Catalpol ameliorates inflammation and oxidative stress via regulating Sirt1 and activating Nrf2/HO‐1 signaling against acute kidney injury

Abstract Background Septic acute kidney injury (SAKI) is usually caused by sepsis. It has been shown that catalpol (Cat) impairs sepsis‐evoked organ dysfunction to a certain degree. The current work aims to evaluate the protective effects of Cat on SAKI and potential mechanisms in vivo and in vitro. Methods SAKI cellular and murine model were set up using lipopolysaccharide (LPS) in vitro and in vivo. Cell apoptosis in cells was determined by TUNEL assay. Levels of inflammatory cytokines were detected by enzyme‐linked immunosorbent assay (ELISA). The levels of the markers of oxidative injury were evaluated by corresponding commercial kits. Protein levels were assayed via western blotting and immunohistochemistry (IHC) staining. Results The results demonstrated that LPS upregulated TNF‐α, IL‐6, and malondialdehyde levels, and downregulated superoxide dismutase, whereas Cat treated cells have the opposite results. Functional assays displayed that Cat remarkably reversed the LPS‐challenged damage as the impairment of TNF‐α and IL‐6 levels, oxidative stress, and the apoptosis in HK‐2 cells. Moreover, knockdown of Sirtuin 1 (Sirt1) counteracted the suppressive impact of Cat on LPS‐triggered inflammatory response, oxidative stress, and renal damage. Further, Cat elevated Sirt1 expression and activated the Nrf2/HO‐1 signaling in LPS‐engendered SAKI in vivo and in vitro. Conclusion Our study clearly proved that Cat protected against LPS‐induced SAKI via synergic antioxidant and anti‐inflammatory actions by regulating Sirt1 and Nrf2/HO‐1 signaling pathways.