Excitation–contraction coupling properties in women with work-related myalgia: a preliminary study

Author:

Green Howard J.12,Ranney Don123,Burnett Margaret1,Galvin Patti4,Kyle Natasha1,Lounsbury David1,Ouyang Jing1,Smith Ian C.1,Stewart Riley1,Tick Heather56,Tupling A. Russell12

Affiliation:

1. Department of Kinesiology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.

2. Centre of Research Expertise for the Prevention of Musculoskeletal Disorders (CRE-MSD), Faculty of Applied Health Sciences, University of Waterloo, 200 University Avenue West, Waterloo, ON N2L 3G1, Canada.

3. Disability Assessment Services, Inc., RR#1 Arthur, Waterloo, ON N0G 1A0, Canada.

4. Wellington Orthopaedic and Rehabilitation Centre, 86 Dawson Road, Unit 3, Guelph, ON N1H 1A8, Canada.

5. Mind-Body Medicine, The RSI Clinic, 79 St. Clair Avenue East, Toronto, ON M4T 1M6, Canada.

6. Departments of Family Medicine and Anaesthesiology & Pain Medicine, University of Washington, 1959 NE Pacific Street, BB-1469, Seattle, WA 98195-6540, USA.

Abstract

We investigated the potential role of selected excitation–contraction coupling processes in females with work-related myalgia (WRM) by comparing WRM with healthy controls (CON) using tissue from extensor carpi radialis brevis (ECRB) and trapezius (TRAP) muscles. For the ECRB, age (mean ± SE) was 29.6 ± 3.5 years for CON (n = 9) and 39.2 ± 2.8 years for WRM (n = 13), while for the TRAP, the values were 26.0 ± 2.1 years for CON (n = 7) and 44.6 ± 2.9 years for WRM (n = 11). For the sarcoplasmic reticulum (SR) of the ECRB, WRM displayed concentrations (nmol·(mg protein)−1·min−1) that were lower (P < 0.05) for Total (202 ± 4.4 vs 178 ± 7.1), Basal (34 ± 1.6 vs 30.1 ± 1.3), and maximal Ca2+-ATPase activity (Vmax, 168 ± 4.9 vs 149 ± 6.3), and Ca2+-uptake (5.06 ± 0.31 vs 4.13 ± 0.29), but not SERCA1a and SERCA2a isoforms, by comparison with CON. When age was incorporated as a co-variant, Total, Basal, and Ca2+-uptake remained different from CON (P < 0.05), but not Vmax (P = 0.13). For TRAP, none of the ATPase properties differed between groups (P > 0.05) either before or following adjustment for age. No differences (P > 0.05) were observed between the groups for Ca2+-release in the SR for either TRAP or ECRB. Similarly, no deficiencies, regardless of muscle, were noted for either the Na+–K+-ATPase content or the α and β subunit isoform distribution in WRM. This preliminary study provides a basis for further research, with expanded numbers, investigating the hypothesis that abnormalities in SR Ca2+-regulation are involved in the cellular etiology of WRM.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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