Microvascular adaptations to resistance training are independent of load in resistance-trained young men

Am J Physiol Regul Integr Comp Physiol. 2018 Aug 1;315(2):R267-R273. doi: 10.1152/ajpregu.00118.2018. Epub 2018 Jun 13.

Abstract

Resistance training promotes microvasculature expansion; however, it remains unknown how different resistance training programs contribute to angiogenesis. Thus, we recruited experienced resistance-trained participants and determined the effect of 12 wk of either high-repetition/low-load or low-repetition/high-load resistance training performed to volitional fatigue on muscle microvasculature. Twenty men performed either a high-repetition [20-25 repetitions, 30-50% of 1-repetition maximum (1RM); n = 10] or a low-repetition (8-12 repetitions, 75-90% of 1RM; n = 10) resistance training program. Muscle biopsies were taken before and after resistance training, and immunohistochemistry was used to assess fiber type (I and II)-specific microvascular variables. High-repetition/low-load and low-repetition/high-load groups were not different in any variable before resistance training. Both protocols resulted in an increase in capillarization. Specifically, after resistance training, the capillary-to-fiber ratio, capillary contacts, and capillary-to-fiber perimeter exchange index were elevated, and sharing factor was reduced. These data demonstrate that resistance training performed to volitional failure, using either high repetition/low load or low repetition/high load, induced similar microvascular adaptations in recreationally resistance-trained young men.

Keywords: capillary; health; resistance training; skeletal muscle.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Age Factors
  • Body Composition
  • Humans
  • Male
  • Microvessels / metabolism
  • Microvessels / physiology*
  • Mitochondria, Muscle / metabolism
  • Muscle Contraction*
  • Muscle Strength
  • Muscle, Skeletal / blood supply*
  • Muscle, Skeletal / metabolism
  • Neovascularization, Physiologic*
  • Nitric Oxide Synthase Type III / metabolism
  • Ontario
  • Oxidative Phosphorylation
  • Resistance Training*
  • Sex Factors
  • Time Factors
  • Vascular Endothelial Growth Factor A / metabolism
  • Young Adult

Substances

  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III