Suppr超能文献

胰岛素对人体游离脂肪酸代谢的调节:脂解作用和再酯化作用的角色

Regulation of free fatty acid metabolism by insulin in humans: role of lipolysis and reesterification.

作者信息

Campbell P J, Carlson M G, Hill J O, Nurjhan N

机构信息

Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2230.

出版信息

Am J Physiol. 1992 Dec;263(6):E1063-9. doi: 10.1152/ajpendo.2006.263.6.E1063.

Abstract

The regulation of lipolysis, free fatty acid appearance into plasma (FFA R(a)), an FFA reesterification and oxidation were examined in seven healthy humans infused intravenously with insulin at rates of 4, 8, 25, and 400 mU.m-2.min-1. Glycerol and FFA R(a) were determined by isotope dilution methods, and FFA oxidation was calculated by indirect calorimetry or by measurement of expired 14CO2 from infused [1-14C]palmitate. These measurements were used to calculate total FFA reesterification, primary FFA reesterification occurring within the adipocyte, and secondary reesterification of circulating FFA molecules. Lipolysis, FFA R(a), and secondary FFA reesterification were exquisitely insulin sensitive [the insulin concentrations that produced half-maximal suppression (EC50), 106 +/- 26, 91 +/- 20 vs. 80 +/- 16 pM, P = not significant] in contrast to insulin suppression of FFA oxidation (EC50, 324 +/- 60, all P < 0.01). The absolute rate of primary FFA reesterification was not affected by the increase in insulin concentration, but the proportion of FFA molecules undergoing primary reesterification doubled over the physiological portion of the insulin dose-response curve (from 0.23 +/- 0.06 to 0.44 +/- 0.07, P < 0.05). This served to magnify insulin suppression of FFA R(a) twofold. In conclusion, insulin regulates FFA R(a) by inhibition of lipolysis while maintaining a constant rate of primary FFA reesterification.

摘要

在7名健康受试者中,以4、8、25和400 mU·m⁻²·min⁻¹的速率静脉输注胰岛素,研究了脂解、游离脂肪酸进入血浆(FFA R(a))、FFA再酯化和氧化的调节情况。通过同位素稀释法测定甘油和FFA R(a),通过间接量热法或测量输注的[1-¹⁴C]棕榈酸呼出的¹⁴CO₂来计算FFA氧化。这些测量用于计算总FFA再酯化、脂肪细胞内发生的初级FFA再酯化以及循环FFA分子的次级再酯化。脂解、FFA R(a)和次级FFA再酯化对胰岛素极为敏感[产生半数最大抑制的胰岛素浓度(EC50),分别为106±26、91±20与80±16 pM,P无显著差异],与之形成对比的是胰岛素对FFA氧化的抑制作用(EC50,324±60,所有P<0.01)。初级FFA再酯化的绝对速率不受胰岛素浓度增加的影响,但在胰岛素剂量-反应曲线的生理范围内,经历初级再酯化的FFA分子比例增加了一倍(从0.23±0.06增至0.44±0.07,P<0.05)。这使得胰岛素对FFA R(a)的抑制作用放大了两倍。总之,胰岛素通过抑制脂解来调节FFA R(a),同时维持初级FFA再酯化的恒定速率。

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