Correlation Engine 2.0
Clear Search sequence regions


  • ampa receptor (3)
  • child (1)
  • gamma (3)
  • homeostasis (1)
  • interneuron (4)
  • mice (6)
  • nitriles (2)
  • parvalbumin (5)
  • perampanel (4)
  • phenotypes (1)
  • Ras GTPase (3)
  • seizures (1)
  • sleep (2)
  • somas (1)
  • subunit (2)
  • Syngap1 (12)
  • Sizes of these terms reflect their relevance to your search.

    Loss-of-function SYNGAP1 mutations cause a neurodevelopmental disorder characterized by intellectual disability and epilepsy. SYNGAP1 is a Ras GTPase-activating protein that underlies the formation and experience-dependent regulation of postsynaptic densities. The mechanisms that contribute to this proposed monogenic cause of intellectual disability and epilepsy remain unresolved. We established the phenotype of the epileptogenesis in a Syngap1+/- mouse model using 24-hour video electroencephalography (vEEG)/electromyography recordings at advancing ages. We administered an acute low dose of perampanel, a Food and Drug Administration-approved AMPA receptor (AMPAR) antagonist, during a follow-on 24-hour vEEG to investigate the role of AMPARs in Syngap1 haploinsufficiency. Immunohistochemistry was performed to determine the region- and location-specific differences in the expression of the GluA2 AMPAR subunit. A progressive worsening of the epilepsy with emergence of multiple seizure phenotypes, interictal spike frequency, sleep dysfunction, and hyperactivity was identified in Syngap1+/- mice. Interictal spikes emerged predominantly during non-rapid eye movement sleep in 24-hour vEEG of Syngap1+/- mice. Myoclonic seizures occurred at behavioral-state transitions both in Syngap1+/- mice and during an overnight EEG from a child with SYNGAP1 haploinsufficiency. In Syngap1+/- mice, EEG spectral power analyses identified a significant loss of gamma power modulation during behavioral-state transitions. A significant region-specific increase of GluA2 AMPAR subunit expression in the somas of parvalbumin-positive interneurons was identified. Acute dosing with perampanel significantly rescued behavioral state-dependent cortical gamma homeostasis, identifying a novel mechanism implicating Ca2+-impermeable AMPARs on parvalbumin-positive interneurons underlying circuit dysfunction in SYNGAP1 haploinsufficiency. Copyright © 2020 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

    Citation

    Brennan J Sullivan, Simon Ammanuel, Pavel A Kipnis, Yoichi Araki, Richard L Huganir, Shilpa D Kadam. Low-Dose Perampanel Rescues Cortical Gamma Dysregulation Associated With Parvalbumin Interneuron GluA2 Upregulation in Epileptic Syngap1+/- Mice. Biological psychiatry. 2020 May 01;87(9):829-842

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 32107006

    View Full Text