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幼鼠小肠黏膜中酮体生成及磷酸烯醇式丙酮酸羧激酶活性的调节

Regulation of ketone formation and phosphoenolpyruvate carboxykinase activity in the small intestinal mucosa of infant rats.

作者信息

Hahn P, Taller M, Srubiski L, Kirby L

机构信息

Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada.

出版信息

Biol Neonate. 1991;60(1):1-6. doi: 10.1159/000243382.

DOI:10.1159/000243382
PMID:1912094
Abstract

We studied the effect of different hormones added in vivo or in vitro on ketogenesis and phosphoenolpyruvate carboxykinase (PEPCK) activity in the small intestinal mucosa of suckling rats. Injection of insulin or dexamethasone in vivo or of an antiglucagon antiserum decreased the rate of ketone formation in the mucosa whereas injection of anti-insulin antiserum led to increased mucosal ketogenesis. PEPCK activity in the mucosa was decreased by the antiglucagon serum but was not affected by insulin or anti-insulin serum injections. Both liver and brown fat PEPCK responded as expected with the activity being elevated by anti-insulin serum and depressed by both insulin and antiglucagon serum. In the in vitro experiments, no effect of any of the agents on PEPCK was found. Ketone formation was suppressed in vitro by insulin or dexamethasone addition to the medium.

摘要

我们研究了体内或体外添加不同激素对乳鼠小肠黏膜生酮作用及磷酸烯醇式丙酮酸羧激酶(PEPCK)活性的影响。体内注射胰岛素或地塞米松,或注射抗胰高血糖素抗血清,均可降低黏膜中的酮生成速率,而注射抗胰岛素抗血清则会导致黏膜生酮作用增强。抗胰高血糖素血清可降低黏膜中的PEPCK活性,但胰岛素或抗胰岛素血清注射对其无影响。肝脏和棕色脂肪中的PEPCK活性变化符合预期,抗胰岛素血清可使其活性升高,胰岛素和抗胰高血糖素血清均可使其活性降低。在体外实验中,未发现任何一种试剂对PEPCK有影响。向培养基中添加胰岛素或地塞米松可在体外抑制酮生成。

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Biol Neonate. 1991;60(1):1-6. doi: 10.1159/000243382.
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引用本文的文献

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Biochem J. 1999 Mar 15;338 ( Pt 3)(Pt 3):569-82.
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The effect of dexamethasone treatment on the expression of the regulatory genes of ketogenesis in intestine and liver of suckling rats.地塞米松治疗对乳鼠肠道和肝脏中酮体生成调节基因表达的影响。
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Developmental changes in mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase gene expression in rat liver, intestine and kidney.
大鼠肝脏、肠道和肾脏中线粒体3-羟基-3-甲基戊二酰辅酶A合酶基因表达的发育变化。
Biochem J. 1993 Jun 1;292 ( Pt 2)(Pt 2):493-6. doi: 10.1042/bj2920493.