Literature DB >> 24423646

Mice with a deletion of the major central myelin protein exhibit hypersensitivity to noxious thermal stimuli: involvement of central sensitization.

Bérengère Petit1, Fabrice Giraudet2, Céline Béchon1, Laurent Bardin3, Paul Avan2, Odile Boespflug-Tanguy4, Mélina Bégou5.   

Abstract

Null mutations in the gene encoding the major myelin protein of the central nervous system, proteolipid protein 1 (PLP1), cause an X-linked form of spastic paraplegia (SPG2) associated with axonal degeneration. While motor symptoms are the best known manifestations of this condition, its somatosensory disturbances have been described but poorly characterized. We carried out a longitudinal study in an animal model of SPG2 - mice carrying a deletion of the Plp1 gene (Plp-null mice). Plp-null mice exhibited severe early-onset thermal hyperalgesia, in the absence of thermal allodynia. We first performed an electrophysiological testing which showed an early decrease in peripheral and spinal conduction velocities in Plp null mice. Such as the abnormal sensitive behaviors, this slowing of nerve conduction was observed before the development of myelin abnormalities at the spinal level, from 3months of age, and without major morphological defects in the sciatic nerve. To understand the link between a decrease in nerve velocity and an increased response to thermal stimuli before the appearance of myelin abnormalities, we focused our attention on the dorsal horn of the spinal cord, the site of integration of somatosensory information. Immunohistochemical studies revealed an early-onset activation of astrocytes and microglia that worsened with age, associated later in age with perturbation of the expression of the sensory neuropeptides calcitonin-gene-related peptide and galanin. Taken together, these results represent complementary data supporting the hypothesis that Plp-null mice suffer from ganglionopathy associated with late onset central demyelination but with few peripheral nerve alterations, induced by the glial-cell-mediated sensitization of the spinal cord. The mechanism suggested here could underlie pain experiments in other leukodystrophies as well as in other non-genetic demyelinating diseases such as multiple sclerosis.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Central sensitization; Dysmyelinating disease; Pain; Transgenic mice

Mesh:

Substances:

Year:  2014        PMID: 24423646     DOI: 10.1016/j.nbd.2014.01.005

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  4 in total

1.  Mild myelin disruption elicits early alteration in behavior and proliferation in the subventricular zone.

Authors:  Elizabeth A Gould; Nicolas Busquet; Douglas Shepherd; Robert M Dietz; Paco S Herson; Fabio M Simoes de Souza; Anan Li; Nicholas M George; Diego Restrepo; Wendy B Macklin
Journal:  Elife       Date:  2018-02-13       Impact factor: 8.140

Review 2.  How Do Cells of the Oligodendrocyte Lineage Affect Neuronal Circuits to Influence Motor Function, Memory and Mood?

Authors:  Renee E Pepper; Kimberley A Pitman; Carlie L Cullen; Kaylene M Young
Journal:  Front Cell Neurosci       Date:  2018-11-16       Impact factor: 5.505

3.  Absence of Tau triggers age-dependent sciatic nerve morphofunctional deficits and motor impairment.

Authors:  Sofia Lopes; André Lopes; Vítor Pinto; Marco R Guimarães; Vanessa Morais Sardinha; Sara Duarte-Silva; Sara Pinheiro; João Pizarro; João Filipe Oliveira; Nuno Sousa; Hugo Leite-Almeida; Ioannis Sotiropoulos
Journal:  Aging Cell       Date:  2016-01-08       Impact factor: 9.304

4.  Heat Exposure and Multiple Sclerosis-A Regional and Temporal Analysis.

Authors:  Gill Chacko; Sneh Patel; Anat Galor; Naresh Kumar
Journal:  Int J Environ Res Public Health       Date:  2021-06-02       Impact factor: 3.390

  4 in total

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