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帕金森病中昼夜节律与NLRP3炎性小体信号通路之间的分子串扰

Molecular crosstalk between circadian clock and NLRP3 inflammasome signaling in Parkinson's disease.

作者信息

Huang Jiahua, Li Wenwei

机构信息

Laboratory of Neuropathology and Neuropharmacology, Department of Neurology, Shanghai Public Health Clinical Center, Fudan University, 201500, Shanghai, China.

Institute of Neurology, Institutes of Integrative Medicine, Fudan University, 201500, Shanghai, China.

出版信息

Heliyon. 2024 Jan 14;10(2):e24752. doi: 10.1016/j.heliyon.2024.e24752. eCollection 2024 Jan 30.

Abstract

Parkinson's disease (PD) is one of the most common neurodegenerative diseases. Research has recently found that both animal models and patients with PD have circadian dysfunction, accompanied by abnormal expression of circadian genes and proteins, which implies that the circadian clock plays a crucial role in PD etiopathogenesis. In addition, a strong relationship between NLRP3 inflammasome signaling and PD has been observed. Meanwhile, the activation of the NLRP3 inflammasome is highly relevant to dysfunctions of the molecular clock. Therefore, alleviating the neuroinflammation caused by NLRP3 inflammasome signaling by adjusting the abnormal molecular clock may be a potential strategy for preventing and treating PD. In this article, we have reviewed the potential or direct relationship between abnormalities of the circadian clock and NLRP3 inflammasome signaling in PD.

摘要

帕金森病(PD)是最常见的神经退行性疾病之一。最近的研究发现,PD的动物模型和患者均存在昼夜节律功能障碍,伴有昼夜节律基因和蛋白质的异常表达,这意味着生物钟在PD的发病机制中起关键作用。此外,已观察到NLRP3炎性小体信号与PD之间存在密切关系。同时,NLRP3炎性小体的激活与分子时钟功能障碍高度相关。因此,通过调节异常的分子时钟来减轻NLRP3炎性小体信号引起的神经炎症可能是预防和治疗PD的潜在策略。在本文中,我们综述了PD中生物钟异常与NLRP3炎性小体信号之间的潜在或直接关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49d/10803942/418181fd745b/gr1.jpg

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