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肥胖和非肥胖人群血浆瘦素与胰岛素的关系。

Plasma leptin and insulin relationships in obese and nonobese humans.

作者信息

Dagogo-Jack S, Fanelli C, Paramore D, Brothers J, Landt M

机构信息

Division of Endocrinology, Diabetes and Metabolism, Washington School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Diabetes. 1996 May;45(5):695-8. doi: 10.2337/diab.45.5.695.

Abstract

Hyperinsulinemia. is associated with an overexpression of mRNA for the ob protein leptin in rodent models of genetic obesity, and insulin has been reported to directly stimulate leptin mRNA in rat adipocytes. Human obesity is also associated with increased leptin mRNA as well as plasma levels, but there have been no reports of the effect of insulin on leptin secretion. We, therefore, tested the hypothesis that insulin stimulates leptin secretion in humans. Using a newly developed leptin assay, immunoreactive leptin was measured in fasting and postprandial plasma samples from 27 healthy adults and in samples before and during euglycemic-hyperinsulinemic then stepped hypoglycemic (hourly steps at 85, 75, 65, 55, and 45 mg/dl) clamps from 10 healthy subjects and 11 patients with IDDM. Plasma leptin was correlated (r = 0.84, P = 0.0005) with BMI in obese but not nonobese subjects and with fasting (r = 0.75, P = 0.008) but not postprandial plasma insulin levels. (Leptin levels did not change postprandially.) Euglycemic hyperinsulinemia did not alter leptin levels, nor did hyperinsulinemic hypoglycemia. Thus, because circulating leptin levels are not increased during postprandial hyperinsulinemia or during euglycemic (or hypoglycemic) hyperinsulinemia, we conclude that, at least in the short term, insulin does not increase leptin secretion in humans and that hyperleptinemia in obese individuals is not likely the result of hyperinsulinemia.

摘要

高胰岛素血症。在遗传性肥胖的啮齿动物模型中与肥胖蛋白瘦素的mRNA过度表达有关,并且据报道胰岛素可直接刺激大鼠脂肪细胞中的瘦素mRNA。人类肥胖也与瘦素mRNA以及血浆水平升高有关,但尚无关于胰岛素对瘦素分泌影响的报道。因此,我们检验了胰岛素刺激人类瘦素分泌这一假设。使用新开发的瘦素检测方法,对27名健康成年人的空腹和餐后血浆样本以及10名健康受试者和11名胰岛素依赖型糖尿病患者在正常血糖-高胰岛素血症然后逐步低血糖(每小时步长分别为85、75、65、55和45mg/dl)钳夹期间及之前的样本中的免疫反应性瘦素进行了测量。血浆瘦素在肥胖但非肥胖受试者中与BMI相关(r = 0.84,P = 0.0005),与空腹血浆胰岛素水平相关(r = 0.75,P = 0.008)但与餐后血浆胰岛素水平无关。(瘦素水平餐后未改变。)正常血糖高胰岛素血症未改变瘦素水平,高胰岛素血症低血糖也未改变。因此,由于餐后高胰岛素血症期间或正常血糖(或低血糖)高胰岛素血症期间循环瘦素水平未升高,我们得出结论,至少在短期内,胰岛素不会增加人类瘦素分泌,肥胖个体中的高瘦素血症不太可能是高胰岛素血症的结果。

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