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

被引:16
作者
Baker, BA [1 ]
Rao, KMK [1 ]
Mercer, RR [1 ]
Geronilla, KB [1 ]
Kashon, ML [1 ]
Miller, GR [1 ]
Cutlip, RG [1 ]
机构
[1] NIOSH, Hlth Effects Lab Div, Morgantown, WV 26505 USA
关键词
muscle injury; stretch; shortening cycles; stereology; mRNA expression;
D O I
10.1249/01.mss.0000191419.67030.69
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
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 D-eater 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.
引用
收藏
页码:463 / 471
页数:9
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