Bone plasticity in response to exercise is sex-dependent in rats

PLoS One. 2013 May 31;8(5):e64725. doi: 10.1371/journal.pone.0064725. Print 2013.

Abstract

Purpose: To characterize the potential sexual dimorphism of bone in response to exercise.

Methods: Young male and female Wistar rats were either submitted to 12 weeks of exercise or remained sedentary. The training load was adjusted at the mid-trial (week 6) by the maximal speed test. A mechanical test was performed to measure the maximal force, resilience, stiffness, and fracture load. The bone structure, formation, and resorption were obtained by histomorphometric analyses. Type I collagen (COL I) mRNA expression and tartrate-resistant acid phosphatase (TRAP) mRNA expression were evaluated by quantitative real-time PCR (qPCR).

Results: The male and female trained rats significantly improved their maximum speed during the maximal exercise test (main effect of training; p<0.0001). The male rats were significantly heavier than the females, irrespective of training (main effect of sex; p<0.0001). Similarly, both the weight and length of the femur were greater for the male rats when compared with the females (main effect of sex; p<0.0001 and p<0.0001, respectively). The trabecular volume was positively affected by exercise in male and female rats (main effect of training; p = 0.001), whereas the trabecular thickness, resilience, mineral apposition rate, and bone formation rate increased only in the trained males (within-sex comparison; p<0.05 for all parameters), demonstrating the sexual dimorphism in response to exercise. Accordingly, the number of osteocytes increased significantly only in the trained males (within-sex comparison; p<0.05). Pearson's correlation analyses revealed that the COL I mRNA expression and TRAP mRNA expression were positively and negatively, respectively, related to the parameters of bone remodeling obtained from the histomorphometric analysis (r = 0.59 to 0.85; p<0.05).

Conclusion: Exercise yielded differential adaptations with respect to bone structure, biomechanical proprieties, and molecular signaling in male and female rats.

MeSH terms

  • Acid Phosphatase / genetics
  • Acid Phosphatase / metabolism
  • Animals
  • Biomarkers / metabolism
  • Collagen Type I / genetics
  • Collagen Type I / metabolism
  • Elasticity
  • Female
  • Femur / anatomy & histology
  • Femur / cytology
  • Femur / physiology*
  • Fractures, Bone / prevention & control
  • Gene Expression
  • Hardness
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Male
  • Osteocytes / cytology
  • Osteocytes / physiology*
  • Physical Conditioning, Animal / physiology*
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Sex Factors
  • Tartrate-Resistant Acid Phosphatase

Substances

  • Biomarkers
  • Collagen Type I
  • Isoenzymes
  • RNA, Messenger
  • Acid Phosphatase
  • Tartrate-Resistant Acid Phosphatase

Grants and funding

The authors have no support or funding to report.