PHYSIOLOGICAL INSULINEMIA ACUTELY MODULATES PLASMA LEPTIN

Citation
Mf. Saad et al., PHYSIOLOGICAL INSULINEMIA ACUTELY MODULATES PLASMA LEPTIN, Diabetes, 47(4), 1998, pp. 544-549
Citations number
48
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00121797
Volume
47
Issue
4
Year of publication
1998
Pages
544 - 549
Database
ISI
SICI code
0012-1797(1998)47:4<544:PIAMPL>2.0.ZU;2-#
Abstract
Whether insulin acutely regulates plasma leptin in humans is controver sial. We examined the dosage-response and time-course characteristics of the effect of insulin on leptin in 10 men (age 42 +/- 2 years [mean +/- SE]; BMI 29.3 +/- 2.0 kg/m(2)). Each individual underwent four 9- h euglycemic clamps (insulin at 20, 40, 80, and 400 mU.m(-2).min(-1)) and a control saline infusion. Although plasma glucose and insulin lev els remained constant, leptin diminished from 9.1 +/- 3.0 to 5.9 +/- 2 .1 ng/ml (P < 0.001) by the end of the control experiment. Conversely, plasma leptin showed a dosage-dependent increase during the insulin i nfusions that was evident within 30-60 min. The insulin-induced increa se in leptin was proportionately lower in obese insulin-resistant men. Free fatty acids (FFAs) decreased during insulin and did not change d uring saline infusions. ED50 (the dose producing half-maximal effect) for insulin's effect on leptin and FFA was similar (138 +/- 36 vs. 102 +/- 24 pmol/l, respectively; P = 0.11). To further define the role of physiological insulinemia, we compared the effect of a very low dosag e insulin infusion (10 mU.m(-2).min(-1)) with that of a control saline infusion in another group of 10 men (mean age 39 +/- 3 years; BMI 27. 1 +/- 1.0 kg/m(2)). Plasma leptin remained stable during that insulin infusion, but fell. by 37 +/- 2% in the control experiment. Thus physi ological insulinemia can acutely regulate plasma leptin. Insulin could mediate the effect of caloric intake on leptin and could be a determi nant of its plasma concentration. Inadequate insulin-induced leptin pr oduction in obese and insulin-resistant subjects may contribute to the development or worsening of obesity.