Perillaldehyde inhibits oxidative stress, NLRP3-mediated inflammation and fibrosis in diabetic nephropathy through regulating HMOX1.

Abstract

Diabetic nephropathy (DN) is a frequently occurred complication of diabetes mellitus (DM) worldwide. Perillaldehyde is a natural terpenoid compound exerted beneficial effects on diabetic cardiomyopathy (DCM), which is another important part of DM complication. However, the effect of perillaldehyde on DN has not been reported. In the present study, we demonstrated that perillaldehyde prevented ROS-driven oxidative stress, with decreased ROS and MDA levels and increased GSH level in high glucose (HG)-treated HK-2 cells. Perillaldehyde also reversed HG-induced NLRP3-mediated inflammation and fibrosis in HK-2 cells, as evidenced by decreased pro-inflammatory cytokines and fibrogenic factors. Furthermore, we observed that perillaldehyde directly targeted HMOX1 and regulated its expression in HK-2 cells. Knockdown of HMOX1 prevented the effects of perillaldehyde on HG-treated HK-2 cells, implying that perillaldehyde exerted its effects via regulating HMOX1. In a high fat diet (HFD)/streptozocin (STZ) mouse model, perillaldehyde also exerted renoprotective, antioxidant, anti-inflammatory and anti-fibrotic activities. In conclusion, our study clearly demonstrated the beneficial effects of perillaldehyde on DN both in vivo and in vitro, which indicated that perillaldehyde might serve as a potential application in treating or preventing DN.