The antioxidant potential of bacoside and its derivatives in Alzheimer's disease: The molecular mechanistic paths and therapeutic prospects

Q1 Environmental Science
Dipanjan Karati , Swarupananda Mukherjee , Souvik Roy
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引用次数: 0

Abstract

Central nervous system disorders are likely to have a substantial effect on the worldwide healthcare demands of humanity in this era. Alzheimer’s disease (AD) is a senile decay of neurons. Extracellular beta-amyloid accumulation and intracellular tau hyperphosphorylation are two key characteristics of the pathogenesis of AD. Because of the multifactorial character of many disorders, new medicine-based psychoactive treatments have had limited success. As a result, there is a growing demand for innovative products that can target different receptors and improve behavioral abilities on their own or in combination with established treatments. In recent years, both industrialized and developing countries have seen a surge in herbal products based on traditional knowledge. According to recent research, bacoside and its congeners can dramatically lower the build-up of amyloid-β plaques, which are a defining feature of AD. This decrease is explained by bacoside's capacity to regulate β-secretase activity, which lowers the production of amyloid-β. Ayurveda is a medical science that focuses on the use of naturally occurring plant products to treat ailments. Many neuroprotective plants are said to be found in Ayurveda. The key physiological dysfunctions linked to tau aggregates, which contribute to dementia and behavioral inconsistencies, include the formation of reactive oxygen species, augmented neuronal swelling, and neurotoxicity. Here, we have focused on bacopa as an anti-Alzheimer medication. Bacoside A, Baccoside B, Apigenin, Betullinic acid, etc. are the pharmacologically active congeners of Brahmi belonging to several chemical families. In this review, the neuroprotective properties, pharmacological effectiveness, and molecular mechanism of bacoside scaffolds against AD have been discussed.
马齿苋苷及其衍生物在阿尔茨海默病中的抗氧化潜力:分子机制途径和治疗前景
在这个时代,中枢神经系统疾病可能对人类的全球医疗保健需求产生重大影响。阿尔茨海默病(AD)是一种神经元的老年性衰退。细胞外β -淀粉样蛋白积累和细胞内tau蛋白过度磷酸化是AD发病机制的两个关键特征。由于许多疾病的多因素特征,新的基于药物的精神活性治疗取得了有限的成功。因此,对创新产品的需求不断增长,这些产品可以针对不同的受体,单独或与已有的治疗方法相结合,提高行为能力。近年来,工业化国家和发展中国家都看到了基于传统知识的草药产品的激增。根据最近的研究,马尾草苷及其同系物可以显著降低淀粉样蛋白-β斑块的形成,而淀粉样蛋白-β斑块是AD的一个决定性特征。这种减少是由于马尾草苷能够调节β分泌酶活性,从而降低淀粉样蛋白-β的产生。阿育吠陀是一门医学科学,专注于使用天然植物产品来治疗疾病。据说在阿育吠陀中发现了许多神经保护植物。与tau聚集体相关的关键生理功能障碍,导致痴呆和行为不一致,包括活性氧的形成,神经元肿胀增强和神经毒性。在这里,我们关注的是马齿苋作为一种抗阿尔茨海默病的药物。马齿苋苷A、马齿苋苷B、芹菜素、白桦酸等是布罗米属几个化学科的具有药理活性的同系物。本文就马齿苋苷支架抗AD的神经保护特性、药理作用及分子机制进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Toxicology Reports
Toxicology Reports Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
7.60
自引率
0.00%
发文量
228
审稿时长
11 weeks
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