[Participation of the cytochrome P450-dependent biotransformation system in realizing the toxic effects of acrylamide].

Voprosy meditsinskoi khimii Pub Date : 2000-03-01
T A Romanova
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Abstract

Neuro-, hepato- and geno-toxic effects of the industrial xenobiotic, acrylamide, were studied in intact rats and in rats with induced phenobarbital- and 3-methylholanthren-dependent isoforms of cytochrome P-450. The induction of the first isoform increased neuro- and hepato-toxic effects of acrylamide and decreased the extent of cell genome damage. Activation of the 3-methylholanthren-dependent cytochrome had no influence on the toxicity of this xenobiotic. Realisation of toxic effects of acrylamide may involve a decrease of the carbohydrate energy metabolism, but in the intact organism these processes precede the induction of the phenobarbital-dependent cytochrome P450.

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[细胞色素p450依赖性生物转化系统在实现丙烯酰胺毒性作用中的参与]。
在完整的大鼠和诱导细胞色素P-450依赖苯巴比妥和3-甲基蒽醌异构体的大鼠中,研究了工业外源物丙烯酰胺的神经、肝和基因毒性作用。第一种异构体的诱导增加了丙烯酰胺的神经和肝毒性作用,降低了细胞基因组损伤的程度。3-甲基蒽醌依赖性细胞色素的激活对这种外源药物的毒性没有影响。丙烯酰胺的毒性作用的实现可能涉及碳水化合物能量代谢的减少,但在完整的生物体中,这些过程先于苯巴比妥依赖性细胞色素P450的诱导。
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