4.7 Article

Protective effect of Schisandra chinensis bee pollen extract on liver and kidney injury induced by cisplatin in rats

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 95, 期 -, 页码 1765-1776

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2017.09.083

关键词

Schisandra chinensis bee pollen extract; Cisplatin toxicity; Liver injury; Kidney injury; Oxidative stress; Inflammation; Apoptotic

资金

  1. Modern Agro-industry Technology Research System [CARS-45-KXJ19]
  2. Fujian Agriculture and Forestry University Foundation for excellent youth teachers [xjq201414]
  3. Fujian Agriculture and Forestry University Technology Development Fund [KF2015022]

向作者/读者索取更多资源

Cisplatin (CP) has been used to cure numerous forms of cancers effectively in clinics, however, it could induce some toxic effects. Bee pollen is a natural compound, produced by honey bees. It is obtained from collected flower pollen and nectar, mixed with bee saliva. Bee pollen produced from Schisandra chinensis plants is described to exert potent antioxidant effects and to be a free radical scavenger. The purpose of this study was to investigate the effects of therapeutic treatment with Schisandra chinensis bee pollen extract (SCBPE) on liver and kidney injury induced by CP. The rats were intragastrically administrated with different doses of SCBPE (400 mg/kg/day, 800 mg/kg/day, 1200 mg/kg/day) and vitamin C (400 mg/kg/day, positive control group) for 12 days, and the liver and kidney injury models were established by single intraperitoneal injection of CP (8 mg/kg) at seventh day. The effect of SCBPE on CP toxicity was evaluated by measuring markers of liver and kidney injury in serum, levels of lipid peroxidation and antioxidants in liver and kidney, observing pathological changes of tissue, and quantified expression of NF kappa B, IL-1 beta, IL-6, cytochrome C, caspase3, caspase9, p53 and Bax in liver and kidney. Compared with the model group, the activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and the content of blood urea nitrogen (BUN), creatinine (Cr) in serum all decreased in SCBPE high dose group. Meanwhile, the activities of superoxide dismutase (SOD), catalase (CAT) and the content of reduced glutathione (GSH) in liver and kidney increased, and the content of malondialdehyde (MDA) and inducible nitric oxide synthase (iNOS) decreased. In addition, the histopathologic aspects showed that the pathological changes of liver and kidney were found in the model group, and SCBPE group reduced to varying degrees. Moreover, the expression of NF kappa B, IL-1 beta, IL-6, cytochrome C, caspase3, caspase9, p53 and Bax in liver and kidney decreased. Therefore, SCBPE could reduce the damage of liver and kidney caused by CP by reducing the level of oxidative stress, and improving the antioxidant, anti-inflammatory and anti-apoptotic capacity of the body.

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