Hasselmann Helge
Faculty of Psychology and Neuroscience, Maastricht University, The Netherlands.
CNS Neurol Disord Drug Targets. 2014;13(4):673-83. doi: 10.2174/1871527313666140618105710.
Depressive disorders have, for a sizeable extent, proven resilient to pharmacotherapy. Established drugs such as selective serotonin reuptake inhibitors (SSRIs) or serotonin-noradrenaline reuptake inhibitors (SNRIs) often provide inadequate symptom relief and sometimes fail altogether. Recently, interest in antidepressant effects of scopolamine, a non-selective muscarinic acetylcholine receptor (mAChR) antagonist, has arisen. Initial evidence suggests that scopolamine provides relatively rapid and long-lasting symptom alleviation for unipolar and bipolar depressed patients. At the same time, side effects of medical dosages appear mild and transient in nature. The aim of the present review is to tentatively discuss the antidepressant potential of scopolamine and to outline putative neurobiological pathways. Clearly, mAChR antagonism provides an intriguing novel therapeutical approach for treating depressive disorders.
在很大程度上,抑郁症已被证明对药物治疗具有耐受性。诸如选择性5-羟色胺再摄取抑制剂(SSRIs)或5-羟色胺-去甲肾上腺素再摄取抑制剂(SNRIs)等已确立的药物通常只能提供不充分的症状缓解,有时甚至完全无效。最近,人们对东莨菪碱(一种非选择性毒蕈碱型乙酰胆碱受体(mAChR)拮抗剂)的抗抑郁作用产生了兴趣。初步证据表明,东莨菪碱能为单相和双相抑郁症患者提供相对快速且持久的症状缓解。与此同时,药物剂量的副作用在性质上似乎轻微且短暂。本综述的目的是初步探讨东莨菪碱的抗抑郁潜力,并概述假定的神经生物学途径。显然,mAChR拮抗作用为治疗抑郁症提供了一种引人入胜的新治疗方法。