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Erschienen in: Drugs & Aging 11/2017

31.10.2017 | Review Article

The Potential of β-Hydroxy-β-Methylbutyrate as a New Strategy for the Management of Sarcopenia and Sarcopenic Obesity

verfasst von: Andrea P. Rossi, Alessia D’Introno, Sofia Rubele, Cesare Caliari, Stefano Gattazzo, Elena Zoico, Gloria Mazzali, Francesco Fantin, Mauro Zamboni

Erschienen in: Drugs & Aging | Ausgabe 11/2017

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Abstract

Sarcopenia is defined as an age-related loss of skeletal muscle mass and function and is recognized as a major clinical problem for older people. Essential amino acid supplementation, particularly β-hydroxy-β-methylbutyrate (HMB), a metabolite of leucine that is produced in skeletal muscle, has been evaluated in several studies as a nutritional approach to enhancing muscle protein synthesis in healthy or frail elderly subjects. Studies performed in in vitro conditions show that HMB may be effective in the treatment of muscle wasting, increasing myogenesis, reducing muscle apoptosis, and having a positive effect on muscle protein turnover; however, studies of the effects of HMB conducted in old animals have reported conflicting results. Clinical trials performed in older adults confirm that HMB can attenuate the progression of sarcopenia in elderly subjects. HMB supplementation results in an increase in skeletal muscle mass and strength in the elderly and its effect is even greater when combined with physical exercise. The role of HMB in sarcopenic obesity management is still under debate and a general lack of intervention studies in this population must be recognized. In conclusion, HMB appears to be effective for enhancing muscle mass and strength in the elderly. Less certain is the role of HMB supplementation in reducing fat mass and, thus, in the treatment of sarcopenic obesity.
Literatur
1.
Zurück zum Zitat Cruz-Jentoft AJ, Baeyens JP, Bauer JM, et al. Sarcopenia: European consensus on definition and diagnosis: report of the European Working Group on Sarcopenia in Older People. Age Ageing. 2010;39(4):412–23.CrossRefPubMedPubMedCentral Cruz-Jentoft AJ, Baeyens JP, Bauer JM, et al. Sarcopenia: European consensus on definition and diagnosis: report of the European Working Group on Sarcopenia in Older People. Age Ageing. 2010;39(4):412–23.CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Volpi E, Rasmussen BB. Nutrition and muscle protein metabolism in the elderly. Diabetes Nutr Metab. 2000;13:99–107.PubMed Volpi E, Rasmussen BB. Nutrition and muscle protein metabolism in the elderly. Diabetes Nutr Metab. 2000;13:99–107.PubMed
3.
Zurück zum Zitat Morley JE, Argiles JM, Evans WJ, Society for Sarcopenia, Cachexia, and Wasting Disease, et al. Nutritional recommendations for the management of sarcopenia. J Am Med Dir Assoc. 2010;11:391–6.CrossRefPubMedPubMedCentral Morley JE, Argiles JM, Evans WJ, Society for Sarcopenia, Cachexia, and Wasting Disease, et al. Nutritional recommendations for the management of sarcopenia. J Am Med Dir Assoc. 2010;11:391–6.CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Kerstetter JE, O’Brien KO, Insogna KL. Low protein intake: the impact on calcium and bone homeostasis in humans. J Nutr. 2003;133:855S–61S.PubMed Kerstetter JE, O’Brien KO, Insogna KL. Low protein intake: the impact on calcium and bone homeostasis in humans. J Nutr. 2003;133:855S–61S.PubMed
5.
Zurück zum Zitat Fulgoni VL 3rd. Current protein intake in America: analysis of the National Health and Nutrition Examination Survey, 2003–2004. Am J Clin Nutr. 2008;87:1554S–7S.PubMed Fulgoni VL 3rd. Current protein intake in America: analysis of the National Health and Nutrition Examination Survey, 2003–2004. Am J Clin Nutr. 2008;87:1554S–7S.PubMed
6.
Zurück zum Zitat Eley HL, Russell ST, Baxter JH, et al. Signaling pathways initiated by beta-hydroxy-beta-methylbutyrate to attenuate the depression of protein synthesis in skeletal muscle in response to cachectic stimuli. Am J Physiol Endocrinol Metab. 2007;293:E923–31.CrossRefPubMed Eley HL, Russell ST, Baxter JH, et al. Signaling pathways initiated by beta-hydroxy-beta-methylbutyrate to attenuate the depression of protein synthesis in skeletal muscle in response to cachectic stimuli. Am J Physiol Endocrinol Metab. 2007;293:E923–31.CrossRefPubMed
7.
Zurück zum Zitat Girón MD, Vílchez JD, Salto R, et al. Conversion of leucine to β-hydroxy-β-methylbutyrate by α-keto isocaproate dioxygenase is required for a potent stimulation of protein synthesis in L6 rat myotubes. Cachexia Sarcopenia Muscle. 2016;7:68–78.CrossRef Girón MD, Vílchez JD, Salto R, et al. Conversion of leucine to β-hydroxy-β-methylbutyrate by α-keto isocaproate dioxygenase is required for a potent stimulation of protein synthesis in L6 rat myotubes. Cachexia Sarcopenia Muscle. 2016;7:68–78.CrossRef
8.
Zurück zum Zitat Schiaffino S, Dyar KA, Ciciliot S, et al. Mechanisms regulating skeletal muscle growth and atrophy. FEBS J. 2013;280:4294–314.CrossRefPubMed Schiaffino S, Dyar KA, Ciciliot S, et al. Mechanisms regulating skeletal muscle growth and atrophy. FEBS J. 2013;280:4294–314.CrossRefPubMed
9.
Zurück zum Zitat Eley HL, Russell ST, Tisdale MJ. Attenuation of depression of muscle protein synthesis induced by lipopolysaccharide, tumor necrosis factor, and angiotensin II by beta-hydroxy-beta-methylbutyrate. Am J Physiol Endocrinol Metab. 2008;295:E1409–16.CrossRefPubMed Eley HL, Russell ST, Tisdale MJ. Attenuation of depression of muscle protein synthesis induced by lipopolysaccharide, tumor necrosis factor, and angiotensin II by beta-hydroxy-beta-methylbutyrate. Am J Physiol Endocrinol Metab. 2008;295:E1409–16.CrossRefPubMed
10.
Zurück zum Zitat Aversa Z, Alamdari N, Castillero E, et al. β-hydroxy-β-methylbutyrate (HMB) prevents dexamethasone-induced myotube atrophy. Biochem Biophys Res Commun. 2012;423:739–43.CrossRefPubMedPubMedCentral Aversa Z, Alamdari N, Castillero E, et al. β-hydroxy-β-methylbutyrate (HMB) prevents dexamethasone-induced myotube atrophy. Biochem Biophys Res Commun. 2012;423:739–43.CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Kornasio R, Riederer I, Butler-Browne G, et al. Beta-hydroxy-beta-methylbutyrate (HMB) stimulates myogenic cell proliferation, differentiation and survival via the MAPK/ERK and PI3K/Akt pathways. Biochim Biophys Acta. 2009;1793:755–63.CrossRefPubMed Kornasio R, Riederer I, Butler-Browne G, et al. Beta-hydroxy-beta-methylbutyrate (HMB) stimulates myogenic cell proliferation, differentiation and survival via the MAPK/ERK and PI3K/Akt pathways. Biochim Biophys Acta. 2009;1793:755–63.CrossRefPubMed
12.
Zurück zum Zitat Eley HL, Russell ST, Tisdale MJ. Mechanism of attenuation of muscle protein degradation induced by tumor necrosis factor-alpha and angiotensin II by beta-hydroxy-beta-methylbutyrate. Am J Physiol Endocrinol Metab. 2008;295:E1417–26.CrossRefPubMed Eley HL, Russell ST, Tisdale MJ. Mechanism of attenuation of muscle protein degradation induced by tumor necrosis factor-alpha and angiotensin II by beta-hydroxy-beta-methylbutyrate. Am J Physiol Endocrinol Metab. 2008;295:E1417–26.CrossRefPubMed
13.
Zurück zum Zitat Hao Y, Jackson JR, Wang Y, et al. β-Hydroxy-β-methylbutyrate reduces myonuclear apoptosis during recovery from hind limb suspension-induced muscle fiber atrophy in aged rats. Am J Physiol Regul Integr Comp Physiol. 2011;301:R701–15.CrossRefPubMedPubMedCentral Hao Y, Jackson JR, Wang Y, et al. β-Hydroxy-β-methylbutyrate reduces myonuclear apoptosis during recovery from hind limb suspension-induced muscle fiber atrophy in aged rats. Am J Physiol Regul Integr Comp Physiol. 2011;301:R701–15.CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Smith HJ, Mukerji P, Tisdale MJ. Attenuation of proteasome-induced proteolysis in skeletal muscle by (beta)-hydroxy-(beta)-methylbutyrate in cancer-induced muscle loss. Cancer Res. 2005;65:277–83.CrossRefPubMed Smith HJ, Mukerji P, Tisdale MJ. Attenuation of proteasome-induced proteolysis in skeletal muscle by (beta)-hydroxy-(beta)-methylbutyrate in cancer-induced muscle loss. Cancer Res. 2005;65:277–83.CrossRefPubMed
15.
Zurück zum Zitat Girón MD, Vílchez JD, Shreeram S, et al. β-Hydroxy-β-methylbutyrate (HMB) normalizes dexamethasone-induced autophagy-lysosomal pathway in skeletal muscle. PLoS One. 2015;10:e0117520.CrossRefPubMedPubMedCentral Girón MD, Vílchez JD, Shreeram S, et al. β-Hydroxy-β-methylbutyrate (HMB) normalizes dexamethasone-induced autophagy-lysosomal pathway in skeletal muscle. PLoS One. 2015;10:e0117520.CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Nissen S, Sharp R, Ray M, et al. The effect of the leucine metabolite β-hydroxy β-methylbutyrate on muscle metabolism during resistance-exercise training. J Appl Physiol (1985). 1996;81:2095–104. Nissen S, Sharp R, Ray M, et al. The effect of the leucine metabolite β-hydroxy β-methylbutyrate on muscle metabolism during resistance-exercise training. J Appl Physiol (1985). 1996;81:2095–104.
17.
Zurück zum Zitat Wilson JM, Grant SC, Lee SR, et al. Beta-hydroxy-beta-methyl-butyrate blunts negative age-related changes in body composition, functionality and myofiber dimensions in rats. J Int Soc Sports Nutr. 2012;9:18.CrossRefPubMedPubMedCentral Wilson JM, Grant SC, Lee SR, et al. Beta-hydroxy-beta-methyl-butyrate blunts negative age-related changes in body composition, functionality and myofiber dimensions in rats. J Int Soc Sports Nutr. 2012;9:18.CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Alway SE, Pereira SL, Edens NK, et al. β-Hydroxy-β-methylbutyrate (HMB) enhances the proliferation of satellite cells in fast muscles of aged rats during recovery from disuse atrophy. Exp Gerontol. 2013;48:973–84.CrossRefPubMed Alway SE, Pereira SL, Edens NK, et al. β-Hydroxy-β-methylbutyrate (HMB) enhances the proliferation of satellite cells in fast muscles of aged rats during recovery from disuse atrophy. Exp Gerontol. 2013;48:973–84.CrossRefPubMed
19.
Zurück zum Zitat Vallejo J, Spence M, Cheng AL, et al. Cellular and physiological effects of dietary supplementation with β-hydroxy-β-methylbutyrate (HMB) and β-alanine in late middle-aged mice. PLoS One. 2016;11:e0150066.CrossRefPubMedPubMedCentral Vallejo J, Spence M, Cheng AL, et al. Cellular and physiological effects of dietary supplementation with β-hydroxy-β-methylbutyrate (HMB) and β-alanine in late middle-aged mice. PLoS One. 2016;11:e0150066.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Park BS, Henning PC, Grant SC, et al. HMB attenuates muscle loss during sustained energy deficit induced by calorie restriction and endurance exercise. Metabolism. 2013;62:1718–29.CrossRefPubMed Park BS, Henning PC, Grant SC, et al. HMB attenuates muscle loss during sustained energy deficit induced by calorie restriction and endurance exercise. Metabolism. 2013;62:1718–29.CrossRefPubMed
21.
Zurück zum Zitat Baptista IL, Silva WJ, Artioli GG, et al. Leucine and HMB differentially modulate proteasome system in skeletal muscle under different sarcopenic conditions. PLoS One. 2013;8:e76752.CrossRefPubMedPubMedCentral Baptista IL, Silva WJ, Artioli GG, et al. Leucine and HMB differentially modulate proteasome system in skeletal muscle under different sarcopenic conditions. PLoS One. 2013;8:e76752.CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Russ DW, Acksel C, Boyd IM, et al. Dietary HMB and β-alanine co-supplementation does not improve in situ muscle function in sedentary, aged male rats. Appl Physiol Nutr Metab. 2015;40:1294–301.CrossRefPubMed Russ DW, Acksel C, Boyd IM, et al. Dietary HMB and β-alanine co-supplementation does not improve in situ muscle function in sedentary, aged male rats. Appl Physiol Nutr Metab. 2015;40:1294–301.CrossRefPubMed
23.
Zurück zum Zitat Van Someren KA, Edwards AJ, Howatson G. Supplementation with β-hydroxy-β-methylbutyrate (HMB) and α-ketoisocaproic acid (KIC) reduces signs and symptoms of exercise-induced muscle damage in man. Int J Sport Nutr Exerc Metab. 2005;15:413–24.CrossRefPubMed Van Someren KA, Edwards AJ, Howatson G. Supplementation with β-hydroxy-β-methylbutyrate (HMB) and α-ketoisocaproic acid (KIC) reduces signs and symptoms of exercise-induced muscle damage in man. Int J Sport Nutr Exerc Metab. 2005;15:413–24.CrossRefPubMed
24.
Zurück zum Zitat Wilkinson DJ, Hossain T, Hill DS, et al. Effects of leucine and its metabolite β-hydroxy-β-methylbutyrate on human skeletal muscle protein metabolism. J Physiol. 2013;591:2911–23.CrossRefPubMedPubMedCentral Wilkinson DJ, Hossain T, Hill DS, et al. Effects of leucine and its metabolite β-hydroxy-β-methylbutyrate on human skeletal muscle protein metabolism. J Physiol. 2013;591:2911–23.CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Vukovich MD, Stubbs NB, Bohlken RM, et al. The effect of dietary β-hydroxy-β-methylbutyrate (HMB) on strength gains and body composition changes in older adults. FASEB J. 1997;11:A376. Vukovich MD, Stubbs NB, Bohlken RM, et al. The effect of dietary β-hydroxy-β-methylbutyrate (HMB) on strength gains and body composition changes in older adults. FASEB J. 1997;11:A376.
26.
Zurück zum Zitat Vukovich MD, Stubbs NB, Bohlken RM. Body composition in 70-year-old adults responds to dietary beta-hydroxy-beta-methylbutyrate similarly to that of young adults. J Nutr. 2001;131:2049–52.PubMed Vukovich MD, Stubbs NB, Bohlken RM. Body composition in 70-year-old adults responds to dietary beta-hydroxy-beta-methylbutyrate similarly to that of young adults. J Nutr. 2001;131:2049–52.PubMed
27.
Zurück zum Zitat Panton L, Rathmacher J, Fuller J, et al. Effect of β-hydroxy-β-ethylbutyrate and resistance training on strength and functional ability in the elderly. Med Sci Sports Exerc. 1998;30:194.CrossRef Panton L, Rathmacher J, Fuller J, et al. Effect of β-hydroxy-β-ethylbutyrate and resistance training on strength and functional ability in the elderly. Med Sci Sports Exerc. 1998;30:194.CrossRef
28.
Zurück zum Zitat Berton L, Bano G, Carraro S, et al. Effect of oral beta-hydroxy-beta-methylbutyrate (HMB) supplementation on physical performance in healthy old women over 65 years: an open label randomized controlled trial. PLoS One. 2015;10:e0141757.CrossRefPubMedPubMedCentral Berton L, Bano G, Carraro S, et al. Effect of oral beta-hydroxy-beta-methylbutyrate (HMB) supplementation on physical performance in healthy old women over 65 years: an open label randomized controlled trial. PLoS One. 2015;10:e0141757.CrossRefPubMedPubMedCentral
29.
Zurück zum Zitat Flakoll P, Sharp R, Baier S, et al. Effect of beta-hydroxy-beta-methylbutyrate, arginine, and lysine supplementation on strength, functionality, body composition, and protein metabolism in elderly women. Nutrition. 2004;20:445–51.CrossRefPubMed Flakoll P, Sharp R, Baier S, et al. Effect of beta-hydroxy-beta-methylbutyrate, arginine, and lysine supplementation on strength, functionality, body composition, and protein metabolism in elderly women. Nutrition. 2004;20:445–51.CrossRefPubMed
30.
Zurück zum Zitat Baier S, Johannsen D, Abumrad N, et al. Year-long changes in protein metabolism in elderly men and women supplemented with a nutrition cocktail of beta-hydroxy-beta-methylbutyrate (HMB), l-arginine, and l-lysine. J Parenter Enteral Nutr. 2009;33:71–82.CrossRef Baier S, Johannsen D, Abumrad N, et al. Year-long changes in protein metabolism in elderly men and women supplemented with a nutrition cocktail of beta-hydroxy-beta-methylbutyrate (HMB), l-arginine, and l-lysine. J Parenter Enteral Nutr. 2009;33:71–82.CrossRef
31.
Zurück zum Zitat Fuller JC Jr, Baier S, Flakoll PJ, et al. Vitamin D status affects strength gains in older adults supplemented with a combination of β-hydroxy-β-methylbutyrate, arginine and lysine: a cohort study. J Parenter Enteral Nutr. 2011;35:757–62.CrossRef Fuller JC Jr, Baier S, Flakoll PJ, et al. Vitamin D status affects strength gains in older adults supplemented with a combination of β-hydroxy-β-methylbutyrate, arginine and lysine: a cohort study. J Parenter Enteral Nutr. 2011;35:757–62.CrossRef
32.
Zurück zum Zitat de Luis DA, Izaola O, Bachiller P, et al. Effect on quality of life and handgrip strength by dynamometry of an enteral specific supplements with beta-hydroxy-beta-methylbutyrate and vitamin D in elderly patients. Nutr Hosp. 2015;32:202–7.PubMed de Luis DA, Izaola O, Bachiller P, et al. Effect on quality of life and handgrip strength by dynamometry of an enteral specific supplements with beta-hydroxy-beta-methylbutyrate and vitamin D in elderly patients. Nutr Hosp. 2015;32:202–7.PubMed
33.
Zurück zum Zitat Stout JR, Smith-Ryan AE, Fukuda DH, et al. Effect of calcium β-hydroxy-β-methylbutyrate (CaHMB) with and without resistance training in men and women 65 + yrs: a randomized, double-blind pilot trial. Exp Gerontol. 2013;48:1303–10.CrossRefPubMed Stout JR, Smith-Ryan AE, Fukuda DH, et al. Effect of calcium β-hydroxy-β-methylbutyrate (CaHMB) with and without resistance training in men and women 65 + yrs: a randomized, double-blind pilot trial. Exp Gerontol. 2013;48:1303–10.CrossRefPubMed
34.
Zurück zum Zitat Cramer JT, Cruz-Jentoft AJ, Landi F, et al. Impacts of high-protein oral nutritional supplements among malnourished men and women with sarcopenia: a multicenter, randomized, double-blinded, controlled trial. J Am Med Dir Assoc. 2016;17:1044–55.CrossRefPubMed Cramer JT, Cruz-Jentoft AJ, Landi F, et al. Impacts of high-protein oral nutritional supplements among malnourished men and women with sarcopenia: a multicenter, randomized, double-blinded, controlled trial. J Am Med Dir Assoc. 2016;17:1044–55.CrossRefPubMed
35.
Zurück zum Zitat Wu H, Xia Y, Jiang J, et al. Effect of beta-hydroxy-beta-methylbutyrate supplementation on muscle loss in older adults: a systematic review and meta-analysis. Arch Gerontol Geriatr. 2015;61:168–75.CrossRefPubMed Wu H, Xia Y, Jiang J, et al. Effect of beta-hydroxy-beta-methylbutyrate supplementation on muscle loss in older adults: a systematic review and meta-analysis. Arch Gerontol Geriatr. 2015;61:168–75.CrossRefPubMed
36.
Zurück zum Zitat Hasselgren PO. Beta-hydroxy-beta-methylbutyrate (HMB) and prevention of muscle wasting. Metabolism. 2014;63:5–8.CrossRefPubMed Hasselgren PO. Beta-hydroxy-beta-methylbutyrate (HMB) and prevention of muscle wasting. Metabolism. 2014;63:5–8.CrossRefPubMed
37.
Zurück zum Zitat Deutz NE, Matheson EM, Matarese LE, et al. NOURISH Study Group. Readmission and mortality in malnourished, older, hospitalized adults treated with a specialized oral nutritional supplement: a randomized clinical trial. Clin Nutr. 2016;35:18–26.CrossRefPubMed Deutz NE, Matheson EM, Matarese LE, et al. NOURISH Study Group. Readmission and mortality in malnourished, older, hospitalized adults treated with a specialized oral nutritional supplement: a randomized clinical trial. Clin Nutr. 2016;35:18–26.CrossRefPubMed
38.
Zurück zum Zitat Deutz NE, Pereira SL, Hays NP, et al. Effect of β-hydroxy-β-methylbutyrate (HMB) on lean body mass during 10 days of bed rest in older adults. Clin Nutr. 2013;32:704–12.CrossRefPubMed Deutz NE, Pereira SL, Hays NP, et al. Effect of β-hydroxy-β-methylbutyrate (HMB) on lean body mass during 10 days of bed rest in older adults. Clin Nutr. 2013;32:704–12.CrossRefPubMed
39.
Zurück zum Zitat Hsieh LC, Chow CJ, Chang WC, et al. Effect of beta-hydroxy-beta-methylbutyrate on protein metabolism in bed-ridden elderly receiving tube feeding. Asia Pac J Clin Nutr. 2010;19:200–8.PubMed Hsieh LC, Chow CJ, Chang WC, et al. Effect of beta-hydroxy-beta-methylbutyrate on protein metabolism in bed-ridden elderly receiving tube feeding. Asia Pac J Clin Nutr. 2010;19:200–8.PubMed
40.
Zurück zum Zitat Hsieh LC, Chien SL, Huang MS, et al. Anti-inflammatory and anticatabolic effects of short-term beta-hydroxy-beta-methylbutyrate supplementation on chronic obstructive pulmonary disease patients in intensive care unit. Asia Pac J Clin Nutr. 2006;15:544–50.PubMed Hsieh LC, Chien SL, Huang MS, et al. Anti-inflammatory and anticatabolic effects of short-term beta-hydroxy-beta-methylbutyrate supplementation on chronic obstructive pulmonary disease patients in intensive care unit. Asia Pac J Clin Nutr. 2006;15:544–50.PubMed
41.
Zurück zum Zitat Panton LB, Rathmacher JA, Baier S, et al. Nutritional supplementation of the leucine metabolite beta-hydroxy-beta-methylbutyrate (HMB) during resistance training. Nutrition. 2000;16:734–9.CrossRefPubMed Panton LB, Rathmacher JA, Baier S, et al. Nutritional supplementation of the leucine metabolite beta-hydroxy-beta-methylbutyrate (HMB) during resistance training. Nutrition. 2000;16:734–9.CrossRefPubMed
42.
Zurück zum Zitat Stout JR, Fukuda DH, Kendall KL, et al. β-Hydroxy-β-methylbutyrate (HMB) supplementation and resistance exercise significantly reduce abdominal adiposity in healthy elderly men. Exp Gerontol. 2015;64:33–4.CrossRefPubMed Stout JR, Fukuda DH, Kendall KL, et al. β-Hydroxy-β-methylbutyrate (HMB) supplementation and resistance exercise significantly reduce abdominal adiposity in healthy elderly men. Exp Gerontol. 2015;64:33–4.CrossRefPubMed
43.
Zurück zum Zitat Gerlinger-Romero F, Guimaraes-Ferreira L, Giannocco G, et al. Chronic supplementation of beta-hydroxy-beta methylbutyrate (HMbeta) increases the activity of the GH/IGF-I axis and induces hyperinsulinemia in rats. Growth Horm IGF Res. 2011;21:57–62.CrossRefPubMed Gerlinger-Romero F, Guimaraes-Ferreira L, Giannocco G, et al. Chronic supplementation of beta-hydroxy-beta methylbutyrate (HMbeta) increases the activity of the GH/IGF-I axis and induces hyperinsulinemia in rats. Growth Horm IGF Res. 2011;21:57–62.CrossRefPubMed
44.
Zurück zum Zitat Pinheiro CH, Gerlinger-Romero F, Guimaraes-Ferreira L, et al. Metabolic and functional effects of beta-hydroxy-beta-methylbutyrate (HMB) supplementation in skeletal muscle. Eur J Appl Physiol. 2012;112:2531–7.CrossRefPubMed Pinheiro CH, Gerlinger-Romero F, Guimaraes-Ferreira L, et al. Metabolic and functional effects of beta-hydroxy-beta-methylbutyrate (HMB) supplementation in skeletal muscle. Eur J Appl Physiol. 2012;112:2531–7.CrossRefPubMed
45.
Zurück zum Zitat Ransone J, Neighbors K, Lefavi R, et al. The effect of β-hydroxy β-methylbutyrate on muscular strength and body composition in collegiate football players. J Strength Cond Res. 2003;17:34–9.PubMed Ransone J, Neighbors K, Lefavi R, et al. The effect of β-hydroxy β-methylbutyrate on muscular strength and body composition in collegiate football players. J Strength Cond Res. 2003;17:34–9.PubMed
46.
Zurück zum Zitat Toledo FG, Watkins S, Kelley DE. Changes induced by physical activity and weight loss in the morphology of inter-myofibrillar mitochondria in obese men and women. J Clin Endocrinol Metab. 2006;92:1827–33. Toledo FG, Watkins S, Kelley DE. Changes induced by physical activity and weight loss in the morphology of inter-myofibrillar mitochondria in obese men and women. J Clin Endocrinol Metab. 2006;92:1827–33.
47.
Zurück zum Zitat Sun X, Zemel MB. Leucine and calcium regulate fat metabolism and energy partitioning in murine adipocytes and muscle cells. Lipids. 2007;42:297–305.CrossRefPubMed Sun X, Zemel MB. Leucine and calcium regulate fat metabolism and energy partitioning in murine adipocytes and muscle cells. Lipids. 2007;42:297–305.CrossRefPubMed
48.
Zurück zum Zitat Sun X, Zemel MB. Leucine modulation of mitochondrial mass and oxygen consumption in skeletal muscle cells and adipocytes. Nutr Metab. 2009;6:26.CrossRef Sun X, Zemel MB. Leucine modulation of mitochondrial mass and oxygen consumption in skeletal muscle cells and adipocytes. Nutr Metab. 2009;6:26.CrossRef
49.
Zurück zum Zitat Bruckbauer A, Zemel MB, Thorpe T, et al. Synergistic effects of leucine and resveratrol on insulin sensitivity and fat metabolism in adipocytes and mice. Nutr Metab. 2012;9:77.CrossRef Bruckbauer A, Zemel MB, Thorpe T, et al. Synergistic effects of leucine and resveratrol on insulin sensitivity and fat metabolism in adipocytes and mice. Nutr Metab. 2012;9:77.CrossRef
50.
Zurück zum Zitat Liang C, Curry BJ, Brown PL, et al. Leucine modulates mitochondrial biogenesis and SIRT1-AMPK signaling in C2C12 myotubes. J Nutr Metab. 2014;2014:239750.CrossRefPubMedPubMedCentral Liang C, Curry BJ, Brown PL, et al. Leucine modulates mitochondrial biogenesis and SIRT1-AMPK signaling in C2C12 myotubes. J Nutr Metab. 2014;2014:239750.CrossRefPubMedPubMedCentral
51.
Zurück zum Zitat Sharawy MH, El-Awady MS, Megahed N, et al. The ergogenic supplement β-hydroxy-β-methylbutyrate (HMB) attenuates insulin resistance through suppressing GLUT-2 in rat liver. Can J Physiol Pharmacol. 2016;94:488–97.CrossRefPubMed Sharawy MH, El-Awady MS, Megahed N, et al. The ergogenic supplement β-hydroxy-β-methylbutyrate (HMB) attenuates insulin resistance through suppressing GLUT-2 in rat liver. Can J Physiol Pharmacol. 2016;94:488–97.CrossRefPubMed
52.
Zurück zum Zitat Yonamine CY, Teixeira SS, Campello RS, et al. Beta hydroxy beta methylbutyrate supplementation impairs peripheral insulin sensitivity in healthy sedentary Wistar rats. Acta Physiol. 2014;212:62–74.CrossRef Yonamine CY, Teixeira SS, Campello RS, et al. Beta hydroxy beta methylbutyrate supplementation impairs peripheral insulin sensitivity in healthy sedentary Wistar rats. Acta Physiol. 2014;212:62–74.CrossRef
Metadaten
Titel
The Potential of β-Hydroxy-β-Methylbutyrate as a New Strategy for the Management of Sarcopenia and Sarcopenic Obesity
verfasst von
Andrea P. Rossi
Alessia D’Introno
Sofia Rubele
Cesare Caliari
Stefano Gattazzo
Elena Zoico
Gloria Mazzali
Francesco Fantin
Mauro Zamboni
Publikationsdatum
31.10.2017
Verlag
Springer International Publishing
Erschienen in
Drugs & Aging / Ausgabe 11/2017
Print ISSN: 1170-229X
Elektronische ISSN: 1179-1969
DOI
https://doi.org/10.1007/s40266-017-0496-0

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Der GLP-1-Agonist Semaglutid hat in der FLOW-Studie bewiesen, dass sich damit die Progression chronischer Nierenerkrankungen bei Patienten mit Typ-2-Diabetes bremsen lässt. Auch in kardiovaskulärer Hinsicht war die Therapie erfolgreich.

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