在肥胖相关的胰岛素抵抗中,随着胰岛素水平升高,游离胰岛素样生长因子-I(free IGF-I)并未降低。
No decrease in free IGF-I with increasing insulin in obesity-related insulin resistance.
作者信息
Ricart W, Fernández-Real J M
机构信息
Unit of Diabetes, Endocrinology and Nutrition, University Hospital of Girona, Spain.
出版信息
Obes Res. 2001 Oct;9(10):631-6. doi: 10.1038/oby.2001.83.
OBJECTIVE
Different facts suggest that the insulin growth factor (IGF)/ insulin growth factor-binding protein (IGFBP) system may be regulated by factors other than growth hormone. It has been proposed that, in healthy subjects, free IGF-I plays a role in glucose metabolism. The role of free IGF-I in glucose homeostasis in insulin resistance is poorly understood. This study was undertaken to evaluate the effects of acute changes in plasma glucose and insulin levels on free IGF-I and IGFBP-1 in obese and non-obese subjects.
RESEARCH METHODS AND PROCEDURES
Nineteen lean and 24 obese subjects were investigated. A frequently sampled intravenous glucose tolerance test was performed. Free IGF-I and IGFBP-1 were determined at 0, 19, 22, 50, 100, and 180 minutes.
RESULTS
Basal free IGF-I levels tended to be higher and IGFBP-1 lower in obese than in lean subjects. IGFBP-1 levels inversely correlated with basal insulin concentration. To determine the effects of insulin on the availability of free IGF-I and IGFBP-1, changes in their plasma concentrations were measured during a frequently sampled intravenous glucose tolerance test. After insulin administration, a significant suppression of free IGF-I at 22% was observed in lean subjects. In contrast, plasma-free IGF-I levels remained essentially unchanged in the obese group. The differences between both groups were statistically significant at 100 minutes (p < 0.01) and 180 minutes (p < 0.05). Serum IGFBP-1 was suppressed to a similar extent in both groups.
DISCUSSION
These data suggest that the concentrations of free IGF-I and IGFBP-1 are differentially regulated by obesity. Obesity-related insulin resistance leads to unsuppressed free IGF-I levels.
目的
不同事实表明,胰岛素生长因子(IGF)/胰岛素生长因子结合蛋白(IGFBP)系统可能受生长激素以外的因素调节。有人提出,在健康受试者中,游离IGF-I在葡萄糖代谢中起作用。游离IGF-I在胰岛素抵抗的葡萄糖稳态中的作用尚不清楚。本研究旨在评估肥胖和非肥胖受试者血浆葡萄糖和胰岛素水平的急性变化对游离IGF-I和IGFBP-1的影响。
研究方法和步骤
对19名瘦人和24名肥胖受试者进行了研究。进行了频繁采样的静脉葡萄糖耐量试验。在0、19、22、50、100和180分钟时测定游离IGF-I和IGFBP-1。
结果
肥胖受试者的基础游离IGF-I水平往往高于瘦人,而IGFBP-1水平则较低。IGFBP-1水平与基础胰岛素浓度呈负相关。为了确定胰岛素对游离IGF-I和IGFBP-1可用性的影响,在频繁采样的静脉葡萄糖耐量试验期间测量了它们的血浆浓度变化。给予胰岛素后,瘦人组游离IGF-I显著抑制22%。相比之下,肥胖组血浆游离IGF-I水平基本保持不变。两组之间的差异在100分钟时具有统计学意义(p<0.01),在180分钟时具有统计学意义(p<0.05)。两组血清IGFBP-1的抑制程度相似。
讨论
这些数据表明,游离IGF-I和IGFBP-1的浓度受肥胖的差异调节。肥胖相关的胰岛素抵抗导致游离IGF-I水平不受抑制。