Nordquist Lina, Lai En Yin, Sjöquist Mats, Jansson Leif, Persson A Erik G
Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Diabetes Metab Res Rev. 2008 Feb;24(2):165-8. doi: 10.1002/dmrr.805.
Pancreatic islet blood flow is regulated separately from that of the exocrine pancreas, and a consistent finding during impaired glucose tolerance is an increased blood perfusion. The aim of the present study was to investigate whether C-peptide affects pancreatic islet arterioles in normal and diabetic mice.
Control and diabetic C57-Bl mice were studied after 2 weeks of alloxan-induced diabetes. Islet arterioles were dissected and microperfused with Dulbecco's modified Eagle medium (DMEM) solution. The effect of luminal application of mouse C-peptide was investigated.
C-peptide reduced the diameter of islet arterioles from diabetic mice (-10+/-4%, P<0.05) compared to base-line values, whilst arterioles from normoglycaemic animals did not respond to C-peptide (P=0.2).
These findings suggest a role for C-peptide in the regulation of islet blood flow, especially during conditions with impaired glucose tolerance.
胰岛血流的调节与外分泌胰腺的血流调节相互独立,糖耐量受损期间的一个一致发现是血液灌注增加。本研究的目的是调查C肽是否影响正常和糖尿病小鼠的胰岛小动脉。
对用四氧嘧啶诱导糖尿病2周后的对照和糖尿病C57-Bl小鼠进行研究。解剖胰岛小动脉,并用杜氏改良 Eagle 培养基(DMEM)溶液进行微量灌注。研究了向管腔内应用小鼠C肽的效果。
与基线值相比,C肽使糖尿病小鼠胰岛小动脉的直径减小(-10±4%,P<0.05),而血糖正常动物的小动脉对C肽无反应(P=0.2)。
这些发现表明C肽在调节胰岛血流中起作用,尤其是在糖耐量受损的情况下。