Modulation of NADPH oxidase and Nrf2/HO-1 pathway by vanillin in cisplatin-induced nephrotoxicity in rats
Autor: | Mohamed A. Shaheen, Mohamed M. Elseweidy, Nahla N Younis, Nehal M. Elsherbiny |
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Rok vydání: | 2020 |
Předmět: |
Male
Necrosis NF-E2-Related Factor 2 Anti-Inflammatory Agents Pharmaceutical Science Apoptosis Pharmacology Kidney Antioxidants Nitric oxide Nephrotoxicity 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine medicine Animals Rats Wistar 030304 developmental biology Cisplatin 0303 health sciences Creatinine NADPH oxidase biology Malondialdehyde Fibrosis Disease Models Animal Oxidative Stress chemistry NADPH Oxidase 4 Benzaldehydes 030220 oncology & carcinogenesis Heme Oxygenase (Decyclizing) biology.protein Kidney Diseases medicine.symptom Signal Transduction medicine.drug |
Zdroj: | Journal of Pharmacy and Pharmacology. 72:1546-1555 |
ISSN: | 2042-7158 0022-3573 |
DOI: | 10.1111/jphp.13340 |
Popis: | Objectives To investigate the protective effect of vanillin in cisplatin (CP)-induced nephrotoxicity in rats and elucidate the role of nrf-2 and its downstream antioxidant molecules. Methods Rats received vanillin (100 mg/kg orally) for 10 constitutive days and CP (7.5 mg/kg, once, ip) on day 6 of vanillin administration. Key findings Cisplatin suppressed body weight gain, increased serum urea and creatinine and renal malondialdehyde and nitric oxide while decreased renal total antioxidant capacity. Up-regulation of NADPH oxidase-4 (NOX-4) was marked in renal tissue of CP-treated rats along with down-regulation of the antioxidant genes (nuclear factor erythroid 2-related factor2 (NRF2) and haem oxygenase-1(HO-1)). Increased tumour necrosis factor-α and decreased interleukin-10 with increased myeloperoxidase activity were apparent in renal tissue of CP-treated rats along with marked tubular injury, neutrophil infiltration and increased apoptosis (caspase-3) and some degree of interstitial fibrosis. Vanillin prophylactic administration prevented the deterioration of kidney function, oxidative and nitrosative stress. It also suppressed NOX-4 and up-regulated NRF2 and HO-1 expression in renal tissue. Inflammation, apoptosis and tubular injury were also inhibited by vanillin. Conclusions The antioxidant mechanism by which vanillin protected against CP-induced nephrotoxicity involved the inhibition of NOX-4 along with the stimulation of Nrf2/HO-1 signalling pathway. These in turn inhibited inflammation and apoptosis. |
Databáze: | OpenAIRE |
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