膳食锌缺乏对fisher -344大鼠药物代谢I期和II期相关酶活性的影响:锌缺乏对药物代谢酶活性的影响

Drug-nutrient interactions Pub Date : 1988-01-01
V Jagadeesan, F Oesch
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引用次数: 0

摘要

进行了一项研究,以测定锌缺乏症的各种I期和II期药物代谢酶。对断奶雄性Fischer大鼠进行为期7周的缺锌治疗。对照组和缺锌组的锌水平分别为30 mg/kg和1.1 mg/kg。在实验结束时,测定各种肝细胞质和微粒体酶的活性。观察到微粒体环氧化物水解酶(以苯(a)芘4-5氧化物为底物)、尿苷二磷酸葡萄糖醛基转移酶(以1-萘酚为底物)和胞质谷胱甘肽- s转移酶(以氯二硝基苯为底物)的活性仅因缺锌而改变。以下酶的活性发生了变化,这可能是由于缺乏锌和/或食物限制造成的:1)芳烃羟化酶;2)细胞色素b;3)细胞色素c;4)细胞色素b5。研究的其他酶,即胞质环氧化水解酶,微粒体EHSTO和UDPGT睾酮在对照组和实验组中没有差异。研究结果与锌缺乏致癌物的激活和肿瘤的形成有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of dietary zinc deficiency on the activity of enzymes associated with phase I and II of drug metabolism in Fischer-344 rats: activities of drug metabolising enzymes in zinc deficiency.

A study was undertaken to assay the various phase I and phase II drug metabolising enzymes in zinc deficiency. Male weanling Fischer rats were subjected to zinc deficiency for a period of 7 weeks. Zinc levels in the control and deficient diets were 30 mg and 1.1 mg/kg diet, respectively. At the end of the experimental period, the activities of various hepatic cytosolic and microsomal enzymes were estimated. It was observed that the activities of microsomal epoxide hydrolase (with benz(a)pyrene 4-5 oxide as substrate), uridine diphospho glucuronyl transferase (with 1-naphthol as substrate) and cytosolic glutathione-S-transferase (with chlorodinitrobenzene as substrate) were altered exclusively due to zinc deficiency. There was a change in the activities of the following enzymes, which could be due either to zinc deficiency and/or food restriction: 1) aryl hydrocarbon hydroxylase; 2) cytochrome b; 3) cytochrome c; and 4) cytochrome b5. Other enzymes studied, i.e., cytosolic epoxide hydrolases, microsomal EHSTO, and UDPGT testosterone were not different in the control and experimental groups. The results are discussed in relation to the activation of carcinogens and neoplastic formation in zinc deficiency.

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