Changes in indices of antioxidant status, lipid peroxidation and inflammation in human skeletal muscle after eccentric muscle actions

Author:

CHILD R.1,BROWN S.2,DAY S.3,DONNELLY A.4,ROPER H.5,SAXTON J.6

Affiliation:

1. Muscle Research Centre, Department of Medicine, University Clinical Departments, Liverpool University, c/o The Duncan Building, Daulby Street, Liverpool L69 3GA, U.K.

2. School of Health and Sport Science, University of North London, London N7 8DB, U.K.

3. Department of Health, Staffordshire University, Stafford ST4 2DF, U.K.

4. Department of Physical Education and Sport Science, Limerick University, Limerick, Ireland

5. Department of Paediatrics, Birmingham Heartlands Hospital, Birmingham B9 5SS, U.K.

6. Institute of Sports Medicine and Exercise Science, Sheffield University, Sheffield S10 2TA, U.K.

Abstract

This study investigated the effects of chronic muscle inflammation on indices of antioxidant status and muscle injury after eccentric exercise. Eight subjects each performed 70 maximal voluntary eccentric muscle actions on an isokinetic dynamometer, using the knee extensors of a single leg. Venous blood samples were collected into serum and EDTA tubes 5 and 3 days before exercise, immediately before exercise, and then again on days 3, 4, 5, 6, 7, 10 and 12 after the bout. Needle biopsies were taken from the vastus lateralis of six subjects, a week before exercise (baseline), and again on days 4 and 7 post-exercise. The concentrations of malondialdehyde in plasma and muscle were used as markers of lipid peroxidation. Creatine kinase activity, β-glucuronidase activity and total antioxidant capacity were determined in serum. In muscle, aqueous and bound total antioxidant capacity, the aqueous sulphydryl concentration, and β-glucuronidase and glucose-6-phosphate dehydrogenase activity were determined. No changes were detected in serum total antioxidant capacity, serum creatine kinase and β-glucuronidase after the baseline biopsy. After exercise serum creatine kinase and β-glucuronidase were elevated although other serum measures were unchanged. In muscle, aqueous and bound total antioxidant capacity, sulphydryls, glucose-6-phosphate dehydrogenase and β-glucuronidase were all elevated. Despite evidence of inflammation in this study, muscle antioxidant status was not compromised, and malondialdehyde was unaltered in muscle and plasma. Therefore, this study provides no evidence that chronic muscle inflammation compromises antioxidant status or increases lipid peroxidation.

Publisher

Portland Press Ltd.

Subject

General Medicine

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