Home LiteratureArticle Details
PMID: 8603766 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Plasma free fatty acids decrease insulin-stimulated skeletal muscle glucose uptake by suppressing glycolysis in conscious rats.

Diabetes ·Vol. 45 ·No. 4 ·1996-04-00 ·Pages 446-53

Kim JK, Wi JK, Youn JH

Abstract

The effects of elevated plasma free fatty acid (FFA) levels on insulin -stimulated whole-body and skeletal muscle glucose transport, glucose uptake, glycolysis, and glycogen synthesis were studied in conscious rats during hyperinsulinemic-euglycemic clamps with (n = 26) or without (n = 23) Intralipid and heparin infusion. Whole-body and skeletal muscle glucose uptake, glycolysis, and glycogen synthesis were estimated using D-[3-3H]glucose and 2-[14C]deoxyglucose (study 1), and glucose transport activity was assessed by analyzing plasma kinetics of L-[14C]glucose and 3-O-[3H]-methylglucose (study 2). Plasma FFA levels decreased during the clamps without intralipid but increased above basal during the clamps with Intralipid infusion (P < 0.01 for both). Elevated plasma FFA levels decreased insulin-stimulated whole-body glucose uptake by approximately 15% and approximately 20% during physiological and maximal insulin clamps, respectively (P < 0.01). Similarly, insulin-stimulated glucose uptake was also decreased in individual skeletal muscles with Intralipid infusion (P < 0.05). The most profound effect of elevated plasma FFA levels was a 30-50% suppression of insulin-stimulated glycolysis in whole body and individual skeletal muscles in both clamps. In contrast, physiological insulin-stimulated glycogen synthesis was increased with elevated plasma FFA levels in whole body and individual skeletal muscles (P < 0.05). Glucose-6-phosphate (G-6-P) levels were increased in soleus and extensor digitorum longus (EDL) muscles with Intralipid infusion in both clamps (P < 0.05). Intralipid infusion did not alter the time profiles of plasma L-glucose and 3-O-methylglucose after an intravenous injection during maximal insulin clamps, and compartmental analysis indicated no significant effect of elevated FFA levels on glucose transport activity in insulin-sensitive tissues (P > 0.05). Thus, elevated plasma FFA decreased insulin-stimulated glucose uptake in skeletal muscle by suppressing glycolysis and increasing G-6-P levels. These findings suggest that the classic glucose-fatty acid cycle was the predominant mechanism underlying the inhibitory effect of FFA on skeletal muscle glucose uptake.

MeSH Terms
3-O-Methylglucose Animals Biological Transport/drug effects Blood Glucose/metabolism Carbon Radioisotopes Deoxyglucose/metabolism Fatty Acids, Nonesterified/blood Glucose/metabolism Glucose Clamp Technique Glycogen/biosynthesis Glycolysis/drug effects Infusions, Intravenous Insulin/administration & dosage,pharmacology Kinetics Male Mathematics Methylglucosides/metabolism Models, Biological Muscle, Skeletal/drug effects,metabolism Rats Rats, Wistar Time Factors Tritium
Chemicals
Blood Glucose Carbon Radioisotopes Fatty Acids, Nonesterified Insulin Methylglucosides Tritium 3-O-Methylglucose Glycogen Deoxyglucose Glucose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kim J K
Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles, 90033, USA.
Wi J K
Youn J H
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
1996-04-00
Pages
446-53
Language
English
Region
United States
NLM ID
0372763
Subset
IM
Grants
NIDDK NIH HHS · DK-47947-01 · United States
NIA NIH HHS · NIA T32-AG00093 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]