Respiration physiology
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Respiration physiology · Mar 1996
How does positive end-expiratory pressure decrease CO2 elimination from the lung?
Six chloralose-urethane anesthetized dogs (23 +/- 2 kg) underwent median thoracotomy (open pleural spaces) and constant mechanical ventilation with O2. We conducted measurements at baseline and during 25 min of ventilation with 3.3 cmH2O positive end-expiratory pressure (PEEP3) or 10.7 cmH2O PEEP (PEEP 11), including breath-by-breath values in the first 2 min after PEEP began. PEEP 11 immediately decreased pulmonary CO2 elimination per breath (VCO2,br, digital integration and multiplication of exhaled flow and FCO2) from 8.4 +/- 2.0 to 4.5 +/- 1.6 ml (P < 0.05) by significantly decreasing alveolar ventilation (VA) (29% increase in anatomical dead space (VDana) and generation of high VA/Q regions) and by decreasing alveolar PCO2 (PACO2) from 42.5 +/- 3.5 to 35.9 +/- 3.5 Torr (decreased CO2 transfer to the lung as electromagnetic aortic cardiac output (QT) decreased by 51%). ⋯ However, CO2 transport was still in unsteady state at 25 min of PEEP. Peripheral tissue retention of CO2 and the significant increase in mixed venous PCO2 (PVCO2, 62.4 +/- 6.2 Torr) were not enough to normalize CO2 transfer to the lung and to sufficiently increase PACO2, especially during the continued depression in QT that occurred at higher PEEP. The sustained decrease in VCO2,br during PEEP was not mirrored by changes in end-tidal PCO2 (PETCO2).
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Respiration physiology · Feb 1996
Self-control of level of mechanical ventilation to minimize CO2 induced air hunger.
Hypercapnia produces an uncomfortable urge to breathe ('air hunger'), which is alleviated by increasing breathing. It has been postulated that awake humans control breathing partly to minimize these sensations; such behavioral control presumably involves the forebrain. To test this postulate, we compared the ventilatory response to hypercapnia when the subject breathed spontaneously to the response when the subject used forebrain commands to control ventilation--on the basis of minimizing air hunger (achieved with subject-controlled positive pressure ventilation). ⋯ This suggests that spontaneous breathing is not behaviorally controlled to minimize discomfort. Alternatively, mechanical ventilation confers an additional relief of air hunger beyond that provided by spontaneous breathing. Since mechanical ventilation (with reduced respiratory muscle contraction) was more effective than spontaneous breathing in relieving air hunger, our results also suggest afferents that signal the degree of respiratory muscle contraction do not contribute to air hunger relief.
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Respiration physiology · Dec 1995
Hematocrit in oxygen transport and swimming in rainbow trout (Oncorhynchus mykiss).
The optimal hematocrit (Hctopt) hypothesis was tested by altering Hct (and arterial blood oxygen content, CaO2) between extreme states of anemia and polycythemia (Hct = 8-55%) in the rainbow trout. Since blood viscosity (eta) effects on cardiac output (Q) and O2 transport (TO2) are likely to be greatest when O2 demand and Q are maximal, we challenged fish to swim to their critical swimming velocity (Ucrit) in a swim-tunnel respirometer at 13 degrees C and measured maximal oxygen uptake (VO2max), maximum Q(Qmax), and other cardiovascular variables. In addition, experimental temperature was lowered to 5 degrees C to increase eta. ⋯ These results clearly demonstrate that eta is not significant in setting normocythemia in rainbow trout. The novel finding of an Hct-dependent relationship for exercise-induced arterial hypoxemia may be indicative of a diffusion limitation to normocythemia. We suggest that factors involved in setting normocythemia in vertebrates should include diffusion limitations to oxygen transfer in addition to blood viscosity and oxygen transport constraints.
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Respiration physiology · Dec 1995
Contribution of opening and closing of lung units to lung hysteresis.
The recruitment and derecruitment of lung units is one explanation of the hysteresis observed in an excised lung during inflation and deflation. A simplified model has been proposed in which the recruitment-derecruitment process is a function of end-expiratory pressure (Frazer, D. G., K. ⋯ Volumes of air were then withdrawn and replaced so that the initial volume was restored in sinusoidal fashion as the amplitude of the volume excursions increased. For PL-VL loops with end-expiratory pressures between +4 and -2 cmH2O, pressure amplitudes rose and the hysteresis index (loop area/tidal volume) increased, regardless of the initial lung volume. These results are consistent with the previously described model of Frazer et al. (1985) which assumed that PL-VL curves can be divided into an 'opening' region, an 'open' region and a 'closing' region and that the demarcation of these regions depends on transpulmonary pressure, specifically end-expiratory pressure, and to a much lesser degree on lung volume.
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Respiration physiology · Oct 1995
Wave speed during maximal expiratory flow and phase velocity from forced oscillations.
To test the hypothesis that pressure waves in the airways propagate at the speed obtained from maximal expiratory flow we compared wave speeds (WS) associated with flow limitation and phase velocities (PV) of oscillatory pressure waves in four excised calf tracheae for transmural pressures (Ptm) between 0 and -10 kPa. WS was calculated from static area-Ptm curves using the acoustic reflection technique. PV was determined by the forced oscillation method between 16 and 1024 Hz. ⋯ In one additional trachea we found that PV decreased from approximately 200 m / sec at 7 Hz to approximately 130 m / sec at 0.23 Hz approaching WS. We suggest that VP is larger than WS because of the differences in airway wall mechanics during small-amplitude oscillations and large amplitude oscillations and large amplitude unidirectional wall motion such as a forced expiration. These results may provide an additional explanation why expiratory flow during rapid breathing or expiratory transients can exceed the maximum expiratory flow-volume envelope.