Effects of human placental extract on hepatic drug metabolizing enzyme.

A Bishayee, K K Banerjee, M Chatterjee
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Abstract

Effects of acute or subchronic administration of human placental extract (HPE), a worldwide clinically used agent, on hepatic drug metabolizing enzyme activities were evaluated in rats. Hepatic microsomal cytochrome P-450 (Cyt. P450) and cytochrome b5 (Cyt. b5) contents and cytosolic glutathione S-transferase (GST) activities were maximally induced after various periods of time following a single intraperitoneal injection of HPE (4 ml/kg) whereas microsomal UDP-glucuronyltransferase (UDPGT) activities were inhibited significantly. All these altered effects were returned almost to the basal levels after 96 h of treatment. Subchronic treatment (30 days) with HPE (1,2 or 4 ml/kg) afforded a significant induction of Cyt. P-450 and Cyt. b5 levels and that of GST activities with a concurrent suppression of the activities of UDPGT and these results were found to be dose-dependent. However, microsomal NADPH cytochrome c reductase activity was not affected either by acute or subchronic treatment. The observed variations in the levels and activities of above house-keeping enzymes were discussed in relation to the possible carcinogenic risk of long-term treatment with this pharmaceutical agent.

人胎盘提取物对肝脏药物代谢酶的影响。
研究了急性或亚慢性给药人胎盘提取物(HPE)对大鼠肝脏药物代谢酶活性的影响。肝微粒体细胞色素P-450。P450)和细胞色素b5 (Cyt。b5)单次腹腔注射HPE (4 ml/kg)后,不同时间对细胞内谷胱甘肽s -转移酶(GST)活性和细胞内谷胱甘肽s -转移酶(GST)含量的影响最大,而对微体内udp -葡萄糖醛酸转移酶(UDPGT)活性的影响显著。在处理96小时后,所有这些改变的效应几乎恢复到基础水平。用HPE(1、2或4 ml/kg)进行亚慢性治疗(30天)可显著诱导Cyt。P-450和Cyt。b5水平和GST活性同时抑制UDPGT活性,这些结果被发现是剂量依赖性的。然而,微粒体NADPH细胞色素c还原酶活性不受急性或亚慢性治疗的影响。观察到的上述管家酶的水平和活动的变化,讨论了与长期使用这种药物治疗可能的致癌风险的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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