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Upper airway CO2 receptors in tegu lizards: localization and ventilatory sensitivity

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Summary

  1. 1.

    Tidal volume, end-tidal CO2, and ventilatory frequency inTupinambis nigropunctatus were measured in response to CO2 (1–4%) delivered to either the mouth or nares. Additionally, the sensitivity of the ventilatory response to nasal CO2 was evaluated at CO2 concentrations less than 1%. The ventilatory parameters were also measured in response to CO2 (1–4%) delivered to the nares after the olfactory peduncle was transected.

  2. 2.

    It was found that (0.4–4%) nasal CO2 depressed ventilatory frequency by 9% to 83% respectively, while tidal volume was not significantly altered. CO2 (1–4%) delivered to the mouth produced no apparent changes in any of the ventilatory parameters. Following transection of the olfactory peduncle, nasal CO2 was ineffective in producing any change in ventilatory frequency or depth.

  3. 3.

    These findings indicate that CO2-sensitive receptors are located in either the nasal or vomeronasal membranes of tegu lizards and that the olfactory peduncle must be intact for these receptors to affect ventilatory changes in response to elevated CO2 concentrations. The receptors are capable of mediating a ventilatory response to CO2 concentrations lower than those found in either expired air or in confined spaces such as occupied burrows.

  4. 4.

    The discrepancies in the ventilatory responses of lizards and snakes to inspired CO2 reported in past experiments may be partially explained by the presence of nasal or vomeronasal CO2-sensitive receptors.

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Abbreviations

f :

respiratory frequency

UA :

upper airways

References

  • Ballam GO (1984) Ventilatory response to inspired CO2 in the lizard,Tupinambis nigropunctatus. Comp Biochem Physiol 78A: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 Biochim 51:379–442

    Google Scholar 

  • Crawford EC Jr, Gatz RN, Piiper J (1977) Ventilatory response of the tegu lizard to inspired CO2 at different body temperatures. Physiologist 20:19 (Abstract)

    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 

  • deJong RH, Hershey WN, Wagman IH (1966) Nerve conduction velocity during hypothermia in man. Anesthesiol 27:805–810

    Google Scholar 

  • Glass M, Johansen K (1976) Control of breathing inAcrochordus javanicus, an aquatic snake. Physiol Zool 49:328–340

    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 (1979) Ventilatory response of the diamondback water snake,Natrix rhombifera to hypoxia, hypercapnia and increased oxygen demand. J Comp Physiol 129:105–110

    Google Scholar 

  • Halpern M, Frumin N (1979) Roles of the vomeronasal and olfactory systems in prey attack and feeding in adult garter snakes. Physiol Behav 22:1183–1189

    Google Scholar 

  • Heller SB, Halpern M (1982) Laboratory observations of aggregative behavior of garter snakes,Thamnophis sirtalis: Roles of the visual, olfactory, and vomeronasal senses. J Comp Physiol Psychol 96:984–999

    Google Scholar 

  • Jackson DC, Kraus DR, Prange HD (1979) Ventilatory response to inspired CO2 in the sea turtle: effects of body size and temperature. Respir Physiol 38:71–81

    Google Scholar 

  • Kubie JL, Halpern M (1979) Chemical senses involved in garter snake prey trailing. J Comp Physiol Psychol 93:648–667

    Google Scholar 

  • Kubie JL, Vagvolgyi A, Halpern M (1978) Roles of the vomeronasal and olfactory behavior of male garter snakes. J Comp Physiol Psychol 92:627–641

    Google Scholar 

  • McDonald HS (1976) Methods for the physiological study of reptiles. In: Gans C, Dawson WR Biology of the Reptilia, vol 5. Academic Press, London New York, pp 43–53

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Parsons LC, Huggins SE (1965) Effects of temperature on electroencephalogram of the caiman. Proc Soc Exp Biol Med 120:422–426

    Google Scholar 

  • Parsons TS (1970) The nose and Jacobson's organ. In: Gans C, Parsons TS Biology of the Reptilia, vol 2. Academic Press, London New York, pp 99–185

    Google Scholar 

  • Phifer CB, Terry LM (1986) Use of hypothermia for general anesthesia in preweaning rodents. Physiol Behav 38:887–890

    Google Scholar 

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

    Google Scholar 

  • Randall WC, Stullken DE, Hiestand WA (1944) Respiration of reptiles as influenced by the composition of inspired air. Copeia 3:136–144

    Google Scholar 

  • Saalfeld E von (1934) Die Mechanik der Atmung beiUromastix (Lacertilia). Pflügers Arch 233:431–448

    Google Scholar 

  • Sakakibara Y (1978) Localization of CO2 sensor related to the inhibition of the bullfrog respiration. Jpn J Physiol 28:721–735

    Google Scholar 

  • Scheaffer RL, McClave JT (1982) Statistics for Engineers. Duxbury, Boston, pp 196–216

    Google Scholar 

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

    Google Scholar 

  • Ulinski PS, Peterson EH (1981) Patterns of olfactory projections in the desert IguanaDipsosaurus dorsalis. J Morph 168:189–227

    Google Scholar 

  • Ultsch GR, Anderson JF (1986) The respiratory microenvironment within the burrows of gopher tortoises (Gopherus polyphemus). Copeia 3:787–795

    Google Scholar 

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Coates, E.L., Ballam, G.O. Upper airway CO2 receptors in tegu lizards: localization and ventilatory sensitivity. J Comp Physiol B 157, 483–489 (1987). https://doi.org/10.1007/BF00691833

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