Leucine: a key amino acid in ageing-associated sarcopenia?
During ageing, a progressive loss of muscle mass has been well described in both man and rodents. This loss of proteins results from an imbalance between protein synthesis and degradation rates. Although some authors have shown a decrease of myofibrillar protein synthesis rates in human volunteers,...
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description | During ageing, a progressive loss of muscle mass has been well described in both man and rodents. This loss of proteins results from an imbalance between protein synthesis and degradation rates. Although some authors have shown a decrease of myofibrillar protein synthesis rates in human volunteers, this imbalance is not clearly apparent when basal rates of protein turnover are measured. A decrease in muscle protein synthesis stimulation was detected nevertheless in ageing rats during the postprandial period, suggesting that the ‘meal signal’ was altered during ageing. Many results now suggest that aged muscle is less sensitive to the stimulatory effect of amino acids at physiological concentrations but is still able to respond if the increase in aminoacidaemia is sufficiently large. Indeed amino acids play an important role in regulating muscle protein turnover both in vitro and in vivo. At the molecular level, amino acids modulate gene expression. Amino acid response elements have been characterised in the promoter of transcriptional factor CCAAT-enhancer binding protein homologous protein and asparagine synthetase genes. Among amino acids, leucine seems to play the major role in regulating the metabolic function. It inhibits proteolysis and stimulates muscle protein synthesis independently of insulin. Leucine has been shown to act as a real mediator by modulating specifically the activities of intracellular kinases linked to the translation of proteins such as phosphatidylinosinol 3′ kinase and mammalian target of rapamycin–70 kDa ribosomal protein S6 (p70S6K) kinases. We recently demonstrated in vitro that protein synthesis of ageing rat muscles becomes resistant to the stimulatory effect of leucine in its physiological concentration range. However, when leucine concentration was increased greatly above its postprandial level, protein synthesis was stimulated normally. Moreover, we studied the effect of meal leucine supplementation on in vivo protein synthesis in adult and ageing rats. Leucine supplementation had no additional effect on muscle protein synthesis in adults but totally restored its stimulation in ageing rats. Whether chronic oral leucine supplementation would be beneficial for maintaining muscle protein mass in elderly men and women remains to be studied. |
doi_str_mv | 10.1079/NRR200252 |
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This loss of proteins results from an imbalance between protein synthesis and degradation rates. Although some authors have shown a decrease of myofibrillar protein synthesis rates in human volunteers, this imbalance is not clearly apparent when basal rates of protein turnover are measured. A decrease in muscle protein synthesis stimulation was detected nevertheless in ageing rats during the postprandial period, suggesting that the ‘meal signal’ was altered during ageing. Many results now suggest that aged muscle is less sensitive to the stimulatory effect of amino acids at physiological concentrations but is still able to respond if the increase in aminoacidaemia is sufficiently large. Indeed amino acids play an important role in regulating muscle protein turnover both in vitro and in vivo. At the molecular level, amino acids modulate gene expression. Amino acid response elements have been characterised in the promoter of transcriptional factor CCAAT-enhancer binding protein homologous protein and asparagine synthetase genes. Among amino acids, leucine seems to play the major role in regulating the metabolic function. It inhibits proteolysis and stimulates muscle protein synthesis independently of insulin. Leucine has been shown to act as a real mediator by modulating specifically the activities of intracellular kinases linked to the translation of proteins such as phosphatidylinosinol 3′ kinase and mammalian target of rapamycin–70 kDa ribosomal protein S6 (p70S6K) kinases. We recently demonstrated in vitro that protein synthesis of ageing rat muscles becomes resistant to the stimulatory effect of leucine in its physiological concentration range. However, when leucine concentration was increased greatly above its postprandial level, protein synthesis was stimulated normally. Moreover, we studied the effect of meal leucine supplementation on in vivo protein synthesis in adult and ageing rats. Leucine supplementation had no additional effect on muscle protein synthesis in adults but totally restored its stimulation in ageing rats. Whether chronic oral leucine supplementation would be beneficial for maintaining muscle protein mass in elderly men and women remains to be studied.</description><identifier>ISSN: 0954-4224</identifier><identifier>EISSN: 1475-2700</identifier><identifier>DOI: 10.1079/NRR200252</identifier><identifier>PMID: 19079937</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Aging ; Amino acids ; Biological and medical sciences ; Development. Metamorphosis. Moult. Ageing ; Fundamental and applied biological sciences. Psychology ; Kinases ; Metabolism ; Muscles ; Musculoskeletal system ; Nutrition research ; Older people ; Physiology ; Protein synthesis ; Proteins ; Sarcopenia ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Women</subject><ispartof>Nutrition research reviews, 2003-06, Vol.16 (1), p.61-70</ispartof><rights>Copyright © CABI Publishing 2003</rights><rights>2003 INIST-CNRS</rights><rights>CABI Publishing</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c378t-e167a6402fa6dfc5300e91b2fa675d71db8977aadaa791ce003a31202a7f46543</citedby><cites>FETCH-LOGICAL-c378t-e167a6402fa6dfc5300e91b2fa675d71db8977aadaa791ce003a31202a7f46543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14888748$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19079937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dardevet, Dominique</creatorcontrib><creatorcontrib>Rieu, Isabelle</creatorcontrib><creatorcontrib>Fafournoux, Pierre</creatorcontrib><creatorcontrib>Sornet, Claire</creatorcontrib><creatorcontrib>Combaret, Lydie</creatorcontrib><creatorcontrib>Bruhat, Alain</creatorcontrib><creatorcontrib>Mordier, Sylvie</creatorcontrib><creatorcontrib>Mosoni, Laurent</creatorcontrib><creatorcontrib>Grizard, Jean</creatorcontrib><title>Leucine: a key amino acid in ageing-associated sarcopenia?</title><title>Nutrition research reviews</title><addtitle>Nutr. Res. Rev</addtitle><description>During ageing, a progressive loss of muscle mass has been well described in both man and rodents. This loss of proteins results from an imbalance between protein synthesis and degradation rates. Although some authors have shown a decrease of myofibrillar protein synthesis rates in human volunteers, this imbalance is not clearly apparent when basal rates of protein turnover are measured. A decrease in muscle protein synthesis stimulation was detected nevertheless in ageing rats during the postprandial period, suggesting that the ‘meal signal’ was altered during ageing. Many results now suggest that aged muscle is less sensitive to the stimulatory effect of amino acids at physiological concentrations but is still able to respond if the increase in aminoacidaemia is sufficiently large. Indeed amino acids play an important role in regulating muscle protein turnover both in vitro and in vivo. At the molecular level, amino acids modulate gene expression. Amino acid response elements have been characterised in the promoter of transcriptional factor CCAAT-enhancer binding protein homologous protein and asparagine synthetase genes. Among amino acids, leucine seems to play the major role in regulating the metabolic function. It inhibits proteolysis and stimulates muscle protein synthesis independently of insulin. Leucine has been shown to act as a real mediator by modulating specifically the activities of intracellular kinases linked to the translation of proteins such as phosphatidylinosinol 3′ kinase and mammalian target of rapamycin–70 kDa ribosomal protein S6 (p70S6K) kinases. We recently demonstrated in vitro that protein synthesis of ageing rat muscles becomes resistant to the stimulatory effect of leucine in its physiological concentration range. However, when leucine concentration was increased greatly above its postprandial level, protein synthesis was stimulated normally. Moreover, we studied the effect of meal leucine supplementation on in vivo protein synthesis in adult and ageing rats. Leucine supplementation had no additional effect on muscle protein synthesis in adults but totally restored its stimulation in ageing rats. Whether chronic oral leucine supplementation would be beneficial for maintaining muscle protein mass in elderly men and women remains to be studied.</description><subject>Aging</subject><subject>Amino acids</subject><subject>Biological and medical sciences</subject><subject>Development. Metamorphosis. Moult. Ageing</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kinases</subject><subject>Metabolism</subject><subject>Muscles</subject><subject>Musculoskeletal system</subject><subject>Nutrition research</subject><subject>Older people</subject><subject>Physiology</subject><subject>Protein synthesis</subject><subject>Proteins</subject><subject>Sarcopenia</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Women</subject><issn>0954-4224</issn><issn>1475-2700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpl0M9LwzAUB_AgipvTg_-AFMGDSPUlTZtmlyHDXzAUhp7La5KOzLWdyXrYf2_Gijt4egQ-ed_Hl5BLCvcUhHx4n88ZAEvZERlSLtKYCYBjMgSZ8pgzxgfkzPslBCNlckoGVIZvMhFDMp6ZTtnGjCOMvs02wto2bYTK6sg2ES6MbRYxet8qixujI49OtWvTWJyck5MKV95c9HNEvp6fPqev8ezj5W36OItVIvJNbGgmMOPAKsx0pdIEwEha7p4i1YLqMpdCIGpEIakyAAkmlAFDUfEs5cmIXO_3rl370xm_KZZt55oQWTBGmaB5LgK63SPlWu-dqYq1szW6bUGh2JVU_JUU7FW_sCtrow-ybyWAmx6gV7iqHDbK-oPjeYjkeXB3fSjWpbN6YQ6n_Y_9Bamwehs</recordid><startdate>20030601</startdate><enddate>20030601</enddate><creator>Dardevet, Dominique</creator><creator>Rieu, Isabelle</creator><creator>Fafournoux, Pierre</creator><creator>Sornet, Claire</creator><creator>Combaret, Lydie</creator><creator>Bruhat, Alain</creator><creator>Mordier, Sylvie</creator><creator>Mosoni, Laurent</creator><creator>Grizard, Jean</creator><general>Cambridge University Press</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RQ</scope><scope>7RV</scope><scope>7TK</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20030601</creationdate><title>Leucine: a key amino acid in ageing-associated sarcopenia?</title><author>Dardevet, Dominique ; Rieu, Isabelle ; Fafournoux, Pierre ; Sornet, Claire ; Combaret, Lydie ; Bruhat, Alain ; Mordier, Sylvie ; Mosoni, Laurent ; Grizard, Jean</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c378t-e167a6402fa6dfc5300e91b2fa675d71db8977aadaa791ce003a31202a7f46543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aging</topic><topic>Amino acids</topic><topic>Biological and medical sciences</topic><topic>Development. Metamorphosis. Moult. Ageing</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kinases</topic><topic>Metabolism</topic><topic>Muscles</topic><topic>Musculoskeletal system</topic><topic>Nutrition research</topic><topic>Older people</topic><topic>Physiology</topic><topic>Protein synthesis</topic><topic>Proteins</topic><topic>Sarcopenia</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dardevet, Dominique</creatorcontrib><creatorcontrib>Rieu, Isabelle</creatorcontrib><creatorcontrib>Fafournoux, Pierre</creatorcontrib><creatorcontrib>Sornet, Claire</creatorcontrib><creatorcontrib>Combaret, Lydie</creatorcontrib><creatorcontrib>Bruhat, Alain</creatorcontrib><creatorcontrib>Mordier, Sylvie</creatorcontrib><creatorcontrib>Mosoni, Laurent</creatorcontrib><creatorcontrib>Grizard, Jean</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Career & Technical Education Database</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Neurosciences Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Nutrition research reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dardevet, Dominique</au><au>Rieu, Isabelle</au><au>Fafournoux, Pierre</au><au>Sornet, Claire</au><au>Combaret, Lydie</au><au>Bruhat, Alain</au><au>Mordier, Sylvie</au><au>Mosoni, Laurent</au><au>Grizard, Jean</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leucine: a key amino acid in ageing-associated sarcopenia?</atitle><jtitle>Nutrition research reviews</jtitle><addtitle>Nutr. Res. Rev</addtitle><date>2003-06-01</date><risdate>2003</risdate><volume>16</volume><issue>1</issue><spage>61</spage><epage>70</epage><pages>61-70</pages><issn>0954-4224</issn><eissn>1475-2700</eissn><abstract>During ageing, a progressive loss of muscle mass has been well described in both man and rodents. This loss of proteins results from an imbalance between protein synthesis and degradation rates. Although some authors have shown a decrease of myofibrillar protein synthesis rates in human volunteers, this imbalance is not clearly apparent when basal rates of protein turnover are measured. A decrease in muscle protein synthesis stimulation was detected nevertheless in ageing rats during the postprandial period, suggesting that the ‘meal signal’ was altered during ageing. Many results now suggest that aged muscle is less sensitive to the stimulatory effect of amino acids at physiological concentrations but is still able to respond if the increase in aminoacidaemia is sufficiently large. Indeed amino acids play an important role in regulating muscle protein turnover both in vitro and in vivo. At the molecular level, amino acids modulate gene expression. Amino acid response elements have been characterised in the promoter of transcriptional factor CCAAT-enhancer binding protein homologous protein and asparagine synthetase genes. Among amino acids, leucine seems to play the major role in regulating the metabolic function. It inhibits proteolysis and stimulates muscle protein synthesis independently of insulin. Leucine has been shown to act as a real mediator by modulating specifically the activities of intracellular kinases linked to the translation of proteins such as phosphatidylinosinol 3′ kinase and mammalian target of rapamycin–70 kDa ribosomal protein S6 (p70S6K) kinases. We recently demonstrated in vitro that protein synthesis of ageing rat muscles becomes resistant to the stimulatory effect of leucine in its physiological concentration range. However, when leucine concentration was increased greatly above its postprandial level, protein synthesis was stimulated normally. Moreover, we studied the effect of meal leucine supplementation on in vivo protein synthesis in adult and ageing rats. Leucine supplementation had no additional effect on muscle protein synthesis in adults but totally restored its stimulation in ageing rats. Whether chronic oral leucine supplementation would be beneficial for maintaining muscle protein mass in elderly men and women remains to be studied.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>19079937</pmid><doi>10.1079/NRR200252</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging Amino acids Biological and medical sciences Development. Metamorphosis. Moult. Ageing Fundamental and applied biological sciences. Psychology Kinases Metabolism Muscles Musculoskeletal system Nutrition research Older people Physiology Protein synthesis Proteins Sarcopenia Vertebrates: anatomy and physiology, studies on body, several organs or systems Women |
title | Leucine: a key amino acid in ageing-associated sarcopenia? |
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