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Effects of long-term tea polyphenols consumption on hepatic microsomal drug-metabolizing enzymes and liver function in Wistar rats

机译:长期食用茶多酚对Wistar大鼠肝微粒体药物代谢酶和肝功能的影响

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摘要

AIM: To investigate the effects of long-term tea polyphenols (TPs) consumption on hepatic microsomal drug-metabolizing enzymes and liver function in rats.METHODS: TPs were administered intragastrically to rats at the doses of 833 mg·kg-1·d–1 (n = 20) and 83.3 mg·kg-1·d-1 (n = 20) respectively for six months. Controlled group (n = 20) was given same volume of saline solution. Then the contents of cytochrome P450, b5, enzyme activities of aminopyrine N-demethylase (ADM), glutathione S-trasferase (GST) and the biochemical liver function of serum were determined.RESULTS: The contents of cytochrome P450 and b5 in the livers of male rats in high dose groups (respectively 2.66 ± 0.55, 10.43 ± 2.78 nmol·mg MS pro-1) were significantly increased compared with the control group (1.08 ± 1.04, 5.51 ± 2.98 nmol·mg MS pro- 1; P < 0.01, respectively). The enzymatic activities of ADM in the livers of female rats in high dose groups (0.91 ± 0.08 mmol·mg MS pro-1min-1) were increased compared with the control group (0.82 ± 0.08 mmol·mg MS pro-1·min-1; P < 0.05). The GST activity was unchanged in all treated groups, and the function of liver was not obviously changed.CONCLUSION: The antidotal capability of rats’ livers can be significantly improved after long-term consumption of TPs. There are differences in changes of drug-metabolizing enzymes between the sexes induced by TPs and normal condition.
机译:目的:研究长期摄入茶多酚(TPs)对大鼠肝微粒体药物代谢酶和肝功能的影响。方法:以大鼠胃内给药茶多酚的量为833 mg·kg -1 ·d –1 (n = 20)和83.3 mg·kg -1 ·d -1 (n = 20)分别六个月。对照组(n = 20)给予相同体积的盐溶液。分别测定了人肝细胞色素P450,b5的含量,氨基嘌呤N-脱甲基酶(ADM)的酶活性,谷胱甘肽S-转移酶(GST)的含量以及血清生化肝功能。高剂量组(分别为2.66±0.55,10.43±2.78 nmol·mg MS pro -1 )的雄性大鼠与对照组相比(1.08±1.04,5.51±2.98 nmol·mg MS pro -1 ;分别为P <0.01)。与对照组相比,高剂量组(0.91±0.08 mmol·mg MS pro -1 min -1 )雌性大鼠肝脏中ADM的酶活性增加。组(0.82±0.08 mmol·mg MS pro -1 ·min -1 ; P <0.05)。结论:长期服用TPs可明显改善大鼠肝脏的解毒能力。结论:所有处理组的GST活性均未改变,肝功能未见明显改变。 TP诱导的性别与正常人之间药物代谢酶的变化存在差异。

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