Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 181, P. 117636 - 117636
Published: Nov. 2, 2024
Language: Английский
Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 181, P. 117636 - 117636
Published: Nov. 2, 2024
Language: Английский
Journal of Biochemical and Molecular Toxicology, Journal Year: 2024, Volume and Issue: 38(11)
Published: Oct. 21, 2024
Abstract Coenzyme Q10 (CoQ10) plays an important role in improving mitochondrial function and has many beneficial effects on the kidney. However, whether CoQ10 protects against diquat (DQ)‐induced acute kidney injury (AKI) remains unclear. In this study, we investigated protective mechanism of action DQ‐induced AKI. Institute Cancer Research (ICR) mice were intraperitoneally injected with DQ to induce The expression levels serum creatinine (Cr), urea, molecule‐1 (KIM‐1) increased, those aquaporin 1 (AQP‐1) decreased, reactive oxygen species (ROS) increased depolarization membranes rupture. contrast, treatment significantly improved reduced Cr, KIM‐1 contents, AQP‐1 expression, ROS contents poisoning. Our results suggest that AKI caused by poisoning may be related disruption homeostasis kinetic homeostasis. Thus, represents a new therapeutic option for prevention
Language: Английский
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0Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 181, P. 117636 - 117636
Published: Nov. 2, 2024
Language: Английский
Citations
0