4.6 Article

Human muscle gene expression following resistance exercise and blood flow restriction

Journal

MEDICINE AND SCIENCE IN SPORTS AND EXERCISE
Volume 40, Issue 4, Pages 691-698

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1249/MSS.0b013e318160ff84

Keywords

mRNA; HIF-1 alpha; REDD1; mTOR; ischemia-reperfusion

Categories

Funding

  1. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [K12HD055929] Funding Source: NIH RePORTER
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [S10RR016650, M01RR000073] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR049877] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE ON AGING [P30AG024832] Funding Source: NIH RePORTER
  5. NCRR NIH HHS [M01 RR00073, S10 RR16650, M01 RR000073] Funding Source: Medline
  6. NIAMS NIH HHS [R01 AR049877] Funding Source: Medline
  7. NIA NIH HHS [P30 AG024832] Funding Source: Medline
  8. NICHD NIH HHS [K12 HD055929] Funding Source: Medline

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Introduction: Blood flow restriction in combination with low-intensity resistance exercise (REFR) increases skeletal muscle size to a similar extent as compared with traditional high-intensity resistance exercise training. However, there are limited data describing the molecular adaptations that occur after REFR. Purpose: To determine whether hypoxia inducible factor-1 alpha (HIF-1 alpha) and REDD1 mRNA are expressed differently in REFR compared with low-intensity resistance exercise with no blood flow restriction (CONTROL). Secondly, to determine whether low-intensity resistance exercise is able to induce changes in mRNA expression of several anabolic and catabolic genes as typically seen with high-intensity resistance exercise. Methods: Six subjects were studied at baseline and 3 h after a bout of leg resistance exercise (20% 1RM) in REFR and CONTROL subjects. Each subject participated in both groups, with 3 wk separating each visit. Muscle biopsy samples were analyzed for mRNA expression, using qRT-PCR. Results: Our primary finding was that there were no differences between CONTROL and REFR for any of the selected genes at 3 h after exercise (P > 0.05). However, low-intensity resistance exercise increased HIF-1 alpha, p21, MyoD, and muscle RING finger 1 (MuRF1) mRNA expression and decreased REDD1 and myostatin mRNA expression in both groups (P < 0.05). Conclusion: Low-intensity resistance exercise can alter skeletal muscle mRNA expression of several genes associated with muscle growth and remodeling, such as REDD1, HIF-1 alpha, MyoD, MuRF1, and myostatin. Further, the results from REFR and CONTROL were similar, indicating that the changes in early postexercise gene expression were attributable to the low-intensity resistance exercise bout, and not blood flow restriction.

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