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PMID: 2384600 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effects of altered glucose homeostasis on glucose transporter expression in skeletal muscle of the rat.

The Journal of clinical investigation ·Vol. 86 ·No. 2 ·1990-08-00 ·Pages 542-7

Bourey RE, Koranyi L, James DE, Mueckler M, Permutt MA

Abstract

Previous studies have suggested that alteration in the expression of the insulin-regulatable glucose transporter of muscle (GLUT-4 protein) may be an important determinant of insulin action. In the present studies, we have examined GLUT-4 mRNA and protein concentrations in muscle after variations in the metabolic status of the intact animal (i.e., 7 d streptozotocin-induced diabetes, 7 d insulin-induced hypoglycemia, and 3 d fasting). These changes in glucose homeostasis were associated with the following changes in GLUT-4 gene products: a decrease of approximately 30% in both mRNA and protein with diabetes; a 50% increase in mRNA and a 2.4-fold increase in protein with insulin injection; and normal mRNA in spite of a 2.7-fold increase in protein with fasting. Fasted diabetics exhibited an increase of 50% in GLUT-4 mRNA and a 2.4-fold increase in protein relative to fed diabetics. In diabetic and insulin-injected groups, the changes in GLUT-4 protein were similar to changes in mRNA, but in fasting, GLUT-4 protein increased without a concomitant change in mRNA. Overall there was no correlation between muscle concentrations of GLUT-4 protein and mRNA. Muscle GLUT-4 protein concentration tended to correlate with plasma glucose (r = -0.57, P less than 0.001), but not with plasma insulin. These results indicate that (a) chronic changes in glucose homeostasis are associated with changes in expression of GLUT-4 protein in muscle; (b) GLUT-4 protein increased in fasted soleus muscle without change in mRNA, thereby differing from fasted adipocytes in which both GLUT-4 products diminish; and (c) no simple relationship exists between total muscle GLUT-4 protein content and whole-body insulin sensitivity.

MeSH Terms
Animals Blood Glucose/physiology Blotting, Western Diabetes Mellitus, Experimental/physiopathology Fasting Gene Expression Homeostasis Hypoglycemia/physiopathology Male Monosaccharide Transport Proteins/genetics,metabolism Muscles/physiology RNA, Messenger/genetics Rats Rats, Inbred Strains
Chemicals
Blood Glucose Monosaccharide Transport Proteins RNA, Messenger
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Bourey R E
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
Koranyi L
James D E
Mueckler M
Permutt M A
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1990-08-00
Pages
542-7
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC296758
Subset
IM
Grants
NIA NIH HHS · AG-00078 · United States
NIDDK NIH HHS · DK-07140 · United States
NIDDK NIH HHS · DK-16746 · United States
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