Protein Feeding Promotes Redistribution of Endogenous Glucose Production to the Kidney and Potentiates Its Suppression by Insulin

被引:53
作者
Pillot, Bruno
Soty, Maud
Gautier-Stein, Amandine
Zitoun, Carine
Mithieux, Gilles
机构
[1] INSERM, U855, F-69008 Lyon, France
[2] Univ Lyon, F-69008 Lyon, France
[3] Univ Lyon 1, F-69622 Villeurbanne, France
关键词
RAT SMALL-INTESTINE; BLOOD-GLUCOSE; PHOSPHATASE-ACTIVITY; MESSENGER-RNA; FOOD-INTAKE; LIVER; GLUCONEOGENESIS; GLUCOSE-6-PHOSPHATASE; METABOLISM; GENE;
D O I
10.1210/en.2008-0601
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to assess in rats the effect of protein feeding on the: 1) distribution of endogenous glucose production (EGP) among gluconeogenic organs, and 2) repercussion on the insulin sensitivity of glucose metabolism. We used gene expression analyses, a combination of glucose tracer dilution and arteriovenous balance to quantify specific organ release, and hyper-insulinemic euglycemic clamps to assess EGP and glucose uptake. Protein feeding promoted a dramatic induction of the main regulatory gluconeogenic genes (glucose-6 phosphatase and phosphoenolpyruvate carboxykinase) in the kidney, but not in the liver. As a consequence, the kidney glucose release was markedly increased, compared with rats fed a normal starch diet. Protein feeding ameliorated the suppression of EGP by insulin and the sparing of glycogen storage in the liver but had no effect on glucose uptake. Combined with the previously reported induction of gluconeogenesis in the small intestine, the present work strongly suggests that a redistribution of glucose production among gluconeogenic organs might occur upon protein feeding. This phenomenon is in keeping with the improvement of insulin sensitivity of EGP, most likely involving the hepatic site. These data shed a new light on the improvement of glucose tolerance, previously observed upon increasing the amount of protein in the diet, in type 2 diabetic patients. ( Endocrinology 150: 616-624, 2009)
引用
收藏
页码:616 / 624
页数:9
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