Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1991 Dec;444:567–578. doi: 10.1113/jphysiol.1991.sp018894

Role of the carotid bodies in the respiratory compensation for the metabolic acidosis of exercise in humans.

S M Rausch 1, B J Whipp 1, K Wasserman 1, A Huszczuk 1
PMCID: PMC1179949  PMID: 1822563

Abstract

1. In response to an acute exercise-induced metabolic acidosis, the fall of arterial pH is constrained by the magnitude of the compensatory hyperventilation. To determine the role of the carotid bodies in this regulatory process, subjects performed prolonged (24 min) square-wave cycle ergometry from a background of unloaded cycling at inspired oxygen fractions (FI,O2) of 0.12 O2 (high carotid body gain), 0.21 O2 (normal carotid body gain) and 0.80 O2 (low carotid body gain). The work rates were selected to provide the same exercise intensity, despite the different inspirates; i.e. resulting in a constant increase in arterial blood [lactate] (delta [L-] approximately 4 mequiv l-1. 2. Ventilatory and pulmonary gas exchange variables were computed breath-by-breath and arterial blood was sampled at intervals throughout the tests and analysed subsequently for [lactate], [pyruvate], arterial partial pressures of oxygen and carbon dioxide (PO2, PCO2), pH, [bicarbonate] and [potassium]. 3. Hypoxia markedly reduced, and hyperoxia magnified, the transient decrease in arterial pH following exercise onset. However, there was a slow acid-base compensatory component, even when carotid chemosensitivity was suppressed by hyperoxia. We therefore conclude that, in humans, carotid body chemosensitivity plays a dominant role in constraining variations of arterial pH in response to the acute metabolic acidosis of heavy exercise, but that secondary-presumably central chemosensory-mechanisms subserve a slower compensatory role.

Full text

PDF
567

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Band D. M., Linton R. A., Kent R., Kurer F. L. The effect of peripheral chemodenervation on the ventilatory response to potassium. Respir Physiol. 1985 May;60(2):217–225. doi: 10.1016/0034-5687(85)90105-7. [DOI] [PubMed] [Google Scholar]
  2. Band D. M., Linton R. A. The effect of hypoxia on the response of the carotid body chemoreceptor to potassium in the anaesthetized cat. Respir Physiol. 1988 Jun;72(3):295–301. doi: 10.1016/0034-5687(88)90088-6. [DOI] [PubMed] [Google Scholar]
  3. Beaver W. L., Lamarra N., Wasserman K. Breath-by-breath measurement of true alveolar gas exchange. J Appl Physiol Respir Environ Exerc Physiol. 1981 Dec;51(6):1662–1675. doi: 10.1152/jappl.1981.51.6.1662. [DOI] [PubMed] [Google Scholar]
  4. Beaver W. L., Wasserman K., Whipp B. J. A new method for detecting anaerobic threshold by gas exchange. J Appl Physiol (1985) 1986 Jun;60(6):2020–2027. doi: 10.1152/jappl.1986.60.6.2020. [DOI] [PubMed] [Google Scholar]
  5. Boetger C. L., Ward D. S. Effect of dopamine on transient ventilatory response to exercise. J Appl Physiol (1985) 1986 Dec;61(6):2102–2107. doi: 10.1152/jappl.1986.61.6.2102. [DOI] [PubMed] [Google Scholar]
  6. Burger R. E., Estavillo J. A., Kumar P., Nye P. C., Paterson D. J. Effects of potassium, oxygen and carbon dioxide on the steady-state discharge of cat carotid body chemoreceptors. J Physiol. 1988 Jul;401:519–531. doi: 10.1113/jphysiol.1988.sp017176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Casaburi R., Stremel R. W., Whipp B. J., Beaver W. L., Wasserman K. Alteration by hyperoxia of ventilatory dynamics during sinusoidal work. J Appl Physiol Respir Environ Exerc Physiol. 1980 Jun;48(6):1083–1091. doi: 10.1152/jappl.1980.48.6.1083. [DOI] [PubMed] [Google Scholar]
  8. DEJOURS P. Control of respiration by arterial chemoreceptors. Ann N Y Acad Sci. 1963 Jun 24;109:682–695. doi: 10.1111/j.1749-6632.1963.tb13497.x. [DOI] [PubMed] [Google Scholar]
  9. Eldridge F. L., Kiley J. P., Millhorn D. E. Respiratory responses to medullary hydrogen ion changes in cats: different effects of respiratory and metabolic acidoses. J Physiol. 1985 Jan;358:285–297. doi: 10.1113/jphysiol.1985.sp015551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Griffiths T. L., Henson L. C., Whipp B. J. Influence of inspired oxygen concentration on the dynamics of the exercise hyperpnoea in man. J Physiol. 1986 Nov;380:387–403. doi: 10.1113/jphysiol.1986.sp016292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kozlowski S., Rasmussen B., Wilkoff W. G. The effect of high oxygen tensions on ventilation during severe exercise. Acta Physiol Scand. 1971 Mar;81(3):385–395. doi: 10.1111/j.1748-1716.1971.tb04913.x. [DOI] [PubMed] [Google Scholar]
  12. Lahiri S., DeLaney R. G. Stimulus interaction in the responses of carotid body chemoreceptor single afferent fibers. Respir Physiol. 1975 Sep;24(3):249–266. doi: 10.1016/0034-5687(75)90017-1. [DOI] [PubMed] [Google Scholar]
  13. Linnarsson D. Dynamics of pulmonary gas exchange and heart rate changes at start and end of exercise. Acta Physiol Scand Suppl. 1974;415:1–68. [PubMed] [Google Scholar]
  14. Linton R. A., Band D. M. The effect of potassium on carotid chemoreceptor activity and ventilation in the cat. Respir Physiol. 1985 Jan;59(1):65–70. doi: 10.1016/0034-5687(85)90019-2. [DOI] [PubMed] [Google Scholar]
  15. Miller J. P., Cunningham D. J., Lloyd B. B., Young J. M. The transient respiratory effects in man of sudden changes in alveolar CO2 in hypoxia and in high oxygen. Respir Physiol. 1974 Feb;20(1):17–31. doi: 10.1016/0034-5687(74)90015-2. [DOI] [PubMed] [Google Scholar]
  16. Oren A., Whipp B. J., Wasserman K. Effect of acid-base status on the kinetics of the ventilatory response to moderate exercise. J Appl Physiol Respir Environ Exerc Physiol. 1982 Apr;52(4):1013–1017. doi: 10.1152/jappl.1982.52.4.1013. [DOI] [PubMed] [Google Scholar]
  17. PERRET C. [Hyperoxia and regulation of ventilation during muscular exercise]. Helv Physiol Pharmacol Acta. 1960;18:72–97. [PubMed] [Google Scholar]
  18. Roston W. L., Whipp B. J., Davis J. A., Cunningham D. A., Effros R. M., Wasserman K. Oxygen uptake kinetics and lactate concentration during exercise in humans. Am Rev Respir Dis. 1987 May;135(5):1080–1084. doi: 10.1164/arrd.1987.135.5.1080. [DOI] [PubMed] [Google Scholar]
  19. SELDINGER S. I. Catheter replacement of the needle in percutaneous arteriography; a new technique. Acta radiol. 1953 May;39(5):368–376. doi: 10.3109/00016925309136722. [DOI] [PubMed] [Google Scholar]
  20. Teppema L. J., Barts P. W., Evers J. A. Effects of metabolic arterial pH changes on medullary ecf pH, csf pH and ventilation in peripherally chemodenervated cats with intact blood-brain barrier. Respir Physiol. 1984 Oct;58(1):123–136. doi: 10.1016/0034-5687(84)90050-1. [DOI] [PubMed] [Google Scholar]
  21. Ward S. A., Blesovsky L., Russak S., Ashjian A., Whipp B. J. Chemoreflex modulation of ventilatory dynamics during exercise in humans. J Appl Physiol (1985) 1987 Nov;63(5):2001–2007. doi: 10.1152/jappl.1987.63.5.2001. [DOI] [PubMed] [Google Scholar]
  22. Wasserman K., Whipp B. J., Koyal S. N., Cleary M. G. Effect of carotid body resection on ventilatory and acid-base control during exercise. J Appl Physiol. 1975 Sep;39(3):354–358. doi: 10.1152/jappl.1975.39.3.354. [DOI] [PubMed] [Google Scholar]
  23. Whipp B. J., Davis J. A., Torres F., Wasserman K. A test to determine parameters of aerobic function during exercise. J Appl Physiol Respir Environ Exerc Physiol. 1981 Jan;50(1):217–221. doi: 10.1152/jappl.1981.50.1.217. [DOI] [PubMed] [Google Scholar]
  24. Whipp B. J., Ward S. A., Wasserman K. Respiratory markers of the anaerobic threshold. Adv Cardiol. 1986;35:47–64. doi: 10.1159/000413438. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES