Literature DB >> 10842225

Delayed loss of small dorsal root ganglion cells after transection of the rat sciatic nerve.

T Tandrup1, C J Woolf, R E Coggeshall.   

Abstract

The present study deals with changes in numbers and sizes of primary afferent neurons (dorsal root ganglion [DRG] cells) after sciatic nerve transection. We find that this lesion in adult rats leads to death of some DRG cells by 8 weeks and 37% by 32 weeks after the lesion. The loss of cells appears earlier in and is more severe in B-cells (small, dark cells with unmyelinated axons) than A-cells (large, light cells with myelinated axons). With regard to mean cell volumes, there is a tendency for both categories of DRG cells to be smaller, but except for isolated time points, these differences are not statistically significant. These findings differ from most earlier reports in that the cell loss takes place later than usually reported, that the loss is more severe for B-cells, and that neither A- or B-cells change size significantly. Accordingly, we conclude that sciatic nerve transection in adult rats leads to a slowly developing but relatively profound loss of primary afferent neurons that is more severe for B-cells. These results can serve as a basis for studies to determine the effectiveness of trophic or survival factors in avoiding axotomy induced cell death. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10842225     DOI: 10.1002/(sici)1096-9861(20000626)422:2<172::aid-cne2>3.0.co;2-h

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  53 in total

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4.  Frozen-section fluorescence microscopy and stereology in the quantification of neuronal death within dorsal root ganglia.

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7.  The effects of delayed nerve repair on neuronal survival and axonal regeneration after seventh cervical spinal nerve axotomy in adult rats.

Authors:  Sharmila Jivan; Liudmila N Novikova; Mikael Wiberg; Lev N Novikov
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Review 9.  Activation of JNK pathway in persistent pain.

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10.  Activated polymorphonuclear cells promote injury and excitability of dorsal root ganglia neurons.

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