Suppr超能文献

非肥胖和肥胖男性中胰岛素反馈抑制的缺乏。

Lack of insulin feedback inhibition in non-obese and obese men.

作者信息

Peiris A N, Stagner J I, Vogel R L, Samols E, Nakagawa A

机构信息

Department of Medicine, University of Louisville, KY 40202.

出版信息

Metabolism. 1993 Mar;42(3):371-5. doi: 10.1016/0026-0495(93)90089-7.

Abstract

The existence of insulin feedback inhibition is a controversial issue. The present study adopted a novel approach to determine whether insulin feedback inhibition exists in vivo during physiologic hyperinsulinemia and if it could contribute to enhanced insulin secretion in obesity. Serial plasma insulin and C-peptide levels were determined during a basal state and a hyperinsulinemic clamp (287 pmol/min/m2) and following discontinuation of the insulin infusion under euglycemic conditions. Insulin secretion rates were derived from plasma C-peptide levels and individual C-peptide kinetics using a two-compartment model. Eight non-obese and nine obese men were recruited for the studies, which were performed in random order. Men with significant variations in glucose levels during hyperinsulinemia were excluded from the analysis. Plasma glucose levels were similar between the non-obese and obese groups during all phases of the study, and similar plasma insulin levels were achieved in both groups during euglycemic hyperinsulinemia. In obese men, C-peptide levels were significantly greater compared with non-obese men during euglycemic hyperinsulinemia (P < .05). However, neither the non-obese nor the obese group demonstrated significant suppression of insulin secretion rates during euglycemic hyperinsulinemia. Expressing the data in absolute terms or as a percent of basal did not alter the results. Moreover, there was no significant change between the non-obese and the obese group during the rapid onset and cessation of hyperinsulinemia. Under euglycemic conditions, physiologic hyperinsulinemia does not induce suppression of endogenous insulin secretion in non-obese or obese men.

摘要

胰岛素反馈抑制的存在是一个有争议的问题。本研究采用了一种新方法来确定在生理性高胰岛素血症期间体内是否存在胰岛素反馈抑制,以及它是否有助于肥胖时胰岛素分泌增加。在基础状态和高胰岛素钳夹(287 pmol/min/m²)期间以及在正常血糖条件下停止胰岛素输注后,测定系列血浆胰岛素和C肽水平。使用双室模型从血浆C肽水平和个体C肽动力学推导胰岛素分泌率。招募了8名非肥胖男性和9名肥胖男性进行研究,研究按随机顺序进行。排除在高胰岛素血症期间血糖水平有显著变化的男性进行分析。在研究的所有阶段,非肥胖组和肥胖组的血浆葡萄糖水平相似,在正常血糖高胰岛素血症期间两组的血浆胰岛素水平也相似。在正常血糖高胰岛素血症期间,肥胖男性的C肽水平显著高于非肥胖男性(P <.05)。然而,无论是非肥胖组还是肥胖组在正常血糖高胰岛素血症期间均未显示出胰岛素分泌率的显著抑制。以绝对值或基础值的百分比表示数据并未改变结果。此外,在高胰岛素血症快速开始和停止期间,非肥胖组和肥胖组之间没有显著变化。在正常血糖条件下,生理性高胰岛素血症不会诱导非肥胖或肥胖男性内源性胰岛素分泌的抑制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验