A review of studies on the implication of NLRP3 inflammasome for Parkinson’s disease and related candidate treatment targets

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nannan Zeng , Qi Wang , Chong Zhang , Yali Zhou , Jianguo Yan
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引用次数: 0

Abstract

Parkinson's disease (PD) is a neurodegenerative disease for which the prevalence is second only to Alzheimer's disease (AD). This disease primarily affects people of middle and old age, significantly impacting their health and quality of life. The main pathological features include the degenerative nigrostriatal dopaminergic (DA) neuron loss and Lewy body (LB) formation. Currently, available PD medications primarily aim to alleviate clinical symptoms, however, there is no universally recognized therapy worldwide that effectively prevents, clinically treats, stops, or reverses the disease. Consequently, the evaluation and exploration of potential therapeutic targets for PD are of utmost importance. Nevertheless, the pathophysiology of PD remains unknown, and neuroinflammation mediated by inflammatory cytokines that prompts neuron death is fundamental for the progression of PD. The nucleotide-binding oligomerization domain-like receptor pyrin domain-containing 3 (NLRP3) inflammasome is a key complex of proteins linking the neuroinflammatory cascade in PD. Moreover, mounting evidence suggests that traditional Chinese medicine (TCM) alleviates PD by suppressing the NLRP3 inflammasome. This article aims to comprehensively review the available studies on the composition and activating mechanism of the NLRP3 inflammasome, along with its significance in PD pathogenesis and potential treatment targets. We also review natural products or synthetic compounds which reduce neuroinflammation via modulating NLRP3 inflammasome activity, aiming to identify new targets for future PD diagnosis and treatment through the exploration of NLRP3 inhibitors. Additionally, this review offers valuable references for developing new PD treatment methods.

NLRP3炎症小体对帕金森病的影响及相关候选治疗靶点的研究综述。
帕金森病(PD)是一种神经退行性疾病,其患病率仅次于阿尔茨海默病(AD)。这种疾病主要影响中老年人,严重影响他们的健康和生活质量。主要病理特征包括退行性黑质纹状体多巴胺能(DA)神经元丢失和路易体(LB)形成。目前,可用的PD药物主要旨在缓解临床症状,然而,世界范围内还没有公认的有效预防、临床治疗、停止或逆转疾病的疗法。因此,评估和探索PD的潜在治疗靶点至关重要。然而,帕金森病的病理生理学仍然未知,炎症细胞因子介导的神经炎症是导致神经元死亡的帕金森病进展的基础。核苷酸结合寡聚结构域样受体pyrin结构域含3(NLRP3)炎症小体是连接帕金森病神经炎症级联反应的关键蛋白质复合体。此外,越来越多的证据表明,中药通过抑制NLRP3炎症小体来减轻PD。本文旨在全面综述关于NLRP3炎症小体的组成和激活机制的现有研究,以及其在PD发病机制中的意义和潜在的治疗靶点。我们还综述了通过调节NLRP3炎症小体活性来减少神经炎症的天然产物或合成化合物,旨在通过探索NLRP3抑制剂来确定未来PD诊断和治疗的新靶点。此外,这篇综述为开发新的帕金森病治疗方法提供了有价值的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurochemistry international
Neurochemistry international 医学-神经科学
CiteScore
8.40
自引率
2.40%
发文量
128
审稿时长
37 days
期刊介绍: Neurochemistry International is devoted to the rapid publication of outstanding original articles and timely reviews in neurochemistry. Manuscripts on a broad range of topics will be considered, including molecular and cellular neurochemistry, neuropharmacology and genetic aspects of CNS function, neuroimmunology, metabolism as well as the neurochemistry of neurological and psychiatric disorders of the CNS.
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