Received January 20, 2006
Revised March 8, 2006
Accepted after revision April 28, 2006
31PMRS evaluated metabolism of perfused intercostal muscles
Brian Lindegaard Pedersen 1*,
Henrik Arendrup 2,
Niels Henry Secher 3,
Bjørn Quistorff 4
1 IMBG-A, NMR-center
2 Department of Thoracic Surgery,Rigshospitalet, University of Copenhagen, Denmark.
3 Department of Anaesthesia, Rigshospitalet, University of Copenhagen, Denmark.
4 IMBG-A. NMR-center
* To whom correspondence should be addressed. E-mail: brlp{at}imbg.ku.dk.
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Abstract |
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Summary
This study presents a perfused preparation for evaluation of metabolism in pig intercostal muscle in vitro. Preserved vessels and nerves to an intercostal segment including two adjacent ribs allowed for tissue perfusion and electrical stimulation with measurement of contraction force, oxygen consumption, and 31P-magnetic resonance spectroscopy (MRS). When perfused at rest with Krebs-Ringer buffer the preparation maintained physiological levels of PCr, Pi, ATP and pH at a stable oxygen consumption of ~ 0.5 µmoles min-1g-1 for more than 2 h. Tonic stimulation of the nerve caused anaerobic energy consumption as PCr and pH decreased and both variables recovered after the contraction with t1/2 values of ~ 7 min. Force increased to 0.040 N g-1 (range 0.031-0.103) and it gradually decreased by about 70% during the subsequent 5 min of stimulation. The calculated free ADP concentration increased from 7.4±2.1 at rest to 28±12 nmoles g-1 (mean ±SD) by the end of the stimulation. Thus anaerobic ATP turnover was 0 at rest, 6.1±2 µmoles min-1 g-1 during the first minute of stimulation and 3.5±0.5 during the two last minutes, corresponding to the drop in force. When the preparation was left unperfused anaerobic ATP turnover averaged 0.40±0.15 µmoles min-1 g-1 for the first 10 min. The preparation can also be applied to human intercostal muscles, as demonstrated for one biopsy. The results demonstrate a stable and functional in vitro preparation of intact perfused intercostal muscles in the pig.
Key words: ATP; PCr; force; phosphorous magnetic resonance spectroscopy; oxygen consumption; intramuscular pH.
Key Words:
Muscle, Nuclear magnetic resonance, Perfusion