Literature DB >> 345071

An explanation of axonal regeneration in peripheral nerves and its failure in the central nervous system.

J A Kiernan.   

Abstract

Nerve fibres severed within peripheral nerves are able to regenerate and reinnervate the structures they formerly supplied. Most axons severed within the mammalian central nervous system (CNS) do not regenerate in this way. Regenerative axonal growth begins to occur in the CNS but ceases about two weeks after injury. Five earlier theories purporting to explain this difference are reviewed and found not to account satisfactorily for many experimental observations. A new hypothesis is advanced in which it is held that in order for regeneration to take place, the growing tips of the axons must be surrounded by extracellular fluid containing proteins (of specified identity) derived from the blood plasma. Such proteins are thought to be imbibed by the tips of the fibres and transported retrogradely to the neuronal cell-bodies. With this hypothesis it is possible to explain the success of axonal regeneration in peripheral nerves and its failure in the CNS. It is also possible to account for the exceptional circumstances in which axons do regenerate in the CNS. Various experiments are suggested for testing the validity of the new hypothesis.

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Year:  1978        PMID: 345071     DOI: 10.1016/0306-9877(78)90022-1

Source DB:  PubMed          Journal:  Med Hypotheses        ISSN: 0306-9877            Impact factor:   1.538


  12 in total

1.  A reappraisal of the effects of ACTH on the response of the central nervous system to injury.

Authors:  M Berry; J Knowles; P Willis; A C Riches; G P Morgans; D Steers
Journal:  J Anat       Date:  1979-06       Impact factor: 2.610

2.  Electrophysiological effect of HeNe laser on normal and injured sciatic nerve in the rat.

Authors:  S Rochkind; M Nissan; N Razon; M Schwartz; A Bartal
Journal:  Acta Neurochir (Wien)       Date:  1986       Impact factor: 2.216

3.  Collagen-omental graft in experimental spinal cord transection.

Authors:  J C de la Torre; H S Goldsmith
Journal:  Acta Neurochir (Wien)       Date:  1990       Impact factor: 2.216

4.  Failure of central axonal regeneration after immunosuppressive treatment.

Authors:  M Berry; A C Riches; J Knowles; P Willis; D Steers
Journal:  J Anat       Date:  1979-09       Impact factor: 2.610

5.  Uptake and retrograde transport of proteins by regenerating axons.

Authors:  J R Sparrow; J A Kiernan
Journal:  Acta Neuropathol       Date:  1979-06-15       Impact factor: 17.088

6.  Vascular permeability and axonal regeneration in tissues autotransplanted into the brain.

Authors:  E A Heinicke
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

7.  Axonal and vascular changes following injury to the rat's optic nerve.

Authors:  J A Kiernan
Journal:  J Anat       Date:  1985-08       Impact factor: 2.610

8.  Endoneurial vascular permeability in degenerating and regenerating peripheral nerves.

Authors:  J R Sparrow; J A Kiernan
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

9.  Vascular permeability associated with axonal regeneration in the optic system of the goldfish.

Authors:  J A Kiernan; A Contestabile
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

10.  The effect of acute ethanol intoxication and chronic ethanol consumption on vascular permeability around cerebral stab wounds in mice.

Authors:  E A Heinicke
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

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