Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1978 May 1;71(5):559–580. doi: 10.1085/jgp.71.5.559

Kinetics of oxygen consumption after a single isometric tetanus of frog sartorius muscle at 20 degrees C

PMCID: PMC2215108  PMID: 307047

Abstract

The time-course of the rate of oxygen consumption (QO2) has been measured in the excised frog sartorius muscle after single isometric tetani of 0.1-1.0 s at 20 degrees C. To measure deltaQO2(t), the change in QO2 from its basal level, a novel method was devised, based on the validity in this tissue of the one-dimensional diffusion equation for oxygen, established in the preceding paper. After a tetanus, deltaQO2 reached a peak within 45-90 s, then declined exponentially, and could be well fit by deltaQO2(t) = QO + Q1(epsilon -k1t - epsilon-k2t). tau2 (= 1/k2), which characterized the rise of deltaQO2, was a decreasing function of tetanus duration (range: from 1.1 +/- 0.28 min [nu = 5] for a 0.1-s tetanus, to 0.34 +/- 0.05 min [nu = 8] for a 1.0-sec tetanus). tau1 (= 1/k1), which characterized the decline of deltaQO2, was not dependent on tetanus duration, with mean 3.68 +/- -.24 min (nu = 46). A forthcoming paper in this series shows that these kinetics of deltaQO2 are the responses to impulse-like changes in the rate of ATP hydrolysis. The variation of tau2 with tetanus duration thus indicates the involvement of a nonlinear process in the coupling of O2 consumption to ATP hydrolysis. However, the monoexponential decline of deltaQO2(t), with time constant independent of tetanus duration, suggests that during this phase, the coupling is rate-limited by a single reaction with apparent first order kinetics.

Full Text

The Full Text of this article is available as a PDF (1.1 MB).

Selected References

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

  1. BASKIN R. J., GAFFIN S. OXYGEN CONSUMPTION IN FROG SARTORIUS MUSCLE. I. THE ISOMETRIC TWITCH. J Cell Physiol. 1965 Feb;65:19–25. doi: 10.1002/jcp.1030650104. [DOI] [PubMed] [Google Scholar]
  2. Casaburi R., Whipp B. J., Wasserman K., Beaver W. L., Koyal S. N. Ventilatory and gas exchange dynamics in response to sinusoidal work. J Appl Physiol Respir Environ Exerc Physiol. 1977 Feb;42(2):300–301. doi: 10.1152/jappl.1977.42.2.300. [DOI] [PubMed] [Google Scholar]
  3. Gore R. W., Whalen W. J. Relations among tissue PO2, QO2, and resting heat production of frog sartorius muscle. Am J Physiol. 1968 Feb;214(2):277–286. doi: 10.1152/ajplegacy.1968.214.2.277. [DOI] [PubMed] [Google Scholar]
  4. HILL A. V. Myothermic methods. Proc R Soc Lond B Biol Sci. 1949 Jun 23;136(883):228–241. doi: 10.1098/rspb.1949.0022. [DOI] [PubMed] [Google Scholar]
  5. Hartree W., Hill A. V. The recovery heat-production in muscle. J Physiol. 1922 Jul 21;56(5):367–381. doi: 10.1113/jphysiol.1922.sp002019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hill D. K. Oxygen tension and the respiration of resting frog's muscle. J Physiol. 1948 Sep 30;107(4):479–495. doi: 10.1113/jphysiol.1948.sp004293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hill D. K. The time course of evolution of oxidative recovery heat of frog's muscle. J Physiol. 1940 Sep 14;98(4):454–459. doi: 10.1113/jphysiol.1940.sp003863. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hill D. K. The time course of the oxygen consumption of stimulated frog's muscle. J Physiol. 1940 May 14;98(2):207–227. doi: 10.1113/jphysiol.1940.sp003845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jacobus W. E., Lehninger A. L. Creatine kinase of rat heart mitochondria. Coupling of creatine phosphorylation to electron transport. J Biol Chem. 1973 Jul 10;248(13):4803–4810. [PubMed] [Google Scholar]
  10. Kawashiro T., Nüsse W., Scheid P. Determination of diffusivity of oxygen and carbon dioxide in respiring tissue: results in rat skeletal muscle. Pflugers Arch. 1975 Sep 9;359(3):231–251. doi: 10.1007/BF00587382. [DOI] [PubMed] [Google Scholar]
  11. Mahler M. Diffusion and consumption of oxygen in the resting frog sartorius muscle. J Gen Physiol. 1978 May;71(5):533–557. doi: 10.1085/jgp.71.5.533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Owen C. S., Wilson D. F. Control of respiration by the mitochondrial phosphorylation state. Arch Biochem Biophys. 1974 Apr 2;161(2):581–591. doi: 10.1016/0003-9861(74)90341-5. [DOI] [PubMed] [Google Scholar]
  13. Piiper J., Di Prampero P. E., Cerretelli P. Oxygen debt and high-energy phosphates in gastrocnemius muscle of the dog. Am J Physiol. 1968 Sep;215(3):523–531. doi: 10.1152/ajplegacy.1968.215.3.523. [DOI] [PubMed] [Google Scholar]
  14. Saks V. A., Chernousova G. B., Voronkov I. I., Smirnov V. N., Chazov E. I. Study of energy transport mechanism in myocardial cells. Circ Res. 1974 Sep;35 (Suppl 3):138–149. [PubMed] [Google Scholar]
  15. Saks V. A., Lipina N. V., Smirnov V. N., Chazov E. I. Studies of energy transport in heart cells. The functional coupling between mitochondrial creatine phosphokinase and ATP ADP translocase: kinetic evidence. Arch Biochem Biophys. 1976 Mar;173(1):34–41. doi: 10.1016/0003-9861(76)90231-9. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES