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Gifford 2016 J Physiol

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Publications in the MiPMap
Gifford JR, Garten RS, Nelson AD, Trinity JD, Layec G, Witman MA, Weavil JC, Mangum T, Hart C, Etheredge C, Jessop J, Bledsoe A, Morgan DE, Wray DW, Richardson RS (2015) Symmorphosis and skeletal muscle VO2max: in vivo and in vitro measures reveal differing constraints in the exercise-trained and untrained human. J Physiol [Epub ahead of print].

» PMID: 26614395

Gifford JR, Garten RS, Nelson AD, Trinity JD, Layec G, Witman MA, Weavil JC, Mangum T, Hart C, Etheredge C, Jessop J, Bledsoe A, Morgan DE, Wray DW, Richardson RS (2015) J Physiol

Abstract: The concept of symmorphosis postulates a matching of structural capacity to functional demand within a defined physiological system, regardless of endurance exercise training status. Whether this concept applies to oxygen (O2) supply and demand during maximal skeletal muscle O2 consumption (VO2max) in humans is unclear. Therefore, in vitro skeletal muscle mitochondrial VO2max (Mito VO2max, mitochondrial respiration of fibers biopsied from vastus lateralis) was compared to in vivo skeletal muscle VO2max during single leg knee extensor exercise (KEVO2max, direct Fick by femoral arterial and venous blood samples and Doppler ultrasound blood flow measurements) and whole-body VO2max during cycling (BodyVO2max, indirect calorimetry) in 10 endurance-exercise trained and 10 untrained young males. In untrained subjects, during KE exercise, maximal O2 supply (KEQO2max) exceeded (462 ± 37 ml∙kg-1 ∙min-1, P<0.05) and KEVO2max matched (340 ± 22 ml∙kg-1 ∙min-1, P>0.05) Mito VO2max (364 ± 16 ml∙kg-1 ∙min-1). Conversely, in trained subjects both KEQO2max (557 ± 35 ml∙kg-1 ∙min-1) and KEVO2max (458 ± 24 ml∙kg-1 ∙min-1) fell far short of MitoVO2max (743 ± 35 ml∙kg-1 ∙min-1, P<0.05). While MitoVO2max was related to KEVO2max (r = 0.69, P<0.05) and BodyVO2max (r = 0.91, P<0.05) in the untrained subjects, these variables were entirely unrelated in the trained subjects. Therefore, in the untrained, VO2max is limited by mitochondrial O2 demand, with evidence of adequate O2 supply, while in trained subjects an exercise training-induced mitochondrial reserve results in skeletal muscle VO2max being markedly limited by O2 supply. Together these in vivo and in vitro measures reveal clearly differing limitations and excesses at VO2max in untrained and trained humans and challenge the concept of symmorphosis as it applies to O2 supply and demand in humans. This article is protected by copyright. All rights reserved. Keywords: BMI, VO2max


Labels: MiParea: Respiration, Exercise physiology;nutrition;life style 


Organism: Human  Tissue;cell: Skeletal muscle  Preparation: Permeabilized cells 

Regulation: Oxygen kinetics  Coupling state: OXPHOS 

HRR: O2k-Protocol