LIVER-INJURY BY THE FALSE MOREL POISON GYROMITRIN

被引:12
作者
BRAUN, R
GREEFF, U
NETTER, KJ
机构
[1] Institute of Pharmacology and Toxicology, University of Marburg
关键词
D O I
10.1016/0300-483X(79)90042-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
After oral application of the mushroom poison gyromitrin a time and dose dependent decrease of cytochrome P-450 was found in rat liver microsomes. The maximal decrease to about 50-60% of the control (after 200 mg/kg, 80% of LD50) was observed 8-12 h after application, a normalization after 48 h. The inhibition of cytochrome P-450 mediated metabolism of aminopyrine and p-nitroanisole corresponds to the decrease of cytochrome P-450. The specific activity of cytochrome P-450 remains unchanged while that of cytochrome P-448 is decreased as shown by means of the metabolism of ethoxycoumarin or ethoxyresorufin. Comparable results were obtained after application of N-methyl-N-formylhydrazine (MFH) which is formed from gyromitrin rapidly by hydrolysis. An attack on the endoplasmatic membrane with a stimulation of lipid peroxidation is discussed. © 1979.
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页码:155 / 163
页数:9
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