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天然产物在 NLRP3 炎性小体介导的阿尔茨海默病和帕金森病神经炎症中的新治疗策略。

A Novel Treatment Strategy by Natural Products in NLRP3 Inflammasome-Mediated Neuroinflammation in Alzheimer's and Parkinson's Disease.

机构信息

College of Korea Medicine, Woosuk University, Jeonju-si, Jeollabuk-do 54986, Korea.

BK21plus Team, College of Pharmacy, The Catholic University of Korea, Bucheon 14662, Korea.

出版信息

Int J Mol Sci. 2021 Jan 28;22(3):1324. doi: 10.3390/ijms22031324.

Abstract

Alzheimer's disease (AD) and Parkinson's disease (PD) are the most common neurodegenerative diseases. Many studies have demonstrated that the release of NLRP3 inflammasome-mediated proinflammatory cytokines by the excessive activation of microglia is associated with the pathogenesis of AD and PD and suggested that the NLRP3 inflammasome plays an important role in AD and PD development. In both diseases, various stimuli, such as Aβ and α-synuclein, accelerate the formation of the NLRP3 inflammasome in microglia and induce pyroptosis through the expression of interleukin (IL)-1β, caspase-1, etc., where neuroinflammation contributes to gradual progression and deterioration. However, despite intensive research, the exact function and regulation of the NLRP3 inflammasome has not yet been clearly identified. Moreover, there have not yet been any experiments of clinical use, although many studies have recently been conducted to improve treatment of inflammatory diseases using various inhibitors for NLRP3 inflammasome pathways. However, recent studies have reported that various natural products show improvement effects in the in vivo models of AD and PD through the regulation of NLRP3 inflammasome assembly. Therefore, the present review provides an overview of natural extraction studies aimed at the prevention or treatment of NLRP3 inflammasome-mediated neurological disorders. It is suggested that the discovery and development of these various natural products could be a potential strategy for NLRP3 inflammasome-mediated AD and PD treatment.

摘要

阿尔茨海默病(AD)和帕金森病(PD)是最常见的神经退行性疾病。许多研究表明,小胶质细胞过度激活释放 NLRP3 炎性体介导体炎性细胞因子与 AD 和 PD 的发病机制有关,并提示 NLRP3 炎性体在 AD 和 PD 发展中起重要作用。在这两种疾病中,各种刺激物,如 Aβ和α-突触核蛋白,加速小胶质细胞中 NLRP3 炎性体的形成,并通过白细胞介素(IL)-1β、半胱天冬酶-1 等的表达诱导细胞焦亡,其中神经炎症有助于疾病的逐渐进展和恶化。然而,尽管进行了深入的研究,但 NLRP3 炎性体的确切功能和调节仍未明确。此外,尽管最近有许多研究使用各种 NLRP3 炎性体途径抑制剂来改善炎症性疾病的治疗,但尚未有任何临床应用的实验。然而,最近的研究报告称,各种天然产物通过调节 NLRP3 炎性体组装,在 AD 和 PD 的体内模型中显示出改善效果。因此,本综述概述了旨在预防或治疗 NLRP3 炎性体介导的神经紊乱的天然产物提取研究。提示发现和开发这些各种天然产物可能是 NLRP3 炎性体介导的 AD 和 PD 治疗的一种潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591b/7866084/bcdfb41a5b66/ijms-22-01324-g001.jpg

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