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PMID: 1936601 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Development of muscle insulin resistance after liver insulin resistance in high-fat-fed rats.

Diabetes ·Vol. 40 ·No. 11 ·1991-11-00 ·Pages 1397-403

Kraegen EW, Clark PW, Jenkins AB, Daley EA, Chisholm DJ, Storlien LH

Abstract

Muscle and hepatic insulin resistance are two major defects of non-insulin-dependent diabetes mellitus. Dietary factors may be important in the etiology of insulin resistance. We studied progressive changes in the development of high-fat-diet-induced insulin resistance in tissues of the adult male Wistar rat. In vivo insulin action was compared 3 days and 3 wk after isocaloric synthetic high-fat or high-starch feeding (59 and 10% cal as fat, respectively). Basal and insulin-stimulated glucose metabolism were assessed in the conscious 5- to 7-h fasted state with the euglycemic clamp (600 pM insulin) with a [3-3H]-glucose infusion. Fat feeding significantly reduced suppressibility of hepatic glucose output by insulin after both 3 days and 3 wk of diet (P less than 0.01). However, a significant impairment of insulin-mediated peripheral glucose disposal was only present after 3 wk of diet. Further in vivo [3H]-2-deoxyglucose uptake studies supported this finding and demonstrated adipose but not muscle insulin resistance after 3 days of high-fat feeding. Muscle triglyceride accumulation due to fat feeding was not significant at 3 days but had doubled by 3 wk in red muscle (P less than 0.001) compared with starch-fed controls. By 3 wk, high-fat-fed animals had developed significant glucose intolerance. We conclude that fat feeding induces insulin resistance in liver and adipose tissue before skeletal muscle with early metabolic changes favoring an oversupply of energy substrate to skeletal muscle relative to metabolic needs. This may generate later muscle insulin resistance.

MeSH Terms
Animals Dietary Fats/pharmacology Glucose/metabolism Insulin/pharmacology Insulin Resistance/physiology Liver/metabolism,physiology Male Muscles/chemistry,metabolism,physiology Rats Rats, Inbred Strains Starch/pharmacology Triglycerides/analysis,metabolism
Chemicals
Dietary Fats Insulin Triglycerides Starch Glucose
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kraegen E W
Garvan Institute of Medical Research, St. Vincent's Hospital, Sydney, New South Wales, Australia.
Clark P W
Jenkins A B
Daley E A
Chisholm D J
Storlien L H
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
1991-11-00
Pages
1397-403
Language
English
Region
United States
NLM ID
0372763
Subset
IM
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