Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
1987-12-22
pubmed:abstractText
We have shown that bullfrog sciatic nerves respond to a conditioning lesion similarly to goldfish optic nerve and rat or mouse sciatic nerve; that is, following a crush the rate of regeneration is faster in nerves that have received a conditioning lesion compared to nerves that have not. Also, damaged nerve fibres show initial growth or sprouting earlier in a previously conditioned nerve compared to nerves that have not received a prior conditioning lesion. We have not detected changes in the transport of fast axonally transported proteins with the conditioning lesion paradigm, other than those changes seen in regenerating nerves after receiving a single lesion. However, more label was present in a few fast axonally transported proteins at the lesion site in conditioned nerves compared to non-conditioned nerves, and this difference is not apparently due to increased transport. It seems that changes in fast axonally transported proteins probably do not contribute directly to the mechanism underlying the conditioning lesion effect of higher out growth rates, although some of the fast transported proteins may be involved in functions, possibly at the growing tip of damaged fibres, which promote or result from the conditioning effect.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0006-8993
pubmed:author
pubmed:issnType
Print
pubmed:day
13
pubmed:volume
423
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1-12
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1987
pubmed:articleTitle
Effects of a conditioning lesion on bullfrog sciatic nerve regeneration: analysis of fast axonally transported proteins.
pubmed:affiliation
Department of Physiology and Biophysics, School of Medicine, University of Miami, FL 33101.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.