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Biochemical effects of three carcinogenic chlorinated methanes in rat liver

机译:三种致癌氯化甲烷在大鼠肝脏中的生化作用

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AbstractThree chlorinated methanes, carbon tetrachloride, chloroform, and methylene chloride, known to cause liver tumors in rodents, were given by oral gavage to adult female rats both 21 h and 4 h before sacrifice. Then hepatic DNA damage, ornithine decarboxylase (ODC), cytochrome P‐450, glutathione content, and serum alanine aminotransferase (SGPT) activity assays were performed. Carbon tetrachloride increased rat hepatic ODC activity and decreased cytochrome P‐450 content at doses both below and above cytotoxicity (as measured by increased SGPT activity). At 54 and 160 mg/kg, chloroform increased hepatic ODC activity with minimal or no elevation in SGPT activity. At 480 mg/kg chloroform increased hepatic ODC and SGPT activity. A dose of 1,275 mg/kg methylene chloride caused a small, but significant amount of hepatic DNA damage. When these three compounds are compared on either an equimolar or equitoxic (1/5 LD50) basis, their ability to induce hepatic ODC or increase SGPT activity was carbon tetrachloride>chloroform>methylene chloride. The results of this biochemical study are interpreted with respect to the ability of chemicals to cause hepatic cancer by either genetic or epigenetic mechani
机译:摘要 以成年雌性大鼠为原料,分别在处死前21 h和4 h口服强饲法对成年雌性大鼠给予已知可引起啮齿动物肝肿瘤的3种氯化甲烷、四氯化碳、氯仿和二氯甲烷。然后进行肝DNA损伤、鸟氨酸脱羧酶(ODC)、细胞色素P-450、谷胱甘肽含量和血清丙氨酸氨基转移酶(SGPT)活性测定。四氯化碳在低于和高于细胞毒性的剂量下增加大鼠肝脏ODC活性并降低细胞色素P-450含量(通过增加SGPT活性测量)。在 54 和 160 mg/kg 时,氯仿增加了肝脏 ODC 活性,而 SGPT 活性升高极少或没有升高。在480mg/kg氯仿时,肝脏ODC和SGPT活性增加。1,275 mg/kg 二氯甲烷的剂量会引起少量但大量的肝脏 DNA 损伤。当在等摩尔或等毒性(1/5 LD50)的基础上比较这三种化合物时,它们诱导肝脏ODC或增加SGPT活性的能力是四氯化碳>氯仿>二氯甲烷。这项生化研究的结果被解释为化学物质通过遗传或表观遗传机制引起肝癌的能力

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