A COX-2 inhibitor reduces muscle soreness, but does not influence recovery and adaptation after eccentric exercise

Scand J Med Sci Sports. 2010 Feb;20(1):e195-207. doi: 10.1111/j.1600-0838.2009.00947.x. Epub 2009 Jun 3.

Abstract

The aim of this study was to investigate the effect of a cyclooxygenase (COX)-2 inhibitor on the recovery of muscle function, inflammation, regeneration after, and adaptation to, unaccustomed eccentric exercise. Thirty-three young males and females participated in a double-blind, placebo-controlled experiment. Seventy unilateral, voluntary, maximal eccentric actions with the elbow flexors were performed twice (bouts 1 and 2) with the same arm, separated by 3 weeks. The test group participants were administered 400 mg/day of celecoxib for 9 days after bout 1. After both bouts 1 and 2, concentric and isometric force-generating capacity was immediately reduced (approximately 40-50%), followed by the later appearance of muscle soreness and increased serum creatine kinase levels. Radiolabelled autologous leukocytes (detected by scintigraphy) and monocytes/macrophages (histology) accumulated in the exercised muscles, simultaneously with increased satellite cell activity. These responses were reduced and recovery was faster after bout 2 than 1, demonstrating a repeated-bout effect. No differences between the celecoxib and placebo groups were detected, except for muscle soreness, which was attenuated by celecoxib. In summary, celecoxib, a COX-2 inhibitor, did not detectably affect recovery of muscle function or markers of inflammation and regeneration after unaccustomed eccentric exercise, nor did the drug influence the repeated-bout effect. However, it alleviated muscle soreness.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / drug effects
  • Adult
  • Arm / physiology
  • Celecoxib
  • Cyclooxygenase 2 Inhibitors / pharmacology*
  • Dinoprostone / metabolism
  • Double-Blind Method
  • Exercise / physiology*
  • Female
  • Humans
  • Immunohistochemistry
  • Isometric Contraction / drug effects
  • Leukocytes / metabolism
  • Male
  • Microdialysis
  • Muscle Contraction / drug effects*
  • Muscle Contraction / physiology
  • Muscle, Skeletal / diagnostic imaging
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Pain / physiopathology
  • Pain / prevention & control*
  • Pyrazoles / pharmacology*
  • Radionuclide Imaging
  • Recovery of Function / drug effects*
  • Recovery of Function / physiology
  • Satellite Cells, Skeletal Muscle / metabolism
  • Sulfonamides / pharmacology*
  • Young Adult

Substances

  • Cyclooxygenase 2 Inhibitors
  • Pyrazoles
  • Sulfonamides
  • Celecoxib
  • Dinoprostone