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三七总皂苷对大鼠肝脏药物代谢酶酶活性、mRNA及蛋白表达的影响
引用本文:陈艳进,王宇光,马增春,肖成荣,谭洪玲,梁乾德,汤响林,赵永红,王东根,高月. 三七总皂苷对大鼠肝脏药物代谢酶酶活性、mRNA及蛋白表达的影响[J]. 中国中药杂志, 2014, 39(19): 3824-3828
作者姓名:陈艳进  王宇光  马增春  肖成荣  谭洪玲  梁乾德  汤响林  赵永红  王东根  高月
作者单位:中南大学 药学院, 湖南 长沙 410000;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850;军事医学科学院 野战输血研究所, 北京 100850;军事医学科学院 放射与辐射医学研究所, 北京 100850
基金项目:国家"重大新药创制"科技重大专项(2012ZX09101201)
摘    要:研究三七总皂苷对大鼠肝脏药物代谢酶酶活性、mRNA及蛋白表达的影响。将Wistar雄性大鼠随机分为9组,给予受试药后,提取肝脏微粒体,肝脏总RNA和总蛋白,分别采用底物探针法、荧光定量PCR技术和Western blot,检测三七总皂苷对肝脏药物代谢酶相关亚型酶活性、mRNA和蛋白质表达3个水平的调节作用。实验的结果是三七总皂苷能显著诱导CYP1A2和CYP2E1酶活性和mRNA表达,同时对CYP2E1的蛋白表达水平也有显著诱导作用;三七总皂苷显著诱导CYP3A mRNA表达,但对CYP3A酶活性水平无明显的影响;三七总皂苷对CYP1A1和CYP2B mRNA表达和酶活性均无明显影响。三七总皂苷对不同的P450亚型的调节作用具有选择性,主要的调节亚型是CYP1A2和CYP2E1,临床应用时,尤其是与CYP1A2和CYP2E1代谢有关药物合用时,应充分考虑到可能产生的药物相互作用以避免潜在的不良反应和毒副作用,同时对CYP2E1的诱导作用是否与人参皂苷清除自由基作用有关值得进一步研究。

关 键 词:三七总皂苷  细胞色素P450  荧光定量PCR技术
收稿时间:2014-02-18

Effect of Panax notoginseng saponins on liver drug metablic enzyme activity, mrna and protein expressions in rats
CHEN Yan-jin,WANG Yu-guang,MA Zeng-chun,XIAO Cheng-rong,TAN Hong-ling,LIANG Qian-de,TANG Xiang-lin,ZHAO Yong-hong,WANG Dong-gen and GAO Yue. Effect of Panax notoginseng saponins on liver drug metablic enzyme activity, mrna and protein expressions in rats[J]. China Journal of Chinese Materia Medica, 2014, 39(19): 3824-3828
Authors:CHEN Yan-jin  WANG Yu-guang  MA Zeng-chun  XIAO Cheng-rong  TAN Hong-ling  LIANG Qian-de  TANG Xiang-lin  ZHAO Yong-hong  WANG Dong-gen  GAO Yue
Affiliation:College of Pharmacy, Central South University, Changsha 410000, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Blood Transfusion, Academy of Military Medical Sciences, Beijing 100850, China;Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China
Abstract:To study the effect of Panax notoginseng saponins(PNS) on liver drug metabolic enzyme activity, mRNA and protein expressions in rats. Male Wistar rats were randomly divided into nine groups. After administration of the test drugs, their liver microsomes, liver total RNA and total protein were extracted to detect the regulating effect of PNS on liver drug metabolic enzyme activity-related subtype enzymatic activity, mRNA and protein expression by substrate probe, quantitative PCR and Western Blot technology. The result of this experiment was that PNS could significantly induce CYP1A2 and CYP2E1 enzyme activity, mRNA expression, CYP2E1 protein expression level. PNS significantly induced CYP3A mRNA expression, but with no significant effect in CYP3A enzyme activity level. PNS had no significant effect CYP1A1 and CYP2B mRNA expressions and enzyme activity levels. PNS had selective regulations on different P450 subtypes, and the major subtypes were CYP1A2 and CYP2E1. In clinical practice, particularly in the combination with CYP1A2 and CYP2E1 metabolism-related drugs, full consideration shall be given to the possible drug interactions in order to avoid potential toxic and side effects. Meanwhile, whether the induction effect of CYP2E1 gets involved in ginsenoside's effect incavenging free radicals deserves further studies.
Keywords:Panax notoginseng saponins  cytochrome P450  fluorescent quantitation PCR technique
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