摘要
目的:研究虎杖苷(polydatin)对肝脏药物代谢酶的影响。方法:小鼠灌服虎杖苷240、120和60mg/kg,给药7天,测定肝微粒体细胞色素P450、b5含量和NADPH细胞色素c还原酶、尿苷二磷酸葡萄糖醛酸转移酶(UDPGT)和谷胱甘肽-S-转移酶(GST)活性。结果:小鼠连续多次灌服虎杖苷后可显著提高其肝脏蛋白质含量,肝指数、肝微粒体细胞色素P450、b5含量和NADPH细胞色素c还原酶活性未见明显变化,肝GST和UDPGT活性显著下降。结论:虎杖苷对小鼠肝微粒体Ⅰ相酶没有明显作用,但抑制II相酶UDPGT和GST。
To observe the effects of polyda.tin on cytochrome P450 and phase Ⅱ transferase. Methods: Polydatin was administered at 60,120,240mg/kg · d in mice for seven days orally. Then total eytochrome P450 and b5 contents, NADPH-eytoehrome P450 reduetase and activities of phase il transferase were detected by speetrophotometer respectively. Results: Compared with the control group, polydatin increased protein content of liver significantly, while didnt affect the hver index, total P450 and b5 contents and the activity of NADPH-eytochrome P450 reduetase( P 〉0.05 ). And activities of GST and UDPGT in liver mierosome were decreased significantly by polydatin (P 〈 0. 01 ), Conclusion: Polydatin has no obvious influence on phase I transferase contents, while it has strong inhibition effects on activities of GST and UDPGT in the mice liver.
出处
《中药药理与临床》
CAS
CSCD
北大核心
2007年第2期12-14,共3页
Pharmacology and Clinics of Chinese Materia Medica