Skip to main content
PMC home page
The Journal of Physiology logoLink to The Journal of Physiology
. 1961 Dec;159(3):410–435. doi: 10.1113/jphysiol.1961.sp006818

Anion permeability of the synaptic and non-synaptic motoneurone membrane

T Araki, M Ito, O Oscarsson
PMCID: PMC1359542  PMID: 13861983

Full text

PDF
414

Selected References

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

  1. ARAKI T., EOCLES J. C., ITO M. Correlation of the inhibitory post-synaptic potential of motoneurones with the latency and time course of inhibition of monosynaptic reflexes. J Physiol. 1960 Dec;154:354–377. doi: 10.1113/jphysiol.1960.sp006584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. ARAKI T., ITO M., OSCARSSON O. Anionic permeability of the inhibitory postsynaptic membrane of motoneurones. Nature. 1961 Jan 7;189:65–65. doi: 10.1038/189065a0. [DOI] [PubMed] [Google Scholar]
  3. BOISTEL J., FATT P. Membrane permeability change during inhibitory transmitter action in crustacean muscle. J Physiol. 1958 Nov 10;144(1):176–191. doi: 10.1113/jphysiol.1958.sp006094. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BRADLEY K., ECCLES J. C. Analysis of the fast afferent impulses from thigh muscles. J Physiol. 1953 Dec 29;122(3):462–473. doi: 10.1113/jphysiol.1953.sp005014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BROCK L. G., COOMBS J. S., ECCLES J. C. The recording of potentials from motoneurones with an intracellular electrode. J Physiol. 1952 Aug;117(4):431–460. doi: 10.1113/jphysiol.1952.sp004759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Boyle P. J., Conway E. J. Potassium accumulation in muscle and associated changes. J Physiol. 1941 Aug 11;100(1):1–63. doi: 10.1113/jphysiol.1941.sp003922. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. CALDWELL P. C. Studies on the internal pH of large muscle and nerve fibres. J Physiol. 1958 Jun 18;142(1):22–62. doi: 10.1113/jphysiol.1958.sp005998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. COOMBS J. S., CURTIS D. R., ECCLES J. C. The electrical constants of the motoneurone membrane. J Physiol. 1959 Mar 12;145(3):505–528. doi: 10.1113/jphysiol.1959.sp006158. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. COOMBS J. S., ECCLES J. C., FATT P. Excitatory synaptic action in motoneurones. J Physiol. 1955 Nov 28;130(2):374–395. doi: 10.1113/jphysiol.1955.sp005413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. COOMBS J. S., ECCLES J. C., FATT P. The specific ionic conductances and the ionic movements across the motoneuronal membrane that produce the inhibitory post-synaptic potential. J Physiol. 1955 Nov 28;130(2):326–374. doi: 10.1113/jphysiol.1955.sp005412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. CURTIS D. R., ECCLES J. C. The time courses of excitatory and inhibitory synaptic actions. J Physiol. 1959 Mar 12;145(3):529–546. doi: 10.1113/jphysiol.1959.sp006159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. ECCLES J. C., ECCLES R. M., LUNDBERG A. Synaptic actions on motoneurones caused by impulses in Golgi tendon organ afferents. J Physiol. 1957 Sep 30;138(2):227–252. doi: 10.1113/jphysiol.1957.sp005849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. ECCLES J. C., ECCLES R. M., LUNDBERG A. The convergence of monosynaptic excitatory afferents on to many different species of alpha motoneurones. J Physiol. 1957 Jun 18;137(1):22–50. doi: 10.1113/jphysiol.1957.sp005794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. ECCLES J. C., FATT P., KOKETSU K. Cholinergic and inhibitory synapses in a pathway from motor-axon collaterals to motoneurones. J Physiol. 1954 Dec 10;126(3):524–562. doi: 10.1113/jphysiol.1954.sp005226. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. ECCLES J. C., FATT P., LANDGREN S., WINSBURY G. J. Spinal cord potentials generated by volleys in the large muscle afferents. J Physiol. 1954 Sep 28;125(3):590–606. doi: 10.1113/jphysiol.1954.sp005183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. ECCLES R. M., LUNDBERG A. Supraspinal control of interneurones mediating spinal reflexes. J Physiol. 1959 Oct;147:565–584. doi: 10.1113/jphysiol.1959.sp006262. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. GERARD R. W., DOTY R. W. Nerve conduction without increased oxygen consumption; the action of azide and fluoroacetate. Biochim Biophys Acta. 1950 Jan;4(1-3):115–117. doi: 10.1016/0006-3002(50)90013-8. [DOI] [PubMed] [Google Scholar]
  18. HAGIWARA S., KUSANO K., SAITO S. Membrane changes in crayfish stretch receptor neutron during synaptic inhibition and under action of gamma-aminobutyric acid. J Neurophysiol. 1960 Sep;23:505–515. doi: 10.1152/jn.1960.23.5.505. [DOI] [PubMed] [Google Scholar]
  19. HARRIS E. J. Anion interaction in frog muscle. J Physiol. 1958 Apr 30;141(2):351–365. doi: 10.1113/jphysiol.1958.sp005979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. HILL A. V., MACPHERSON L. The effect of nitrate, iodide and bromide on the duration of the active state in skeletal muscle. Proc R Soc Lond B Biol Sci. 1954 Dec 15;143(910):81–102. doi: 10.1098/rspb.1954.0055. [DOI] [PubMed] [Google Scholar]
  21. HODGKIN A. L., KATZ B. The effect of sodium ions on the electrical activity of giant axon of the squid. J Physiol. 1949 Mar 1;108(1):37–77. doi: 10.1113/jphysiol.1949.sp004310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. HUTTER O. F., NOBLE D. The chloride conductance of frog skeletal muscle. J Physiol. 1960 Apr;151:89–102. [PMC free article] [PubMed] [Google Scholar]
  23. HUTTER O. F., PADSHA S. M. Effect of nitrate and other anions on the membrane resistance of frog skeletal muscle. J Physiol. 1959 Apr 23;146(1):117–132. doi: 10.1113/jphysiol.1959.sp006182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. KUNO M. Excitability following antidromic activation in spinal motoneurones supplying red muscles. J Physiol. 1959 Dec;149:374–393. doi: 10.1113/jphysiol.1959.sp006345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. LING G., GERARD R. W. The membrane potential and metabolism of muscle fibers. J Cell Physiol. 1949 Dec;34(3):413–438. doi: 10.1002/jcp.1030340307. [DOI] [PubMed] [Google Scholar]
  26. LUFT J. H. Permanganate; a new fixative for electron microscopy. J Biophys Biochem Cytol. 1956 Nov 25;2(6):799–802. doi: 10.1083/jcb.2.6.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. MULLINS L. J., MOORE R. D. The movement of thallium ions in muscle. J Gen Physiol. 1960 Mar;43:759–773. doi: 10.1085/jgp.43.4.759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. MULLINS Lj. The penetration of some cations into muscle. J Gen Physiol. 1959 Mar 20;42(4):817–829. doi: 10.1085/jgp.42.4.817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. SHANES A. M. Electrochemical aspects of physiological and pharmacological action in excitable cells. I. The resting cell and its alteration by extrinsic factors. Pharmacol Rev. 1958 Mar;10(1):59–164. [PubMed] [Google Scholar]
  30. SIMON S. E., JOHNSTONE B. M., SHANKLY K. H., SHAW F. H. Muscle: a three phase system. The partition of monovalent ions across the cell membrane. J Gen Physiol. 1959 Sep;43:55–79. doi: 10.1085/jgp.43.1.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. SJODIN R. A. Rubidium and cesium fluxes in muscle as related to the membrane potential. J Gen Physiol. 1959 May 20;42(5):983–1003. doi: 10.1085/jgp.42.5.983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. SOLOMON A. K. Red cell membrane structure and ion transport. J Gen Physiol. 1960 May;43:1–15. doi: 10.1085/jgp.43.5.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. SPYROPOULOS C. S., TASAKI I. Nerve excitiation and synaptic transmission. Annu Rev Physiol. 1960;22:407–432. doi: 10.1146/annurev.ph.22.030160.002203. [DOI] [PubMed] [Google Scholar]

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

RESOURCES