Quantitative histology and MGF gene expression in rats following SSC exercise in vivo

Med Sci Sports Exerc. 2006 Mar;38(3):463-71. doi: 10.1249/01.mss.0000191419.67030.69.

Abstract

Purpose: We investigated the effects of muscle length during stretch-shortening cycles (SSC) in vivo on changes in MGF gene expression and quantitative morphometry in rat skeletal muscle.

Methods: Dorsiflexor muscles of male Sprague-Dawley rats were exposed to seven sets of 10 SSC at 500 degrees .s(-1). Animals were randomly assigned to a long muscle length injury group (L-inj), short muscle length injury group (S-inj), or isometric group (Iso), with recoveries examined at 6 or 48 h post-injury for each group. Following exposure, animals were euthanized, and the tissue was prepared for either histology (quantitative morphometry) or RNA isolation, followed by quantitative real-time reverse transcriptase polymerase chain reaction. mRNA levels were measured for mechano-growth factor (MGF), while 18S ribosomal RNA served as the internal reference sample.

Results: Stereological measures indicative of edema and myofiber degeneration were significantly increased in the L-inj SSC group at 48 h when compared with the S-inj or Iso group. MGF mRNA was increased transiently at 6 h in the isometric group. In contrast, MGF mRNA was increased at 48 h in the S-inj, but was not increased at either time point in the L-inj group.

Conclusion: These data strongly indicate that exposure to SSC at longer muscle lengths result in greater morphometric indices of inflammation and degeneration than SSC conducted at a shorter muscle lengths or isometric contractions, at the same time that the adaptation to SSC was prolonged and, apparently, not resolved in the L-inj group that was manifested by the lack of up-regulation in MGF mRNA.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Animals
  • Gene Expression / genetics*
  • Isometric Contraction / physiology*
  • Male
  • Musculoskeletal System / injuries*
  • Musculoskeletal System / physiopathology
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • West Virginia

Substances

  • RNA, Messenger