Exercise-induced muscle damage is reduced in resistance-trained males by branched chain amino acids: a randomized, double-blind, placebo controlled study - PubMed (original) (raw)

Exercise-induced muscle damage is reduced in resistance-trained males by branched chain amino acids: a randomized, double-blind, placebo controlled study

Glyn Howatson et al. J Int Soc Sports Nutr. 2012.

Abstract

Background: It is well documented that exercise-induced muscle damage (EIMD) decreases muscle function and causes soreness and discomfort. Branched-chain amino acid (BCAA) supplementation has been shown to increase protein synthesis and decrease muscle protein breakdown, however, the effects of BCAAs on recovery from damaging resistance training are unclear. Therefore, the aim of this study was to examine the effects of a BCAA supplementation on markers of muscle damage elicited via a sport specific bout of damaging exercise in trained volunteers.

Methods: Twelve males (mean ± SD age, 23 ± 2 y; stature, 178.3 ± 3.6 cm and body mass, 79.6 ± 8.4 kg) were randomly assigned to a supplement (n = 6) or placebo (n = 6) group. The damaging exercise consisted of 100 consecutive drop-jumps. Creatine kinase (CK), maximal voluntary contraction (MVC), muscle soreness (DOMS), vertical jump (VJ), thigh circumference (TC) and calf circumference (CC) were measured as markers of muscle damage. All variables were measured immediately before the damaging exercise and at 24, 48, 72 and 96 h post-exercise.

Results: A significant time effect was seen for all variables. There were significant group effects showing a reduction in CK efflux and muscle soreness in the BCAA group compared to the placebo (P<0.05). Furthermore, the recovery of MVC was greater in the BCAA group (P<0.05). The VJ, TC and CC were not different between groups.

Conclusion: The present study has shown that BCAA administered before and following damaging resistance exercise reduces indices of muscle damage and accelerates recovery in resistance-trained males. It seems likely that BCAA provided greater bioavailablity of substrate to improve protein synthesis and thereby the extent of secondary muscle damage associated with strenuous resistance exercise.

Clinical trial registration number: NCT01529281.

Keywords: BCAA; Muscle damage; Recovery; Resistance training.

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Figures

Figure 1

Figure 1

Experimental design and a flow diagram of the participants allocation to groups.

Figure 2

Figure 2

Plasma creatine kinase concentration before and up to 96 h after the damaging bout of exercise. * denotes a significant group effect. Values are means ± SD; N = 12.

Figure 3

Figure 3

Delayed onset muscle soreness before and up to 96 h after the damaging bout of exercise. * denotes a significant group effect. Values are means ± SD; N = 12.

Figure 4

Figure 4

Maximal voluntary force before and up to 96 h after the damaging bout of exercise. * denotes a significant group effect. Values are means ± SD; N = 12.

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References

    1. Adams GR, Cheng DC, Haddad F, Baldwin KM. Skeletal muscle hypertrophy in response to isometric, lengthening, and shortening training bouts of equivalent duration. J Appl Physiol. 2004;96:1613–1618. doi: 10.1152/japplphysiol.01162.2003. - DOI - PubMed
    1. Higbie EJ, Cureton KJ, Warren GL, Prior BM. Effects of concentric and eccentric training on muscle strength, cross-sectional area, and neural activation. J Appl Physiol. 1996;81:2173–2181. - PubMed
    1. Hortobagyi T, Hill JP, Houmard JA, Fraser DD, Lambert NJ, Israel RG. Adaptive responses to muscle lengthening and shortening in humans. J Appl Physiol. 1996;80:765–772. - PubMed
    1. Howatson G, van Someren KA. The prevention and treatment of exercise-induced muscle damage. Sports Med. 2008;38:483–503. doi: 10.2165/00007256-200838060-00004. - DOI - PubMed
    1. Howatson G, Hough P, Pattison J, Hill JA, Blagrove R, Glaister M, Thompson KG. Trekking poles reduce exercise-induced muscle injury during mountain walking. Med Sci Sports Exerc. 2010;43:140–145. - PubMed

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