RESUMO
Specific oscillatory patterns are considered biomarkers of pathological neuronal network in brain diseases, such as epilepsy. However, the dynamics of underlying oscillations during the epileptogenesis throughout the hippocampal formation in the temporal lobe epilepsy is not clear. Here, we characterized in vitro oscillatory patterns within the hippocampal formation of epileptic rats, under 4-aminopyridine (4-AP)-induced hyperexcitability and during the spontaneous network activity, at two periods of epileptogenesis. First, at the beginning of epileptic chronic phase, 30 days post-pilocarpine-induced Status Epilepticus (SE). Second, at the established epilepsy, 60 days post-SE. The 4-AP-bathed slices from epileptic rats had increased susceptibility to ictogenesis in CA1 at 30 days post-SE, and in entorhinal cortex and dentate gyrus at 60 days post-SE. Higher power and phase coherence were detected mainly for gamma and/or high frequency oscillations (HFOs), in a region- and stage-specific manner. Interestingly, under spontaneous network activity, even without 4-AP-induced hyperexcitability, slices from epileptic animals already exhibited higher power of gamma and HFOs in different areas of hippocampal formation at both periods of epileptogenesis, and higher phase coherence in fast ripples at 60 days post-SE. These findings reinforce the critical role of gamma and HFOs in each one of the hippocampal formation areas during ongoing neuropathological processes, tuning the neuronal network to epilepsy.
Assuntos
Epilepsia do Lobo Temporal , Epilepsia , Estado Epiléptico , Animais , Modelos Animais de Doenças , Epilepsia/induzido quimicamente , Hipocampo , Pilocarpina/toxicidade , Ratos , Roedores , Estado Epiléptico/induzido quimicamenteRESUMO
ABSTRACT Objective: To verify if, by three distinct quantifiers, the measured electroencephalographic signal at rest is different from the signal measured during a word reading situation, especially considering the faster rhythms, gamma and high-gamma, as it occurs in clinical rhythms (delta to beta). Methods: A total of 96 electroencephalographic signals measured from neurologically healthy volunteers were evaluated at two moments: resting and word reading. Each signal segment was measured by three quantifiers that separately assess normalized power, percent power, and right and left hemisphere coherence. The Mann-Whitney test was used to compare the results of the quantifiers in each brain range. Results: The gamma and high-gamma rhythms presented a more distinct behavior when comparing the analyzed moments (resting and reading) than the clinical rhythms. Conclusion: This finding contributes to the scarce literature on faster rhythms, which can contain information that is normally disregarded in neurological clinical practice.
RESUMO Objetivo: Verificar se, por meio de três quantificadores distintos, o sinal eletroencefalográfico medido em repouso é diferente do sinal medido durante o processo de leitura, especialmente considerando os ritmos rápidos, gama e supergama, assim como ocorre nos ritmos clínicos delta a beta. Métodos: Foram avaliados 96 sinais eletroencefalográficos medidos em voluntários neurologicamente saudáveis, em dois momentos: repouso e leitura de palavras. Cada trecho do sinal foi mensurado por três quantificadores que medem, de maneira isolada, a potência normalizada e a potência percentual, bem como a coerência entre os hemisférios direito e esquerdo. O teste estatístico de Mann-Whitney foi usado para comparar os resultados dos quantificadores em cada faixa cerebral. Resultados: Os ritmos gama e supergama apresentaram comportamento mais distinto entre os momentos analisados (repouso e leitura) que os ritmos clinicamente analisados. Conclusão: Esse achado contribui com a escassa literatura segundo a qual os ritmos rápidos podem conter informações que normalmente são descartadas na neurologia clínica.
Assuntos
Leitura , Encéfalo/diagnóstico por imagem , Eletroencefalografia/métodos , Ritmo Gama , Ritmo beta , Ritmo DeltaRESUMO
Our understanding of the brain's functional organisation has greatly benefited from occasional exploratory sessions during electrophysiological studies, trying various manipulations of an animal's environment to trigger responses in particular neurons. Famous examples of such exploration have unveiled various unexpected response properties, such as those of mirror neurons. This approach, which relies on the possibility to test online the reactivity of precise neural populations has no equivalent so far in humans. The present study proposes and applies a radically novel framework for mapping human brain functions in ecological situations based on a combination of a) exploratory sessions, using real-time electrophysiology to formulate hypotheses about the functional role of precise cortical regions and b) controlled experimental protocols specifically adapted to test these hypotheses. Using this two-stage approach with an epileptic patient candidate for surgery and implanted with intracerebral electrodes, we were able to precisely map high-level auditory functions in the patients' superior temporal lobe. We propose that this procedure constitutes at the least a useful complement of electrical cortical stimulations to map eloquent brain areas in epileptic patients before their surgery, but also a path of discovery for human functional brain mapping.