The Effects and Mechanisms of Xanthones in Alzheimer's Disease: A Systematic Review

被引:5
|
作者
Pang, Li Wen [1 ]
Hamzah, Sharina [1 ,2 ]
Tan, Sui Ling Janet [3 ]
Mah, Siau Hui [4 ]
Yow, Hui Yin [1 ,5 ]
机构
[1] Taylors Univ, Fac Hlth & Med Sci, Sch Pharm, Subang Jaya 47500, Selangor, Malaysia
[2] Taylors Univ, Med Advancement Better Qual Life Impact Lab, Subang Jaya 47500, Selangor, Malaysia
[3] Univ Malaya, Fac Pharm, Dept Pharmaceut Technol, Kuala Lumpur 50603, Malaysia
[4] Taylors Univ, Fac Hlth & Med Sci, Sch Biosci, Subang Jaya 47500, Selangor, Malaysia
[5] Univ Malaya, Fac Pharm, Dept Pharmaceut Life Sci, Kuala Lumpur 50603, Malaysia
关键词
Xanthone; Alzheimer's disease; Neuroinflammation; Acetylcholinesterase; Memory impairment; ALPHA-MANGOSTIN; OXIDATIVE STRESS; MANGIFERIN; BETA; CHOLINESTERASE; SCOPOLAMINE;
D O I
10.1007/s11064-023-04005-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Xanthones are natural secondary metabolites that possess great potential as neuroprotective agents due to their prominent biological effects on Alzheimer's disease (AD). However, their underlying mechanisms in AD remain unclear. This study aimed to systematically review the effects and mechanisms of xanthones in cell culture and animal studies, gaining a better understanding of their roles in AD. A comprehensive literature search was conducted in the Medline and Scopus databases using specific keywords to identify relevant articles published up to June 2023. After removing duplicates, all articles were imported into the Rayyan software. The article titles were screened based on predefined inclusion and exclusion criteria. Relevant full-text articles were assessed for biases using the OHAT tool. The results were presented in tables. Xanthones have shown various pharmacological effects towards AD from the 21 preclinical studies included. Cell culture studies demonstrated the anti-cholinesterase activity of xanthones, which protects against the loss of acetylcholine. Xanthones exhibited neuroprotective effects by promoting cell viability, reducing the accumulation of & beta;-amyloid and tau aggregation. The administration of xanthones in animal models resulted in a reduction in neuronal inflammation by decreasing microglial and astrocyte burden. In terms of molecular mechanisms, xanthones prevented neuroinflammation through the modulation of signaling pathways, including TLR4/TAK1/NF-& kappa;B and MAPK pathways. Mechanisms such as activation of caspase-3 and -9 and suppression of endoplasmic reticulum stress were also reported. Despite the various neuroprotective effects associated with xanthones, there are limited studies reported on their underlying mechanisms in AD. Further studies are warranted to fully understand their potential roles in AD.
引用
收藏
页码:3485 / 3511
页数:27
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