Literature DB >> 30051354

Dp71-Dystrophin Deficiency Alters Prefrontal Cortex Excitation-Inhibition Balance and Executive Functions.

Rémi Chaussenot1, Muriel Amar1,2, Philippe Fossier1, Cyrille Vaillend3.   

Abstract

In the Duchenne muscular dystrophy (DMD) syndrome, mutations affecting expression of Dp71, the main dystrophin isoform of the multipromoter dmd gene in brain, have been associated with intellectual disability and neuropsychiatric disturbances. Patients' profile suggests alterations in prefrontal cortex-dependent executive processes, but the specific dysfunctions due to Dp71 deficiency are unclear. Dp71 is involved in brain ion homeostasis, and its deficiency is expected to increase neuronal excitability, which might compromise the integrity of neuronal networks undertaking high-order cognitive functions. Here, we used electrophysiological (patch clamp) and behavioral techniques in a transgenic mouse that display a selective loss of Dp71 and no muscular dystrophy, to identify changes in prefrontal cortex excitatory/inhibitory (E/I) balance and putative executive dysfunctions. We found prefrontal cortex E/I balance is shifted toward enhanced excitation in Dp71-null mice. This is associated with a selective alteration of AMPA receptor-mediated glutamatergic transmission and reduced synaptic plasticity, while inhibitory transmission is unaffected. Moreover, Dp71-null mice display deficits in cognitive processes that depend on prefrontal cortex integrity, such as cognitive flexibility and sensitivity of spatial working memory to proactive interference. Our data suggest that impaired cortical E/I balance and executive dysfunctions contribute to the intellectual and behavioral disturbances associated with Dp71 deficiency in DMD, in line with current neurobehavioral models considering these functions as key pathophysiological factors in various neurodevelopmental disorders. These new insights in DMD neurobiology also suggest new directions for therapeutic developments targeting excitatory neurotransmission, as well as for guidance of academic environment in severely affected DMD children.

Entities:  

Keywords:  Cognitive flexibility; Cortical network plasticity; Glia; Intellectual disability; Mouse models; Working memory

Mesh:

Substances:

Year:  2018        PMID: 30051354     DOI: 10.1007/s12035-018-1259-6

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  5 in total

1.  Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies.

Authors:  Eric P Hoffman
Journal:  Acta Myol       Date:  2020-12-01

2.  Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophy.

Authors:  Amel Saoudi; Faouzi Zarrouki; Catherine Sebrié; Charlotte Izabelle; Aurélie Goyenvalle; Cyrille Vaillend
Journal:  Dis Model Mech       Date:  2021-09-21       Impact factor: 5.758

3.  The Expanding Spectrum of Dystrophinopathies: HyperCKemia to Manifest Female Carriers.

Authors:  Renu Suthar; Shivan Kesavan; Indar K Sharawat; Manisha Malviya; Titiksha Sirari; Bhupendra K Sihag; Arushi G Saini; Vishalavath Jyothi; Naveen Sankhyan
Journal:  J Pediatr Neurosci       Date:  2021-07-02

Review 4.  Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy.

Authors:  Michael Naidoo; Karen Anthony
Journal:  Mol Neurobiol       Date:  2019-12-13       Impact factor: 5.590

5.  Defects of full-length dystrophin trigger retinal neuron damage and synapse alterations by disrupting functional autophagy.

Authors:  Elisabetta Catalani; Silvia Bongiorni; Anna Rita Taddei; Marta Mezzetti; Federica Silvestri; Marco Coazzoli; Silvia Zecchini; Matteo Giovarelli; Cristiana Perrotta; Clara De Palma; Emilio Clementi; Marcello Ceci; Giorgio Prantera; Davide Cervia
Journal:  Cell Mol Life Sci       Date:  2020-08-04       Impact factor: 9.261

  5 in total

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