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Chloroform induction of ornithine decarboxylase activity in rats.

机译:在大鼠中氯仿诱导鸟氨酸脱羧酶活性。

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摘要

Chloroform is a drinking water contaminant that has been demonstrated to be carcinogenic to mice and rats resulting in an increased incidence of liver and kidney tumors, respectively. The mechanism of chloroform carcinogenicity might be by tumor initiation and/or promotion. Since induction of ornithine decarboxylase (ODC) activity has been proposed as a molecular marker for tumor promoters, we have investigated the effect of chloroform on ODC activity in rats. Chloroform induced a dose-dependent increase of hepatic ODC with an apparent threshold at 100 mg/kg body weight. Female rats were two to four times more susceptible to to chloroform. Upon daily dosing of chloroform for 7 days the liver became less susceptible, with the last dose of chloroform resulting in only 10% of the activity observed after a single dose. Nuclear RNA polymerase I activity was also induced by chloroform. Chloroform, rather than increasing the activity of renal ODC, resulted in a 35% reduction. The induction by chloroform of hepatic ODC activity might be associated with regenerative hyperplasia while the renal carcinogenicity of chloroform could not be demonstrated to be associated with ODC induction.
机译:三氯甲烷是一种饮用水污染物,已被证明对小鼠和大鼠具有致癌性,分别导致肝脏和肾脏肿瘤的发生率增加。氯仿致癌的机制可能是通过肿瘤的引发和/或促进。由于鸟氨酸脱羧酶(ODC)活性的诱导已被提出作为肿瘤启动子的分子标记,我们已经研究了氯仿对大鼠ODC活性的影响。三氯甲烷诱导肝ODC剂量依赖性增加,其表观阈值为100 mg / kg体重。雌性大鼠对氯仿的敏感性是后者的2至4倍。每天服用氯仿7天后,肝脏变得较不敏感,最后一剂氯仿导致单次给药后仅观察到10%的活性。氯仿也可诱导核RNA聚合酶I活性。三氯甲烷没有增加肾脏ODC的活性,而是减少了35%。氯仿诱导肝ODC活性可能与再生增生有关,而氯仿的肾致癌性不能被证明与ODC诱导有关。

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