| Literature DB >> 35545730 |
Fahadul Islam1, Mohamed H Nafady2, Md Rezaul Islam1, Susmita Saha1, Salma Rashid1, Aklima Akter1, Md Harun- Or-Rashid1, Muhammad Furqan Akhtar3, Asma Perveen4, Ghulam Md Ashraf5,6, Md Habibur Rahman7,8, Sherouk Hussein Sweilam9,10.
Abstract
Alzheimer's disease (AD) is the most common cause of dementia and cognitive impairment; yet, there is currently no treatment. A buildup of Aβ, tau protein phosphorylation, oxidative stress, and inflammation in AD is pathogenic. The accumulation of amyloid-beta (Aβ) peptides in these neurocognitive areas is a significant characteristic of the disease. Therefore, inhibiting Aβ peptide aggregation has been proposed as the critical therapeutic approach for AD treatment. Resveratrol has been demonstrated in multiple studies to have a neuroprotective, anti-inflammatory, and antioxidant characteristic and the ability to minimize Aβ peptides aggregation and toxicity in the hippocampus of Alzheimer's patients, stimulating neurogenesis and inhibiting hippocampal degeneration. Furthermore, resveratrol's antioxidant effect promotes neuronal development by activating the silent information regulator-1 (SIRT1), which can protect against the detrimental effects of oxidative stress. Resveratrol-induced SIRT1 activation is becoming more crucial in developing novel therapeutic options for AD and other diseases that have neurodegenerative characteristics. This review highlighted a better knowledge of resveratrol's mechanism of action and its promising therapeutic efficacy in treating AD. We also highlighted the therapeutic potential of resveratrol as an AD therapeutic agent, which is effective against neurodegenerative disorders.Entities:
Keywords: Alzheimer’s disease; Autophagy induction; Neuroinflammation; Oxidative stress; Resveratrol; SIRT1
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Year: 2022 PMID: 35545730 DOI: 10.1007/s12035-022-02859-7
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590