spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by GUTMANN, E.
Right arrow Articles by YOUNG, J. Z.
Right arrow Search for Related Content
PubMed
Right arrow Articles by GUTMANN, E.
Right arrow Articles by YOUNG, J. Z.
Journal of Experimental Biology 19,14-44 (1942)
Published by Company of Biologists 1942


The Rate of Regeneration of Nerve

E. GUTMANN 1, L. GUTTMANN 1, P. B. MEDAWAR 1, and J. Z. YOUNG 1

1 Department of Zoology and Comparative Anatomy, Oxford

1. Five different methods have been used to estimate the rate of advance of regeneration along nerves in the rabbit. Not all give the same result. When the advance of the axon tips is studied a higher rate is recorded than when the times necessary for functional recovery are considered. In the latter case the experiment gives a measure of the rate of advance not of the tips of the axons but of completed nerve fibres, able to function.

2. The ‘scar delay’, or period before arrival of new axon tips in the peripheral stump, is nearly constant in all well-made sutures (7.3 days). After interruption of a nerve by complete crushing at one spot this delay is only slightly shorter (5.2 days).

3. There is a further delay before maturation to the level of functional completion begins to advance down the nerve, so that the total latent period before advance of recovery begins is about 36 days after suture and 20 days after crushing a nerve.

4. The rate of advance of the fastest axon tips was determined by finding the furthest point from the lesion at which reflexes could be elicited by pinching the nerve. After suture of the n. peroneus in the rabbit this rate was 3.5 and after crushing 4.4 mm./day.

5. This rate of the axon tips is not significantly different after crushing the nerve at different distances from the nerve cell body, namely high in the thigh or below the knee.

6. This rate is similar in the tibial, peroneal and sural divisions of the sciatic in the rabbit.

7. The rate of advance of functional, completion of nerve fibres was measured by making lesions at various levels and studying (a) the time necessary for return of response to nociceptive stimuli to a given point on the skin and (b) the time for recovery of a given motor function, namely, spreading of the toes. Both methods give rates of 2.0 mm./day after suture, and 3.0 mm./day after crushing.

8. Analgesic areas on the foot shrink at the rate of 2.1 mm./day during recovery after crushing the nerve, 1.6 mm./day after suture.

9. Comparison of the times of recovery of muscles at varying distances from a lesion gives an estimate of rate of advance of functional completion of 2.2 mm./day after crushing a nerve, but this method is only approximate in the rabbit.

10. In rabbits of 1 month old the rate of advance of the axon tips is not greatly different from that in adults, but the delay in the scar is less, and maturation of the nerve fibres proceeds more rapidly.

Submitted on October 23, 1941




This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
J. W. Lichtman and J. R. Sanes
TRANSLATIONAL NEUROSCIENCE DURING THE SECOND WORLD WAR
J. Exp. Biol., September 15, 2006; 209(18): 3485 - 3487.
[Full Text] [PDF]


Home page
J. Neurosci.Home page
C. K. Franz, U. Rutishauser, and V. F. Rafuse
Polysialylated Neural Cell Adhesion Molecule Is Necessary for Selective Targeting of Regenerating Motor Neurons
J. Neurosci., February 23, 2005; 25(8): 2081 - 2091.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
A. P. Mizisin, Y. Vu, M. Shuff, and N. A. Calcutt
Ciliary Neurotrophic Factor Improves Nerve Conduction and Ameliorates Regeneration Deficits in Diabetic Rats
Diabetes, July 1, 2004; 53(7): 1807 - 1812.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
Y. A. Pan, T. Misgeld, J. W. Lichtman, and J. R. Sanes
Effects of Neurotoxic and Neuroprotective Agents on Peripheral Nerve Regeneration Assayed by Time-Lapse Imaging In Vivo
J. Neurosci., December 10, 2003; 23(36): 11479 - 11488.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. B. Siconolfi and N. W. Seeds
Induction of the Plasminogen Activator System Accompanies Peripheral Nerve Regeneration after Sciatic Nerve Crush
J. Neurosci., June 15, 2001; 21(12): 4336 - 4347.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. B. Siconolfi and N. W. Seeds
Mice Lacking tPA, uPA, or Plasminogen Genes Showed Delayed Functional Recovery after Sciatic Nerve Crush
J. Neurosci., June 15, 2001; 21(12): 4348 - 4355.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. A. Al-Majed, C. M. Neumann, T. M. Brushart, and T. Gordon
Brief Electrical Stimulation Promotes the Speed and Accuracy of Motor Axonal Regeneration
J. Neurosci., April 1, 2000; 20(7): 2602 - 2608.
[Abstract] [Full Text] [PDF]


Home page
J Hand Surg Eur VolHome page
A. M. RAJI
An Experimental Study of the Effects of Pulsed Electromagnetic Field (Diapulse) on Nerve Repair
J Hand Surg Eur Vol., April 1, 1984; 9(2): 105 - 112.
[Abstract] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
F. E. Holmes, S. Mahoney, V. R. King, A. Bacon, N. C. H. Kerr, V. Pachnis, R. Curtis, J. V. Priestley, and D. Wynick
Targeted disruption of the galanin gene reduces the number of sensory neurons and their regenerative capacity
PNAS, October 10, 2000; 97(21): 11563 - 11568.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1942