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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Veröffentlicht in:Diabetologia 2009-09, Vol.52 (9), p.1889-1898
Hauptverfasser: Fujita, S, Glynn, E. L, Timmerman, K. L, Rasmussen, B. B, Volpi, E
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container_end_page 1898
container_issue 9
container_start_page 1889
container_title Diabetologia
container_volume 52
creator Fujita, S
Glynn, E. L
Timmerman, K. L
Rasmussen, B. B
Volpi, E
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 &lt; 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 &lt; 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 &lt; 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 &lt; 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 &amp; dosage ; Insulin - pharmacology ; Insulin resistance ; Insulin Resistance - physiology ; Internal Medicine ; Kinases ; Leg - blood supply ; Male ; Medical sciences ; Medicine ; Medicine &amp; 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. 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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 &lt; 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 &lt; 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 &lt; 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 &lt; 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 &amp; 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 &amp; 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. 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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. 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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 &lt; 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 &lt; 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 &lt; 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 &lt; 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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