Renal inflammation combined with renal function reserve reduction accelerate kidney aging via pentose phosphate pathway

Aging is closely associated with inflammation, which affects renal function reserve (RFR) in the kidneys. This study aims to investigate the impact of reduced RFR reduction on kidney aging and the influence of renal inflammation and RFR reduction on this process. Natural aging rats and those subject...

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Veröffentlicht in:iScience 2024-06, Vol.27 (6), p.110045, Article 110045
Hauptverfasser: Han, Bing, Zhang, YiXuan, Liu, Chao, Ji, Pengcheng, Xing, Zenghui, Geng, Xiaodong, Chi, Kun, Gong, Ming, Li, Yingying, Zhang, Ying, Fu, Zhangning, Hong, Quan, Cai, Guangyan, Chen, Xiangmei, Sun, Xuefeng
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Sprache:eng
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Zusammenfassung:Aging is closely associated with inflammation, which affects renal function reserve (RFR) in the kidneys. This study aims to investigate the impact of reduced RFR reduction on kidney aging and the influence of renal inflammation and RFR reduction on this process. Natural aging rats and those subjected to unilateral nephrectomy (UNX), 1/6 nephrectomy (1/6NX), and unilateral ureteral obstruction (UUO) were observed at 6, 12, 18, and 21 months. Our findings suggest that RFR reduction and renal inflammation can accelerate kidney aging, and inflammation contributes more. Metabolomics analysis revealed alterations in amino acid metabolism contribute to RFR decline. Furthermore, experiments in vitro confirmed the involvement of pentose phosphate pathway (PPP) in promoting aging though inflammation. Our research provides novel insights into for the mechanism of kidney aging and provides indirect support for clinical treatment decisions, such as addressing kidney inflammation, stones, or tumors that may necessitate partial or complete nephrectomy. [Display omitted] •Renal inflammation and RFR decline can accelerate kidney aging•RFR decline may be associated with alterations in amino acid metabolism•PPP plays an important role in inflammation promoting aging•PPP can promote aging through oxidative stress Biochemistry; Cell biology; Immunology; Molecular biology
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2024.110045