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Glucose generates coincident insulin and somatostatin pulses and antisynchronous glucagon pulses from human pancreatic islets.

机译:葡萄糖产生重合的胰岛素和生长抑制素脉冲和来自人胰岛胰岛的抗生素胰胰酚。

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摘要

The kinetics of insulin, glucagon and somatostatin release was studied in human pancreatic islets. Batches of 10-15 islets were perifused and the hormones measured with RIA in 30-sec fractions. Increase of glucose from 3 to 20 mm resulted in a brief pulse of glucagon coinciding with suppression of basal insulin and somatostatin release. There was a subsequent drop of glucagon release concomitant with the appearance of a pronounced pulse of insulin and a slightly delayed pulse of somatostatin. Continued exposure to 20 mm glucose generated pulsatile release of the three hormones with 7- to 8-min periods accounting for 60-70% of the secreted amounts. Glucose caused pronounced stimulation of average insulin and somatostatin release. However, the nadirs between the glucagon pulses were lower than the secretion at 3 mm glucose, resulting in 18% suppression of average release. The repetitive glucagon pulses were antisynchronous to coincident pulses of insulin and somatostatin. The resulting greater than 20-fold variations of the insulin to glucagon ratio might be essential for minute-to-minute regulation of the hepatic glucose production.
机译:在人胰岛胰岛中研究了胰岛素,胰高血糖素和生长抑素释放的动力学。已经泛化了10-15个胰岛的批次,并用RIA在30秒馏分中测量激素。从3到20毫米的葡萄糖的增加导致了胰高血糖素的短暂脉冲,与抑制基底胰岛素和生长抑制素释放。随后的胰高血糖素释放伴随着外观的胰岛素的外观和生长抑制素的略微延迟脉冲。持续暴露于20毫米葡萄糖产生的三个激素的脉动释放,7-8分钟,占分泌量的60-70%。葡萄糖引起平均胰岛素和生长抑素释放的发音刺激。然而,胰高血糖素脉冲之间的Nadirs低于3mm葡萄糖的分泌,导致平均释放的18%抑制。重复性胰高血糖素脉冲是胰岛素和生长抑素的一致脉冲的反异步。由此产生的胰岛素与胰高血糖素比的20倍变化可能对肝葡萄糖产生的微小细微调节至关重要。

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