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

被引:184
作者
Bruce, CR
Anderson, MJ
Carey, AL
Newman, DG
Bonen, A
Kriketos, AD
Cooney, GJ
Hawley, JA
机构
[1] RMIT Univ, Sch Med Sci, Exercise Metab Grp, Bundoora, Vic 3083, Australia
[2] RMIT Univ, Sch Med Sci, Skeletal Muscle Res Lab, Bundoora, Vic 3083, Australia
[3] Univ Melbourne, Dept Physiol, Exercise Physiol & Metab Lab, Parkville, Vic 3052, Australia
[4] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
[5] St Vincents Hosp, Garvan Inst Med Res, Sydney, NSW 2010, Australia
关键词
D O I
10.1210/jc.2003-030791
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We determined whole-body insulin sensitivity, long-chain fatty acyl coenzyme A (LCACoA) content, skeletal muscle triglyceride (TG(m)) 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 O(2) 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. TG(m) 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 beta-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; beta-hydroxyacylCoAdehydrogenase, 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 TG(m) 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 TG(m) concentration or long-chain fatty acyl CoA content.
引用
收藏
页码:5444 / 5451
页数:8
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