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Am J Physiol Regul Integr Comp Physiol 279: R1224-R1229, 2000;
0363-6119/00 $5.00
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Vol. 279, Issue 4, R1224-R1229, October 2000

Intraportal glucose infusion and pancreatic islet blood flow in anesthetized rats

Per-Ola Carlsson, Masanori Iwase, and Leif Jansson

Department of Medical Cell Biology, Uppsala University, SE-751 23 Uppsala, Sweden

The aim of the study was to evaluate whether a selective increase in portal vein blood glucose concentration can affect pancreatic islet blood flow. Anesthetized rats were infused (0.1 ml/min for 3 min) directly into the portal vein with saline, glucose, or 3-O-methylglucose. The infused dose of glucose (1 mg · kg body wt-1 · min-1) was chosen so that the systemic blood glucose concentration was unaffected. Intraportal infusion of D-glucose increased insulin release and islet blood flow; the osmotic control substance 3-O-methylglucose had no such effect. A bilateral vagotomy performed 20 min before the infusions potentiated the islet blood flow response and also induced an increase in whole pancreatic blood flow, whereas the insulin response was abolished. Administration of atropine to vagotomized animals did not change the blood flow responses to intraportal glucose infusions. When the vagotomy was combined with a denervation of the hepatic artery, there was no stimulation of islet blood flow or insulin release after intraportal glucose infusion. We conclude that a selective increase in portal vein blood glucose concentration may participate in the islet blood flow increase in response to hyperglycemia. This effect is probably mediated via periarterial nerves and not through the vagus nerve. Furthermore, this blood flow increase can be dissociated from changes in insulin release.

pancreatic blood flow; hepatic glucoreceptors; denervation; vagus nerve


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