Background: Vancomycin (VCM) is a first-line antibiotic for severe infections, but its clinical utility is limited by nephrotoxicity. Atorvastatin (ATO), a widely used lipid-lowering agent, has shown renoprotective potential. However, whether ATO mitigates vancomycin-induced nephrotoxicity (VIN) remains unclear. Methods: We investigated the effects of ATO on VIN using male C57BL/6 mice and HK-2 cells. Renal function, histopathology, inflammation, oxidative stress, and apoptosis were assessed. Transcriptome sequencing of renal tissue was performed to explore underlying mechanisms. Results: In vivo, ATO significantly improved VCM-induced renal dysfunction and renal pathological damage in mice. It significantly suppressed the release of inflammatory cytokines, enhanced renal antioxidant capacity, and reduced renal cell apoptosis. In vitro, ATO significantly increased HK-2 cell viability while reducing inflammation, reactive oxygen species (ROS) production, and renal cell apoptosis. Transcriptomic analysis revealed that ATO modulated peroxisome proliferator-activated receptor α (PPARα) signaling activity, which was accompanied by upregulated expression of solute carrier (SLC) transporters. Conclusion: This preclinical study demonstrates for the first time that ATO attenuates VIN by a PPARα-associated signaling pathway that orchestrates the upregulation of SLC transporters (including OAT1, OAT3, OCT2, and MATE1) to promote the excretion of endogenous toxins, with concomitant integrated protective effects against inflammation, oxidative stress, and apoptosis. These findings identify a novel mechanism and potential therapeutic strategy for VIN. Keywords: atorvastatin, vancomycin, nephrotoxicity, PPARα, SLC transporters
Lin et al. (Wed,) studied this question.