Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism

Aims/hypothesis: This study aimed to examine if beta-aminoisobutyric acid (BAIBA) is (i) secreted by skeletal muscle in humans during exercise, (ii) associated with insulin secretory function in vivo, and (iii) directly linked with acute glucose-mediated insulin release by pancreatic beta cells in v...

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Main Authors: Jonathan P. Barlow, Kristian Karstoft, Andreas Vigelsø, Martin Gram, Jørn W. Helge, Flemming Dela, Kirk Pappan, Donna O’Neil, Warwick Dunn, Thomas P.J. Solomon
Format: Article
Language:English
Published: Elsevier 2020-09-01
Series:Metabolism Open
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589936820300335
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spelling doaj-841acbf5f0ba462dae19c286578b2d5e2020-11-25T01:38:26ZengElsevierMetabolism Open2589-93682020-09-017100053Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolismJonathan P. Barlow0Kristian Karstoft1Andreas Vigelsø2Martin Gram3Jørn W. Helge4Flemming Dela5Kirk Pappan6Donna O’Neil7Warwick Dunn8Thomas P.J. Solomon9School of Sport, Exercise, and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, UK; Mitochondrial Profiling Centre, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, UK; Corresponding author. Mitochondrial Profiling Centre, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, B15 2TT, UK.Centre of Inflammation and Metabolism, Rigshospitalet, Copenhagen, Denmark; Centre for Physical Activity Research, Rigshospitalet, Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Geriatrics, Bispebjerg-Frederiksberg University Hospital, Bispebjerg, DenmarkMetabolon Inc, Durham, NC, USASchool of Biosciences and Phenome Centre Birmingham, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, UKSchool of Biosciences and Phenome Centre Birmingham, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, UK; Institute for Metabolism and Systems Research, College of Medical Sciences, University of Birmingham, Edgbaston, UKSchool of Sport, Exercise, and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, UK; Institute for Metabolism and Systems Research, College of Medical Sciences, University of Birmingham, Edgbaston, UKAims/hypothesis: This study aimed to examine if beta-aminoisobutyric acid (BAIBA) is (i) secreted by skeletal muscle in humans during exercise, (ii) associated with insulin secretory function in vivo, and (iii) directly linked with acute glucose-mediated insulin release by pancreatic beta cells in vitro. Methods: Following 2-weeks of single-leg immobilization, plasma BAIBA concentrations were measured in the brachial artery and the femoral veins of each leg in healthy male subjects, at rest and during two-legged dynamic knee-extensor exercise. During a 2-h hyperglycamic clamp, insulin secretory function and levels of plasma BAIBA were assessed in non-diabetic individuals, non-diabetic individuals following 24-h hyperglycemia and patients with type 2 diabetes. Direct effects of BAIBA on acute glucose-mediated insulin release were probed in INS-1832/3 cells under normal and ‘diabetes-like’ conditions. Finally, the effect of BAIBA on mitochondrial function was assessed in INS-1832/3 cells using extracellular flux analysis. Results: (i) BAIBA is released from skeletal muscle at rest and during exercise under healthy conditions but is suppressed during exercise following leg immobilization, (ii) plasma BAIBA concentrations inversely associate with insulin secretory function in humans, (iii) BAIBA lowers mitochondrial energy metabolism in INS-1 832/3 cells in parallel with decreased insulin secretionConclusion/interpretation: BAIBA is a myokine released by skeletal muscle during exercise and indepedantly alters the triggering pathway of insulin secretion in cultured INS-1832/3 cells.http://www.sciencedirect.com/science/article/pii/S2589936820300335ExerciseMuscle contractionMyokineType 2 diabetesGlucolipotoxicityPancreatic beta-cell
collection DOAJ
language English
format Article
sources DOAJ
author Jonathan P. Barlow
Kristian Karstoft
Andreas Vigelsø
Martin Gram
Jørn W. Helge
Flemming Dela
Kirk Pappan
Donna O’Neil
Warwick Dunn
Thomas P.J. Solomon
spellingShingle Jonathan P. Barlow
Kristian Karstoft
Andreas Vigelsø
Martin Gram
Jørn W. Helge
Flemming Dela
Kirk Pappan
Donna O’Neil
Warwick Dunn
Thomas P.J. Solomon
Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism
Metabolism Open
Exercise
Muscle contraction
Myokine
Type 2 diabetes
Glucolipotoxicity
Pancreatic beta-cell
author_facet Jonathan P. Barlow
Kristian Karstoft
Andreas Vigelsø
Martin Gram
Jørn W. Helge
Flemming Dela
Kirk Pappan
Donna O’Neil
Warwick Dunn
Thomas P.J. Solomon
author_sort Jonathan P. Barlow
title Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism
title_short Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism
title_full Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism
title_fullStr Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism
title_full_unstemmed Beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from INS-1 832/3 cells by mediating mitochondrial energy metabolism
title_sort beta-aminoisobutyric acid is released by contracting human skeletal muscle and lowers insulin release from ins-1 832/3 cells by mediating mitochondrial energy metabolism
publisher Elsevier
series Metabolism Open
issn 2589-9368
publishDate 2020-09-01
description Aims/hypothesis: This study aimed to examine if beta-aminoisobutyric acid (BAIBA) is (i) secreted by skeletal muscle in humans during exercise, (ii) associated with insulin secretory function in vivo, and (iii) directly linked with acute glucose-mediated insulin release by pancreatic beta cells in vitro. Methods: Following 2-weeks of single-leg immobilization, plasma BAIBA concentrations were measured in the brachial artery and the femoral veins of each leg in healthy male subjects, at rest and during two-legged dynamic knee-extensor exercise. During a 2-h hyperglycamic clamp, insulin secretory function and levels of plasma BAIBA were assessed in non-diabetic individuals, non-diabetic individuals following 24-h hyperglycemia and patients with type 2 diabetes. Direct effects of BAIBA on acute glucose-mediated insulin release were probed in INS-1832/3 cells under normal and ‘diabetes-like’ conditions. Finally, the effect of BAIBA on mitochondrial function was assessed in INS-1832/3 cells using extracellular flux analysis. Results: (i) BAIBA is released from skeletal muscle at rest and during exercise under healthy conditions but is suppressed during exercise following leg immobilization, (ii) plasma BAIBA concentrations inversely associate with insulin secretory function in humans, (iii) BAIBA lowers mitochondrial energy metabolism in INS-1 832/3 cells in parallel with decreased insulin secretionConclusion/interpretation: BAIBA is a myokine released by skeletal muscle during exercise and indepedantly alters the triggering pathway of insulin secretion in cultured INS-1832/3 cells.
topic Exercise
Muscle contraction
Myokine
Type 2 diabetes
Glucolipotoxicity
Pancreatic beta-cell
url http://www.sciencedirect.com/science/article/pii/S2589936820300335
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