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肥胖受试者中碳水化合物无法节省亮氨酸氧化。

Failure of carbohydrate to spare leucine oxidation in obese subjects.

作者信息

Nair K S, Halliday D, Ford G C, Heels S, Garrow J S

机构信息

Nutrition Research Group, Clinical Research Centre, Harrow, UK.

出版信息

Int J Obes. 1987;11(5):537-44.

PMID:3323087
Abstract

Leucine kinetics were studied in six obese subjects (W/H2 = 39 +/- 4) and six normal subjects (W/H2 = 21 +/- 3) before and after an oral load of 150 g glucose. An intravenous infusion of 1(-13)C leucine was given to the fasting subjects for 450 min: a steady state of plasma leucine enrichment was established 90 min after the start of the infusion, and the glucose load was given 220 min after the start of the infusion. Compared with the lean controls the obese subjects showed a greater area under the curve of blood glucose after the glucose load (P less than 0.025) and higher insulin and glucagon levels both before and after the meal (P less than 0.05), thus indicating the well-known insulin insensitivity of obese (but not diabetic) subjects with respect to glucose metabolism. After the glucose load the lean subjects showed a significant and sustained decrease in leucine oxidation (from 20.0 +/- 2.2 to 13.3 +/- 1.5 mumol/kg LBM/h: P less than 0.01). This response is similar to that observed when insulin-dependent diabetic subjects are given insulin. However the obese subjects showed no decrease in leucine oxidation after the glucose meal (20.3 +/- 1.9 before, and 21.2 +/- 3.6 after). This indicates that obese subjects show insensitivity to the action of insulin with respect to protein metabolism as well as carbohydrate metabolism.

摘要

在六名肥胖受试者(体重指数W/H2 = 39 ± 4)和六名正常受试者(体重指数W/H2 = 21 ± 3)口服150克葡萄糖前后,对其亮氨酸动力学进行了研究。对空腹受试者静脉输注1-¹³C亮氨酸450分钟:输注开始90分钟后建立血浆亮氨酸富集的稳定状态,并在输注开始220分钟后给予葡萄糖负荷。与瘦对照组相比,肥胖受试者在葡萄糖负荷后血糖曲线下面积更大(P < 0.025),且餐前和餐后胰岛素及胰高血糖素水平均更高(P < 0.05),这表明肥胖(但非糖尿病)受试者在葡萄糖代谢方面存在众所周知的胰岛素不敏感性。葡萄糖负荷后,瘦受试者亮氨酸氧化显著且持续下降(从20.0 ± 2.2降至13.3 ± 1.5微摩尔/千克瘦体重/小时:P < 0.01)。这种反应与给胰岛素依赖型糖尿病受试者注射胰岛素时观察到的反应相似。然而,肥胖受试者在进葡萄糖餐后亮氨酸氧化没有下降(餐前为20.3 ± 1.9,餐后为21.2 ± 3.6)。这表明肥胖受试者在蛋白质代谢以及碳水化合物代谢方面对胰岛素的作用不敏感。

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