Literature DB >> 15979797

Heritability of symptoms in the neuroma model of neuropathic pain: replication and complementation analysis.

Marshall Devor1, Sonia del Canho, Pnina Raber.   

Abstract

Applying genetic selection pressure to an outbred population of albino rats, we have derived lines that show consistently high versus low pain phenotype in the neuroma model of neuropathic pain. Trait segregation developed rapidly, replicating earlier observations using this methodology. The resulting novel selection lines, designated nHA and nLA, share a common genetic background but have dramatically contrasting neuropathic pain behavior. In addition to confirming that the pain trait selected is heritable (estimated realized heritability h(2)=0.31), we have refreshed the availability of this research resource, namely animals of uniform genetic background but with contrasting pain phenotype. Crossing nHA rats with animals of the high (recessive) line from the earlier selection program (HA) yielded offspring almost uniformly high in pain phenotype. This complementation analysis indicates that the same gene(s) was selected in both selection programs, attesting to its unique salience in determining pain phenotype in the neuroma model.

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Year:  2005        PMID: 15979797     DOI: 10.1016/j.pain.2005.04.025

Source DB:  PubMed          Journal:  Pain        ISSN: 0304-3959            Impact factor:   6.961


  5 in total

1.  The genetics of pain and analgesia in laboratory animals.

Authors:  William R Lariviere; Jeffrey S Mogil
Journal:  Methods Mol Biol       Date:  2010

2.  Expression of the dopaminergic D1 and D2 receptors in the anterior cingulate cortex in a model of neuropathic pain.

Authors:  J Manuel Ortega-Legaspi; Patricia de Gortari; René Garduño-Gutiérrez; María Isabel Amaya; Martha León-Olea; Ulises Coffeen; Francisco Pellicer
Journal:  Mol Pain       Date:  2011-12-15       Impact factor: 3.395

3.  A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain.

Authors:  Weihua Meng; Harshal A Deshmukh; Louise A Donnelly; Nicola Torrance; Helen M Colhoun; Colin N A Palmer; Blair H Smith
Journal:  EBioMedicine       Date:  2015-08-04       Impact factor: 8.143

4.  Sources of individual variability: miRNAs that predispose to neuropathic pain identified using genome-wide sequencing.

Authors:  Kiran Kumar Bali; Michael Hackenberg; Avigail Lubin; Rohini Kuner; Marshall Devor
Journal:  Mol Pain       Date:  2014-03-19       Impact factor: 3.395

5.  A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain.

Authors:  W Meng; H A Deshmukh; N R van Zuydam; Y Liu; L A Donnelly; K Zhou; A D Morris; H M Colhoun; C N A Palmer; B H Smith
Journal:  Eur J Pain       Date:  2015-03       Impact factor: 3.931

  5 in total

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