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微生物代谢产物氧化三甲胺与肾脏疾病

The microbial metabolite trimethylamine N-oxide and the kidney diseases.

作者信息

Su Jin-Qi, Wu Xiang-Qi, Wang Qi, Xie Bo-Yang, Xiao Cui-Yan, Su Hong-Yong, Tang Ji-Xin, Yao Cui-Wei

机构信息

Guangdong Provincial Key Laboratory of Autophagy and Major Chronic Non-communicable Diseases, Institute of Nephrology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.

Key Laboratory of Prevention and Management of Chronic Kidney Diseases of Zhanjiang City, Institute of Nephrology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.

出版信息

Front Cell Infect Microbiol. 2025 Mar 11;15:1488264. doi: 10.3389/fcimb.2025.1488264. eCollection 2025.

Abstract

Trimethylamine N-oxide (TMAO), a metabolite, is a co-metabolite produced by both gut microbiota and livers, originating from foods rich in choline or carnitine. Emerging evidence suggests that TMAO may play a role in the pathogenesis of various kidney diseases, including acute kidney injury and chronic kidney disease. Research has demonstrated that heightened levels of TMAO are correlated with a heightened likelihood of kidney disease advancement and cardiovascular incidents among individuals with chronic kidney disease. Furthermore, TMAO has been observed to stimulate inflammation, oxidative stress, and fibrosis in animal models of kidney disease. Mechanistically, TMAO may contribute to kidney disease pathogenesis by inhibiting autophagy, activating the NLRP3 inflammasome, and inducing mitochondrial dysfunction. Therefore, targeting TMAO may represent a promising therapeutic strategy for the treatment of kidney diseases. Future studies are needed to further investigate the role of TMAO in kidney disease pathogenesis and to develop TMAO-targeted therapies for the prevention and treatment of kidney diseases.

摘要

氧化三甲胺(TMAO)是一种代谢产物,是由肠道微生物群和肝脏共同产生的一种共代谢产物,源自富含胆碱或肉碱的食物。新出现的证据表明,TMAO可能在包括急性肾损伤和慢性肾病在内的各种肾脏疾病的发病机制中起作用。研究表明,氧化三甲胺水平升高与慢性肾病患者肾病进展和心血管事件的可能性增加相关。此外,在肾病动物模型中观察到TMAO会刺激炎症、氧化应激和纤维化。从机制上讲,TMAO可能通过抑制自噬、激活NLRP3炎性小体和诱导线粒体功能障碍来促进肾病发病机制。因此,针对TMAO可能是治疗肾脏疾病的一种有前景的治疗策略。需要进一步的研究来进一步调查TMAO在肾病发病机制中的作用,并开发针对TMAO的疗法来预防和治疗肾脏疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2555/11933022/b4b5e7b77e49/fcimb-15-1488264-g001.jpg

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