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胰岛素抵抗对肥胖患者亮氨酸和葡萄糖动力学的不同影响。

Differential effects of insulin resistance on leucine and glucose kinetics in obesity.

作者信息

Caballero B, Wurtman R J

机构信息

Clinical Research Center, Massachusetts Institute of Technology, Cambridge.

出版信息

Metabolism. 1991 Jan;40(1):51-8. doi: 10.1016/0026-0495(91)90192-y.

Abstract

The effects of insulin resistance on glucose and amino acid metabolism were studied in obese nondiabetic women (body mass index [BMI], (32.8 +/- 2) and in lean controls. Glucose disposal rate, hepatic glucose production, and leucine carbon flux and oxidation were simultaneously measured during the postabsorptive state and during euglycemic hyperinsulinemia, by means of primed, constant infusions of D-[6,6-2H2]glucose and L-[1-13C]leucine. Each subject participated in two insulin clamp studies on separate days, at infusion rates of 10 and 40 mU (m2.min)-1, producing plasma insulin levels of 20 to 25 and 70 to 80 microU/mL, respectively. Fat-free mass (FFM) was calculated from underwater weighing measurements. Insulin-mediated glucose disposal rate was significantly slower in the obese group: 2.05 +/- 0.05 versus 3.84 +/- 0.18 mg (kg.min)-1 in controls during the 10-mU insulin clamp, and 3.80 +/- 0.23 versus 9.16 +/- 0.47 mg (kg.min)-1 during the 40-mU clamp. The insulin-induced decrease in plasma levels of branched chain amino acids was also significantly blunted in the obese group. Baseline leucine flux was similar in lean and obese subjects (78 +/- 3 and 71 +/- 2 mumol (kg.h)-1, respectively), and its decline in response to insulin infusion was also comparable (8% and 10% during the 10-mU/m2 clamp, and of 17% and 18% during the 40-mU/m2 clamp in lean and obese, respectively). Basal leucine carbon oxidation (from [13C]leucine and [13C]alpha ketoisocaproate [alpha-KIC] plasma enrichments) was also similar in lean and obese, and did not change significantly with insulin infusion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在肥胖非糖尿病女性(体重指数[BMI]为(32.8±2))和瘦对照组中研究了胰岛素抵抗对葡萄糖和氨基酸代谢的影响。通过给予负荷剂量、持续输注D-[6,6-2H2]葡萄糖和L-[1-13C]亮氨酸,在空腹状态和正常血糖高胰岛素血症期间同时测量葡萄糖处置率、肝脏葡萄糖生成以及亮氨酸碳通量和氧化。每个受试者在不同日期参加两项胰岛素钳夹研究,输注速率分别为10和40 mU/(m2·min)-1,分别产生血浆胰岛素水平为20至25和70至80 μU/mL。通过水下称重测量计算无脂肪量(FFM)。在肥胖组中,胰岛素介导的葡萄糖处置率显著较慢:在10-mU胰岛素钳夹期间,肥胖组为2.05±0.05 mg/(kg·min)-1,对照组为3.84±0.18 mg/(kg·min)-1;在40-mU钳夹期间,肥胖组为3.80±0.23 mg/(kg·min)-1,对照组为9.16±0.47 mg/(kg·min)-1。肥胖组中胰岛素诱导的支链氨基酸血浆水平下降也明显减弱。瘦受试者和肥胖受试者的基线亮氨酸通量相似(分别为78±3和71±2 μmol/(kg·h)-1),其对胰岛素输注的下降也相当(在10-mU/m2钳夹期间,瘦受试者和肥胖受试者分别为8%和10%;在40-mU/m2钳夹期间,分别为17%和18%)。瘦受试者和肥胖受试者的基础亮氨酸碳氧化(来自[13C]亮氨酸和[13C]α-酮异己酸[α-KIC]血浆富集)也相似,并且随着胰岛素输注没有显著变化。(摘要截短至250字)

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