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. 1980 Apr;301:271–280. doi: 10.1113/jphysiol.1980.sp013204

Levels of high-energy phosphates in crayfish nerve during prolonged repetitive impulse activity.

D O Smith
PMCID: PMC1279397  PMID: 7411433

Abstract

1. Levels of ATP and arginine phosphate (ArgP) in the mixed nerve bundle of the crayfish walking leg were assayed in fresh tissue and after prolonged repetitive stimulation. 2. In fresh tissue, ATP and ArgP levels were estimated to be about 34 n-mole/mg protein and 157 n-mole/mg protein, respectively, corresponding to concentrations of 3 . 0 and 13 . 9 mM. 3. Following 5 min of repetitive stimulation at 30 impulses/sec, the ATP concentration in the nerve increased by 0 . 52 mM; after 10 and 20 min of stimulation, the concentrations returned to values similar to those of fresh tissue. 4. The ArgP concentrations were similar to those of fresh tissue after 5 min of stimulation at 30 impulses/sec but dropped to about 85% of those values after 10 and 20 min of stimulation. 5. Increased K+ in the physiological saline reduced [ATP] following stimulation; decreased Na+ in the saline increased the content of ATP in unstimulated nerves. 6. It is concluded that repetitive action potential activity may be associated with relatively constant and perhaps increased production of ATP.

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Selected References

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

  1. Alnaes E., Rahamimoff R. On the role of mitochondria in transmitter release from motor nerve terminals. J Physiol. 1975 Jun;248(2):285–306. doi: 10.1113/jphysiol.1975.sp010974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Atwood H. L., Lang F., Morin W. A. Synaptic vesicles: selective depletion in crayfish excitatory and inhibitory axons. Science. 1972 Jun 23;176(4041):1353–1355. doi: 10.1126/science.176.4041.1353. [DOI] [PubMed] [Google Scholar]
  3. Baker P. F., Blaustein M. P., Keynes R. D., Manil J., Shaw T. I., Steinhardt R. A. The ouabain-sensitive fluxes of sodium and potassium in squid giant axons. J Physiol. 1969 Feb;200(2):459–496. doi: 10.1113/jphysiol.1969.sp008703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Banay-Schwartz M., Teller D. N., Gergely A., Lajtha A. The effects of metabolic inhibitors on amino acid uptake and the levels of ATP, Na+, and K+ in incubated slices of mouse brain. Brain Res. 1974 May 10;71(1):117–131. doi: 10.1016/0006-8993(74)90195-4. [DOI] [PubMed] [Google Scholar]
  5. Brinley F. J., Jr, Mullins L. J. Sodium extrusion by internally dialyzed squid axons. J Gen Physiol. 1967 Nov;50(10):2303–2331. doi: 10.1085/jgp.50.10.2303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. CALDWELL P. C. The phosphorus metabolism of squid axons and its relationship to the active transport of sodium. J Physiol. 1960 Jul;152:545–560. doi: 10.1113/jphysiol.1960.sp006508. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cohen L. B., Landowne D. The temperature dependence of the movement of sodium ions associated with nerve impulses. J Physiol. 1974 Jan;236(1):95–111. doi: 10.1113/jphysiol.1974.sp010424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. DUDEL J., KUFFLER S. W. The quantal nature of transmission and spontaneous miniature potentials at the crayfish neuromuscular junction. J Physiol. 1961 Mar;155:514–529. doi: 10.1113/jphysiol.1961.sp006644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FRANKENHAEUSER B., HODGKIN A. L. The after-effects of impulses in the giant nerve fibres of Loligo. J Physiol. 1956 Feb 28;131(2):341–376. doi: 10.1113/jphysiol.1956.sp005467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. GREENGARD P., STRAUB R. W. Effect of frequency of electrical stimulation on the concentration of intermediary metabolites in mammalian non-myelinated fibres. J Physiol. 1959 Oct;148:353–361. doi: 10.1113/jphysiol.1959.sp006292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. HEALD P. J. Rapid changes in creatine phosphate level in cerebral cortex slices. Biochem J. 1954 Aug;57(4):673–679. [PMC free article] [PubMed] [Google Scholar]
  12. HODGKIN A. L., KEYNES R. D. Active transport of cations in giant axons from Sepia and Loligo. J Physiol. 1955 Apr 28;128(1):28–60. doi: 10.1113/jphysiol.1955.sp005290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hatt H., Smith D. O. Synaptic depression related to presynaptic axon conduction block. J Physiol. 1976 Jul;259(2):367–393. doi: 10.1113/jphysiol.1976.sp011471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kline M. H., Hexum T. D., Dahl J. L., Hokin L. E. Studies on the characterization of the sodium-potassium transport adenosinetriphosphatase. VII. Comparison of the properties of the membrane-bound and partially purified soluble and insoluble forms of the enzyme. Arch Biochem Biophys. 1971 Dec;147(2):781–787. doi: 10.1016/0003-9861(71)90439-5. [DOI] [PubMed] [Google Scholar]
  15. LOWRY O. H., PASSONNEAU J. V., HASSELBERGER F. X., SCHULZ D. W. EFFECT OF ISCHEMIA ON KNOWN SUBSTRATES AND COFACTORS OF THE GLYCOLYTIC PATHWAY IN BRAIN. J Biol Chem. 1964 Jan;239:18–30. [PubMed] [Google Scholar]
  16. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  17. Montant P., Chmouliovsky M. Energy-rich metabolites in stimulated mammalian non-myelinated nerve fibres. Experientia. 1968 Aug 15;24(8):782–783. doi: 10.1007/BF02144864. [DOI] [PubMed] [Google Scholar]
  18. Nassar-Gentina V., Passonneau J. V., Vergara J. L., Rapoport S. I. Metabolic correlates of fatigue and of recovery from fatigue in single frog muscle fibers. J Gen Physiol. 1978 Nov;72(5):593–606. doi: 10.1085/jgp.72.5.593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Okada Y., McDougal D. B., Jr Physiological and biochemical changes in frog sciatic nerve during anoxia and recovery. J Neurochem. 1971 Dec;18(12):2335–2353. doi: 10.1111/j.1471-4159.1971.tb00189.x. [DOI] [PubMed] [Google Scholar]
  20. SHANES A. M. Potassium movement in relation to nerve activity. J Gen Physiol. 1951 Jul;34(6):795–807. doi: 10.1085/jgp.34.6.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Smith D. O., Hatt H. Axon conduction block in a region of dense connective tissue in crayfish. J Neurophysiol. 1976 Jul;39(4):794–801. doi: 10.1152/jn.1976.39.4.794. [DOI] [PubMed] [Google Scholar]
  22. Smith D. O. Mechanisms of action potential propagation failure at sites of axon branching in the crayfish. J Physiol. 1980 Apr;301:243–259. doi: 10.1113/jphysiol.1980.sp013202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Smith D. O. Morphological aspects of the safety factor for action potential propagation at axon branch points in the crayfish. J Physiol. 1980 Apr;301:261–269. doi: 10.1113/jphysiol.1980.sp013203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Smith D. O. Ultrastructural basis of impulse propagation failure in a nonbranching axon. J Comp Neurol. 1977 Dec 15;176(4):659–669. doi: 10.1002/cne.901760413. [DOI] [PubMed] [Google Scholar]
  25. Weibel E. R. Stereological principles for morphometry in electron microscopic cytology. Int Rev Cytol. 1969;26:235–302. doi: 10.1016/s0074-7696(08)61637-x. [DOI] [PubMed] [Google Scholar]
  26. Zucker R. S. Characteristics of crayfish neuromuscular facilitation and their calcium dependence. J Physiol. 1974 Aug;241(1):91–110. doi: 10.1113/jphysiol.1974.sp010642. [DOI] [PMC free article] [PubMed] [Google Scholar]

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