Bishayee A, Banerjee K K, Chatterjee M
Department of Pharmaceutical Technology, Jadavpur University, Calcutta, India.
Riv Eur Sci Med Farmacol. 1995 Jan-Feb;17(1):19-26.
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.
在大鼠中评估了全球临床使用的药物人胎盘提取物(HPE)急性或亚慢性给药对肝脏药物代谢酶活性的影响。单次腹腔注射HPE(4 ml/kg)后,在不同时间段,肝微粒体细胞色素P-450(Cyt. P450)和细胞色素b5(Cyt. b5)含量以及胞质谷胱甘肽S-转移酶(GST)活性被最大程度诱导,而微粒体UDP-葡萄糖醛酸转移酶(UDPGT)活性则受到显著抑制。在治疗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水平以及GST活性,同时抑制UDPGT的活性,并且这些结果呈剂量依赖性。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。针对该药物长期治疗可能的致癌风险,讨论了上述看家酶水平和活性的观察变化。