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PMID: 2662408 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Pretranslational suppression of an insulin-responsive glucose transporter in rats with diabetes mellitus.

Science (New York, N.Y.) ·Vol. 245 ·No. 4913 ·1989-07-07 ·Pages 60-3

Garvey WT, Huecksteadt TP, Birnbaum MJ

Abstract

A prominent feature of diabetes mellitus is the inability of insulin to appropriately increase the transport of glucose into target tissues. The contributions of different glucose transport proteins to insulin resistance in rats with streptozotocin-induced diabetes was evaluated. A glucose transporter messenger RNA and its cognate protein that are exclusively expressed in muscle and adipose tissue were specifically depleted in diabetic animals, and these effects were reversed after insulin therapy; a different glucose transporter and its messenger RNA that exhibit a less restricted tissue distribution were not specifically modulated in this way. Depletion of the muscle- and adipose-specific glucose transporter species correlates with and may account for the major portion of cellular insulin resistance in diabetes in these animals.

MeSH Terms
3-O-Methylglucose Adipose Tissue/metabolism Animals Blood Glucose/metabolism Brain/metabolism Diabetes Mellitus, Experimental/drug therapy,metabolism Insulin/therapeutic use Male Methylglucosides/metabolism Monosaccharide Transport Proteins/biosynthesis,genetics Muscles/metabolism Organ Specificity RNA, Messenger/genetics Rats Rats, Inbred Strains Reference Values Suppression, Genetic Transcription, Genetic
Chemicals
Blood Glucose Insulin Methylglucosides Monosaccharide Transport Proteins RNA, Messenger 3-O-Methylglucose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Garvey W T
Section of Endocrinology and Metabolism, VA Medical Center, Indianapolis, IN.
Huecksteadt T P
Birnbaum M J
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1989-07-07
Pages
60-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDDK NIH HHS · DK 38765 · United States
NIDDK NIH HHS · DK 39519 · United States
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