Boswellic Acids as Promising Leads in Drug Development against Alzheimer's Disease

被引:8
作者
Haghaei, Hossein [1 ]
Soltani, Somaieh [2 ,3 ]
Arefhosseini, Seyedrafie [1 ]
Rashidi, Mohammad-Reza [2 ,3 ,4 ]
Karima, Saeed [5 ]
机构
[1] Tabriz Univ Med Sci, Nutr & Food Sci Fac, Tabriz, Iran
[2] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Pharm Fac, Tabriz, Iran
[4] Tabriz Univ Med Sci, Res Ctr Pharmaceut Nanotechnol, Tabriz, Iran
[5] Shahid Beheshti Univ Med Sci SBMU, Dept Clin Biochem, Sch Med, Tehran, Iran
关键词
Alzheimer's disease; Boswellic acids; Disease-modifying therapy; Multi-target drug; Plant derived scaffolds; DOUBLE-BLIND; AMYLOID-BETA; OXIDATIVE STRESS; IN-VITRO; COGNITIVE IMPAIRMENT; SERRATA EXTRACT; CATHEPSIN-G; ACETYL-11-KETO-BETA-BOSWELLIC ACID; ACETYLCHOLINESTERASE INHIBITORS; ANTIINFLAMMATORY PROPERTIES;
D O I
10.34172/PS.2020.25
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Biological activity of Boswellia extract (BE) has been attributed to its main active ingredients; i.e. Boswellic acids (BAs). BE/BAs possess a promising therapeutic potential in neurodegenerative disorders; including Alzheimer's disease (AD). The multifactorial nature of AD pathophysiology necessitates the development of the disease-modifying agents (DMA). Recent multi-targeting approaches for the DMAs development have brought more attention to the plant-derived compounds regarding their better human compatibility because of their biological origin. This review addresses the current knowledge on the anti-AD activity of BE/BAs based on the available in silico, in vitro, in vivo studies and clinical trials. The contribution of BE/BAs in inflammatory pathways, Tau and beta-amyloid proteins, microtubule functions, oxidative stress, cholinesterase and diabetes/insulin pathways involved in AD have been discussed. BAs efficacy in different AD-related pathways has been confirmed in vitro and in vivo. They can be considered as valuable scaffold/lead compounds for multi-targeted DMAs in anti-AD drug discovery and development.
引用
收藏
页码:14 / 31
页数:18
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