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Biomedical subjects

P Scheid

Publications and source records attributed to P Scheid.

At least 163 records · Page 9Linked to original sources
PubMed1978

Estimation of effective parabronchial gas volume during intermittent ventilatory flow: theory and application in the duck.

The difference in gas exchange performance between continuous and intermittent ventilatory flow is theoretically studied in the alveolar lung model. When measurements obtained with intermittent flow are analyzed assuming continuous flow, an apparent diffusing capacity. Dapp, results which is an underestimate of the true value, D. This true value, D, may be assessed from measurements at continuous flow. With decreasing effective lung gas volume, Veff, Dapp increasingly deviates D. The dependence of Dapp/D on Veff in the parabronchial lung seems to be similar to that in the alveolar lung. Experimental data of Dapp/D (Scheid et al., 1977) are used to assess Veff for the duck lung. The average value of Veff thus obtained, 93 ml, exceeds the anatomical estimate of parabronchial gas volume. Gas transfer across the open parabronchial ends may contribute in enlarging the parabronchial gas volume to the volume, Veff, that is effective as gas capacity in conditions of non-steady ventilatory flow.

Animals↗
PubMed1978

Analysis of gas exchange between air capillaries and blood capillaries in avian lungs.

A number of models is analyzed to study gas exchange between blood capillaries and air capillaries in the avian parabronchial wall when diffusion is the only transport mechanism in the air capillaries. The existing anatomical arrangement of blood capillaries that traverse the periparabronchial tissue from peripherally located arterioles to draining venules at the luminal surface appears to provide a particularly high gas exchange efficiency. Application of the theory to measurements in the hen using histological estimates suggests that substantial concentration gradients exist inside the air capillary gas whose magnitude vary along the parabronchus. Thus at the gas inflow end of the parabronchus the partial pressure drop within the air capillaries could amount, for both O2 and CO2, to about 10--15 torr at rest and to 30--40 torr during exercise. Due to the peculiar arrangement of capillary blood flow to the air capillaries the effects of these gradients on gas exchange are very slight during rest. During exercise, however, the diffusional resistance inside the air capillaries may become limiting for the over-all gas exchange, and other mechanisms may be needed to secure respiratory gas transfer.

Animals↗
PubMed1978

Blood flow distribution in the duck lung and its control by respiratory gases.

Blood flow to subunits of the lung was studied in the duck by use of radioactive microspheres. In spontaneously breathing, unanesthetized animals (series I) neopulmo was slightly better perfused than the average lung and along the paleopulmonic parabronchi, blood flow was found to decrease in the direction of ventilatory gas flow and thus of decreasing PO2 and increasing PCO2 in lung gas. The effects of respiratory gases on regional lung perfusion were investigated in unidirectionally ventilated animals (series II) in which gas mixtures offered to both lungs could be controlled independently. Local hypoxia resulted in reduction of local blood flow, whereas effects from hyperoxia or CO2 could not be substantiated. Reversal of the direction of unidirectional ventilatory flow (series III), and thus reversal of the profiles of respired gas concentrations along the parabronchi, suggest that the inhomogeneity in blood flow observed in spontaneously breathing animals of series I can only in part be explained as an acute adjustment to the local hypoxia. Calculations show that this inhomogeneity of blood flow constitutes an only minor impairment of the overall gas exchange efficacy of the parabronchial lung.

Animals↗
PubMed1978

Mixing technique for study of oxygen-hemoglobin equilibrium: a critical evaluation.

In the mixing technique for study of oxygen-hemoglobin equilibrium, the O2 saturation (SO2) of a blood mixture is calculated from the volume ratio at which an oxygenated sample is mixed with a deoxygenated sample, and the PO2 in the mixture is measured polarographically. Any predetermined level of SO2 may be obtained by proper choice of the volume ratio. It is shown that the volume and oxygen saturation of the mixed samples are by far the most critical parameters in calculating SO2, and a method is suggested by which the volume ratio is accurately measured by weighing the blood samples before mixing. Other parameters that influence determination of SO2, e.g., the O2 capacity of the blood, are much less important. The method has been applied to establish the O2 dissociation curve in human blood, and good reproducibility and agreement with standard curves were obtained. Measurements in rabbit blood yielded similarly satisfactory results. The technique is particularly applicable to problems that require exact adjustment of SO2 to a predetermined value, such as determination of the half-saturation pressure or of the Bohr effect at various levels of O2 saturation.

Animals↗
PubMed1977

Oxygen affinity of duck blood determined by in vivo and in vitro technique.

Half saturation partial pressure of O2,P50, was determined in domestic Muscovy ducks (Cairina moschata) both by in vivo and in vitro techniques. For in vivo determination, blood samples were drawn from the anesthetized, artificially ventilated animals and analyzed both for O2 content, Co2, and O2 partial pressure, Po2. O2 capacity was detemined in arterial samples during hyperoxic ventilation (arterial Po2 about 180 torr). P50 was calculated from measurements in venous blood samples (O2 saturation near 50%). For in vitro determinations, Co2 was measured in blood samples equilibrated with Po2 close to P50. No significant difference was found between P50 values determined by both techniques. At 41 C and pH 7.50, P50 averaged 41.7 torr when analyzed by in vivo technique and 41.4 torr when determined in vitro. The variability between animals was less than 1 torr (SD) and could be explained by the experimental error. The partially discordant literature data on P50 of duck blood are reviewed and critically discussed.

Animals↗
PubMed1977

Intrapulmonary receptors in the Tegu lizard: I. Sensitivity to CO2.

Single unit vagal recordings from intrapulmonary receptors were obtained in decerebrate, paralyzed lizards both during pump ventilation and during unidirectional ventilation on the cannulated, sack-shaped lung. Two types of receptors were identified: (1) CO2-receptors, which increased their discharge frequency as intrapulmonary CO2 concentration decreased but were not sensitive to stretch of the lung. (2) Mechanoreceptors, which rapidly increased discharge frequency when the lung was stretched. These receptors' CO2 sensitivity varied. Lungs of lizards thus appeared to possess both CO2 receptors, which have functional characteristics similar to those in birds, and mechanoreceptors with properties similar to stretch receptors in mammals.

Animals↗
PubMed1977

Intrapulmonary receptors in the Tegu lizard: II. Functional characteristics and localization;.

Intrapulmonary receptors identified in the Tegu lizard by single-unit vagal recording (Fedde et al., 1977) were subjected to a number of stimuli and localized within the lung. Some carbon dioxide receptors could follow periodic changes in intrapulmonary CO2 concentrations as rapidly as 1.3 Hz; No oxygen sensitivity was observed with this receptor type, and halothane markedly depressed the discharge frequency. In response to intravenously injected acetazolamide they increased their discharge frequency and became almost totally insensitive to CO2, suggesting molecular per se is not the direct controller of receptor discharge; These receptors show many of the functional characteristics described for those in the avian lung. Afferent activity from both CO2 and mechanoreceptors could be elicited by electrically stimulating the lung surface. The CO2 receptors appeared to be organized in a receptive field covering more than 1 cm2 of lung surface, multiple receptors being innervated by a single afferent fiber. Activity in afferent fibers from mechanoreceptors could be evoked from only one distinct spot on the lung surface. Conduction velocities of afferent fibers from CO2 receptors ranged from 1 to 3 m-sec-1; from mechanoreceptors, from 1.9 to 5.2 m-sec-1.

Acetazolamide↗
PubMed1976

Measurement of Krogh's diffusion constant of CO2 in respiring muscle at various CO2 levels: evidence for facilitated diffusion.

Krogh's diffusion constant for CO2, KCO2, was determined in respiring muscle tissue at various levels of tissue PCO2, between 10 and 160 torr, using a technique described previously (Kawashiro et atl, 1975). With increasing mean tissue PCO2, KCO2 declined towards an apparently asymptotic value. The relationship between KCO2 (10(-9) mmol-cm(-1)-min(-1)-tor(-1)) and PCO2 (torr) at 37 degrees C could be approximated by the equation KCO2 = 17.3 [1 + 1.72 - exp(--0.027 - PCO2)]-At PCO2 = 0 torr KCO2 exceeded the asymptotic value, which was virtually attained at PCO2 = 100 torr, by more than a factor of two. Thus CO2 diffusion in muscle appears to be facilitated in the low PCO2 range. Specific CO2 production rate of tissue, which was determined simultaneously, did not vary with CO2 in the PCO2 range studied. Effects of facilitated CO2 transport on CO2 exchange in muscle are assessd using simple models. In the presence of CO2 facilitation muscle PCO2 is reduced, particularly during exercise.

Animals↗
PubMed1976

Problems in determination of oxygen dissociation of avian blood.

No appreciable errors are expected in determination of blood gas values and pH using classical techniques provided time of anaerobic storage is kept small and is, if unavoidable performed on ice. In particular, dissociation curves may safely be analyzed with the Van Slyke technique which is in disagreement with the conclusions of Lutz et al. (1973). For measurement of PO2 and PCO2, delay time is mainly dictated by response time of the electrodes; measurements may have to be corrected for metabolism, particularly in high PO2 range.

Animals↗
PubMed1976

Measurement of diffusivity and metabolic rate of O2 and CO2 in respiring tissue.

The method described is apt to measure, at the same time, Krogh's diffusion constant and specific metabolic rates for O2 and CO2 in intact, respiring tissues. Due to metabolism tissue thickness for this method is limited to about 500 mum unless hyperbaric conditions are used. The results suggest that both KO2 and KCO2 are similar in alive and in dead tissue. Due to tissue inhomogeneity and to possible facilitation of O2 or CO2 transport our values of K have to be considered as effective mean values for the physiological range of PO2 and PCO2 in muscle at rest and at exercise.

Animals↗
PubMed1976

A technique for study of lung function in birds by blocking the primary bronchus.

The technique described allows in vivo placement of a blocking balloon in the avian primary bronchus between the origins of the two sets of secondary bronchi, the medioventrals and mediodorsals. With caudal air sacs cannulated the animal may then be ventilated with a constant flow of gas passing entirely through the gas-exchanging parabronchi. This technique has been found useful particularly in studies of pulmonary gas exchange in birds.

Animals↗
PubMed1976

Effects of CO2 on pulmonary air flow resistance in the duck.

Effects of CO2 on pulmonary smooth muscle were assessed by measuring the air flow resistance of secondary bronchi and parabronchi in ducks unidirectionally ventilated with a constant gas flow through the parabronchial lung, the bypass of the primary bronchus being occluded by a blocking catheter. Pressure differences across the blocking balloon (deltaP), corresponding to the pressure drop in the gas flowing through the mediodorsal and medioventral secondary bronchi (MD and MV) and parabronchi, were measured at flow rates (V) varied from 0.5 to 3 L-min-1 and at CO2 concentrations of ventilating gas (FICO2) varied from 0 to 10%. 1) deltaP increased more than linearly with V. The resulting flow resistance R(= deltaP/V) averaged 43 and 95 cm H2O-L-1-sec at V = 0.5 and 3 L-min-1, respectively. 2) Step changes in FICO2 at constant V were followed within 0.5 to 5 sec by changes in R. 3) Lowering FICO2 from 5% resulted in marked increases in R, the value at FICO2 = 0% being more than twice the average value at 5%. Raising FICO2 from 5% up to 10% was followed by only slight changes in R. 4) Vagotomy did not consistently change R at any level of CO2; it did, however, slightly increase the delay time for changes in R on step changes of FICO2. 5)The medioventral secondary bronchi and their orifices into the primary bronchus appeared to be mainly responsible for the resistance measured and its changes with CO2. The resistance offered by the parabronchi appeared to be much smaller and much less dependent on CO2. The results suggest importance of lung gas CO2 in aerodynamic valving of respiratory flow in avian lungs during normal breathing and particularly during thermal panting to prevent alkalosis.

Airway Resistance↗
PubMed1976

Gas exchange in air sacs: contribution to respiratory gas exchange in ducks.

Air sac gas exchange was studied in ducks by measuring the rates of inert gas uptake and of O2 and CO2 equilibration in caudal thoracic air sac whose ventilation was prevented by surgival sealing of the ostia. The data were analyzed on a model incorporating three possible routes by which air sac gas could be exchanged with the surrounding tissue: (1) into the blood perfusing the air sac walls; (2) into the adjoining air sac via tissue membranes; (3) into the bronchial system of the lung via diffusion through lung tissue bordering upon the caudal thoracic air sac. Exchange rates of gases via the two latter paths were found to be small as compared with the first route. From application of model parameters to O2 and CO2 exchange in air sacs under physiological conditions the following conclusions were drawn: (1) the caudal thoracic air sac makes the major contribution to total gas exchange between air sacs and blood; (2) this exchange can account for less than 5% of total respiratory gas exchange; (3) the exchange is too small to account for the O2 and CO2 partial pressures in caudal thoracic air sacs of ducks. Other mechanisms like gas exchange in neopulmonic parabronchi, which conduct air to the caudal air sacs during inspiration or re-inspiration of dead space appear to play a more significant role in the deviation of O2 and CO2 partial pressures in the caudal air sacs from those in inspired air.

Air Sacs↗