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Alzheimer's disease, enzyme targets and drug discovery struggles: From natural products to drug prototypes

机译:阿尔茨海默氏病,酶靶标和药物发现的斗争:从天然产物到药物原型

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Alzheimer's disease (AD) is an incapacitating neurodegenerative disease that slowly destroys brain cells. This disease progressively compromises both memory and cognition, culminating in a state of full dependence and dementia. Currently, AD is the main cause of dementia in the elderly and its prevalence in the developed world is increasing rapidly. Classic drugs, such as acetylcholinesterase inhibitors (AChEIs), fail to decline disease progression and display several side effects that reduce patient's adhesion to phar-macotherapy. The past decade has witnessed an increasing focus on the search for novel AChEIs and new putative enzymatic targets for AD, like (3- and 7-secretases, sirtuins, caspase proteins and glycogen synthase kinase-3 (GSK-3). In addition, new mechanistic rationales for drug discovery in AD that include autophagy and synaptogenesis have been discovered. Herein, we describe the state-of-the-art of the development of recent enzymatic inhibitors and enhancers with therapeutic potential on the treatment of AD.
机译:阿尔茨海默氏病(AD)是一种失能的神经退行性疾病,会慢慢破坏脑细胞。该疾病逐渐损害记忆力和认知力,最终达到完全依赖和痴呆的状态。当前,AD是老年人痴呆的主要原因,并且其在发达国家的流行正在迅速增加。诸如乙酰胆碱酯酶抑制剂(AChEIs)之类的经典药物无法降低疾病进程,并显示出多种副作用,这些副作用降低了患者对Phar-macotherapy的粘附性。在过去的十年中,目睹了对AD的新颖AChEI和新的假定酶标靶的关注,例如(3-和7-分泌酶,sirtuins,caspase蛋白和糖原合酶激酶3(GSK-3)。在AD中发现了包括自噬和突触发生在内的新的药物发现机理,在此,我们描述了最新的酶抑制剂和增强剂在AD治疗中的发展潜力。

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