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炎性小体:代谢综合征的新型治疗靶点?

Inflammasomes: novel therapeutic targets for metabolic syndrome?

作者信息

Cao Pengyu, Yang Yulin, Zhang Ningning, Wang Bojian, Gong Zhenwei

机构信息

The Second People's Hospital of Changzhou, the Third Affiliated Hospital of Nanjing Medical University, Changzhou, Jiangsu, China.

Changzhou Medical Center, Nanjing Medical University, Changzhou, Jiangsu, China.

出版信息

Front Endocrinol (Lausanne). 2025 May 13;16:1569579. doi: 10.3389/fendo.2025.1569579. eCollection 2025.

Abstract

Chronic inflammation is a hallmark for Metabolic Syndrome (MetS). It is also one of the most important risk factors for insulin resistance and metabolic disorders. Inflammasomes, which are intracellular multiprotein complexes within the innate immune system, regulate the production and maturation of pro-inflammatory cytokines including interleukin-1β (IL-1β) and IL-18 upon sensing pathogens or danger signals in the cytosol. A growing body of evidence indicates that inflammasomes play a pivotal role in the pathophysiology and progression of metabolic diseases, as deficiency in the key component of inflammasomes protects mice from high fat diet induced obesity and insulin resistance. Thus, in this review, we will summarize the role of inflammasomes in MetS and how to treat MetS by targeting inflammasomes. This may provide novel insights and therapeutic targets for treating metabolic disorders.

摘要

慢性炎症是代谢综合征(MetS)的一个标志。它也是胰岛素抵抗和代谢紊乱最重要的危险因素之一。炎性小体是先天性免疫系统中的细胞内多蛋白复合物,在感知细胞溶质中的病原体或危险信号后,调节促炎细胞因子(包括白细胞介素-1β(IL-1β)和IL-18)的产生和成熟。越来越多的证据表明,炎性小体在代谢性疾病的病理生理学和进展中起关键作用,因为炎性小体关键成分的缺乏可保护小鼠免受高脂饮食诱导的肥胖和胰岛素抵抗。因此,在本综述中,我们将总结炎性小体在代谢综合征中的作用以及如何通过靶向炎性小体来治疗代谢综合征。这可能为治疗代谢紊乱提供新的见解和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a5a/12106043/48b10b31452c/fendo-16-1569579-g001.jpg

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