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Dynamics of AMPA receptors regulate epileptogenesis in patients with epilepsy

The excitatory glutamate α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors (AMPARs) contribute to epileptogenesis. Thirty patients with epilepsy and 31 healthy controls are scanned using positron emission tomography with our recently developed radiotracer for AMPARs, [(11)C]K-2, which...

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Detalles Bibliográficos
Autores principales: Eiro, Tsuyoshi, Miyazaki, Tomoyuki, Hatano, Mai, Nakajima, Waki, Arisawa, Tetsu, Takada, Yuuki, Kimura, Kimito, Sano, Akane, Nakano, Kotaro, Mihara, Takahiro, Takayama, Yutaro, Ikegaya, Naoki, Iwasaki, Masaki, Hishimoto, Akitoyo, Noda, Yoshihiro, Miyazaki, Takahiro, Uchida, Hiroyuki, Tani, Hideaki, Nagai, Nobuhiro, Koizumi, Teruki, Nakajima, Shinichiro, Mimura, Masaru, Matsuda, Nozomu, Kanai, Kazuaki, Takahashi, Kazuhiro, Ito, Hiroshi, Hirano, Yoji, Kimura, Yuichi, Matsumoto, Riki, Ikeda, Akio, Takahashi, Takuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213790/
https://www.ncbi.nlm.nih.gov/pubmed/37080205
http://dx.doi.org/10.1016/j.xcrm.2023.101020
Descripción
Sumario:The excitatory glutamate α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors (AMPARs) contribute to epileptogenesis. Thirty patients with epilepsy and 31 healthy controls are scanned using positron emission tomography with our recently developed radiotracer for AMPARs, [(11)C]K-2, which measures the density of cell-surface AMPARs. In patients with focal-onset seizures, an increase in AMPAR trafficking augments the amplitude of abnormal gamma activity detected by electroencephalography. In contrast, patients with generalized-onset seizures exhibit a decrease in AMPARs coupled with increased amplitude of abnormal gamma activity. Patients with epilepsy had reduced AMPAR levels compared with healthy controls, and AMPARs are reduced in larger areas of the cortex in patients with generalized-onset seizures compared with those with focal-onset seizures. Thus, epileptic brain function can be regulated by the enhanced trafficking of AMPAR due to Hebbian plasticity with increased simultaneous neuronal firing and compensational downregulation of cell-surface AMPARs by the synaptic scaling.