Siddiqui M K, Anjum F, Qadri S S
Toxicology Unit, Regional Research Laboratory, Hyderabad A.P., India.
J Environ Sci Health B. 1987 Oct;22(5):553-64. doi: 10.1080/03601238709372572.
Effects of three different doses of endosulfan respectively designated as low, medium and high on cytochrome P450(Cyt.P450), glutathione S-transferase(GST) activity and glutathione content (GSH) of hepatic and extra hepatic tissues of rat were determined after 24 hours of treatment. Endosulfan caused induction of cyt. P450 in liver, lung and brain at all the three doses tested while in kidney, spleen and heart either induction or reduction took place and was unrelated with dosages of endosulfan. Similarly, GST activity significantly changed in extra hepatic tissues while liver GST activity did not record any significant alteration under the experimental conditions. The GSH content also showed changes (increase/decrease) unrelated to endosulfan dosages in different organs. Thus, the effects varied with organ and dosages. As these metabolic parameters are involved in biotransformation of many endogenous molecules as well, the study may throw some light on physiological disturbances due to changes in metabolizing system on one side and organ specificity in toxic action of endosulfan on the other.
在处理24小时后,测定了分别标记为低、中、高剂量的三种不同剂量硫丹对大鼠肝脏和肝外组织细胞色素P450(Cyt.P450)、谷胱甘肽S-转移酶(GST)活性及谷胱甘肽含量(GSH)的影响。在所测试的所有三种剂量下,硫丹均能诱导肝脏、肺和脑中的细胞色素P450,而在肾脏、脾脏和心脏中,要么发生诱导要么发生降低,且与硫丹剂量无关。同样,肝外组织中的GST活性显著变化,而在实验条件下肝脏GST活性未记录到任何显著改变。不同器官中GSH含量也呈现出与硫丹剂量无关的变化(增加/减少)。因此,其影响因器官和剂量而异。由于这些代谢参数也参与许多内源性分子的生物转化,该研究一方面可能揭示代谢系统变化引起的生理紊乱,另一方面可能揭示硫丹毒性作用的器官特异性。