Early alterations in a mouse model of Rett syndrome: the GABA developmental shift is abolished at birth

Autor: M. Billon-Grand, Jean-Luc Gaiarsa, Damien Guimond, Sanaz Eftekhari, Roman Tyzio, Paolo Bonifazi, Yehezkel Ben-Ari, Natalia Lozovaya, Alexandre Pons-Bennaceur, Javier Rasero, T.-T. Bui, Diana C. Ferrari, Morgane Chiesa, Romain Nardou
Přispěvatelé: Gaiarsa, Jean-Luc, APPEL À PROJETS GÉNÉRIQUE 2018 - Invagination et migration des épithéliums - - Migrafolds2018 - ANR-18-CE13-0021 - AAPG2018 - VALID, Neurochlore (Ben-Ari Institute of Neuroarcheology), Institut de Neurobiologie de la Méditerranée [Aix-Marseille Université] (INMED - INSERM U1249), Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU), Biocruces Bizkaia Health Research Institute [Baracaldo], ANR-18-CE13-0021,Migrafolds,Invagination et migration des épithéliums(2018)
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
medicine.medical_specialty
congenital
hereditary
and neonatal diseases and abnormalities

Methyl-CpG-Binding Protein 2
[SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology
Respiratory System
lcsh:Medicine
Rett syndrome
Biology
Synaptic Transmission
Article
MECP2
03 medical and health sciences
Glutamatergic
Mice
0302 clinical medicine
Sodium Potassium Chloride Symporter Inhibitors
Internal medicine
medicine
Rett Syndrome
Premovement neuronal activity
Animals
lcsh:Science
Bumetanide
gamma-Aminobutyric Acid
Mice
Knockout

Neurons
Multidisciplinary
Neuronal Plasticity
lcsh:R
[SDV.NEU.NB] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology
[SDV.BDD.EO] Life Sciences [q-bio]/Development Biology/Embryology and Organogenesis
Synaptic Potentials
medicine.disease
Receptors
GABA-A

3. Good health
Mice
Inbred C57BL

030104 developmental biology
Endocrinology
Metabotropic receptor
[SDV.BDD.EO]Life Sciences [q-bio]/Development Biology/Embryology and Organogenesis
Excitatory postsynaptic potential
GABAergic
lcsh:Q
030217 neurology & neurosurgery
Neurological disorders
medicine.drug
Neuroscience
Zdroj: Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9, pp.9276. ⟨10.1038/s41598-019-45635-9⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-16 (2019)
ISSN: 2045-2322
DOI: 10.1038/s41598-019-45635-9
Popis: Genetic mutations of the Methyl-CpG-binding protein-2 (MECP2) gene underlie Rett syndrome (RTT). Developmental processes are often considered to be irrelevant in RTT pathogenesis but neuronal activity at birth has not been recorded. We report that the GABA developmental shift at birth is abolished in CA3 pyramidal neurons of Mecp2−/y mice and the glutamatergic/GABAergic postsynaptic currents (PSCs) ratio is increased. Two weeks later, GABA exerts strong excitatory actions, the glutamatergic/GABAergic PSCs ratio is enhanced, hyper-synchronized activity is present and metabotropic long-term depression (LTD) is impacted. One day before delivery, maternal administration of the NKCC1 chloride importer antagonist bumetanide restored these parameters but not respiratory or weight deficits, nor the onset of mortality. Results suggest that birth is a critical period in RTT with important alterations that can be attenuated by bumetanide raising the possibility of early treatment of the disorder.
Databáze: OpenAIRE