SIRT3
锡尔图因
医学
线粒体生物发生
自噬
线粒体
疾病
炎症
氧化应激
糖尿病
细胞代谢
生物信息学
肾脏疾病
炎症体
药理学
NAD+激酶
内科学
内分泌学
细胞生物学
新陈代谢
生物
生物化学
细胞凋亡
酶
作者
Yinfeng Chen,Ying Wang,Dongrong Yu,Hailing Zhao,Ping Li
出处
期刊:Renal Failure
[Taylor & Francis]
日期:2025-08-19
卷期号:47 (1): 2543927-2543927
被引量:1
标识
DOI:10.1080/0886022x.2025.2543927
摘要
Diabetic kidney disease (DKD) is a microvascular complication of diabetes and a major cause of kidney failure; current treatment methods still need improvement. Sirtuin 3 (SIRT3) is an NAD+-dependent protein deacetylase located in the mitochondria, where it regulates the activity and biological functions of diverse proteins and influences various mitochondrial functions via deacetylation. Increasing research indicates that SIRT3 holds promise as a therapeutic target for DKD. This review examines SIRT3's impact on mitochondrial functions, including mitochondrial biogenesis, autophagy, dynamics, oxidative homeostasis, and energy metabolism. We summarize that SIRT3 delays the progression of DKD by inhibiting oxidative stress, reducing inflammation, regulating cell death, and modulating energy metabolism. Finally, we categorize the applications of SIRT3 activators in renal diseases. In summary, this review provides a thorough understanding of SIRT3's functional role in DKD and proposes a potential therapeutic approach pending clinical validation.
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