Antagonism by growth hormone of insulin-sensitive hexose transport in 3T3-F442A adipocytes

• Published in: Endocrinology (Philadelphia) Vol. 125; no. 5; p. 2600
• Main Authors: Silverman, M S, Mynarcik, D C, Corin, R E, Haspel, H C, Sonenberg, M
• Format: Journal Article
• Language: English
• Published: United States 01.11.1989
• Subjects: Adipose Tissue - cytology; Adipose Tissue - drug effects; Adipose Tissue - metabolism; Animals; Biological Transport, Active - drug effects; Cell Differentiation; Cells, Cultured; Deoxy Sugars - metabolism; Deoxyglucose - metabolism; Growth Hormone - pharmacology; Insulin - pharmacology; Insulin Antagonists - pharmacology; Kinetics; Mice
• ISSN: 0013-7227
• DOI: 10.1210/endo-125-5-2600

We have studied the effects of GH on basal and insulin-stimulated hexose transport by 3T3-F442A adipocytes in a hormonally defined serum-free medium. Adipocytes preincubated in defined medium exhibit a low level of hexose transport which is acutely (15 min) stimulated (greater than 5-fold) by insulin (EC50, 0.1-0.2 nM). GH has acute (15-45 min) insulin-mimetic (greater than 2-fold) and chronic (4-48 h) diabetogenic (50-80%) effects on basal and insulin-stimulated hexose transport. The insulin-mimetic effect of GH has a higher EC50 (2 nM) than its diabetogenic effect (EC50, 0.2 nM). Chronic GH exposure decreases the maximal responsiveness (50-80%) and the acute sensitivity (approximately 2-fold) of hexose transport to insulin. Insulin-stimulated transport is more (approximately 5-fold) sensitive to the diabetogenic effect of GH than is basal transport. Insulin binding and degradation were not altered by chronic exposure to GH. The diabetogenic effect of GH may occur at a postinsulin binding level.