4.5 Article

Proteolytic mRNA expression in response to acute resistance exercise in human single skeletal muscle fibers

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 101, Issue 5, Pages 1442-1450

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00438.2006

Keywords

gene expression; tumor necrosis factor-alpha; calpain; muscle really interesting novel gene finger-1; atrogin-1; muscle atrophy F-box; caspase-3; Bcl-2-associated X protein; B-cell leukemia/lymphoma-2

Funding

  1. NIA NIH HHS [AG-18409] Funding Source: Medline

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The purpose of this study was to characterize changes in mRNA expression of select proteolytic markers in human slow-twitch [myosin heavy chain (MHC) 1] and fast-twitch (MHC Pi a) single skeletal muscle fibers following a bout of resistance exercise (RE). Muscle biopsies were obtained from the vastus lateralis of eight young healthy sedentary men [23 +/- 2 yr (mean +/- SID), 93 +/- 17 kg, 183 +/- 6 cm] before and 4 and 24 h after 3 X 10 repetitions of bilateral knee extensions at 65% of one repetition maximum. The mRNA levels of TNF-alpha, calpains 1 and 2, muscle RING (really interesting novel gene) finger-1 (MuRF-1), atrogin-1, caspase-3, B-cell leukemia/lymphoma (Bcl)-2, and Bcl-2-associated X protein (Bax) were quantified using real-time RT-PCR. Generally, MHC I fibers had higher (1.6- to 5.0-fold, P < 0.05) mRNA expression pre- and post-RE. One exception was a higher (1.6- to 3.9-fold, P < 0.05) Bax-to-Bcl-2 mRNA ratio in MHC Pi a fibers pre- and post-RE. RE increased (1.4- to 4.8-fold, P < 0.05) MuRF-1 and caspase-3 mRNA levels 4-24 h post-RE in both fiber types, whereas Bax-to-Bcl-2 mRNA ratio increased 2.2-fold (P < 0.05) at 4 It post-RE only in MHC I fibers. These results suggest that MHC I fibers have a greater proteolytic mRNA expression pre- and post-RE compared with MHC Pi a fibers. The greatest mRNA induction following RE was in MuRF-1 and caspase-3 in both fiber types. This altered and specific proteolytic mRNA expression among slow-and fast-twitch muscle fibers indicates that the ubiquitin/proteasomal and caspase pathways may play an important role in muscle remodeling with RE.

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