharmaceutical Sciences and Natural Products, Central University of Punjab, Bathinda, Punjab, 151001-India.
Curr Drug Targets. 2017;18(1):87-97. doi: 10.2174/1389450117666151209123402.
The monoamine oxidase (MAO) enzyme is responsible for the deamination of monoamine neurotransmitters and regulates their concentration in the central and peripheral nervous systems. Imbalance in the concentration of neurotransmitters in the brain and central nervous system is linked with the biochemical pathology of various neurogenic disorders. Irreversible MAO inhibitors were the first line drugs developed for the management of severe depression but most of these were withdrawn from the clinical practice due to their fatal side effects including food-drug interactions. New generations of MAO inhibitors were developed which were reversible and selective for one of the enzyme isoform and showed improved pharmacological profile. The discovery of crystal structure of MAO-A & MAO-B isoforms helped in understanding the drug-receptor interactions at the molecular level and designing of ligands with selectivity for either of the isoforms. The current article provides an overview on the MAO enzyme as potential drug target for different disease states. The article describes catalytic mechanism of MAO enzyme, crystal structures of the two MAO isoforms, traditional MAO inhibitors and various problems associated with their use, new developments in the MAO inhibitors and their potential as therapeutic agents especially in neurological disorders.
单胺氧化酶(MAO)负责单胺类神经递质的脱氨基作用,并调节其在中枢和外周神经系统中的浓度。大脑和中枢神经系统中神经递质浓度的失衡与各种神经源性疾病的生化病理学有关。不可逆的MAO抑制剂是最早开发用于治疗严重抑郁症的一线药物,但由于其致命的副作用(包括食物-药物相互作用),大多数此类药物已从临床实践中撤出。新一代的MAO抑制剂被开发出来,它们是可逆的,并且对其中一种酶亚型具有选择性,显示出改善的药理学特性。MAO-A和MAO-B亚型晶体结构的发现有助于在分子水平上理解药物-受体相互作用,并设计对任一亚型具有选择性的配体。本文概述了MAO酶作为不同疾病状态潜在药物靶点的情况。文章描述了MAO酶的催化机制、两种MAO亚型的晶体结构、传统的MAO抑制剂及其使用中存在的各种问题、MAO抑制剂的新进展及其作为治疗剂的潜力,尤其是在神经疾病方面的潜力。