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Effect of venous (gut) CO2 loading on intrapulmonary gas fractions and ventilation in the tegu lizard

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Summary

Studies were conducted to determine regional pulmonary gas concentrations in the tegu lizard lung. Additionally, changes in pulmonary gas concentrations and ventilatory patterns caused by elevating venous levels of CO2 by gut infusion were measured.

It was found that significant stratification of lung gases was present in the tegu and that dynamic fluctuations of CO2 concentration varied throughout the length of the lung. Mean\(F_{CO_2 } \) was greater and\(F_{O_2 } \) less in the posterior regions of the lung. In the posterior regions gas concentrations remained nearly constant, whereas in the anterior regions large swings were observed with each breath. In the most anterior sections of the lung near the bronchi, CO2 and O2 concentrations approached atmospheric levels during inspiration and posterior lung levels during expiration.

During gut loading of CO2, the rate of rise of CO2 during the breathing pause increased. The mean level of CO2 also increased. Breathing rate and tidal volume increased to produce a doubling ofV E.

These results indicate that the method of introduction of CO2 into the tegu respiratory system determines the ventilatory response. If the CO2 is introduced into the venous blood a dramatic increase in ventilation is observed. If the CO2 is introduced into the inspired air a significant decrease in ventilation is produced. The changes in pulmonary CO2 environment caused by inspiratory CO2 loading are different from those caused by venous CO2 loading. We hypothesize that the differences in pulmonary CO2 environment caused by either inspiratory CO2 loading or fluctuations in venous CO2 concentration act differently on the IPC. The differing response of the IPC to the two methods of CO2 loading is the cause of the opposite ventilatory response seen during either venous or inspiratory loading.

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Abbreviations

IPC :

intrapulmonary chemoreceptors

UAC :

upper airway chemoreceptors

V T :

inspiratory tidal volume

\(F_{CO_2 } \) :

CO2 gas fraction

\(F_{O_2 } \) :

O2 gas fraction

V E :

minute ventilation

References

  • Ballam GO (1984) Ventilatory response to inspired CO2 in the lizard,Tupinambis nigropunctatus. Comp Biochem Physiol 78:757–762

    Google Scholar 

  • Ballam GO (1985) Breathing response of the tegu lizard to 1–4% CO2 in the mouth and nose or inspired into the lungs. Respir Physiol 62:375–386

    Google Scholar 

  • Boelaert R (1941) Sur la physiologie de la respiration des lacertiens. Arch Int Physiol 51:379–442

    Google Scholar 

  • Bradley GW, Noble MIM, Trenchard D (1976) The direct effect on pulmonary stretch receptor discharge produced by changing lung carbon dioxide concentration in dogs on cardiopulmonary bypass and its action on breathing. J Physiol 261:359–373

    Google Scholar 

  • Burggren W, Glass M, Johansen K (1977) Pulmonary ventilation/perfusion relationships in terrestrial and aquatic chelonian reptiles. Can J Zool 55:2024–2034

    Google Scholar 

  • Coates EL, Ballam GO (1987) Upper airway CO2 receptors in tegu lizards: localization and ventilatory sensitivity. J Comp Physiol B 157:483–489

    Google Scholar 

  • Davies DG, Thomas JL, Smith EN (1982) Effect of body temperature on ventilatory control in the alligator. J Appl Physiol: Respir Environ Exercise Physiol 52:114–118

    Google Scholar 

  • Dean JB, Gratz RK (1983) The effect of body temperature and CO2 breathing on ventilation and acid-base status in the northern water snakeNerodia sipedon. Physiol Zool 56:290–301

    Google Scholar 

  • Donnelly P, Woolcock A (1978) Stratification of inspired air in the elongated lungs of the carpet python,Morelia spilotes variegata. Respir Physiol 35:301–315

    Google Scholar 

  • Fedde MR, Kuhlmann WD, Scheid P (1977) Intrapulmonary receptors in the tegu lizard: I. Sensitivity to CO2. Respir Physiol 29:35–48

    Google Scholar 

  • Fisher JT, Sant'Ambrogio FB, Saint'Ambrogio G (1983) Stimulation of tracheal slowly adapting stretch receptors by hypercapnia and hypoxia. Respir Physiol 53:325–339

    Google Scholar 

  • Fordyce WE, Grodins FS (1980) Ventilatory responses to intravenous and airway CO2 administration in anesthetized dogs. J Appl Physiol: Respir Environ Exercise Physiol 48:337–346

    Google Scholar 

  • Gans C, Clark BD (1978) Air flow in reptilian ventilation. J Comp Biochem Physiol 60:453–457

    Google Scholar 

  • Glass ML, Wood SC, Hoyt RW, Johansen K (1979) Chemical control of breathing in the lizard,Varanus exanthematicus. Comp Biochem Physiol 62A:999–1003

    Google Scholar 

  • Gratz RK (1984) Effect of bilateral vagotomy on the ventilatory responses of the water snakeNerodia sipedon. Am J Physiol 246:R221-R227

    Google Scholar 

  • Gratz RK, Ar A, Geiser J (1981) Gas tension profile of the lung of the viper,Vipera xanthina palestinae. Respir Physiol 44:165–176

    Google Scholar 

  • Greco EC Jr, Fordyce WE, Gonzalez F Jr, Reischl P, Grodins FS (1978) Respiratory responses to intravenous and intrapulmonary CO2 in awake dogs. J Appl Physiol: Respir Environ Exercise Physiol 45:109–114

    Google Scholar 

  • Hlastala MP, Standaert YA, Pierson DJ, Luchtel DL (1985) The matching of ventilation and perfusion in the lung of the tegu lizard,Tupinambis nigropunctatus. Respir Physiol 60:277–294

    Google Scholar 

  • Hollander M, Wolfe DL (1973) Nonparametric statistical methods. Wiley, New York, pp 26–38

    Google Scholar 

  • Johansen K (1959) Heart activity during experimental diving of snakes. Am J Physiol 197:604–606

    Google Scholar 

  • Jones DR, Milsom WK, Butler PJ (1985) Ventilatory response to venous CO2 loading by gut ventilation in ducks. Can J Zool 63:1232–1236

    Google Scholar 

  • Kiley JP, Fedde MR (1983) Exercise hyperpnea in the duck without intrapulmonary chemoreceptor involvement. Respir Physiol 53:355–365

    Google Scholar 

  • Milsom W, Jones D (1980) The role of vagal afferent information and hypercapnia in control of the breathing pattern in Chelonia. J Exp Biol 87:53–63

    Google Scholar 

  • Mitchell GS, Gleeson TT, Bennett AF (1981) Ventilation and acid-base balance during graded activity in lizards. Am J Physiol 240:R29-R37

    Google Scholar 

  • Nielsen B (1961) On the regulation of respiration in reptiles. I. The effect of temperature and CO2 on the respiration of lizards (Lacerta). J Exp Biol 38:301–304

    Google Scholar 

  • Nielsen B (1962) On the regulation of respiration in reptiles. II. The effect of hypoxia with and without moderate hypercapnia on the respiration and metabolism of lizards. J Exp Biol 39:107–117

    Google Scholar 

  • Nye PCG, Marsh J (1982) Ventilation and carotid chemoreceptor discharge during venous CO2 loading via the gut. Respir Physiol 50:335–350

    Google Scholar 

  • Pacheco RM, Coates EL, Arman F, Ballam GO (1985) Ventilatory response to pulsed and mean CO2 in the nares of the tegu lizard (Abstract). Fed Proc 44:849

    Google Scholar 

  • Perry SF, Duncker HR (1978) Lung architecture, volume and static mechanics in five species of lizards. Respir Physiol 34:61–81

    Google Scholar 

  • Pough HF (1969) Physiological aspects of the burrowing of sand lizards (Uma, Iguanidae) and other lizards. Comp Biochem Physiol 31:869–884

    Google Scholar 

  • Saalfeld EF von (1934) Die Mechanik der Atmung beiUromastix (Lacertilia). Pflüg Arch Ges Physiol 233:431–448

    Google Scholar 

  • Scheid P, Kuhlmann WD, Fedde MR (1977) Intrapulmonary receptors in the tegu lizard: II. Functional characteristics and localization. Respir Physiol 29:49–62

    Google Scholar 

  • Tallman RD Jr, Grodins FS (1982a) Intrapulmonary CO2 receptors and ventilatory response to lung CO2 loading. J Appl Physiol: Respir Environ Exercise Physiol 52:1272–1277

    Google Scholar 

  • Tallman RD Jr, Grodins FS (1982b) Intrapulmonary CO2 receptor discharge at different levels of venous\(P_{CO_2 } \). J Appl Physiol: Respir Environ Exercise Physiol 53:1386–1391

    Google Scholar 

  • Templeton JR, Dawson WR (1963) Respiration in the lizardCrotaphytus collaris. Physiol Zool 36:104–126

    Google Scholar 

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Ballam, G.O., Donaldson, L.A. Effect of venous (gut) CO2 loading on intrapulmonary gas fractions and ventilation in the tegu lizard. J Comp Physiol B 158, 591–600 (1988). https://doi.org/10.1007/BF00692568

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