Erdmann Johannes, Kallabis Bianca, Oppel Ulrich, Sypchenko Oleg, Wagenpfeil Stefan, Schusdziarra Volker
Else-Kröner-Fresenius Center of Nutritional Medicine, Technical University of Munich, Ismaninger Strasse 22, D-81675 Munich, Germany.
Am J Physiol Endocrinol Metab. 2008 Mar;294(3):E568-75. doi: 10.1152/ajpendo.00560.2007. Epub 2008 Jan 2.
Obesity is associated with insulin resistance and hyperinsulinemia, which is considered to be a core component in the pathophysiology of obesity-related comorbidities. As yet it is unknown whether insulin resistance and hyperinsulinemia already develop during weight gain within the normal range. In 10 healthy male subjects the effect of intentional weight gain by 2 BMI points was examined on insulin. C-peptide and glucose levels following a meal, 75 g of glucose, and a two-step hyperglycemic clamp increased plasma glucose by 1.38 and 2.75 mmol/l, respectively. Baseline insulin, C-peptide, and glucose concentrations were significantly higher after weight gain from 21.8 to 23.8 kg/m(2) BMI within 4(1/2) mo. Calculations of insulin secretion and clearance indicate that reduced insulin clearance contributes more to post-weight gain basal hyperinsulinemia than insulin secretion. Following oral or intravenous stimulation insulin concentrations were significantly higher post-weight gain during all three test conditions, whereas C-peptide and glucose levels did not differ. Calculations of insulin secretion and clearance demonstrated that higher stimulated insulin concentrations are entirely due to clearance but not secretion. Despite significantly higher insulin levels, the rate of intravenous glucose required to maintain the defined elevation of glucose levels was either identical (1.38 mmol/l) or even significantly lower (2.75 mmol/l) following weight gain. The present study demonstrates for the first time that insulin resistance already develops during weight gain within the normal range of body weight. The associated basal and stimulated hyperinsulinemia is the result of differentiated changes of insulin secretion and clearance, respectively.
肥胖与胰岛素抵抗和高胰岛素血症相关,而这被认为是肥胖相关合并症病理生理学的核心组成部分。目前尚不清楚在正常体重范围内体重增加期间胰岛素抵抗和高胰岛素血症是否已经出现。在10名健康男性受试者中,研究了有意使体重增加2个体重指数(BMI)单位对胰岛素、C肽和葡萄糖水平的影响。给予75克葡萄糖餐后,通过两步高血糖钳夹试验,体重增加分别使血浆葡萄糖升高1.38和2.75毫摩尔/升。在4个半月内体重从BMI 21.8增加到23.8千克/平方米后,基线胰岛素、C肽和葡萄糖浓度显著升高。胰岛素分泌和清除率的计算表明,体重增加后基础高胰岛素血症更多是由于胰岛素清除率降低而非胰岛素分泌增加所致。在口服或静脉刺激后,在所有三种测试条件下体重增加后胰岛素浓度均显著更高,而C肽和葡萄糖水平无差异。胰岛素分泌和清除率的计算表明,刺激后较高的胰岛素浓度完全是由于清除率增加而非分泌增加。尽管胰岛素水平显著更高,但体重增加后维持规定血糖水平升高所需的静脉葡萄糖输注速率要么相同(1.38毫摩尔/升),要么甚至显著更低(2.75毫摩尔/升)。本研究首次表明,在正常体重范围内体重增加期间胰岛素抵抗已经出现。相关的基础和刺激后高胰岛素血症分别是胰岛素分泌和清除率差异变化的结果。