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This version published online on December 18, 2007
Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2007-1981
A more recent version of this article appeared on March 1, 2008
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Submitted on September 5, 2007
Accepted on December 6, 2007

Calpain-10 mRNA and protein levels in human skeletal muscle: Effect of acute lipid-induced insulin resistance and type 2 diabetes

L. Norton, T. Parr, K. Chokkalingam, R. G. Bardsley, H. Ye, G. I. Bell, M. M.A.L. Pelsers, L. J.C. van Loon, and K. Tsintzas*

Centre for Integrated Systems Biology and Medicine, School of Biomedical Sciences, Nottingham University Medical School, Queens Medical Centre, Nottingham, NG7 2UH, UK; Division of Nutritional Sciences, School of Biosciences, Sutton Bonington Campus, University of Nottingham, LE12 5RD, UK; Department of Medicine, University of Chicago, Chicago, IL 60637, USA; Department of Movement Sciences, Maastricht University, Maastricht, The Netherlands

* To whom correspondence should be addressed. E-mail: Kostas.Tsintzas{at}nottingham.ac.uk.

Objective: To investigate the effect of lipid-induced insulin resistance and type 2 diabetes on skeletal muscle calpain-10 mRNA and protein levels.

Research design and methods: In the first part of this study, 10 healthy subjects underwent hyperinsulinemic euglycemic (4.5 mmol/l) clamps for 6 h with intravenous infusion of either saline (CON) or a 20% Intralipid emulsion (LIPID). Skeletal muscle biopsies were taken before and after 3 and 6 h of insulin infusion and analyzed for calpain-10 mRNA and protein expression. In the second part of the study, muscle samples obtained after an overnight fast in 10 long-standing, sedentary type 2 diabetes patients, 10 sedentary, weight-matched, normoglycemic controls, and 10 age-matched, endurance trained cyclists were analyzed for calpain-10 mRNA and protein content.

Results: Intralipid infusion in healthy subjects reduced whole body glucose disposal by approximately 50% (P<0.001). Calpain-10 mRNA (P=0.01) but not protein content was reduced following 6 h of insulin infusion in both the CON and LIPID trials. Skeletal muscle calpain-10 mRNA and protein content did not differ between the type 2 diabetes patients and normoglycemic controls, but there was a strong trend for total calpain-10 protein to be greater in the endurance trained athletes (P=0.06).

Conclusions: These data indicate that skeletal muscle calpain-10 expression is not modified by insulin resistance per se, and suggest that hyperinsulinemia and exercise training may modulate human skeletal muscle calpain-10 expression.







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