Betaine Supplementation Enhances Circulating Anabolic Hormones And Akt Muscle Signaling In Humans

PURPOSE: The aim of this study was to further investigate betaine ergogenicity. Specifically, we characterized betaine effects on circulating hormone concentrations and Akt muscle signaling proteins. METHODS: Twelve men (age, 19.7 + or - 1.23 years; body fat, 18.7 + or - 7.0%) performed an Acute Exe...

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Published in:Medicine and science in sports and exercise Vol. 44; no. 5S; p. 949
Main Authors: Apicella, Jenna M, Lee, Elaine C, Bailey, Brooke L, Saenz, Catherine, Anderson, Jeffrey M, Craig, Stuart AS, Kraemer, William J, Volek, Jeff S, Maresh, Carl M
Format: Journal Article
Language:English
Published: 01-05-2012
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Abstract PURPOSE: The aim of this study was to further investigate betaine ergogenicity. Specifically, we characterized betaine effects on circulating hormone concentrations and Akt muscle signaling proteins. METHODS: Twelve men (age, 19.7 + or - 1.23 years; body fat, 18.7 + or - 7.0%) performed an Acute Exercise Test (AET) before and after two weeks of supplementation with either betaine (B) (1.25g BID) or placebo (P) with a two-week washout period between treatments. Circulating (serum/plasma) GH, IGF-1, cortisol, and insulin were measured. Vastus lateralis muscle samples were analyzed for select signaling proteins (Akt, p70 S6k, AMPK). RESULTS: B (vs. P) supplementation increased GH (mean + or - SD (Area Under the Curve, AUC), B: 40.72 + or - 6.14, P: 38.28 + or - 5.54, p = 0.060) and IGF-1 (mean + or - SD (AUC), B: 106.19 + or - 13.44, P: 92.45 + or - 10.14, p = 0.010), but decreased cortisol (mean + or - SD (AUC), B: 1149.63 + or - 80.83, P: 1228.53 + or - 130.32, p = 0.007). There were no differences in insulin (AUC). B increased resting total muscle Akt (p =0.003). B potentiated phosphorylation (relative to P) of Akt (Ser473) and p70 S6k (Thr389) (p =0.016 and p = 0.005, respectively). Phosphorylation of AMPK (Thr172) decreased during both treatments (both p = 0.001). CONCLUSION: Betaine supplementation fostered an anabolic endocrine profile: increased GH and IGF-1 and decreased cortisol. This hormonal profile suggests signaling that promotes increased protein synthesis. We conclude that betaine supplementation may provide ergogenic benefit via a heightened anabolic endocrine profile that supports increases in protein synthesis.
AbstractList PURPOSE: The aim of this study was to further investigate betaine ergogenicity. Specifically, we characterized betaine effects on circulating hormone concentrations and Akt muscle signaling proteins. METHODS: Twelve men (age, 19.7 + or - 1.23 years; body fat, 18.7 + or - 7.0%) performed an Acute Exercise Test (AET) before and after two weeks of supplementation with either betaine (B) (1.25g BID) or placebo (P) with a two-week washout period between treatments. Circulating (serum/plasma) GH, IGF-1, cortisol, and insulin were measured. Vastus lateralis muscle samples were analyzed for select signaling proteins (Akt, p70 S6k, AMPK). RESULTS: B (vs. P) supplementation increased GH (mean + or - SD (Area Under the Curve, AUC), B: 40.72 + or - 6.14, P: 38.28 + or - 5.54, p = 0.060) and IGF-1 (mean + or - SD (AUC), B: 106.19 + or - 13.44, P: 92.45 + or - 10.14, p = 0.010), but decreased cortisol (mean + or - SD (AUC), B: 1149.63 + or - 80.83, P: 1228.53 + or - 130.32, p = 0.007). There were no differences in insulin (AUC). B increased resting total muscle Akt (p =0.003). B potentiated phosphorylation (relative to P) of Akt (Ser473) and p70 S6k (Thr389) (p =0.016 and p = 0.005, respectively). Phosphorylation of AMPK (Thr172) decreased during both treatments (both p = 0.001). CONCLUSION: Betaine supplementation fostered an anabolic endocrine profile: increased GH and IGF-1 and decreased cortisol. This hormonal profile suggests signaling that promotes increased protein synthesis. We conclude that betaine supplementation may provide ergogenic benefit via a heightened anabolic endocrine profile that supports increases in protein synthesis.
Author Volek, Jeff S
Saenz, Catherine
Apicella, Jenna M
Bailey, Brooke L
Kraemer, William J
Anderson, Jeffrey M
Craig, Stuart AS
Maresh, Carl M
Lee, Elaine C
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