Tackling of Renal Carcinogenesis in Wistar Rats by <i>Silybum marianum</i> Total Extract, Silymarin, and Silibinin <i>via</i> Modulation of Oxidative Stress, Apoptosis, Nrf2, PPAR<i>γ</i>, NF‐<i>κ</i>B, and PI3K/Akt Signaling Pathways
Nour Y. S. Yassin, Sameh AbouZid, Asmaa M. El-Kalaawy, Tarek M. Ali, Basem H. Elesawy, Osama M. Ahmed
Abstract
The present work was designed to assess the efficacy of Silybum marianum total extract (STE), silymarin (Sm), and silibinin (Sb) against experimentally induced renal carcinogenesis in male Wistar rats and their roles in regulating oxidative stress, inflammation, apoptosis, and carcinogenesis. The diethylnitrosamine (DEN)/2‐acetylaminofluorene (AAF)/carbon tetrachloride (CCl 4 )‐administered rats were orally treated with STE (200 mg/kg b.w.), Sm (150 mg/kg b.w.), and Sb (5 mg/kg b.w.) every other day either from the 1 st week or from the 16 th week of carcinogen administration to the end of 25 th week. The treatments with STE, Sm, and Sb attenuated markers of toxicity in serum, decreased kidney lipid peroxidation (LPO), and significantly reinforced the renal antioxidant armory. The biochemical results were further confirmed by the histopathological alterations. The treatments also led to suppression of proinflammatory mediators such as NF‐ κβ , p65, I κβα , and IL‐6 in association with inhibition of the PI3K/Akt pathway. Furthermore, they activated the expressions of PPARs, Nrf2, and IL‐4 in addition to downregulation of apoptotic proteins p53 and caspase‐3 and upregulation of antiapoptotic mediator Bcl‐2. The obtained data supply potent proof for the efficacy of STE, Sm, and Sb to counteract renal carcinogenesis via alteration of varied molecular pathways.