4.7 Article

Stereological and somatotopic analysis of the spinal microglial response to peripheral nerve injury

期刊

BRAIN BEHAVIOR AND IMMUNITY
卷 21, 期 5, 页码 624-633

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2006.10.017

关键词

microglia; spinal cord; stereology; somatotopy; pain

资金

  1. Canadian Institutes of Health Research [11219-5] Funding Source: Medline

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The involvement of glia, and glia-neuronal signalling in enhancing nociceptive transmission has become an area of intense scientific interest. In particular, a role has emerged for activated microglia in the development and maintenance of neuropathic, pain following peripheral nerve injury. Following activation, spinal microglia proliferate and release many substances which are capable of modulating neuronal excitability within the spinal cord. Here, we the investigated the response of spinal microglia to a unilateral spared nerve injury (SNI) in terms of the quantitative increase in cell number and the spatial distribution of the increase. Design-based stereological techniques were combined with iba-1 immunohistochemistry to estimate the total number of microglia in the spinal dorsal horn in naive and peripheral nerve-injured adult rats. In addition, by mapping the central terminals of hindlimb nerves, the somatotopic distribution of the microglial response was mapped. Following SNI there was a marked increase in the number of spinal microglia: The total number of microglia (mean +/- SD) in the dorsal horn sciatic territory of the naive rat was estimated to be 28,591 +/- 2715. Following SNI the number of microglia was 82,034 +/- 8828. While the pattern of microglial activation generally followed somatotopic boundaries, with the majority of microglia within the territory occupied by peripherally axotomised primary afferents, some spread was seen into regions occupied by intact, 'spared' central projections of the sural nerve. This study provides a reproducible method of assaying spinal microglial dynamics following peripheral nerve injury both quantitatively and spatially. (c) 2006 Elsevier Inc. All rights reserved.

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