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PMID: 8550560 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Hepatic overexpression of insulin-like growth factor-II in adulthood increases basal and insulin-stimulated glucose disposal in conscious mice.

The Journal of biological chemistry ·Vol. 271 ·No. 1 ·1996-01-05 ·Pages 203-8

Rossetti L, Barzilai N, Chen W, Harris T, Yang D, Rogler CE

Abstract

The physiological role of circulating insulin-like growth factor-II (IGF-II) in adult humans is poorly understood. We recently generated an IGF-II transgenic murine model of persistent IGF-II production (plasma IGF-II approximately 30-fold increased above normal) through over-expression of the transgene driven by the major urinary protein promoter (Rinderknecht, E., and Humbel, R. E. (1978) J. Biol. Chem. 269, 13779-13784). To determine whether in vivo insulin action is improved in these transgenic mice, we performed euglycemic insulin (18 milliunits/kg.min) clamp studies in conscious IGF-II transgenic and in age- and weight-matched control mice. Plasma glucose and insulin concentrations were significantly lower in the IGF-II transgenic compared with both control grouoff Despite decreased plasma glucose concentration, basal hepatic glucose production (HGP) and glucose clearance were increased. During the insulin clamp studies in IGF-II transgenic mice compared with control mice (a) the rates of glucose infusion and glucose uptake were increased by approximately by 65 and approximately 55%, respectively; (b) glycolysis was increased by approximately 12% while glycogen synthesis was approximately 2-fold higher; (c) while the suppression of plasma free fatty acid was similar, the increment in plasma lactate concentration was significantly higher; (d) although HGP was similarly inhibited by insulin, phosphoenolpyruvate gluconeogenesis was enhanced and accounted for a larger portion of HGP (64% versus approximately 40% in control mice). Our data suggest that the persistence of circulating IGF-II in adult mice to levels commonly observed in adult humans (50-70 nM) causes a marked improvement in peripheral (skeletal muscle) insulin action, which is not due to changes in body composition. These results suggest that circulating IGF-II may exert a regulatory role on insulin sensitivity and body composition in humans.

MeSH Terms
Adult Animals Glucokinase/metabolism Glucose/metabolism Glucose Clamp Technique Glucose-6-Phosphatase/metabolism Glycogen/metabolism Glycogen Synthase/metabolism Humans Insulin/metabolism Insulin-Like Growth Factor II/genetics,metabolism Liver/enzymology,metabolism Mice Mice, Inbred C57BL Mice, Inbred CBA Mice, Transgenic Muscle, Skeletal/metabolism Phosphoenolpyruvate Carboxykinase (GTP)/metabolism Tritium
Chemicals
Insulin Tritium Insulin-Like Growth Factor II Glycogen Glycogen Synthase Glucokinase Glucose-6-Phosphatase Phosphoenolpyruvate Carboxykinase (GTP) Glucose
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Rossetti L
Division of Endocrinology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Barzilai N
Chen W
Harris T
Yang D
Rogler C E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-01-05
Pages
203-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · R01-CA 56076 · United States
NIDDK NIH HHS · R01-DK 48321 · United States
NIDDK NIH HHS · R029-DK 45024 · United States
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