首页> 外文期刊>Japanese Journal of Pharmacology >COMPARISON OF EFFECTS OF ACETAMINOPHEN ON LIVER MICROSOMAL DRUG METABOLISM AND LIPID PEROXIDATION IN RATS AND MICE
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COMPARISON OF EFFECTS OF ACETAMINOPHEN ON LIVER MICROSOMAL DRUG METABOLISM AND LIPID PEROXIDATION IN RATS AND MICE

机译:乙胺磷对大鼠和小鼠肝微粒体代谢和脂质过氧化作用的比较

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References(18) Cited-By(3) Studies were conducted to determine the in vivo effect of acetaminophen (AAP) on the lipid peroxidation, drug metabolizing enzyme activity and microsomal electron transfer system of rat and mouse liver. AAP was found to inhibit ethylmorphine N-demethylase activity in the presence of NADPH and this inhibition of the enzyme was due to decrease in cytochrome P-450 content, but not due to change in lipid peroxidation in liver microsomes. Kinetical data showed that AAP administration had no effect on Km values of ethylmorphine N-demethylase, however, a decrease in the Vmax values was seen in rats and mice. There was no significant effect of AAP on both NADPH-cytochrome c reductase and the content of cytochrome b5 3 hours after this administration to rats and mice. On the other hand, AAP induced a significant decrease in NADH-ferricyanide reductase in mice, but not in rats. The greatest decrease in cytochrome P-450 was observed among the components of the liver microsomal electron transfer system of rats and mice.
机译:参考文献(18)引用了By(3)进行研究以确定对乙酰氨基酚(AAP)对大鼠和小鼠肝脏脂质过氧化,药物代谢酶活性和微粒体电子转移系统的体内作用。发现在NADPH存在下,AAP抑制乙基吗啡N-脱甲基酶活性,这种抑制作用是由于细胞色素P-450含量降低,而不是由于肝微粒体脂质过氧化作用的改变。运动学数据表明,AAP给药对乙基吗啡N-脱甲基酶的Km值没有影响,但是,在大鼠和小鼠中发现Vmax值降低。在对大鼠和小鼠给药后3小时,AAP对NADPH-细胞色素c还原酶和细胞色素b5的含量均无显着影响。另一方面,AAP在小鼠中诱导了NADH-铁氰化物还原酶的显着降低,但在大鼠中却没有。在大鼠和小鼠的肝微粒体电子转移系统的组成部分中,细胞色素P-450的减少最大。

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