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Slowed muscle oxygen uptake kinetics with raised metabolism are not dependent on blood flow or recruitment dynamics
Author(s) -
Wüst Rob C. I.,
McDonald James R.,
Sun Yi,
Ferguson Brian S.,
Rogatzki Matthew J.,
Spires Jessica,
Kowalchuk John M.,
Gladden L. Bruce,
Rossiter Harry B.
Publication year - 2014
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2013.267476
Subject(s) - isometric exercise , perfusion , contraction (grammar) , chemistry , stimulation , blood flow , medicine , muscle contraction , gastrocnemius muscle , anatomy , endocrinology , skeletal muscle
Key points A slow adjustment of skeletal muscle oxygen uptake ( V ̇ O 2 ) to produce energy during exercise predisposes to early fatigue. In human studies,V ̇ O 2kinetics are slow when exercise is initiated from an elevated baseline; this is proposed to reflect slow blood flow regulation and/or recruitment of muscle fibres containing few mitochondria. To investigate this, we measuredV ̇ O 2kinetics in canine muscle, with experimental control over muscle activation and blood flow. We found thatV ̇ O 2kinetics remained slow when contractions were initiated from an elevated baseline despite experimentally increased blood flow and uniform fibre activation. These data challenge our current understanding of the control of muscleV ̇ O 2and demand consideration of new alternative mediators forV ̇ O 2control.Abstract Oxygen uptake kinetics (τ V ̇ O 2 ) are slowed when exercise is initiated from a raised metabolic rate. Whether this reflects the recruitment of muscle fibres differing in oxidative capacity, or slowed blood flow ( Q ̇ ) kinetics is unclear. This study determined τ V ̇ O 2in canine muscle in situ , with experimental control over muscle activation and Q ̇ during contractions initiated from rest and a raised metabolic rate. The gastrocnemius complex of nine anaesthetised, ventilated dogs was isolated and attached to a force transducer. Isometric tetanic contractions (50 Hz; 200 ms duration) via supramaximal sciatic nerve stimulation were used to manipulate metabolic rate: 3 min stimulation at 0.33 Hz (S1), followed by 3 min at 0.67 Hz (S2). Circulation was initially intact (SPON), and subsequently isolated for pump‐perfusion (PUMP) above the greatest value in SPON. MuscleV ̇ O 2was determined contraction‐by‐contraction using an ultrasonic flowmeter and venous oximeter, and normalised to tension‐time integral (TTI). τ V ̇ O 2 /TTI and τ Q ̇ were less in S1 SPON (mean ± s.d.: 13 ± 3 s and 12 ± 4 s, respectively) than in S2 SPON (29 ± 19 s and 31 ± 13 s, respectively; P < 0.05). τ V ̇ O 2 /TTI was unchanged by pump‐perfusion (S1 PUMP , 12 ± 4 s; S2 PUMP , 24 ± 6 s; P < 0.001) despite increased O 2 delivery; at S2 onset, venous O 2 saturation was 21 ± 4% and 65 ± 5% in SPON and PUMP, respectively.V ̇ O 2kinetics remained slowed when contractions were initiated from a raised metabolic rate despite uniform muscle stimulation and increased O 2 delivery. The intracellular mechanism may relate to a falling energy state, approaching saturating ADP concentration, and/or slowed mitochondrial activation; but further study is required. These data add to the evidence that muscleV ̇ O 2control is more complex than previously suggested.