母鼠消耗乙醇对后代的肝毒性:乙醇氧化系统个体发育研究的评估。

Alcohol and drug research Pub Date : 1987-01-01
B Rovinski, E A Hosein, H Lee, G L Hin, N K Rastogi
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引用次数: 0

摘要

研究了母体长期摄入乙醇对大鼠肝脏乙醇氧化系统发育的影响。在妊娠第19天首次检测乙醇脱氢酶(ADH)活性。然后迅速增加,在出生后第14天达到成人水平。该酶的个体发生模式、比活性及其对底物或辅因子的亲和力不受母体慢性乙醇消耗的影响。肝微粒体细胞色素P-450含量在出生前首次检测到微量。然后在出生后的前10天迅速增加。母体慢性乙醇摄入不影响发育模式,但诱导P-450在整个出生后检测总量的增加。在胎儿和出生后肝脏中发现脂肪堆积,似乎与胎儿ADH氧化乙醇的新能力有关。ADH和微粒体乙醇氧化系统的晚期出现表明胎儿肝脏将完全依赖于母体氧化子宫内乙醇的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatotoxicity of maternal ethanol consumption in rat offspring: an assessment with a study of the ontogenetic development of ethanol-oxidizing systems.

The effect of chronic maternal ethanol ingestion on the ontogenetic development of rat hepatic ethanol-oxidizing systems was investigated. Alcohol dehydrogenase (ADH) activity was first detected at day 19 of gestation. It then increased rapidly to reach adult levels by day 14 postnatally. The ontogenetic pattern, the specific activity and the affinity of the enzyme for its substrate or cofactor were not affected by chronic maternal ethanol consumption. Hepatic microsomal cytochrome P-450 content was first detected in trace amounts just prior to birth. It then increased rapidly in the first 10 days postnatally. Chronic maternal ethanol ingestion did not affect the developmental pattern but induced an increase in the total amount of P-450 detected throughout the postnatal period studied. Fat accumulation was found in fetal and postnatal livers and appeared to correlate with the emerging ability to oxidize ethanol by fetal ADH. The late appearance of the ADH and microsomal ethanol-oxidizing systems indicates that the fetal liver would be entirely dependent on maternal mechanisms to oxidize in-utero ethanol.

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