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Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity

Aims/hypothesis It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with...

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Published in:Diabetologia 2021-05, Vol.64 (5), p.1158-1168
Main Authors: Koh, Han-Chow E., van Vliet, Stephan, Meyer, Gretchen A., Laforest, Richard, Gropler, Robert J., Klein, Samuel, Mittendorfer, Bettina
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van Vliet, Stephan
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description Aims/hypothesis It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with obesity. The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity. Methods We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [ 2 H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [ 15 O]H 2 O (to assess muscle perfusion) and [ 18 F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition. Results We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg −1  min −1 in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg −1  min −1 , respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate ( r 2  = 0.65, p  
doi_str_mv 10.1007/s00125-021-05383-w
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The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity. Methods We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [ 2 H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [ 15 O]H 2 O (to assess muscle perfusion) and [ 18 F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition. Results We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg −1  min −1 in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg −1  min −1 , respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate ( r 2  = 0.65, p  &lt; 0.05). Conclusions/interpretation Obesity-associated insulin resistance is generalised across all major muscles, and is not caused by alterations in muscle fibre type composition or perfusion. In addition, insulin-stimulated whole-body glucose disposal relative to fat-free mass provides a reliable index of muscle glucose uptake rate. Graphical abstract</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-021-05383-w</identifier><identifier>PMID: 33511440</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adult ; Antidepressants ; Biological Transport - drug effects ; Biopsy ; Diabetes ; Fat-free body mass ; Female ; Fluorodeoxyglucose F18 ; Glucose ; Glucose - metabolism ; Glucose - pharmacokinetics ; Glucose Clamp Technique ; Human Physiology ; Humans ; Insulin ; Insulin - metabolism ; Insulin - pharmacology ; Insulin resistance ; Insulin Resistance - physiology ; Internal Medicine ; Male ; Medicine ; Medicine &amp; Public Health ; Metabolic Diseases ; Middle Aged ; Muscle, Skeletal - diagnostic imaging ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - pathology ; Muscles ; Obesity ; Obesity - diagnostic imaging ; Obesity - metabolism ; Obesity - pathology ; Perfusion ; Positron emission tomography ; Quadriceps muscle ; Quadriceps Muscle - diagnostic imaging ; Quadriceps Muscle - drug effects ; Quadriceps Muscle - metabolism ; Quadriceps Muscle - pathology ; Thinness - diagnostic imaging ; Thinness - metabolism ; Thinness - pathology</subject><ispartof>Diabetologia, 2021-05, Vol.64 (5), p.1158-1168</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-c0ba1e0aeeee6d84e64aaf060719060568bdb086d6cc5d0e44757bcab698cd0f3</citedby><cites>FETCH-LOGICAL-c474t-c0ba1e0aeeee6d84e64aaf060719060568bdb086d6cc5d0e44757bcab698cd0f3</cites><orcidid>0000-0001-8992-555X ; 0000-0002-0238-1439 ; 0000-0003-4784-4967 ; 0000-0001-9268-3993 ; 0000-0001-7127-1156 ; 0000-0003-0049-2677 ; 0000-0002-6550-0570</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33511440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koh, Han-Chow E.</creatorcontrib><creatorcontrib>van Vliet, Stephan</creatorcontrib><creatorcontrib>Meyer, Gretchen A.</creatorcontrib><creatorcontrib>Laforest, Richard</creatorcontrib><creatorcontrib>Gropler, Robert J.</creatorcontrib><creatorcontrib>Klein, Samuel</creatorcontrib><creatorcontrib>Mittendorfer, Bettina</creatorcontrib><title>Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><addtitle>Diabetologia</addtitle><description>Aims/hypothesis It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with obesity. The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity. Methods We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [ 2 H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [ 15 O]H 2 O (to assess muscle perfusion) and [ 18 F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition. Results We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg −1  min −1 in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg −1  min −1 , respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate ( r 2  = 0.65, p  &lt; 0.05). Conclusions/interpretation Obesity-associated insulin resistance is generalised across all major muscles, and is not caused by alterations in muscle fibre type composition or perfusion. In addition, insulin-stimulated whole-body glucose disposal relative to fat-free mass provides a reliable index of muscle glucose uptake rate. 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The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity. Methods We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [ 2 H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [ 15 O]H 2 O (to assess muscle perfusion) and [ 18 F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition. Results We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg −1  min −1 in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg −1  min −1 , respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate ( r 2  = 0.65, p  &lt; 0.05). Conclusions/interpretation Obesity-associated insulin resistance is generalised across all major muscles, and is not caused by alterations in muscle fibre type composition or perfusion. In addition, insulin-stimulated whole-body glucose disposal relative to fat-free mass provides a reliable index of muscle glucose uptake rate. Graphical abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33511440</pmid><doi>10.1007/s00125-021-05383-w</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-8992-555X</orcidid><orcidid>https://orcid.org/0000-0002-0238-1439</orcidid><orcidid>https://orcid.org/0000-0003-4784-4967</orcidid><orcidid>https://orcid.org/0000-0001-9268-3993</orcidid><orcidid>https://orcid.org/0000-0001-7127-1156</orcidid><orcidid>https://orcid.org/0000-0003-0049-2677</orcidid><orcidid>https://orcid.org/0000-0002-6550-0570</orcidid><oa>free_for_read</oa></addata></record>
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source Springer Nature
subjects Adult
Antidepressants
Biological Transport - drug effects
Biopsy
Diabetes
Fat-free body mass
Female
Fluorodeoxyglucose F18
Glucose
Glucose - metabolism
Glucose - pharmacokinetics
Glucose Clamp Technique
Human Physiology
Humans
Insulin
Insulin - metabolism
Insulin - pharmacology
Insulin resistance
Insulin Resistance - physiology
Internal Medicine
Male
Medicine
Medicine & Public Health
Metabolic Diseases
Middle Aged
Muscle, Skeletal - diagnostic imaging
Muscle, Skeletal - drug effects
Muscle, Skeletal - metabolism
Muscle, Skeletal - pathology
Muscles
Obesity
Obesity - diagnostic imaging
Obesity - metabolism
Obesity - pathology
Perfusion
Positron emission tomography
Quadriceps muscle
Quadriceps Muscle - diagnostic imaging
Quadriceps Muscle - drug effects
Quadriceps Muscle - metabolism
Quadriceps Muscle - pathology
Thinness - diagnostic imaging
Thinness - metabolism
Thinness - pathology
title Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity
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