Asano T, Ninomiya H, Kan K, Yamamoto T, Okumura M
First Department of Internal Medicine, School of Medicine, Fukuoka University, Japan.
Endocrinol Jpn. 1989 Oct;36(5):767-73. doi: 10.1507/endocrj1954.36.767.
To investigate glucagon (IRG) and insulin (IRI) responses to alanine infusion in obesity and to assess the effect of body weight reduction with respect to hormonal balance, we compared six obese subjects with nine normal weight controls. None of the subjects were diabetic by OGTT criteria. Plasma IRI and IRG were measured following IV alanine at a rate of 0.1 g/kg over a period of 2 min. Our obese subjects had an increase in IRG response to alanine, which was due to decreased suppression of alpha-cell function due to insulin resistance. Weight reduction via calorie restriction reduced insulin demand, resulting in reduced plasma IRI by restoring beta-cell function, and the IRG response was paradoxically decreased as compared with that before weight loss. It is conceivable that improvements in insulin sensitivity after body weight reduction may re-establish the normalization of pancreatic beta-cell function and the insulin-induced inhibition of IRG secretion. Our obese subjects were characterized by decreased IRG secretion which was reflected in a change in body weight reduction.
为了研究肥胖状态下胰高血糖素(IRG)和胰岛素(IRI)对丙氨酸输注的反应,并评估体重减轻对激素平衡的影响,我们将6名肥胖受试者与9名正常体重对照者进行了比较。根据口服葡萄糖耐量试验(OGTT)标准,所有受试者均无糖尿病。以0.1 g/kg的速率在2分钟内静脉输注丙氨酸后,测量血浆IRI和IRG。我们的肥胖受试者对丙氨酸的IRG反应增加,这是由于胰岛素抵抗导致α细胞功能抑制减弱。通过热量限制减轻体重可降低胰岛素需求,通过恢复β细胞功能导致血浆IRI降低,与体重减轻前相比,IRG反应反而降低。可以想象,体重减轻后胰岛素敏感性的改善可能会重新建立胰腺β细胞功能的正常化以及胰岛素诱导的IRG分泌抑制。我们的肥胖受试者的特征是IRG分泌减少,这反映在体重减轻的变化中。