Limonin mitigates cisplatin-induced acute kidney injury through metabolic reprogramming

Acute kidney injury (AKI) is a known complication of cisplatin administration; currently, there are no effective ways to prevent it. Therefore, it largely limited the use of cisplatin in chemotherapy in the clinic. In this study, we reported that Limonin, a triterpenoid compound extracted from citru...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2023-11, Vol.167, p.115531-115531, Article 115531
Hauptverfasser: Zeng, Xi, Zhou, Xianke, Zhou, Jiayi, Zhou, Hong, Hong, Xue, Li, Dier, Xiang, Yadie, Zhong, Menghua, Chen, Yudan, Liang, Dongning, Fu, Haiyan
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Sprache:eng
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Zusammenfassung:Acute kidney injury (AKI) is a known complication of cisplatin administration; currently, there are no effective ways to prevent it. Therefore, it largely limited the use of cisplatin in chemotherapy in the clinic. In this study, we reported that Limonin, a triterpenoid compound extracted from citrus, alleviated cisplatin-induced AKI through metabolic reprogramming in the diseased kidneys. Cisplatin was employed to induce AKI in mice. Three groups were set up: Sham, cisplatin + vehicle, and cisplatin + Limonin. Using UHPLC-TOF/MS, we conducted metabolomics to profile the kidneys' endogenous metabolites and metabolic pathways. A network pharmacological method was performed to identify the targets of Limonin on AKI. The human proximal tubular epithelial cell line (HK-2) was applied for in vitro studies. Limonin preserved serum creatinine and blood urea nitrogen levels after cisplatin-induced AKI. Employing metabolomics, we identified 33 endogenous differentially expressed metabolites and 7 significantly disturbed metabolic pathways in the diseased kidneys within three groups. After AKI, Limonin significantly reduced linoleic acid and its downstream product, arachidonic acid, thus exerting a protective effect on the kidney. The network pharmacological method identified CYP3A4 as a key target of Limonin in treating AKI, while CYP3A4 also serve as a mediator of arachidonic acid metabolism. In vitro, Limonin markedly reduced the level of arachidonic acid and HK-2 cell apoptosis triggered by cisplatin, mainly related to the targeted inhibition of CYP3A4-mediated arachidonic acid metabolism. Limonin ameliorates cisplatin-induced AKI by inhibiting CYP3A4 activity to regulate arachidonic acid metabolism, ultimately preserving kidney function. [Display omitted] •Limonin is an effective phytochemical with significant clinical potential in preventing cisplatin-induced AKI.•Regulating the kidney metabolic microenvironment change is a key mechanism of limonin treating cisplatin-induced AKI.•As a novel target of limonin, CYP3A4 mediates arachidonic acid metabolism to protect against AKI.
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2023.115531