GABA-A receptor downregulation in brains of subjects with autism.

Gamma-aminobutyric acid A (GABAA) receptors are ligand-gated ion channels responsible for mediation of fast inhibitory action of GABA in the brain. Preliminary reports have demonstrated altered expression of GABA receptors in the brains of subjects with autism suggesting GABA/glutamate system dysreg...

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Publicado en:Journal of Autism & Developmental Disorders Vol. 39; no. 2; pp. 223 - 231
Autores principales: Fatemi SH, Reutiman TJ, Folsom TD, Thuras PD
Formato: pictorial research tables/charts Journal Article
Publicado: Springer Nature Feb2009
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2009
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      pub: Springer Nature
      place: New York, New York
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        atl: GABA-A receptor downregulation in brains of subjects with autism.
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          Fatemi SH
          Reutiman TJ
          Folsom TD
          Thuras PD
        affil: Department of Psychiatry, Division of Neuroscience Research, School of Medicine, University of Minnesota, 420 Delaware St SE, MMC 392 Minneapolis 55455
      sug:
        subj:
          Autism Spectrum Disorder Physiopathology
          Brain Metabolism
          Brain Physiopathology
          GABA
          Receptors, Neurotransmitter Metabolism
          Adult
          Blotting, Western
          Brain Drug Effects
          Descriptive Statistics
          Experimental Studies
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          Matched Case Control
          Middle Age
          T-Tests
          Two-Tailed Test
          Human
          Adult: 19-44 years
          Middle Aged: 45-64 years
          Female
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      ab: Gamma-aminobutyric acid A (GABAA) receptors are ligand-gated ion channels responsible for mediation of fast inhibitory action of GABA in the brain. Preliminary reports have demonstrated altered expression of GABA receptors in the brains of subjects with autism suggesting GABA/glutamate system dysregulation. We investigated the expression of four GABAA receptor subunitsand observed significant reductions in GABRA1, GABRA2, GABRA3, and GABRB3 in parietal cortex (Brodmann='s Area 40 (BA40)), while GABRA1 and GABRB3 were significantly altered in cerebellum, and GABRA1 was significantly altered in superior frontal cortex (BA9). The presence of seizure disorder did not have a significant impact on GABAA receptor subunit expression in the three brain areas. Our results demonstrate that GABAA receptors are reduced in three brain regions that have previously been implicated in the pathogenesis of autism, suggesting widespread GABAergic dysfunction in the brains of subjects with autism.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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