Colella R M, Bonner-Weir S, Braunstein L P, Schwalke M, Weir G C
Life Sci. 1985 Sep 16;37(11):1059-65. doi: 10.1016/0024-3205(85)90597-1.
Glucose metabolism and insulin secretion were studied in isolated rat pancreatic islets of different sizes and the amount of tissue was quantitated by the measurement of DNA. It was found that larger islets (140-210 ng DNA/islet) utilized more glucose (based on the conversion of 3H-5-glucose to [3H]20) per ng of DNA than islets containing less DNA (60-120 ng/islet). However, the insulin secreted per ng of DNA in response to a given glucose concentration was the same in islets of all sizes. Also, the islet insulin and glucagon content when expressed in terms of DNA did not depend upon islet size. Thus, although glucose utilization rates expressed as a function of islet DNA content were greater in larger islets, no such relationship was found for glucose-induced insulin release or insulin and glucagon content.
在分离出的不同大小的大鼠胰岛中研究了葡萄糖代谢和胰岛素分泌,并通过测量DNA对组织量进行了定量。结果发现,较大的胰岛(140 - 210 ng DNA/胰岛)每ng DNA利用的葡萄糖(基于3H - 5 - 葡萄糖转化为[3H]20)比含DNA较少的胰岛(60 - 120 ng/胰岛)更多。然而,在所有大小的胰岛中,每ng DNA对给定葡萄糖浓度反应分泌的胰岛素量是相同的。此外,以DNA表示的胰岛胰岛素和胰高血糖素含量并不取决于胰岛大小。因此,尽管以胰岛DNA含量为函数表示的葡萄糖利用率在较大的胰岛中更高,但在葡萄糖诱导的胰岛素释放或胰岛素和胰高血糖素含量方面未发现这种关系。