Nguyen Thi Hanh, Wang San-Lang, Nguyen Van Bon
Doctoral Program in Applied Sciences, Tamkang University, New Taipei City 25137, Taiwan.
Department of Chemistry, Tamkang University, New Taipei City 25137, Taiwan.
Pharmaceuticals (Basel). 2023 Apr 12;16(4):580. doi: 10.3390/ph16040580.
Alzheimer's disease (AD) is the most common form of dementia. It increases the risk of other serious diseases and causes a huge impact on individuals, families, and socioeconomics. AD is a complex multifactorial disease, and current pharmacological therapies are largely based on the inhibition of enzymes involved in the pathogenesis of AD. Natural enzyme inhibitors are the potential sources for targeting AD treatment and are mainly collected from plants, marine organisms, or microorganisms. In particular, microbial sources have many advantages compared to other sources. While several reviews on AD have been reported, most of these previous reviews focused on presenting and discussing the general theory of AD or overviewing enzyme inhibitors from various sources, such as chemical synthesis, plants, and marine organisms, while only a few reviews regarding microbial sources of enzyme inhibitors against AD are available. Currently, multi-targeted drug investigation is a new trend for the potential treatment of AD. However, there is no review that has comprehensively discussed the various kinds of enzyme inhibitors from the microbial source. This review extensively addresses the above-mentioned aspect and simultaneously updates and provides a more comprehensive view of the enzyme targets involved in the pathogenesis of AD. The emerging trend of using in silico studies to discover drugs concerning AD inhibitors from microorganisms and perspectives for further experimental studies are also covered here.
阿尔茨海默病(AD)是最常见的痴呆形式。它会增加患其他严重疾病的风险,并对个人、家庭和社会经济造成巨大影响。AD是一种复杂的多因素疾病,目前的药物治疗主要基于对参与AD发病机制的酶的抑制。天然酶抑制剂是针对AD治疗的潜在来源,主要从植物、海洋生物或微生物中收集。特别是,与其他来源相比,微生物来源具有许多优势。虽然已经报道了几篇关于AD的综述,但这些先前的综述大多侧重于介绍和讨论AD的一般理论,或概述来自各种来源(如化学合成、植物和海洋生物)的酶抑制剂,而关于针对AD的微生物来源酶抑制剂的综述只有少数几篇。目前,多靶点药物研究是AD潜在治疗的新趋势。然而,尚无综述全面讨论来自微生物来源的各类酶抑制剂。本综述广泛探讨了上述方面,同时更新并提供了关于AD发病机制中涉及的酶靶点的更全面观点。本文还涵盖了利用计算机模拟研究从微生物中发现AD抑制剂的新趋势以及进一步实验研究的前景。