Skip to main content
PMC home page
The Journal of Physiology logoLink to The Journal of Physiology
. 1960 Dec;154(2):288–307. doi: 10.1113/jphysiol.1960.sp006580

Surplus excitation in reflex action of motoneurones as measured by recurrent inhibition

R Granit, L T Rutledge
PMCID: PMC1359802  PMID: 13707845

Full text

PDF
292

Selected References

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

  1. ALVORD E. C., Jr, FUORTES M. G. Reflex activity of extensor motor units following muscular afferent excitation. J Physiol. 1953 Nov 28;122(2):302–321. doi: 10.1113/jphysiol.1953.sp005001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. ARAKI T., OTANI T. Accommodation and local response in motoneurons of toad's spinal cord. Jpn J Physiol. 1959 Mar 25;9(1):69–83. doi: 10.2170/jjphysiol.9.69. [DOI] [PubMed] [Google Scholar]
  3. BROCK L. G., COOMBS J. S., ECCLES J. C. Intracellular recording from antidromically activated motoneurones. J Physiol. 1953 Dec 29;122(3):429–461. doi: 10.1113/jphysiol.1953.sp005013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BROOKS V. B., WILSON V. J. Recurrent inhibition in the cat's spinal cord. J Physiol. 1959 May 19;146(2):380–391. doi: 10.1113/jphysiol.1959.sp006199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Barron D. H., Matthews B. H. The interpretation of potential changes in the spinal cord. J Physiol. 1938 Apr 14;92(3):276–321. doi: 10.1113/jphysiol.1938.sp003603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. CURTIS D. R., ECCLES R. M. The excitation of Renshaw cells by pharmacological agents applied electrophoretically. J Physiol. 1958 May 28;141(3):435–445. doi: 10.1113/jphysiol.1958.sp005987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. 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]
  8. ELDRED E., GRANIT R., MERTON P. A. Supraspinal control of the muscle spindles and its significance. J Physiol. 1953 Dec 29;122(3):498–523. doi: 10.1113/jphysiol.1953.sp005017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FRANK K., FUORTES M. G. Unitary activity of spinal interneurones of cats. J Physiol. 1956 Feb 28;131(2):424–435. doi: 10.1113/jphysiol.1956.sp005472. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. GRANIT R. Neuromuscular interaction in postural tone of the cat's isometric soleus muscle. J Physiol. 1958 Oct 31;143(3):387–402. doi: 10.1113/jphysiol.1958.sp006067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. GRANIT R., PASCOE J. E., STEG G. The behaviour of tonic alpha and gamma motoneurones during stimulation of recurrent collaterals. J Physiol. 1957 Oct 30;138(3):381–400. doi: 10.1113/jphysiol.1957.sp005857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. GRANIT R., PHILLIPS C. G., SKOGLUND S., STEG G. Differentiation of tonic from phasic alpha ventral horn cells by stretch, pinna and crossed extensor reflexes. J Neurophysiol. 1957 Sep;20(5):470–481. doi: 10.1152/jn.1957.20.5.470. [DOI] [PubMed] [Google Scholar]
  13. Granit R., Haase J., Rutledge L. T. Recurrent inhibition in relation to frequency of firing and limitation of discharge rate of extensor motoneurones. J Physiol. 1960 Dec;154(2):308–328. doi: 10.1113/jphysiol.1960.sp006581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. HARTLINE H. K., RATLIFF F. Inhibitory interaction of receptor units in the eye of Limulus. J Gen Physiol. 1957 Jan 20;40(3):357–376. doi: 10.1085/jgp.40.3.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. KOIZUMI K., USHIYAMA J., BROOKS C. M. A study of reticular formation action on spinal interneurons and motoneurons. Jpn J Physiol. 1959 Sep 15;9:282–303. doi: 10.2170/jjphysiol.9.282. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. MATTHEWS P. B., RUSHWORTH G. The selective effect of proCaine on the stretch reflex and tendon jerk of soleus muscle when applied to its nerve. J Physiol. 1957 Feb 15;135(2):245–262. doi: 10.1113/jphysiol.1957.sp005707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Matthews P. B. A study of certain factors influencing the stretch reflex of the decerebrate cat. J Physiol. 1959 Oct;147(3):547–564. doi: 10.1113/jphysiol.1959.sp006261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Matthews P. B. The dependence of tension upon extension in the stretch reflex of the soleus muscle of the decerebrate cat. J Physiol. 1959 Oct;147(3):521–546. doi: 10.1113/jphysiol.1959.sp006260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. PHILLIPS C. G. Actions of antidromic pyramidal volleys on single Betz cells in the cat. Q J Exp Physiol Cogn Med Sci. 1959 Jan;44(1):1–25. doi: 10.1113/expphysiol.1959.sp001364. [DOI] [PubMed] [Google Scholar]
  21. WILSON V. J. Recurrent facilitation of spinal reflexes. J Gen Physiol. 1959 Mar 20;42(4):703–713. doi: 10.1085/jgp.42.4.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. WILSON V. J., TALBOT W. H., DIECKE F. P. Distribution of recurrent facilitation and inhibition in cat spinal cord. J Neurophysiol. 1960 Mar;23:144–153. doi: 10.1152/jn.1960.23.2.144. [DOI] [PubMed] [Google Scholar]
  23. WILSON V. J., TALBOT W. H., DIECKE F. P. Pattern of recurrent conditioning of spinal reflexes. Nature. 1959 Mar 21;183(4664):824–825. doi: 10.1038/183824a0. [DOI] [PubMed] [Google Scholar]
  24. WILSON V. J., TALBOT W. H. Recurrent conditioning in the cat spinal cord. Differential effect of meprobamate on recurrent facilitation and inhibition. J Gen Physiol. 1960 Jan;43:495–502. doi: 10.1085/jgp.43.3.495. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES