Literature DB >> 1822782

Passive avoidance behaviour deficit in the mdx mouse.

F Muntoni1, A Mateddu, G Serra.   

Abstract

Thirty per cent of boys with Duchenne muscular dystrophy (DMD) suffer from various degrees of mental retardation. Since dystrophin, the protein absent in muscles of boys with DMD, is produced also in the brain, it was postulated that the deficiency of brain dystrophin might account for the mental retardation found in DMD boys. The mdx mouse, a mouse model of DMD, fails to produce dystrophin in muscle and brain. This prompted us to study the cognitive function of these animals. Learning and memory processes were studied in 10 mdx females and 9 genetically matched controls using the passive avoidance test. Statistically significant differences in the retention of the passive avoidance response was detected between mdx and control mice, indicating an impairment in passive avoidance learning in mdx mice. Our data reinforce the view that brain dystrophin deficiency is correlated with cognitive dysfunction and indicate that mdx mice might be a model for the mental retardation found in DMD boys.

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Mesh:

Year:  1991        PMID: 1822782     DOI: 10.1016/0960-8966(91)90059-2

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  22 in total

1.  Increased density of dystrophin protein in the lateral versus the vermal mouse cerebellum.

Authors:  Wanda M Snow; Mark Fry; Judy E Anderson
Journal:  Cell Mol Neurobiol       Date:  2013-02-23       Impact factor: 5.046

2.  Dysregulation of Intracellular Ca2+ in Dystrophic Cortical and Hippocampal Neurons.

Authors:  José R Lopez; Juan Kolster; Arkady Uryash; Eric Estève; Francisco Altamirano; José A Adams
Journal:  Mol Neurobiol       Date:  2016-12-15       Impact factor: 5.590

3.  Neurocognitive Impairment in mdx Mice.

Authors:  Clarissa M Comim; Letícia Ventura; Viviane Freiberger; Paula Dias; Daiane Bragagnolo; Matheus L Dutra; Ricardo A Amaral; Ana Lucia S Camargo-Fagundes; Patrícia A Reis; Hugo C Castro-Faria-Neto; Mariz Vainzof; Maria I Rosa
Journal:  Mol Neurobiol       Date:  2019-05-10       Impact factor: 5.590

Review 4.  Cognitive dysfunction in Duchenne muscular dystrophy: a possible role for neuromodulatory immune molecules.

Authors:  Mark G Rae; Dervla O'Malley
Journal:  J Neurophysiol       Date:  2016-07-06       Impact factor: 2.714

5.  Nitric oxide generated by muscle corrects defects in hippocampal neurogenesis and neural differentiation caused by muscular dystrophy.

Authors:  Bo Deng; David Glanzman; James G Tidball
Journal:  J Physiol       Date:  2009-02-23       Impact factor: 5.182

Review 6.  Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.

Authors:  Caroline Perronnet; Cyrille Vaillend
Journal:  J Biomed Biotechnol       Date:  2010-06-17

7.  Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks.

Authors:  C Vaillend; A Rendon; R Misslin; A Ungerer
Journal:  Behav Genet       Date:  1995-11       Impact factor: 2.805

8.  Abnormalities in brain structure and biochemistry associated with mdx mice measured by in vivo MRI and high resolution localized (1)H MRS.

Authors:  Su Xu; Da Shi; Stephen J P Pratt; Wenjun Zhu; Andrew Marshall; Richard M Lovering
Journal:  Neuromuscul Disord       Date:  2015-07-10       Impact factor: 4.296

9.  Enhancing Endogenous Nitric Oxide by Whole Body Periodic Acceleration Elicits Neuroprotective Effects in Dystrophic Neurons.

Authors:  Jose R Lopez; A Uryash; J Kolster; E Estève; R Zhang; J A Adams
Journal:  Mol Neurobiol       Date:  2018-03-26       Impact factor: 5.590

Review 10.  The roles of the dystrophin-associated glycoprotein complex at the synapse.

Authors:  Gonneke S K Pilgram; Saranyapin Potikanond; Richard A Baines; Lee G Fradkin; Jasprina N Noordermeer
Journal:  Mol Neurobiol       Date:  2009-11-09       Impact factor: 5.590

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