It is still uncertain that hyperoxia affects muscle oxygen consumption (VO 2 ) during repetitive contractions [1]. There is both theoretical and experimental support for the idea that all precapillary O 2 losses, i.e., a longitudinal decrease in arteriolar oxygen tension (PO 2 ), an arteriovenous diffusion shunt, and diffusive exchange between arterioles and capillaries contribute significantly to limitations on O 2 extraction in the resting muscle [2]. Furthermore, O 2 -diffusion shunt as an ineffective O 2 supply may affect VO 2 in tetanically contracting muscle during hyperoxia.We examined the influence of hyperoxia on VO 2 and peripheral O 2 exchange during repetitive tetanic contractions with the canine gastrocnemius muscle group. Possible mechanisms for limiting VO 2 by increasing PaO 2 have been discussed in relation to peripheral O 2 diffusion limitation for muscle VO 2 [3-8] using both muscle venous effluent PO 2 (PvO 2 ), reflecting O 2 driving force of diffusion from erythrocyte to mitochondria, and VO 2 /PvO 2 ratio, reflecting O 2 diffusion conductance [9,10].
MethodsEight mongrel dogs (mean weight 13.2Ϯ0.9 kg) were anesthetized with pentobarbital sodium (I.P., 30 mg/kg). The animals were ventilated by a respirator with room air except for hyperoxia. The left gastrocnemius-plantaris muscle group in the 8 dogs was surgically prepared using a method similar to that described by us previously [5,6]. The right femoral artery and vein were exposed, and heparin (1,000 IU kg Ϫ1 ) was administered intravenously. A thermostatically controlled infrared lamp was used to keep the surface of the muscle at 37°C. The isolated gastrocnemius was perfused by blood using methods described previously [6]. The perfusion pressure at the inlet of the arterial supply to the muscle was measured using a pressure transducer. Blood flow was measured using an electromagnetic flow meter (Nihon Kohden, Tokyo), the flow probe being set in the venous line.The tendon was cut close to the calcaneus, clamped and connected to a force transducer (Showa model WBS-50 K, Tokyo). The length of the muscle was adjusted at 10 g force g Ϫ1 muscle weight. Isometric, tetanic contractions were induced by supramaximal stimuli (4 V, 0.2 ms duration) in trains of 200 ms duration. In each train, the frequency was 50 impulses/s. The frequency of trains was 1/s.Each muscle took part in 3 min contraction bouts with 15 min intervals. The order of each bout was randomized in order to avoid the influence of successive 3 min contraction bouts. During hyperoxia, the dogs