Muscle oxidative capacity is a better predictor of insulin sensitivity than lipid status

Bruce, Clinton R., Anderson, Mtichell J., Carey, Andrew L., Newman, David G., Bonen, Arend, Kriketos, Adamandia D., Cooney, Gregory J. and Hawley, John A. 2003, Muscle oxidative capacity is a better predictor of insulin sensitivity than lipid status, Journal of clinical endocrinology and metabolism, vol. 88, no. 11, pp. 5444-5451, doi: 10.1210/jc.2003-030791.

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Title Muscle oxidative capacity is a better predictor of insulin sensitivity than lipid status
Author(s) Bruce, Clinton R.ORCID iD for Bruce, Clinton R. orcid.org/0000-0002-0515-3343
Anderson, Mtichell J.
Carey, Andrew L.
Newman, David G.
Bonen, Arend
Kriketos, Adamandia D.
Cooney, Gregory J.
Hawley, John A.
Journal name Journal of clinical endocrinology and metabolism
Volume number 88
Issue number 11
Start page 5444
End page 5451
Total pages 8
Publisher The Endocrine Society
Place of publication Washington, DC
Publication date 2003
ISSN 0021-972X
1945-7197
Summary We determined whole-body insulin sensitivity, long-chain fatty acyl coenzyme A (LCACoA) content, skeletal muscle triglyceride (TGm) concentration, fatty acid transporter protein content, and oxidative enzyme activity in eight patients with type 2 diabetes (TYPE 2); six healthy control subjects matched for age (OLD), body mass index, percentage of body fat, and maximum pulmonary O2 uptake; nine well-trained athletes (TRAINED); and four age-matched controls (YOUNG). Muscle biopsies from the vastus lateralis were taken before and after a 2-h euglycemic-hyperinsulinemic clamp. Oxidative enzyme activities, fatty acid transporters (FAT/CD36 and FABPpm), and TGm were measured from basal muscle samples, and total LCACoA content was determined before and after insulin stimulation. Whole-body insulin-stimulated glucose uptake was lower in TYPE 2 (P < 0.05) than in OLD, YOUNG, and TRAINED. TGm was elevated in TYPE 2 compared with all other groups (P < 0.05). However, both basal and insulin-stimulated skeletal muscle LCACoA content were similar. Basal citrate synthase activity was higher in TRAINED (P < 0.01), whereas β-hydroxyacyl CoA dehydrogenase activity was higher in TRAINED compared with TYPE 2 and OLD. There was a significant relationship between the oxidative capacity of skeletal muscle and insulin sensitivity (citrate synthase, r = 0.71, P < 0.001; β-hydroxyacyl CoA dehydrogenase, r = 0.61, P = 0.001). No differences were found in FAT/CD36 protein content between groups. In contrast, FABPpm protein was lower in OLD compared with TYPE 2 and YOUNG (P < 0.05). In conclusion, despite markedly elevated skeletal muscle TGm in type 2 diabetic patients and strikingly different levels of whole-body glucose disposal, both basal and insulin-stimulated LCACoA content were similar across groups. Furthermore, skeletal muscle oxidative capacity was a better predictor of insulin sensitivity than either TGm concentration or long-chain fatty acyl CoA content.
Language eng
DOI 10.1210/jc.2003-030791
Field of Research 119999 Medical and Health Sciences not elsewhere classified
Socio Economic Objective 970111 Expanding Knowledge in the Medical and Health Sciences
HERDC Research category C1.1 Refereed article in a scholarly journal
Persistent URL http://hdl.handle.net/10536/DRO/DU:30067063

Document type: Journal Article
Collections: Faculty of Health
School of Health and Social Development
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