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脂质输注诱导肝脏葡萄糖-6-磷酸酶基因表达。

Induction of hepatic glucose-6-phosphatase gene expression by lipid infusion.

作者信息

Massillon D, Barzilai N, Hawkins M, Prus-Wertheimer D, Rossetti L

机构信息

Diabetes Research and Training Center, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

Diabetes. 1997 Jan;46(1):153-7. doi: 10.2337/diab.46.1.153.

Abstract

The distal enzymatic step in the process of glucose output is catalyzed by the glucose-6-phosphatase (Glc-6-Pase) complex. The recently cloned catalytic unit of this complex has been shown to be regulated by insulin, dexamethasone, cAMP, and glucose. Using a combination of intralipid and/or nicotinic acid infusions and a pancreatic clamp technique, we maintained plasma free fatty acids (FFAs) at three different levels (0.26 +/- 0.07, 0.56 +/- 0.09, and 1.59 +/- 0.12 mmol/l) in the presence of well-controlled hormonal and metabolic conditions. An increase in the plasma FFA concentration within the physiological range caused a rapid, greater than threefold increase in the mRNA and protein levels of the catalytic subunit of Glc-6-Pase in the liver. These data indicate that the in vivo gene expression of Glc-6-Pase in the liver is regulated by circulating lipids independent of insulin and thus that prolonged hyperlipidemia may contribute to the increased production of glucose via increased expression of this protein.

摘要

葡萄糖输出过程中的远端酶促步骤由葡萄糖-6-磷酸酶(Glc-6-Pase)复合体催化。最近克隆出的该复合体催化单元已被证明受胰岛素、地塞米松、环磷酸腺苷(cAMP)和葡萄糖的调节。我们通过联合输注脂肪乳剂和/或烟酸并采用胰腺钳夹技术,在激素和代谢条件良好控制的情况下,将血浆游离脂肪酸(FFA)维持在三个不同水平(0.26±0.07、0.56±0.09和1.59±0.12 mmol/L)。生理范围内血浆FFA浓度的升高导致肝脏中Glc-6-Pase催化亚基的mRNA和蛋白质水平迅速增加超过三倍。这些数据表明,肝脏中Glc-6-Pase的体内基因表达受循环脂质调节,独立于胰岛素,因此长期高脂血症可能通过该蛋白表达增加导致葡萄糖生成增加。

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