Stümpel F, Kucera T, Gardemann A, Jungermann K
Institute of Biochemistry and Molecular Cell Biology, Georg-August University, Göttingen, Germany.
Gastroenterology. 1996 Jun;110(6):1863-9. doi: 10.1053/gast.1996.v110.pm8964412.
BACKGROUND & AIMS: Insulin exerts a strict short-term control of glucose disappearance by glucose storage as well as degradation in the liver and peripheral insulin target tissues, but an acute control of glucose appearance by glucose absorption in the intestine is as yet unknown. The aim of the present study was to evaluate, whether insulin acutely modulates intestinal glucose absorption.
In the isolated, nonrecirculating joint perfusion of the small bowel and liver of the rat via the celiac trunc and the superior mesenteric artery, glucose absorption was examined without and with infusion of insulin via the portal vein.
Portal insulin enhanced acutely intestinal glucose absorption. This thus far unknown stimulatory effect of portal insulin was dose-dependent and detectable at physiological insulin concentrations. Atropine infused into the superior mesenteric artery completely prevented the insulin-dependent increase in intestinal glucose absorption, and carbachol caused a similar increase as portal insulin.
Portal insulin dose-dependently generated a signal in the liver or portal vein. This signal was transmitted in a retrograde direction against the blood stream in the portal vein to the small intestine via hepatoenteral muscarinic nerves. This signal markedly increased intestinal glucose absorption.
胰岛素通过在肝脏和外周胰岛素靶组织中储存和降解葡萄糖,对葡萄糖消失发挥严格的短期控制作用,但胰岛素是否对肠道葡萄糖吸收导致的葡萄糖出现进行急性控制尚不清楚。本研究的目的是评估胰岛素是否能急性调节肠道葡萄糖吸收。
在大鼠小肠和肝脏通过腹腔干和肠系膜上动脉进行的离体、非循环联合灌注中,在不通过门静脉输注胰岛素和通过门静脉输注胰岛素的情况下检测葡萄糖吸收情况。
门静脉胰岛素能急性增强肠道葡萄糖吸收。门静脉胰岛素这种迄今为止未知的刺激作用呈剂量依赖性,在生理胰岛素浓度下即可检测到。注入肠系膜上动脉的阿托品完全阻止了胰岛素依赖的肠道葡萄糖吸收增加,而卡巴胆碱引起的增加与门静脉胰岛素相似。
门静脉胰岛素在肝脏或门静脉中剂量依赖性地产生一个信号。该信号通过肝肠毒蕈碱神经逆着门静脉中的血流方向传递至小肠。该信号显著增加肠道葡萄糖吸收。