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慢性胃肠外给予碳水化合物对大鼠肝脏药物代谢的影响。

Effects of chronic parenteral carbohydrate administration on hepatic drug metabolism in the rat.

作者信息

Hartshorn R D, Demers L M, Sultatos L G, Vesell E S, Lang C M, Hughes H C

出版信息

Pharmacology. 1979;18(2):103-11. doi: 10.1159/000137237.

Abstract

Effects of chronic parenteral carbohydrate administration on hepatic microsomal enzyme activity were studied in the rat. Intraperitoneal injections of either glucose or fructose (2.88 g daily for 7 days) significantly decreased hepatic cytochrome P-450 content and ethylmorphine N-demethylase and aniline hydroxylase activities. By the 5th day, cytochrome P-450 content decreased to 70-76% and ethylmorphine N-demethylase activity to 66-69% of control values. Aniline hydroxylase activity was not significantly altered until the 7th day, by which time it was 77-79% of control values. In vivo assessment of hepatic drug-metabolizing capacity using antipyrine as a test drug confirmed these decreases observed in vitro. Two major conclusions of these experiments are that such variables as time and dose of carbohydrate administration can affect the magnitude of the changes produced and that each parameter measured exhibited a distinctive pattern of change with time. Chronic carbohydrate administration produced hepatic fatty infiltration and glycogen depletion. Since all groups received identical amounts of specific nutrients, fatty infiltration was probably due to increased lipogenesis with decreased hepatic oxidative metabolism of fat. During these experiments neither hypoinsulinemia nor increased levels of cyclic AMP were observed. The molecular mechanisms responsible for hepatic glycogen depletion and decreased MFO activities remain to be established.

摘要

在大鼠中研究了长期胃肠外给予碳水化合物对肝微粒体酶活性的影响。腹腔注射葡萄糖或果糖(每天2.88克,共7天)显著降低了肝细胞色素P-450含量以及N-脱甲基酶和苯胺羟化酶的活性。到第5天,细胞色素P-450含量降至对照值的70%-76%,N-脱甲基酶活性降至对照值的66%-69%。苯胺羟化酶活性直到第7天才有显著变化,此时为对照值的77%-79%。以安替比林作为测试药物对肝脏药物代谢能力进行的体内评估证实了体外观察到的这些降低。这些实验的两个主要结论是,诸如碳水化合物给药的时间和剂量等变量会影响所产生变化的幅度,并且所测量的每个参数都呈现出随时间变化的独特模式。长期给予碳水化合物会导致肝脏脂肪浸润和糖原耗竭。由于所有组接受的特定营养素量相同,脂肪浸润可能是由于脂肪生成增加以及肝脏对脂肪的氧化代谢减少所致。在这些实验过程中,未观察到低胰岛素血症或环磷酸腺苷水平升高。导致肝脏糖原耗竭和微粒体混合功能氧化酶(MFO)活性降低的分子机制仍有待确定。

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