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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Hijacking of hippocampal-cortical oscillatory coupling during sleep in temporal lobe epilepsy

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Autor(es):
Mendes, Renan Augusto Viana [1] ; Zacharias, Leonardo Rakauskas [2] ; Ruggiero, Rafael Naime [2] ; Leite, Joao Pereira [2] ; Moraes, Marcio Flavio Dutra [1] ; Lopes-Aguiar, Cleiton [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Fisiol & Biofis, Nucleo Neurociencias, Belo Horizonte, MG - Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Neurociencias & Ciencias Comportamento, Ribeirao Preto - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Epilepsy & Behavior; v. 121, n. B AUG 2021.
Citações Web of Science: 1
Resumo

Memory impairment is the most common cognitive deficit in patients with temporal lobe epilepsy (TLE). This type of epilepsy is currently regarded as a network disease because of its brain-wide alterations in functional connectivity between temporal and extra-temporal regions. In patients with TLE, network dysfunctions can be observed during ictal states, but are also described interictally during rest or sleep. Here, we examined the available literature supporting the hypothesis that hippocampal \& ndash;cortical coupling during sleep is hijacked in TLE. First, we look at studies showing that the coordination between hippocampal sharp-wave ripples (100 \& ndash;200 Hz), corticothalamic spindles (9 \& ndash;16 Hz), and cortical delta waves (1 \& ndash;4 Hz) during nonrapid eye movement (NREM) sleep is critical for spatial memory consolidation. Then, we reviewed studies showing that animal models of TLE display precise coordination between hippocampal interictal epileptiform discharges (IEDs) and spindle oscillations in the prefrontal cortex. This aberrant oscillatory coupling seems to surpass the physiological ripple \& ndash;delta-spindle coordination, which could underlie memory consolidation impairments. We also discuss the role of rapid eye movement (REM) sleep for local synaptic plasticity and memory. Sleep episodes of REM provide windows of opportunity for reactivation of expression of immediate early genes (i.e., zif-268 and Arc). Besides, hippocampal theta oscillations during REM sleep seem to be critical for memory consolidation of novel object place recognition task. However, it is still unclear which extend this particular phase of sleep is affected in TLE. In this context, we show some preliminary results from our group, suggesting that hippocampal theta \& ndash;gamma phase \& ndash;amplitude coupling is exacerbated during REM in a model of basolateral amygdala fast kindling. In conclusion, there is an increasing body of evidence suggesting that circuits responsible for memory consolidation during sleep seem to be gradually coopted and degraded in TLE. This article is part of the Special Issue \& ldquo;NEWroscience 2018{''} (c) 2019 Elsevier Inc. All rights reserved. (AU)

Processo FAPESP: 18/02303-4 - Estudo da conectividade da circuitaria meso-cortico-limbica em animais submetidos a Status epilepticus durante o desenvolvimento e sua relação com comorbidades psiquiátricas
Beneficiário:Rafael Naime Ruggiero
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 16/17882-4 - Epilepsias farmacorresistentes: desafios diagnósticos, estudo das comorbidades associadas e novas abordagens experimentais
Beneficiário:João Pereira Leite
Modalidade de apoio: Auxílio à Pesquisa - Temático