苯对苯巴比妥治疗大鼠混合功能氧化酶影响的年龄相关差异。

A Plewka, D Plewka, M Kamiński
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引用次数: 0

摘要

实验对象为5、10、30、60和540日龄雌性Wistar大鼠。分别给予苯巴比妥(50 mg/kg体重)和苯(250 mg/kg体重)腹腔注射。在光滑(SER)和粗糙(RER)的肝微粒体中,研究了混合功能氧化酶的活性。较早的苯巴比妥诱导降低了苯的负影响。在所有被检查的动物中,蛋白质、细胞色素P-450和去甲基酶4-氨基吡啶活性均观察到这一点。仅对nadph -细胞色素bs和nadh -细胞色素bs还原酶活性的抑制作用部分下降,苯巴比妥对苯的抑制作用无显著影响。
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Age associated differences in effects of benzene on mixed-function oxidases in phenobarbital-treated rats.

These studies were performed on 5, 10, 30, 60 and 540 days old female Wistar rats. The animals were treated i.p. with phenobarbital (50 mg/kg body weight) and benzene (250 mg/kg body weight). In smooth (SER) and rough (RER) hepatic microsomes, the mixed function oxidases activity were studied. The earlier phenobarbital induction decreased the negative benzene influence. In all examined animals this was observed for protein, cytochrome P-450, and demethylase 4-aminopyrine activities. A partial decrease of inhibition was noticed only for activities of NADPH-cytochrome bs and NADH-cytochrome bs reductase activities, phenobarbital did not significantly change the effect of benzene.

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International Code of Ethics for occupational health professionals. International conference on peripheral nerve toxicity. (12-13 June, 1993, Kanazawa, Japan). Increased urinary excretion of the oxidative DNA adduct, 8-hydroxydeoxyguanosine, as a possible early indicator of occupational cancer hazards in the asbestos, rubber, and azo-dye industries. Computer-aided methods for evaluating cancer risk in miners due to radiation exposure. Mutagenicity of B(a)P in the presence of some hydralazine derivatives.
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