首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Effect of glucose/sulfonylurea interaction on release of insulin glucagon and somatostatin from isolated perfused rat pancreas.
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Effect of glucose/sulfonylurea interaction on release of insulin glucagon and somatostatin from isolated perfused rat pancreas.

机译:葡萄糖/磺酰脲相互作用对离体灌注大鼠胰腺中胰岛素胰高血糖素和生长抑素释放的影响。

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摘要

The effect of a sulfonylurea, glibenclamide, on the release of insulin, glucagon, and somatostatin was studied in the isolated perfused rat pancreas. At glucose concentrations of 1.1 mM or less, the drug stimulated somatostatin release, whereas glucagon release, after 2-3 min of increase, was markedly inhibited. Insulin release was moderately stimulated, and maximal release occurred relatively late. A moderate glucose load (6.7 mM) inhibited glibenclamide-induced release of somatostatin, whereas the two in combination exerted an additive action on insulin release. Greater glucose loads, which by themselves would stimulate somatostatin release, only marginally suppressed glibenclamide-induced somatostatin release. The insulinogenic effect of these glucose levels was not modified by glibenclamide. Glibenclamide may thus stimulate both the alpha and beta as well as delta cells of the pancreas, depending on glucose concentration. We suggest a paracrine (local) interaction of somatostatin with the alpha and beta cells, which has an important role in the kinetics of insulin and glucagon release induced by sulfonylureas.
机译:在分离的灌注大鼠胰腺中研究了磺酰脲,格列本脲对胰岛素,胰高血糖素和生长抑素释放的影响。在葡萄糖浓度为1.1 mM或更低的情况下,该药物刺激生长抑素释放,而在增加2-3分钟后,胰高血糖素的释放受到明显抑制。胰岛素释放受到中度刺激,最大释放发生的相对较晚。适度的葡萄糖负荷(6.7 mM)抑制了格列本脲诱导的生长抑素释放,而两者的结合对胰岛素释放产生加和作用。较高的葡萄糖负荷本身会刺激生长抑素的释放,仅略微抑制了格列本脲诱导的生长抑素的释放。格列本脲未改变这些葡萄糖水平的致胰岛素作用。因此,取决于葡萄糖浓度,格列本脲可以刺激胰腺的α和β细胞以及δ细胞。我们建议生长抑素与α和β细胞的旁分泌(局部)相互作用,这在磺酰脲类药物诱导的胰岛素和胰高血糖素释放动力学中具有重要作用。

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