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The impact of early environmental interventions on structural plasticity of the axon initial segment in neocortex.
Nozari, Masoumeh; Suzuki, Toshimitsu; Rosa, Marcello G P; Yamakawa, Kazuhiro; Atapour, Nafiseh.
Afiliación
  • Nozari M; Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.
  • Suzuki T; Laboratory for Neurogenetics, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
  • Rosa MG; Neuroscience Program, Monash Biomedicine Discovery Institute and Department of Physiology, Monash University, Melbourne, Victoria, Australia.
  • Yamakawa K; Australian Research Council, Centre of Excellence for Integrative Brain Function, Monash University Node, Clayton, Victoria, Australia.
  • Atapour N; Laboratory for Neurogenetics, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Dev Psychobiol ; 59(1): 39-47, 2017 01.
Article en En | MEDLINE | ID: mdl-27473368
Plasticity of the axon initial segment (AIS) is a newly discovered type of structural plasticity that regulates cell excitability. AIS plasticity has been reported to happen during normal development of neocortex and also in a few pathological conditions involving disruption of the inhibition/excitation balance. Here we report on the impact of early environmental interventions on structural plasticity of AIS in the mouse neocortex. C57BL/6 mice were raised in standard or enriched environment (EE) from birth up to the time of experiments and were injected with saline or MK-801 [N-Methyl-D-Aspartate (NMDA) receptor antagonist, 1 mg/kg] on postnatal days (P) 6-10. We used Ankyrin G immunoreactivity to mark the AIS of cortical neurons in two sub-regions of frontal cortex (frontal association area, FrA and secondary motor cortex, M2) and in the secondary visual cortex (V2). In 1-month-old mice, the mean AIS length differed between three areas, with the shortest AISs being observed in V2. Postnatal MK-801 or EE led to shortening of AIS only in the frontal areas. However, exposure to EE restored AIS shortening induced by MK-801. Chronic postnatal MK-801 results in structural plasticity of AIS exclusive to the frontal cortex. EE may modify underlying neuronal mechanisms resulting in restoration of AIS length.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Maleato de Dizocilpina / Receptores de N-Metil-D-Aspartato / Antagonistas de Aminoácidos Excitadores / Neocórtex / Ambiente / Segmento Inicial del Axón / Plasticidad Neuronal Límite: Animals Idioma: En Revista: Dev Psychobiol Año: 2017 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Maleato de Dizocilpina / Receptores de N-Metil-D-Aspartato / Antagonistas de Aminoácidos Excitadores / Neocórtex / Ambiente / Segmento Inicial del Axón / Plasticidad Neuronal Límite: Animals Idioma: En Revista: Dev Psychobiol Año: 2017 Tipo del documento: Article País de afiliación: Irán