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白藜芦醇与神经保护:从实验室到临床治疗阿尔茨海默病的潜在治疗方法的新视角。

Resveratrol and neuroprotection: an insight into prospective therapeutic approaches against Alzheimer's disease from bench to bedside.

机构信息

Department of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.

Faculty of Applied Health Science Technology, Misr University for Science and Technology, Giza, Egypt.

出版信息

Mol Neurobiol. 2022 Jul;59(7):4384-4404. doi: 10.1007/s12035-022-02859-7. Epub 2022 May 12.

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.

摘要

阿尔茨海默病(AD)是痴呆和认知障碍最常见的原因;然而,目前尚无治疗方法。AD 中 Aβ、tau 蛋白磷酸化、氧化应激和炎症的积累是致病的。淀粉样β(Aβ)肽在这些神经认知区域的积累是该疾病的一个重要特征。因此,抑制 Aβ 肽聚集已被提议作为 AD 治疗的关键治疗方法。多项研究表明,白藜芦醇具有神经保护、抗炎和抗氧化特性,能够最小化阿尔茨海默病患者海马体中 Aβ 肽的聚集和毒性,刺激神经发生并抑制海马体退化。此外,白藜芦醇的抗氧化作用通过激活沉默信息调节因子-1(SIRT1)促进神经元发育,从而可以防止氧化应激的有害影响。白藜芦醇诱导的 SIRT1 激活在开发 AD 和其他具有神经退行性特征的疾病的新型治疗选择方面变得更加重要。本综述强调了更好地了解白藜芦醇的作用机制及其在治疗 AD 方面的有希望的治疗效果。我们还强调了白藜芦醇作为 AD 治疗剂的治疗潜力,它对神经退行性疾病有效。

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