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PMID: 1733808 Published · ppublish English Journal Article

Glucose transporter levels in tissues of spontaneously diabetic Zucker fa/fa rat (ZDF/drt) and viable yellow mouse (Avy/a).

Diabetes ·Vol. 41 ·No. 2 ·1992-02-00 ·Pages 187-93

Slieker LJ, Sundell KL, Heath WF, Osborne HE, Bue J, Manetta J, Sportsman JR

Abstract

We used antibodies to the fat/muscle glucose transporter (GLUT4) and the liver glucose transporter (GLUT2) to measure levels of these proteins in various tissues of two rodent models of non-insulin-dependent (type II) diabetes mellitus: the obese spontaneously diabetic male Zucker fa/fa rat (ZDF/drt) and the male viable yellow Avy/a obese diabetic mouse. The ZDF/drt strain generally develops overt diabetes associated with decreased plasma insulin levels. Depending on the age of the animals, the ZDF/drt rats can be arbitrarily segregated into age-matched obese, mildly diabetic (blood glucose less than 11 mM) and obese, and severely diabetic (blood glucose greater than 20 mM) groups. Avy/a mice are comparably hyperglycemic but unlike the ZDF/drt rats are severely hyperinsulinemic. In both groups of diabetic animals, GLUT4 in adipose tissue, heart, and skeletal muscle was reduced 25-55%, and GLUT2 in liver was increased 30-40%, relative to lean, age-matched controls. However, when the mildly diabetic ZDF/drt rats were compared to the lean controls, the only significant difference was a 25% reduction of GLUT4 in heart. Within all of the ZDF/drt rats (excluding the lean controls), GLUT2 in liver and GLUT4 in adipose tissue, heart, and skeletal muscle correlated significantly with glycemia. These data suggest that, in these two models of type II diabetes, glucose transporter levels in muscle, adipose tissue, and liver are regulated in a tissue-selective manner in response to changes in insulin and glucose. Furthermore, at least in the ZDF/drt rat, alterations in GLUT2 and/or GLUT4 protein levels appear not to be associated with obesity per se but appear to be secondary to the severely diabetic state.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Adipose Tissue/metabolism Amino Acid Sequence Analysis of Variance Animals Diabetes Mellitus, Experimental/metabolism Liver/metabolism Male Mice Mice, Obese Molecular Sequence Data Monosaccharide Transport Proteins/metabolism Muscles/metabolism Myocardium/metabolism Rats Rats, Zucker
Chemicals
Monosaccharide Transport Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Slieker L J
Diabetes Research Division, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285.
Sundell K L
Heath W F
Osborne H E
Bue J
Manetta J
Sportsman J R
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
1992-02-00
Pages
187-93
Language
English
Region
United States
NLM ID
0372763
Subset
IM
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