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首页> 外文期刊>Biological & pharmaceutical bulletin >Effects of Ganoderma lucidum Polysaccharide on CYP2E1,CYP1A2 and CYP3A Activities in BCG-Immune Hepatic Injury in Rats
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Effects of Ganoderma lucidum Polysaccharide on CYP2E1,CYP1A2 and CYP3A Activities in BCG-Immune Hepatic Injury in Rats

机译:灵芝多糖对大鼠BCG免疫性肝损伤中CYP2E1,CYP1A2和CYP3A活性的影响

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摘要

The purpose of the present study was to investigate the effect of Ganoderma lucidum polysaccharide(GLPS),a major active component in Chinese medicinal fungus,on cytochrome P450 metabolic activity in Bacillus Calmette Guerin(BCG)-induced immune hepatic injury in rats.The enzyme kinetics of the probes including chlorzoxazone(CYP2E1),phenacetin(CYP1A2)and nifedipine(CYP3A)were evaluated by HPLC.The results showed that BCG-pretreatment(125 mg/kg)significantly increased serum levels of alanine transaminase(ALT),nitrite and malondialdehyde(MDA),inhibited activities of superoxide dismutase(SOD)and decreased P450 total content in microsomes(p<0.05).Administration of GLPS(50 and 200 mg/kg)reversed above hepatic injury stimulated by BCG in vivo.Moreover,GLPS dose-dependently inhibited activities of CYP2E1,CYP1A2 and CYP3A in hepatic microsomes in vitro,suggesting that inhibition of GLPS on P450 oxidative metabolism might participate in the hepatoprotective mechanism,and also suggested that pharmacokinetics might be changed by drug-herb interaction.
机译:本研究的目的是研究中药真菌的主要活性成分灵芝多糖(GLPS)对卡介苗(BCG)诱导的大鼠免疫性肝损伤的细胞色素P450代谢活性的影响。用高效液相色谱法测定了氯唑沙宗(CYP2E1),非那西丁(CYP1A2)和硝苯地平(CYP3A)的动力学,结果表明,经卡介苗预处理(125 mg / kg)可显着提高血清丙氨酸转氨酶(ALT),亚硝酸盐和亚硝酸盐的含量。丙二醛(MDA),超氧化物歧化酶(SOD)活性抑制和微粒体中P450总含量降低(p <0.05)。GLPS(50和200 mg / kg)的施用与BCG体内刺激引起的肝损伤相反。 CYP2E1,CYP1A2和CYP3A的剂量依赖性抑制肝微粒体的体外活性,提示GLPS对P450氧化代谢的抑制作用可能参与了肝保护机制,并提示药-药相互作用可能会改变药物代谢动力学。

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