Journal
RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY
Volume 134, Issue 3, Pages 239-246Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/S1569-9048(03)00016-8
Keywords
conductance, O-2,O- muscle; diffusing capacity, O-2, muscle; exercise, maximal O-2 consumption; gas exchange, O-2 supply to muscle; mammals, dog; muscle, O-2 Supply; oxygen, diffusivity, plasma; pharmacological agents, trans sodium crocetinate
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Funding
- PHS HHS [R01 40155, P01 17731] Funding Source: Medline
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The lumped parameter describing skeletal muscle diffusional conductance for O-2, DMO2, reflects all of the resistances for O-2 in moving from red cell to muscle fiber mitochondria. The purpose of our study was to determine if the carotenoid compound, trans sodium crocetinate (TSC), which has been reported to increase the diffusivity of O-2 in plasma, improves DMO2 and thus, V-O2,V-max in maximally contracting in situ skeletal muscle. V-O2,V-max was measured in the isolated perfused canine gastrocnemius (n = 5) during 3 min of isometric tetanic contractions at 1 Hz, while the animal was breathing 12% O-2 (PA(O2) = 32 +/- 2 Torr, mean +/- S.E.) under two experimental conditions. The first was a control contraction period and the second (following 60 min recovery) was performed within 5 min after infusion of a 0.1 mg ml(-1) solution of TSC (total dose 100 mug kg(-1)). There were no significant differences in convective O-2 delivery (11.9 +/- 2.3 vs. 12.1 +/- 2.2 ml min 100 g(-1)), V-O2,V-max (9.5 +/- 1.5 vs. 9.6 +/- 1.5 ml min(-1).100 g(-1)) or calculated DMO2 (0.37 +/- 0.03 vs. 0.37 +/- 0.04 ml min 100 g(-1).Torr(-1)) between contraction periods. As such, our results show that TSC does not improve performance in maximally contracting canine gastrocnemius muscle in situ under moderately hypoxic conditions, suggesting either that TSC in this situation does not increase plasma O-2 diffusivity or that this step in O-2 diffusion from red cell to myocyte does not constrain DMO2. (C) 2003 Elsevier Science B.V. All rights reserved.
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