Kahweol Ameliorates Cisplatin-Induced Acute Kidney Injury through Pleiotropic Effects in Mice.
Jung-Yeon KimJungmin JoJaechan LeemKwan-Kyu ParkPublished in: Biomedicines (2020)
Cisplatin is an effective chemotherapeutic agent, but its clinical use is frequently limited by its nephrotoxicity. The pathogenesis of cisplatin-induced acute kidney injury (AKI) remains incompletely understood, but oxidative stress, tubular cell death, and inflammation are considered important contributors to cisplatin-induced renal injury. Kahweol is a natural diterpene extracted from coffee beans and has been shown to possess anti-oxidative and anti-inflammatory properties. However, its role in cisplatin-induced nephrotoxicity remains undetermined. Therefore, we investigated whether kahweol exerts a protective effect against cisplatin-induced renal injury. Additionally, its mechanisms were also examined. Administration of kahweol attenuated renal dysfunction and histopathological damage together with inhibition of oxidative stress in cisplatin-injected mice. Increased expression of nicotinamide adenine dinucleotide phosphate oxidase 4 and decreased expression of manganese superoxide dismutase and catalase after cisplatin treatment were significantly reversed by kahweol. Moreover, kahweol inhibited cisplatin-induced apoptosis and necroptosis in the kidneys. Finally, kahweol reduced inflammatory cytokine production and immune cell accumulation together with suppression of nuclear factor kappa-B pathway and downregulation of vascular adhesion molecules. Together, these results suggest that kahweol ameliorates cisplatin-induced renal injury via its pleiotropic effects and might be a potential preventive option against cisplatin-induced nephrotoxicity.
Keyphrases
- oxidative stress
- induced apoptosis
- acute kidney injury
- nuclear factor
- cell death
- dna damage
- diabetic rats
- poor prognosis
- cardiac surgery
- toll like receptor
- signaling pathway
- ischemia reperfusion injury
- endoplasmic reticulum stress
- mouse model
- anti inflammatory
- type diabetes
- drug induced
- high fat diet induced
- cystic fibrosis
- immune response
- skeletal muscle
- binding protein
- hydrogen peroxide
- escherichia coli
- climate change
- high resolution
- replacement therapy