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Repeated ischaemic isometric exercise increases muscle fibre conduction velocity in humans: involvement of Na + ‐K + ‐ATPase
Author(s) -
Rongen G. A.,
Dijk J. P.,
Ginneken E. E. van,
Stegeman D. F.,
Smits P.,
Zwarts M. J.
Publication year - 2002
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.2001.014290
Subject(s) - isometric exercise , cardiology , ischemia , medicine , contraction (grammar) , ouabain , nerve conduction velocity , electromyography , muscle contraction , anesthesia , chemistry , physical medicine and rehabilitation , sodium , organic chemistry
This study was performed to test two hypotheses: (1) ischaemic preconditioning (development of tolerance to ischaemia) influences muscle fibre conduction velocity (MFCV) during repeated ischaemic isometric exercise and (2) the increase in MFCV to supranormal levels during recovery from ischaemic exercise is caused by activation of Na + −K + ‐ATPase. For this purpose, MFCV was measured with surface electromyography (sEMG) during repeated ischaemic isometric exercise of the brachioradial muscle (2 min at 30 % of maximal voluntary contraction). The involvement of ischaemic preconditioning was tested by changing the duration of ischaemia and by intra‐arterial infusion of adenosine (brachial artery, 50 μg min −1 dl −1 ). The role of Na + −K + ‐ATPase was explored using ouabain (0.2 μg min −1 dl −1 ). During the exercise, MFCV decreased from 4.4 ± 0.2 m s −1 to 3.7 ± 0.2 m s −1 ( P < 0.01, n = 13 ). Similar reductions in MFCV were observed during repeated exercise, irrespective of the reperfusion time (10 min vs. 18 min) or duration of the ischaemia (2 vs. 10 min). However, initial MFCV gradually increased for each subsequent contraction when contractions were repeated at 10 min intervals (4.4 ± 0.2 m s −1 vs. 4.9 ± 0.2 m s −1 for the first and fourth contraction respectively; P < 0.01 ; n = 13 ). This increase was not observed when contractions were performed at 18 min intervals, nor when additional ischaemia was applied. Intra‐arterial adenosine did not affect MFCV. Intra‐arterial ouabain did not affect the reduction in MFCV during exercise but completely prevented the increase in MFCV during recovery: from 4.7 ± 0.2 m s −1 to 5.2 ± 0.2 m s −1 vs. 4.5 ± 0.1 m s −1 to 4.5 ± 0.1 m s −1 in the absence and presence of ouabain respectively ( P < 0.05 for ouabain effect; n = 6 ). In conclusion, ischaemic preconditioning is not involved in changes in MFCV during repeated ischaemic isometric exercise. The increase in MFCV during recovery from repeated ischaemic isometric exercise is caused by rapid activation of Na + −K + ‐ATPase.