4.2 Article

Hot-processed virgin coconut oil abrogates cisplatin-induced nephrotoxicity by restoring redox balance in rats compared to fermentation-processed virgin coconut oil

期刊

DRUG AND CHEMICAL TOXICOLOGY
卷 45, 期 3, 页码 1373-1382

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/01480545.2020.1831525

关键词

Virgin coconut oil; polyphenols; hot-processed method; fermentation-processed method; cisplatin; nephroprotection; antioxidant activity

资金

  1. Council of Scientific and Industrial Research, India [09/869 (0012)/2012-EMR-I]
  2. Indian Council for Medical Research [3/2/2/8/2018/Online Onco Fship/NCD-III]

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This study compared the phenolic content and nephroprotective effect of hot-processed virgin coconut oil (HPVCO) and fermentation-processed virgin coconut oil (FPVCO). The results showed that HPVCO had higher polyphenol content and greater antioxidant activity, and provided better protection against cisplatin-induced nephrotoxicity.
Virgin coconut oil (VCO) is a functional food oil prepared from fresh coconut kernel either by hot-processed (HPVCO) or fermentation-processed (FPVCO). The FPVCO has been widely explored for its pharmacological efficacy; while HPVCO, which has traditional uses, is less explored. The present study compared the phenolic content and nephroprotective effect of both these oils in male Wistar rats.In vitroantioxidant activity was estimated in terms of 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, ferric reducing antioxidant power andex vivolipid peroxidation inhibition. Inin vivomodels, the rats were pretreated orally with of FPVCO or HPVCO (doses 2 and 4 mL/kg) for seven days and nephrotoxicity was induced by the single intraperitoneal injection of cisplatin (10 mg/kg). The results indicated significantly higher polyphenol content in HPVCO (400.3 +/- 5.8 mu g/mL) than that of FPVCO (255.5 +/- 5.8 mu g/mL). Corroborating with the increased levels of polyphenols, thein vitroantioxidant potential was significantly higher in the HPVCO. Further, pretreatment with these VCO preparations protected the rats against the cisplatin-induced nephrotoxicity, with higher extent by HPVCO. The renal function markers like urea, creatinine and total bilirubin were significantly reduced (p < 0.05) with HPVCO pretreatment. Apart from the nephroprotective effects, HPVCO also abrogated the cisplatin-induced myelosuppression and hepatotoxicity. The restoration of hepato-renal function by the pretreatment of HPVCO was well corroborated with the improvement in functional antioxidants and subsequent reduction in renal lipid peroxidation. Supporting these observations, renal histology revealed reduced glomerular/tubular congestion and necrosis. Thus, the study concludes that HPVCO may be better functional food than FPVCO.

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