Supraphysiological hyperinsulinaemia is necessary to stimulate skeletal muscle protein anabolism in older adults: evidence of a true age-related insulin resistance of muscle protein metabolism
Aims/hypothesis The physiological increase in muscle protein anabolism induced by insulin is blunted in healthy, glucose-tolerant older adults. We hypothesised that the age-related defect in muscle protein anabolism is a true insulin resistance state and can be overridden by supraphysiological hyper...
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description | Aims/hypothesis The physiological increase in muscle protein anabolism induced by insulin is blunted in healthy, glucose-tolerant older adults. We hypothesised that the age-related defect in muscle protein anabolism is a true insulin resistance state and can be overridden by supraphysiological hyperinsulinaemia. Methods We used dye dilution, stable isotopic and immunoblotting techniques to measure leg blood flow, muscle protein synthesis, protein kinase B/mammalian target of rapamycin (Akt/mTOR) signalling, and amino acid kinetics in 14 healthy, glucose-tolerant older volunteers at baseline, and during an insulin infusion at postprandial (PD, 0.15 mU min⁻¹ 100 ml⁻¹) or supraphysiologically high (HD, 0.30 mU min⁻¹ 100 ml⁻¹) doses. Results Leg blood flow, muscle protein synthesis, and Akt/mTOR signalling were not different at baseline. During hyperinsulinaemia, leg blood flow (p < 0.01) and muscle protein synthesis increased in the HD group only (PD [%/h]: from 0.063 ± 0.006 to 0.060 ± 0.005; HD [%/h]: from 0.061 ± 0.007 to 0.098 ± 0.007; p < 0.01). Muscle Akt phosphorylation increased in both groups, but the increase tended to be greater in the HD group (p = 0.07). The level of p70 ribosomal S6 kinase 1 (S6K1) phosphorylation increased in the HD group only (p < 0.05). Net amino acid balance across the leg improved in both groups, but a net anabolic effect was observed only in the HD group (p < 0.05). Conclusions/interpretation We conclude that supraphysiological hyperinsulinaemia is necessary to stimulate muscle protein synthesis and anabolic signalling in healthy older individuals, suggesting the existence of a true age-related insulin resistance of muscle protein metabolism. |
doi_str_mv | 10.1007/s00125-009-1430-8 |
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L ; Timmerman, K. L ; Rasmussen, B. B ; Volpi, E</creator><creatorcontrib>Fujita, S ; Glynn, E. L ; Timmerman, K. L ; Rasmussen, B. B ; Volpi, E</creatorcontrib><description>Aims/hypothesis The physiological increase in muscle protein anabolism induced by insulin is blunted in healthy, glucose-tolerant older adults. We hypothesised that the age-related defect in muscle protein anabolism is a true insulin resistance state and can be overridden by supraphysiological hyperinsulinaemia. Methods We used dye dilution, stable isotopic and immunoblotting techniques to measure leg blood flow, muscle protein synthesis, protein kinase B/mammalian target of rapamycin (Akt/mTOR) signalling, and amino acid kinetics in 14 healthy, glucose-tolerant older volunteers at baseline, and during an insulin infusion at postprandial (PD, 0.15 mU min⁻¹ 100 ml⁻¹) or supraphysiologically high (HD, 0.30 mU min⁻¹ 100 ml⁻¹) doses. Results Leg blood flow, muscle protein synthesis, and Akt/mTOR signalling were not different at baseline. During hyperinsulinaemia, leg blood flow (p < 0.01) and muscle protein synthesis increased in the HD group only (PD [%/h]: from 0.063 ± 0.006 to 0.060 ± 0.005; HD [%/h]: from 0.061 ± 0.007 to 0.098 ± 0.007; p < 0.01). Muscle Akt phosphorylation increased in both groups, but the increase tended to be greater in the HD group (p = 0.07). The level of p70 ribosomal S6 kinase 1 (S6K1) phosphorylation increased in the HD group only (p < 0.05). Net amino acid balance across the leg improved in both groups, but a net anabolic effect was observed only in the HD group (p < 0.05). Conclusions/interpretation We conclude that supraphysiological hyperinsulinaemia is necessary to stimulate muscle protein synthesis and anabolic signalling in healthy older individuals, suggesting the existence of a true age-related insulin resistance of muscle protein metabolism.</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-009-1430-8</identifier><identifier>PMID: 19588121</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Activities of daily living ; Age ; Aging ; Amino acids ; Animals ; Biological and medical sciences ; Biopsy ; Blood Glucose - metabolism ; Body Mass Index ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Exercise ; Female ; Femoral Artery - drug effects ; Femoral Artery - physiology ; Fundamental and applied biological sciences. Psychology ; Glucose ; Human Physiology ; Humans ; Hyperinsulinism - pathology ; Hyperinsulinism - physiopathology ; Insulin - administration & dosage ; Insulin - pharmacology ; Insulin resistance ; Insulin Resistance - physiology ; Internal Medicine ; Kinases ; Leg - blood supply ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; Metabolic Diseases ; Metabolism ; Muscle Proteins - biosynthesis ; Muscle Proteins - drug effects ; Muscle Proteins - metabolism ; Muscle, Skeletal - pathology ; Musculoskeletal system ; Older people ; Phosphorylation ; Physiology ; Protein synthesis ; Proteins ; Reference Values ; Regional Blood Flow - drug effects ; Sarcopenia ; Striated muscle. Tendons ; Veins & arteries ; Vertebrates: osteoarticular system, musculoskeletal system</subject><ispartof>Diabetologia, 2009-09, Vol.52 (9), p.1889-1898</ispartof><rights>Springer-Verlag 2009</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-d99c0b480fa6a6f7bc3fca52ee51a31dd61c66528d27b399bdaae3a202dcd5083</citedby><cites>FETCH-LOGICAL-c533t-d99c0b480fa6a6f7bc3fca52ee51a31dd61c66528d27b399bdaae3a202dcd5083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00125-009-1430-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00125-009-1430-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21859040$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19588121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujita, S</creatorcontrib><creatorcontrib>Glynn, E. L</creatorcontrib><creatorcontrib>Timmerman, K. L</creatorcontrib><creatorcontrib>Rasmussen, B. B</creatorcontrib><creatorcontrib>Volpi, E</creatorcontrib><title>Supraphysiological hyperinsulinaemia is necessary to stimulate skeletal muscle protein anabolism in older adults: evidence of a true age-related insulin resistance of muscle protein metabolism</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><addtitle>Diabetologia</addtitle><description>Aims/hypothesis The physiological increase in muscle protein anabolism induced by insulin is blunted in healthy, glucose-tolerant older adults. We hypothesised that the age-related defect in muscle protein anabolism is a true insulin resistance state and can be overridden by supraphysiological hyperinsulinaemia. Methods We used dye dilution, stable isotopic and immunoblotting techniques to measure leg blood flow, muscle protein synthesis, protein kinase B/mammalian target of rapamycin (Akt/mTOR) signalling, and amino acid kinetics in 14 healthy, glucose-tolerant older volunteers at baseline, and during an insulin infusion at postprandial (PD, 0.15 mU min⁻¹ 100 ml⁻¹) or supraphysiologically high (HD, 0.30 mU min⁻¹ 100 ml⁻¹) doses. Results Leg blood flow, muscle protein synthesis, and Akt/mTOR signalling were not different at baseline. During hyperinsulinaemia, leg blood flow (p < 0.01) and muscle protein synthesis increased in the HD group only (PD [%/h]: from 0.063 ± 0.006 to 0.060 ± 0.005; HD [%/h]: from 0.061 ± 0.007 to 0.098 ± 0.007; p < 0.01). Muscle Akt phosphorylation increased in both groups, but the increase tended to be greater in the HD group (p = 0.07). The level of p70 ribosomal S6 kinase 1 (S6K1) phosphorylation increased in the HD group only (p < 0.05). Net amino acid balance across the leg improved in both groups, but a net anabolic effect was observed only in the HD group (p < 0.05). Conclusions/interpretation We conclude that supraphysiological hyperinsulinaemia is necessary to stimulate muscle protein synthesis and anabolic signalling in healthy older individuals, suggesting the existence of a true age-related insulin resistance of muscle protein metabolism.</description><subject>Activities of daily living</subject><subject>Age</subject><subject>Aging</subject><subject>Amino acids</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Blood Glucose - metabolism</subject><subject>Body Mass Index</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Exercise</subject><subject>Female</subject><subject>Femoral Artery - drug effects</subject><subject>Femoral Artery - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose</subject><subject>Human Physiology</subject><subject>Humans</subject><subject>Hyperinsulinism - pathology</subject><subject>Hyperinsulinism - physiopathology</subject><subject>Insulin - administration & dosage</subject><subject>Insulin - pharmacology</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - physiology</subject><subject>Internal Medicine</subject><subject>Kinases</subject><subject>Leg - blood supply</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Metabolism</subject><subject>Muscle Proteins - biosynthesis</subject><subject>Muscle Proteins - drug effects</subject><subject>Muscle Proteins - metabolism</subject><subject>Muscle, Skeletal - pathology</subject><subject>Musculoskeletal system</subject><subject>Older people</subject><subject>Phosphorylation</subject><subject>Physiology</subject><subject>Protein synthesis</subject><subject>Proteins</subject><subject>Reference Values</subject><subject>Regional Blood Flow - drug effects</subject><subject>Sarcopenia</subject><subject>Striated muscle. Tendons</subject><subject>Veins & arteries</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU-L1TAUxYsoznP0A7jRIIir6k3S9qXuZPAfDLgYB9yV2-T2Tca0fea2wvt2fjRTWhyYhask3N8955CTZc8lvJUA-3cMIFWZA9S5LDTk5kG2SxeVQ6HMw2y3jHNpqh9n2RPmWwDQZVE9zs5kXRojldxlf67mY8TjzYn9GMaDtxjEzelI0Q88Bz8g9R6FZzGQJWaMJzGNgiffzwEnEvyTAk1pqZ_ZBhLHOE7kB4EDtmPw3Iv0GIOjKNDNYeL3gn57R4MlMXYCxRRnEnigPNIi6MRmLCKx5wk38J58nzxX_afZow4D07PtPM-uP338fvElv_z2-evFh8vcllpPuatrC21hoMMKq27fWt1ZLBVRKVFL5yppq6pUxql9q-u6dYikUYFy1pVg9Hn2ZtVNEX7NxFPTe7YUAg40ztzstTagFBSJfHWPvB3nOKRwjZLaFEVRQYLkCtk4MkfqmmP0ffreRkKzlNus5Tap3GYpt1kivNiE57Ynd7extZmA1xuAnIrsYvo9z_84JU1ZQ7GYq5XjNBoOFO8S_s_95brU4djgISbh6ysFUoOsqsrsjf4LJrvLkw</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Fujita, S</creator><creator>Glynn, E. 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L ; Timmerman, K. L ; Rasmussen, B. B ; Volpi, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-d99c0b480fa6a6f7bc3fca52ee51a31dd61c66528d27b399bdaae3a202dcd5083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Activities of daily living</topic><topic>Age</topic><topic>Aging</topic><topic>Amino acids</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Blood Glucose - metabolism</topic><topic>Body Mass Index</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Exercise</topic><topic>Female</topic><topic>Femoral Artery - drug effects</topic><topic>Femoral Artery - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose</topic><topic>Human Physiology</topic><topic>Humans</topic><topic>Hyperinsulinism - pathology</topic><topic>Hyperinsulinism - physiopathology</topic><topic>Insulin - administration & dosage</topic><topic>Insulin - pharmacology</topic><topic>Insulin resistance</topic><topic>Insulin Resistance - physiology</topic><topic>Internal Medicine</topic><topic>Kinases</topic><topic>Leg - blood supply</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic Diseases</topic><topic>Metabolism</topic><topic>Muscle Proteins - biosynthesis</topic><topic>Muscle Proteins - drug effects</topic><topic>Muscle Proteins - metabolism</topic><topic>Muscle, Skeletal - pathology</topic><topic>Musculoskeletal system</topic><topic>Older people</topic><topic>Phosphorylation</topic><topic>Physiology</topic><topic>Protein synthesis</topic><topic>Proteins</topic><topic>Reference Values</topic><topic>Regional Blood Flow - drug effects</topic><topic>Sarcopenia</topic><topic>Striated muscle. Tendons</topic><topic>Veins & arteries</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujita, S</creatorcontrib><creatorcontrib>Glynn, E. L</creatorcontrib><creatorcontrib>Timmerman, K. L</creatorcontrib><creatorcontrib>Rasmussen, B. B</creatorcontrib><creatorcontrib>Volpi, E</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</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 China</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujita, S</au><au>Glynn, E. L</au><au>Timmerman, K. L</au><au>Rasmussen, B. B</au><au>Volpi, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Supraphysiological hyperinsulinaemia is necessary to stimulate skeletal muscle protein anabolism in older adults: evidence of a true age-related insulin resistance of muscle protein metabolism</atitle><jtitle>Diabetologia</jtitle><stitle>Diabetologia</stitle><addtitle>Diabetologia</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>52</volume><issue>9</issue><spage>1889</spage><epage>1898</epage><pages>1889-1898</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>Aims/hypothesis The physiological increase in muscle protein anabolism induced by insulin is blunted in healthy, glucose-tolerant older adults. We hypothesised that the age-related defect in muscle protein anabolism is a true insulin resistance state and can be overridden by supraphysiological hyperinsulinaemia. Methods We used dye dilution, stable isotopic and immunoblotting techniques to measure leg blood flow, muscle protein synthesis, protein kinase B/mammalian target of rapamycin (Akt/mTOR) signalling, and amino acid kinetics in 14 healthy, glucose-tolerant older volunteers at baseline, and during an insulin infusion at postprandial (PD, 0.15 mU min⁻¹ 100 ml⁻¹) or supraphysiologically high (HD, 0.30 mU min⁻¹ 100 ml⁻¹) doses. Results Leg blood flow, muscle protein synthesis, and Akt/mTOR signalling were not different at baseline. During hyperinsulinaemia, leg blood flow (p < 0.01) and muscle protein synthesis increased in the HD group only (PD [%/h]: from 0.063 ± 0.006 to 0.060 ± 0.005; HD [%/h]: from 0.061 ± 0.007 to 0.098 ± 0.007; p < 0.01). Muscle Akt phosphorylation increased in both groups, but the increase tended to be greater in the HD group (p = 0.07). The level of p70 ribosomal S6 kinase 1 (S6K1) phosphorylation increased in the HD group only (p < 0.05). Net amino acid balance across the leg improved in both groups, but a net anabolic effect was observed only in the HD group (p < 0.05). Conclusions/interpretation We conclude that supraphysiological hyperinsulinaemia is necessary to stimulate muscle protein synthesis and anabolic signalling in healthy older individuals, suggesting the existence of a true age-related insulin resistance of muscle protein metabolism.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>19588121</pmid><doi>10.1007/s00125-009-1430-8</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Activities of daily living Age Aging Amino acids Animals Biological and medical sciences Biopsy Blood Glucose - metabolism Body Mass Index Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Exercise Female Femoral Artery - drug effects Femoral Artery - physiology Fundamental and applied biological sciences. Psychology Glucose Human Physiology Humans Hyperinsulinism - pathology Hyperinsulinism - physiopathology Insulin - administration & dosage Insulin - pharmacology Insulin resistance Insulin Resistance - physiology Internal Medicine Kinases Leg - blood supply Male Medical sciences Medicine Medicine & Public Health Metabolic Diseases Metabolism Muscle Proteins - biosynthesis Muscle Proteins - drug effects Muscle Proteins - metabolism Muscle, Skeletal - pathology Musculoskeletal system Older people Phosphorylation Physiology Protein synthesis Proteins Reference Values Regional Blood Flow - drug effects Sarcopenia Striated muscle. Tendons Veins & arteries Vertebrates: osteoarticular system, musculoskeletal system |
title | Supraphysiological hyperinsulinaemia is necessary to stimulate skeletal muscle protein anabolism in older adults: evidence of a true age-related insulin resistance of muscle protein metabolism |
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