Visnagin attenuates thioacetamide-induced kidney damage through suppression of renal injury marker, oxidative stress, inflammation, apoptosis, and TGF-β-mediated renal fibrosis
摘要
Visnagin is a phytochemical constituent that can modulate oxidative stress, mitigate inflammation, and have anti-apoptotic properties. Hence, our study aims to identify the therapeutic potential of visnagin against thioacetamide (TAA)-induced nephrotoxicity. TAA was injected at a dosage of 200 mg/kg via the i.p. route every third day until the 8th week. Visnagin co-treatment was administered at the doses of 5 and 10 mg/kg via the i.p. route every day for 8 weeks. At the end of the treatment, several biochemical, histopathological, and qRT-PCR analyses were done. Visnagin treatment in TAA-treated rats reduces the increased levels of serum creatinine and blood urea nitrogen, with a significant reduction in malondialdehyde and nitrite, and increases the superoxide dismutase levels. Furthermore, visnagin has shown protective action against TAA-induced histopathological changes as it improves the Bowman capsular space, reduces tubule damage, and decreases collagen deposition. At the molecular level, the visnagin therapeutic potential has been assessed. TAA induces an increase in kidney injury markers like kidney injury marker-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL), as well as inflammatory markers such as TNF‐α and IL-6, while visnagin treatment restores these alterations. Subsequently, visnagin treatment downregulated the TAA-induced increased expression of genes related to fibrosis (TGF-β) and apoptosis (caspase 3). Our study demonstrated that visnagin exhibits antioxidant, anti-inflammatory, anti-fibrotic, and anti-apoptotic properties. It protects against TAA-associated oxidative renal damage due to its reactive oxygen species scavenging properties and ability to reduce kidney injury markers. Visnagin possesses promising therapeutic potential against TAA-induced nephrotoxicity.