INTRODUÇÃO: Aproximadamente 20 a 30% dos casos novos de epilepsia se tornam refratários ao tratamento medicamentoso ao longo do tempo e a maioria destes casos está relacionada à esclerose mesial temporal (EMT). Disfunção metabólica tem sido relacionada à EMT por diferentes métodos, como tomografia de emissão de pósitrons, tomografia computadorizada por emissão de fóton único, espectroscopia de próton e fósforo (31P-ERM) por ressonância magnética. A caracterização das alterações metabólicas relacionadas à EMT pode auxiliar na melhor compreensão da epileptogênese, da refratariedade clínica comumente encontrada nestes pacientes e na busca de novas possibilidades terapêuticas. OBJETIVOS: Avaliar pela 31P-ERM o perfil metabólico dos pacientes com EMT e comparar com os dados de controles saudáveis. Verificar a existência de correlação entre o tempo de epilepsia, frequência de crises com os resultados da 31P-ERM nas regiões hipocampais. MÉTODOS: 33 pacientes com EMT unilateral e 31 controles foram estudados pela 31P-ERM, tridimensional em aparelho de 3,0 Tesla. Os voxels selecionados para análise foram os localizados na região hipocampal (RH), região insulonuclear anterior (RINA), região insulonuclear posterior (RINP) e na região frontal (RF). Estes voxels foram considerados ipsilaterais ou contralaterais à EMT, diagnosticada pela ressonância magnética convencional. Os metabólitos estudados foram: fosfodiésteres (PDE), fosfomonoésteres (PME), fosfato inorgânico (Pi), fosfocreatina (PCr) , adenosina trifosfato total (ATPt) compostos pela soma dos ?-, ?- e ?-ATP. Foram ainda avaliadas as razões PCr/ATPt, PCr/?-ATP, PCr/Pi e PME/PDE bem como o pH e magnésio. RESULTADOS: Na RH contralateral, aumento de ?-ATP e redução de PCr/ ?-ATP foram significativos. Na RINA ipsilateral, redução de Pi e PCr/ ?-ATP foram detectados. Na RINA contralateral, houve redução de Pi e aumento de ATPT. Na RINP ipsilateral, foram detectados redução de Pi, PCr/?-ATP e aumento de ?-ATP. Na RF contralateral houve redução de Pi. Não houve diferença entre nenhum dos metabólitos ou razões estudados na RH ipsilateral, RINP contralateral, RF ipsilateral em comparação aos controles. Não houve correlação dos resultados da 31P-ERM com o tempo de epilepsia na RH. Em relação à frequência de crises, houve correlação com ATPT, PME, PDE, PME/PDE na RH ipsilateral e de ?-ATP, ATPT, PCr/ ?-ATP e PCr/ATPT na RH contralateral. Análises adicionais foram feitas com os resultados na RH, separando os pacientes de acordo com a frequência de crises e tempo de epilepsia. No grupo de pacientes com frequência igual ou maior que 10 crises por mês, o PME foi menor na RH ipsilateral enquanto que o ?-ATP foi maior e o PCr/?-ATP menor na RH contralateral. No grupo de pacientes com tempo de epilepsia igual ou maior que 20 anos, o ?-ATP foi maior na RH contralateral. Nos grupos de pacientes com frequência de crises menor que 10 por mês ou tempo de epilepsia menor que 20 anos, nenhuma diferença foi detectada. Dados interpolados nas RH foram avaliados, notando-se redução de PME na RH ipsilateral e tendência a significância de diferenças de ?-ATP e PCr/?-ATP na RH contralateral. CONCLUSÕES: Há alterações energéticas difusas nas regiões não epileptogênicas de pacientes com EMT que podem estar relacionadas à disfunção mitocondrial. Na RH ipsilateral, detectou-se redução de PME na análise de voxels interpolados e no grupo de pacientes com frequência maior que 10 crises por mês, indicando alteração de composição de membrana, provavelmente relacionado à gliose e perda neuronal / INTRODUCTION: Around 20-30% of new cases of epilepsy become drug resistant over time and most of these cases are related to mesial temporal sclerosis (MTS). Metabolic dysfunction has been related to MTS by different methods such as positron emission tomography, single photon emission computed tomography, proton and phosphorus (31P-MRS) magnetic resonance imaging spectroscopy. Characterization of metabolic changes related to MTS can improve the understanding of epileptogenesis and drug resistance commonly found in these patients and in the search of new therapeutic possibilities. OBJETIVES: Evaluate by 31P-MRS the metabolic profile of patients with MTS and compare with data from healthy controls. Check the correlation between time of epilepsy, seizure frequency with the results of 31P-MRS in the hippocampal regions. METHODS: 33 unilateral MTS patients and 31 controls were studied by three-dimensional 31P-MRS in 3.0 Tesla equipment. The voxels selected for analysis were located in the hippocampal region (HR), anterior insulonuclear region (RINA), posterior insulonuclear region (RINP) and frontal region (RF). These voxels were considered ipsilateral or contralateral to MTS, diagnosed by conventional MRI. Analised metabolites were: phosphodiesthers (PDE), phosphomonoesthers (PME), inorganic phosphate (Pi), phosphocreatine (PCr) , total adenosine triphosphate ( ATPt) sum of ?- + ?- + ?-ATP and ?-ATP. We also evaluate PCr/ATPt , PCr/?-ATP, PCr/Pi and PME/PDE ratios as well as pH and magnesium. RESULTS: In the contralateral HR, increase of ?-ATP and decrease of PCr / ?-ATP were significant. In the ipsilateral RINA, reductions of Pi and PCr / ?-ATP were detected. In the contralateral RINA, there were reduction of Pi and increased ATPT. In the ipsilateral RINP, reduction of Pi and PCr / ?-ATP and increased ?-ATP were detected. In the contralateral RF, decreased Pi was found. There was no difference between any of the studied metabolites or ratios in the ipsilateral HR, contralateral RINP, ipsilateral RF compared to controls. There was no correlation between the results of 31P-ERM and time of epilepsy in HR. The following metabolites showed correlation with the seizure frequency in the ipsilateral HR: ATPT, PME, PDE, PME/PDE. The seizure frequency was correlated to ?-ATP, ATPT, PCr/ ?-ATP, PCr/ATPT in the contralateral HR. Aditional analysis was made with the results from HR, dividing the patients according to seizure frequency and time of epilepsy. Patients with 10 or more seizures per month showed reduction of PME in the ipsilateral HR; increase of ?-ATP and decrease of PCr/?- ATP in the contralateral HR. Patients with time of epilepsy of 20 years or more showed increase of ?-ATP in the contralateral HR. Patients with less than 10 seizures per month or time of epilepsy lower than 20 years did not demonstrate any difference. Reduction of PME in the ipsilateral HR and tendency to significant differences in ?-ATP and PCr/?-ATP in the contralateral HR were detected from interpolated data. CONCLUSIONS: There are diffuse energetic changes in non epileptogenic regions of patients with MTS that could be related to mitochondrial dysfunction. In the ipsilateral HR, reduction of PME was found from interpolated data and in the group of patients with 10 or more seizures per month, suggesting changes in membrane composition, probably related to gliosis and neuronal loss

Orientador: Roberto Jose Maria Covolan / Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Fisica Gleb Wataghin / Made available in DSpace on 2018-08-11T17:50:31Z (GMT). No. of bitstreams: 1 Ozelo_HelkaFabbriBroggian_D.pdf: 3528702 bytes, checksum: 523c7cd6259312cc27664736508c3c69 (MD5) Previous issue date: 2008 / Resumo: Neste trabalho, uma técnica multimodal envolvendo eletroencefalografia (EEG) e imagens funcionais por Ressonância Magnética (fMRI) foi implementada a fim de realizar estudos sobre memória operacional em um grupo de indivíduos, incluindo controles e pacientes com epilepsia do lobo temporal mesial (ELTM) associada à atro½a hipocampal esquerda. Para isso, uma série de testes de memória foram implementados. Estes testes foram baseados em um paradigma em blocos dividido em períodos de codificação e retenção de memória, otimizados com relação ao tempo de duração para que se adequassem tanto à análise de EEG quanto para a análise de fMRI. O paradigma foi apresentado aos indivíduos no primeiro momento durante a aquisição de EEG e posteriormente durante a aquisição de fMRI. Os dados de EEG indicaram a presença de oscilações theta (4-8 Hz) na região do córtex frontal e oscilações alfa (9-12 Hz) na região do córtex parieto-occipital, em ambos os grupos durante todo o período de codi.cação. No entanto, durante a retenção só foi observada a presença do ritmo alfa nas regiões mais posteriores, envolvendo principalmente as áreas temporo-parietais. Diferentemente do que é encontrado na literatura, foram estabelecidas correlações entre esses ritmos e respostas BOLD tanto positivas quanto negativas, envolvendo diferentes regiões cerebrais. No entanto, estas áreas de ativação e de desativação não eram concorrentes, mas sim vizinhas ou contralaterais. Embora ambos os grupos, controles e pacientes, tenham apresentado um desempenho semelhante na realização dos testes, houve discrepâncias entre os dois grupos com relação às estruturas corticais envolvidas na tarefa. Durante a codi.cação, o grupo controle apresentou a predominância de áreas de ativação no hemisfério cerebral esquerdo, enquanto que no grupo de pacientes a ativação foi igualmente distribuída entre os dois hemisférios. Esse achado sugere o fenômeno de neuroplasticidade, no qual áreas corticais adicionais seriam recrutadas para compensar as estruturas afetadas pela atrofia / Abstract: In this work, a multimodal approach involving electroencefalography (EEG) and functional Magnetic Resonance Imaging (fMRI) was implemented in order to perform studies on working memory in a group of subjects including controls and patients with mesial temporal lobe epilepsy (MTLE) associated with left hippocampal atrophy. In order to do that, a series of memory tests were implemented. These tests were based on a block paradigm containing epochs of memory codification and memory retention, optimized with respect to the time to fit both analysis of EEG and fMRI. The paradigm was presented to subjects for the first time during EEG acquisition and later during fMRI acquisition. EEG data indicated the presence of theta oscillations (4-8 Hz) in the frontal region and alpha oscillations (9-12 Hz) in the parieto-occipital region, in both groups. In the retention period, it was only observed the presence of the alpha rhythm in the posterior region, involving mainly the temporo-parietal regions. Diÿerently from what is found in the literature, correlations were established among these rhythms and both, positive and negative BOLD responses, but in diÿerent regions. Activation and deactivation zones were detected for all epochs. The deactivation zones were found not only in the neighborhood of the activation regions, but frequently in the homologous regions. Although both groups, controls and patients, presented similar performance for the memory tests, there were discrepancies between these groups in terms of the cortical structures involved in the memory task. In the control group, it was found predominance of activation at the left hemisphere whereas for the patient group activation was predominantly lateralized to the right, probably due to damage in the mesial temporal lobe structures. Such a finding is suggestive of the neuroplasticity phenomenon by which additional cortical areas would be recruited to compensate the structures affected by atrophy / Doutorado / Física Médica / Doutor em Ciências

Made available in DSpace on 2016-03-15T19:39:56Z (GMT). No. of bitstreams: 1 Geraldo Henrique Lemos Barbosa.pdf: 744647 bytes, checksum: a447200460fcb4cfbb7a563e03f92252 (MD5) Previous issue date: 2012-08-16 / Fundo Mackenzie de Pesquisa / Epilepsy is a multifactorial disease, multi-faceted, featuring different variations in severity from person to person, characterized by the emergence of spontaneous seizures due to neuronal hyperactivity. Among the epilepsies, temporal lobe epilepsy (TLE) is a very serious and common, comprising about 40% of all cases, often refractory to medication with a substantial impact on cognitive processes and behavior of the affected person. The ELT is characterized by the presence of complex partial seizures with onset in limbic structures, partially attributed to more frequent primary neuropathology, hippocampal sclerosis. This crisis can cause behavioral and cognitive impairments associated with psychiatric disorders, which Disorder Attention Deficit Hyperactivity Disorder (ADHD). In order to evaluate the locomotor activity and exploration in young rats subjected to status epilepticus. Male Wistar rats aged 25 days postnatal, received intraperitoneal injection of pilocarpine (350mg/kg). Control animals received saline. The model induced by pilocarpine was used in this study, given that their histological, biochemical, electrophysiological and behavioral reliably reproduce those found in human TLE. After induction by pilocarpine SE animals underwent behavioral tests that began five days after SE and were completed in 15 days. They were: the open field and elevated plus maze. The present study showed evidence that young animals subjected to status epilepticus exhibit moderate hyperactivity with increased emotionality in a threatening context. Hyperactivity was observed over time, when the animals were reintroduced to an environment with neutral context (open field) or immediately when exposed to a threatening environment (LCE). The results of this study argue for the simultaneous presence of ADHD in the model of TLE. Evidence shows that behavioral changes are manifested early, even before the installation of behavioral seizures. In this respect, it opens a window of opportunity to get early interventions that may minimize the deleterious consequences of seizures. / A epilepsia é uma doença multifatorial, multifacetada, que apresenta diferentes variações de gravidade de pessoa para pessoa, caracterizada pelo surgimento de crises espontâneas devido à hiperatividade neural. Dentre as epilepsias, a epilepsia do lobo temporal (ELT) é uma forma muito grave e comum, que compreende cerca de 40% de todos os casos, comumente refratária à medicação com um impacto substancial no processo cognitivo e no comportamento da pessoa afetada. A ELT é caracterizada pela presença de crises parciais complexas com início nas estruturas límbicas, parcialmente atribuídas à neuropatologia primária mais frequente, a esclerose hipocampal. Essa crise pode causar prejuízos cognitivos e comportamentais, associados a transtornos psiquiátricos, os quais o Transtorno do Déficit de Atenção e Hiperatividade (TDAH). Com objetivo de avaliar a atividade locomotora e exploratória em ratos jovens submetidos ao status epilepticus. Ratos Wistar machos com idade de 25 dias pós-natal, receberam injeção intraperitoneal de pilocarpina (350mg/kg). Animais controle receberam solução salina. O modelo de indução por pilocarpina foi utilizado nessa pesquisa, tendo em vista que suas características histológicas, bioquímicas, eletrofisiológicas e comportamentais reproduzem de forma fidedigna as encontradas na ELT em humanos. Após a indução ao SE por pilocarpina os animais foram submetidos a testes comportamentais que tiveram início 5 dias após o SE e foram concluídos em 15 dias. Foram eles: o campo aberto e o labirinto em cruz elevado. O presente trabalho mostrou evidências que animais jovens submetidos ao status epilepticus apresentam hiperatividade moderada com aumento da emocionalidade em um contexto ameaçador. A hiperatividade foi observada ao longo do tempo, quando os animais foram reapresentados a um ambiente com contexto neutro (campo aberto) ou imediatamente, quando expostos a um ambiente ameaçador (LCE). Os resultados observados neste estudo argumentam a favor da presença concomitante de TDHA no modelo de ELT. Mostra evidências que as alterações comportamentais se manifestam precocemente, antes mesmo da instalação das crises epilépticas comportamentais. Neste aspecto, abre-se uma janela de oportunidades para se buscar intervenções precoces que possam minimizar as consequências deletérias das crises convulsivas.

Introdução: A lateralização atípica de linguagem (LAL) é mais frequentemente observada em indivíduos com epilepsia no hemisfério esquerdo. Pacientes com epilepsia secundária a esclerose mesial temporal (EMT) apresentam alta frequência de LAL. A presença de EMTE, diretamente ou por efeitos à distância, perturbaria a determinação típica de lateralidade de linguagem (LL). Estudos de LL com RMf, em populações homogêneas de pacientes com EMT são escassos. Os padrões regionais de reorganização, nesta população, assim como os fatores clínicos e funcionais associados à LAL são pouco conhecidos. Os objetivos deste estudo foram (1) Validar paradigma de linguagem em RMf capaz de ativar áreas frontais e temporais de linguagem (2) Avaliar LL regional, em população homogênea de pacientes com EMT e verificar o papel de variáveis clínicas e da atividade epileptiforme na determinação de LAL. Foram avaliados 46 pacientes com EMT unilateral (24 EMTE e 22 EMTD) e 24 controles saudáveis, destros. Todos os participantes foram submetidos a RMf de linguagem com paradigma de nomeação responsiva à leitura (NRL) desenvolvido em língua portuguesa. O paradigma foi eficaz em ativar áreas de linguagem. A correlação entre IL-RMf e IL-Wada foi estatisticamente significativa no GFM (0,387; p < 0,01); GFI (0,594, p < 0,001); GTS (0,357, p < 0,05); GTM (0,509, p < 0,001) e GTI (0,489, p < 0,001). Os pacientes foram classificados em discordantes e concordantes (EEG/RM), após monitorização prolongada por vídeo-EEG. As classificações individuais de LL do teste de Wada e RMf foram concordantes em 84%(GFM), 86% (GFI), 74%(GTS), 83%(GTM) e 86%(GTI) dos casos. A frequência de LAL variou de 17 a 33%, para EMTE; 14 a 17%, para EMTD e de 0 a 10%, no grupo controle. Os grupos EMTEc e EMTEd apresentaram menores valores de IL-RMf, em relação ao grupo controle no GFM e GFI (p <= 0.05). Adicionalmente, o grupo EMTEd apresentou menor IL-RMf no GTM (p <= 0.01) e GTI (p <= 0.05). O grupo EMTDd apresentou menor IL-RMf no GFM; GFI; GTM e GTI (p <= 0.05). A ocorrência de mais de 5 descargas/hora no período interictal associou-se a LAL no GFM (p <= 0.01). Início da epilepsia, maior tempo de epilepsia e presença de IPI não foram associadas a LAL. Concluiu-se que a presença de EMT associou-se a LAL nas regiões frontais e temporais, sugerindo reorganização de linguagem envolvendo amplas regiões cerebrais, distantes da zona epileptogênica. O achado de LAL observada no grupo EMTDd sugere que a atividade epileptiforme temporal esquerda pode influenciar a reorganização de linguagem, independentemente da presença de lesão estrutural à esquerda. A maior frequência de descargas à esquerda associou-se a LAL / Atypical language lateralization (ALL) is associated with left hemisphere epilepsy, especially in epilepsy secondary to left mesial temporal sclerosis (MTS). Recent findings indicate that MTS, directly or by an at-distance effect may disrupt typical language lateralization (LL). Language-fMRI investigations in homogeneous MTS populations are scarce. Frontal and temporal language reorganization patterns in this population remain incompletely understood, as well as clinical factors associated with ALL. Our objectives were (1) To validate an fMRI paradigm effective to activate frontal and temporal language areas (2) To evaluate regional LL patterns in a homogeneous population of MTS patients and to investigate clinical factors associated with ALL. We studied forty-six right-handed patients (24 left MTS and 22 right MTS) and 24 controls. Patients and controls were similar in age and gender. Left and right MTS groups were comparable in terms of clinical variables. All participants underwent a language fMRI with reading response-naming paradigm (RRN) task developed in Brazilian Portuguese. The task effectively activated frontal and temporal language areas, with a high concordance with the Wada test. All patients were classified as concordant and discordant after video-EEG monitoring. Correlation between Wada test and fMRI LIs was significant in MFG (0.387; p < 0.01); IFG (0.594, p < 0.001); STG (0.357, p < 0.05); MTG (0.509, p < 0.001) e ITG (0.489, p < 0.001). Individual LI classifications with Wada test and fMRI were concordant in 84%(MFG), 86% (IFG), 74%(STG), 83%(MTG) e 86%(ITG). The frequency of ALL was 17-33%, in left MTS; 14-17%, in right MTS and 0-10%, in controls. Both concordant and discordant-left MTS patients presented lower LI than controls in MFG and IFG (p<=0.05). Additionally, discordant left MTS group presented lower LI in MTG (p<=0.01) and ITG (p<=0.05). Discordant right MTS group presented lower LI in MFG; IFG; MTG and ITG (p <= 0.05). Interictal left-sided spike frequency (< 5/h) was associated with lower LI (p <= 0.01) in MTG. In conclusion, MTS was associated with frontal and temporal language reorganization. Presence of ALL in discordant RMTS group suggests that left temporal epileptic activity may influence language reorganization, even in the absence of a left structural lesion. Higher left-sided spike frequency in MTS was associated with a left-right shift of speech representation

Introdução: A memória prospectiva (MP) refere-se a um conjunto de habilidades cognitivas que permitem lembrar-se de uma intenção a desempenhar no futuro, no momento adequado. Essa função é pouco avaliada em baterias neuropsicológicas que avaliam pessoas com epilepsia. Objetivo: Estudamos o impacto da cirurgia para epilepsia sobre a MP, componente prospectivo, em pessoas submetidas a lobectomia temporal unilateral para controle de epilepsia refratária ao tratamento clínico. Métodos: Comparamos o desempenho de MP em pessoas com epilepsia associada à esclerose mesial temporal à esquerda (EMTE) ou direita (EMTD) com dois grupos controles. Um grupo foi composto por indivíduos sem epilepsia (controles normais), e o outro por pessoas com epilepsia secundária à EMT, submetidos a avaliação e reavaliação neuropsicológica, sem intervenção cirúrgica (grupo clínico para controle teste/reteste). Resultados: Avaliamos 42 indivíduos sem epilepsia, 20 do grupo clínico (controle teste/reteste) e 39 do grupo cirúrgico (pré e pósoperatório). Comparamos o desempenho entre grupos e também a variação de desempenho individual, pelo índice de mudança confiável. Os grupos não diferiram em idade, escolaridade e quociente de inteligência. Na avaliação inicial, observou-se rebaixamento no desempenho em MP nos grupos clínico e cirúrgico (p < 0,01) (efeito lesão), sem diferença entre os grupos EMTE ou EMTD (efeito lateralidade). Para o grupo cirúrgico, observamos acentuada (p < 0,01) redução de crises e leve, porém significativa, redução de carga de drogas antiepilépticas pós-operatória. Observamos estabilidade em reteste de MP, declínio de memória verbal para o grupo EMTE e estabilidade de memória verbal e visual para o grupo EMTD. Conclusão: Embora exista um sistema de evocação compartilhado entre a MP e a memória episódica, a ressecção de estruturas temporais mesiais acometidas patologicamente não provoca declínio adicional em MP, mesmo quando se observou declínio de memória verbal no grupo EMTE. O comportamento dissociado de declínio de memória verbal para o grupo EMTE e preservação de MP após cirurgia de epilepsia sugere diferentes papeis das estruturas temporais mesiais nestes sistemas de memória. O papel do acometimento de estruturas extratemporais e de estruturas temporais não mesiais na MP em pacientes com EMT deverá ser melhor elucidado em estudos futuros / Introduction: Prospective memory (PM) refers to a set of cognitive abilities that allow recall of a previous intention to perform in the future, in the appropriate setting. This function is not usually evaluated in neuropsychological batteries used to evaluate people with epilepsy. Objective: We evaluated the impact of epilepsy surgery on the prospective component of PM, in people undergoing unilateral temporal lobectomy to treat medically refractory epilepsy. Methods: We compared performance in PM in people with left or right mesial temporal sclerosis (MTS) in the pre and postoperative periods with that of two control groups. One group was composed of people without epilepsy (normal controls), and another group was composed of people with epilepsy associated with mesial temporal sclerosis that underwent neuropsychological testing and retesting without undergoing surgery (clinical test/retest control group). Results: We studied 42 people without epilepsy, 20 clinical controls (test/retest group), and 39 patients that underwent epilepsy surgery (pre and postoperative testing). We compared groups performances and changes in individual performances with the reliable change index. Groups did not differ in age, education, and intelligence quotient. We found decreased preoperative PM performance for the clinical and surgical groups (p < 0.01) (lesion effect), without a difference between right and left groups (laterality effect). Postoperatively, there was a significant (p < 0.01) decrease in number of seizures, a small, but significant reduction in antiepileptic drug load, stable prospective memory, verbal and visual memory for right mesial temporal sclerosis, and decreased verbal memory in the left mesial temporal sclerosis group. Conclusion: In spite of a shared evocation system for episodic and prospective memory, resection of pathologically involved mesial temporal structures does not impact on prospective memory performance, even in the setting verbal memory decline in the left MTS group.The finding of dissociated verbal memory decline and PM stability after epilepsy surgery suggests a different role of mesial temporal lobe structures in these memory systems. The role of extratemporal and nonmesial temporal lobe structures in prospective memory in MTS patients should be evaluated in future studies

Introdução: A epilepsia do lobo temporal mesial (ELTM) é a forma mais comum de epilepsia na população adulta, tendo a esclerose hipocampal como principal substrato neuropatológico. Uma elevada proporção dos pacientes com ELTM apresentam história familiar positiva para a epilepsia, sugerindo a participação de fatores genéticos nesta síndrome. O citoesqueleto neuronal é essencial para os processos fisiológicos das células nervosas e crises epilépticas parecem afetar esta estrutura. O citoesqueleto neuronal possui importantes componentes regulatórios, dentre eles as proteínas associadas aos microtúbulos do tipo 2 (MAP2) e tau. Objetivos: Avaliar a densidade neuronal (células imunomarcadas com NeuN), neobrotamento das fibras musgosas (por histoquímica de neo-Timm) e a expressão imunohistoquímica das proteínas MAP2 e tau no hipocampo de casos cirúrgicos de ELTM (subtipos familiar e esporádico) e controles. As mesmas análises foram conduzidas no modelo animal de lítiopilocarpina. Métodos: Casos ELTM (n=38) foram divididos em ELTM familiar (n=20) e ETLM esporádica (n=18). Hipocampos controles (n=10) foram provenientes de necrópsias de sujeitos sem histórico de problemas neurológicos. No modelo animal de lítio-pilocarpina, animais submetidos ao status epilepticus (SE) foram sacrificados nos seguintes tempos pós-SE: 1, 7, 15 e 60 dias e classificados como grupos SE1, SE7, SE15 e SE60. Animais controle foram injetados com salina. Resultados: O grupo ELTM apresentou menor densidade neuronal que o controle nas regiões da camada granular, hilo, CA4, CA3, CA1 e prosubículo. O grupo ELTM mostrou maior valor de cinza da histoquímica de neo-Timm na camada granular, molecular interna e molecular externa e maior espessura do neobrotamento axonal na camada molecular interna em relação ao grupo controle. O grupo ELTM esporádica teve maior valor de cinza da histoquímica de neo-Timm e tendência à maior espessura do neobrotamento que o grupo ELTM familiar na camada molecular interna. O grupo ELTM apresentou menor expressão de MAP2 que o grupo controle no hilo, CA4, CA3, CA1 e prosubículo e maior expressão que o controle na camada granular, CA2 e parasubículo. O grupo ELTM esporádica teve maior expressão de MAP2 que o grupo ELTM familiar em CA1 e córtex entorrinal. O grupo ELTM apresentou maior expressão de tau que o grupo controle nas regiões da camada granular, hilo, CA3, CA2 e córtex entorrinal. O grupo ELTM esporádica demonstrou menor imunorreatividade para tau que o grupo ELTM familiar no córtex entorrinal. No modelo de lítio-pilocarpina, os grupos submetidos ao SE apresentaram menor densidade neuronal e maior neobrotamento que o grupo salina. Quanto à expressão de MAP2, os grupos SE60 e SE15 apresentaram maiores valores de expressão que os demais grupos em todas as regiões analisadas. A expressão de tau em CA3 não foi diferente entre os grupos animais analisados. Conclusão: Nossos resultados existem perda neuronal, reorganização sináptica das fibras musgosas e alterações na expressão de proteínas MAP2 e tau no hipocampo de pacientes com ELTM. Dentre os casos ELTM, encontramos diferenças no neobrotamento de fibras musgosas e na expressão de MAP2 e tau entre os grupos ELTM familiar e esporádica, indicando que estes grupos se apresentam de forma distinta em relação à epilepsia. Encontramos resultados II semelhantes em relação à densidade neuronal e o neobrotamento de fibras musgosas entre pacientes com ELTM e no modelo experimental. Porém, em relação à expressão das proteínas MAP2 e tau, encontramos algumas diferenças entre humanos e animais com ELTM. Nossos resultados sugerem que apesar do modelo de epilepsia induzida por lítio-pilocarpina ser relevante para o estudo da ELTM humana e mimetizar importantes aspectos neuropatológicos, a correspondência quanto à expressão de algumas proteínas estruturais não é completa. Estudos adicionais de expressão de proteínas do citoesqueleto em outros modelos animais de ELTM serão de grande importância para o melhor entendimento do processo epileptogênco. / Introduction: Mesial temporal lobe epilepsy (MTLE) is the most common form of epilepsy in adults and has hippocampal sclerosis as the main pathological substrate. A high proportion of patients with MTLE have positive familial history for epilepsy, suggesting the involvement of genetic factors in this syndrome. Seizures may affect the neuronal cytoskeleton, an structure that is essential in the physiological processes of nerve cells. Components of the neuronal cytoskeleton include microtubule-associated protein type 2 (MAP2) and tau. Objectives: Our aim was to evaluate neuronal density, mossy fiber sprouting and immunohistochemical expression of MAP2 and tau in the hippocampus of surgical cases of MTLE (familial and sporadic subtypes) and controls. The same analysis were conducted in the MTLE lithiumpilocarpine animal model.Methods: MTLE cases (n = 38) were divided into familial MTLE (n = 20) and sporadic MTLE (n = 18). Control hippocampi (n = 10) were obtained from autopsies of subjects without history of epilepsy. In the lithium-pilocarpine animal model, male Wistar rats were submitted to status epilepticus (SE) and were killed at the following post-SE days: 1, 7, 15 and 60, and were further classified SE1, SE7, SE15 and SE60. Control animals were injected with saline. Results: MTLE showed decreased neuronal density than controls in the granular layer, hilus, CA4, CA3, CA1 and prosubiculum. MTLE group showed increased neo-Timm gray value in the granular layer, inner and outer molecular layer, as well as increased mossy fiber length of mossy fiber in the inner molecular layer when compared to controls. Sporadic MTLE specimens exhibited increased inner molecular layer gray value than familial MTLE. MTLE hihppocampi showed decreased MAP2 expression in the hilus, CA4, CA3, CA1 and prosubiculum. In the granular layer, CA2 and parasubiculum, MAP2 expression was higher in MTLE specimens than in controls. CA1 and entorhinal cortex from sporadic MTLE hippocampi showed increased MAP2 expression than familial MTLE. Tau expression was increased in the granular layer, hilus, CA3, CA2 and entorhinal cortex of MTLE specimens. Sporadic MTLE exhibited lower tau immunoreactivity in the entorhinal cortex than familial MTLE. In the lithiumpilocarpine animal model, rats submitted to SE presented lower values of neuronal density and mossy fiber sprouting than controls. SE15 and SE60 showed increased MAP2 expression in all hippocampal subfields. Tau expression in CA3 was not different among the groups. Conclusion: Our results indicate that besides neuronal loss and axonal sprouting, MTLE specimens also exhibit dendritic abnormalities related to MAP2 expression. Increased tau immunoreactivity in epileptogenic hippocampi indicates possible abnormal expression related to mossy fiber sprouting in chronic MTLE. We found differential sprouting, MAP2 and tau expression between sporadic and familial MTLE. It is possible that different genetic background might result in somehow distinct neuropathological substrates between the two MTLE subtypes, although their clinical manifestation is quite similar. While neuronal loss and axonal sprouting profiles in human MTLE and chronic phase of the lithium-pilocarpine animal model are comparable, we could not find corresponding results regarding MAP2 and tau expression. IV Several studies have shown that chemo-convulsant as pilocarpine and kainic acid result in widespread brain epileptic discharges, which are different from the more focal hippocampal discharges seen in human MTLE. Despite its limitations, the lithium-pilocarpine model stands as an important and widely used animal model of epilepsy. Besides that, other animal models in which ictal discharges and lesions are more limited to the hippocampal formation might better mimic what we see in human MTLE.

Abstract The purpose of the present work was to investigate whether children with non-lesional temporal lobe epilepsy (TLE) have deficits in neuropsychological performance and whether the possible deficits can be investigated using functional magnetic resonance imaging (fMRI). In this population-based study, 21 children aged 8-15 with non-lesional TLE and a normal intelligence quotient were evaluated and compared with 21 healthy, age- and gender-matched controls. Neuropsychological assessments, clinical examinations, electroencephalography (EEG) and structural and functional MRI were performed on all the subjects. Three fMRI methods were used: resting-state regional homogeneity, resting-state functional connectivity and task-induced blood oxygenation level-dependent activation. The patients with non-lesional TLE showed good neuropsychological performance on average, although the girls were found to have significant problems in several neuropsychological tests. The deficits were not restricted to elements of performance involving the classical temporal lobe memory system but were also found in tests requiring frontal and parietal lobe functioning. Early onset of epilepsy and duration of epilepsy had significant negative effects on neuropsychological performance. All the fMRI methods detected significant functional differences between the TLE patients and the healthy controls, not only in the temporal lobes but also in broad networks extending to the frontal, parietal and thalamic areas. These differences seemed to differ markedly in location between the TLE patients depending on the interictal EEG findings. Neuropsychological performance results were supported by the fMRI findings, implying that TLE should be regarded as a widespread disruption of the brain networks and not just malfunction of a single region in the brain within these networks. This needs to be taken into consideration when evaluating learning abilities among TLE patients even at an early stage in epilepsy. / Tiivistelmä Tutkimuksen tarkoituksena oli selvittää onko lapsilla, jotka sairastavat tuntemattomasta syystä aiheutuvaa ohimolohkoepilepsiaa, neuropsykologisia ongelmia ja aiheuttavatko mahdolliset ongelmat aivojen toiminnallisessa magneettikuvauksessa nähtäviä muutoksia. Tähän väestöpohjaiseen tutkimukseen otettiin 21 tuntemattomasta syystä ohimolohkoepilepsiaa sairastavaa normaaliälyistä 8-15-vuotiaista lasta ja verrattiin heitä 21 terveeseen, ikä- ja sukupuolivakioituun kontrollihenkilöön. Kaikille tutkimukseen osallistuneille tehtiin neuropsykologinen tutkimus, kliininen tutkimus, aivosähkökäyrä sekä rakenteellinen ja toiminnallinen aivojen magneettikuvaus. Toiminnallisessa magneettikuvauksessa käytettiin veren happipitoisuudesta riippuvaista (engl. blood oxygenation level-dependent) kontrastia kuvantamaan levossa aivojen paikallista homogeniteettia (engl. regional homogeneity) ja toiminnallista kytkennällisyyttä (engl. functional connectivity) sekä kognitiivisten tehtävien herättämiä aktivaatio-vasteita. Tuntemattomasta syystä ohimolohkoepilepsiaa sairastavien lasten neuropsykologinen suoriutuminen oli keskimäärin hyvää, vaikkakin tytöillä oli nähtävillä tilastollisesti merkitseviä ongelmia useissa eri testeissä. Ongelmat eivät rajoittuneet pelkästään klassisiin ohimolohkoalueen muistitoimintoihin, vaan niitä havaittiin myös otsa- ja päälakilohkojen toimintoja edellyttävissä testeissä. Varhainen sairastumisikä ja epilepsian kesto heikensivät suoriutumista tilastollisesti merkitsevästi osatesteissä, joissa tarvittiin näönvaraisen hahmottamisen taitoja, psykomotorista nopeutta ja työmuistia. Ohimolohkoepilepsiaa sairastavien ja terveiden kontrollien aivoissa löydettiin toiminnallisia eroja kaikilla toiminnallisen magneettikuvauksen menetelmillä. Eroja ei todettu ainoastaan ohimolohkoissa, vaan niitä löytyi myös otsa- ja päälakilohkoon sekä tyvitumakealueelle ylettyvissä laaja-alaisissa hermoverkostoissa. Epilepsiapotilailla erojen paikantuminen riippui kohtaustenvälisestä aivosähkökäyrälöydöksestä. Neuropsykologisen suoriutumisen tulokset tukevat toiminnallisen magneettikuvauksen löydöksiä kuvastaen temporaaliepilepsian olevan laaja-alainen hermoverkostojen häiriö eikä pelkästään tietyn aivoalueen toiminnan häiriö. Tämä tulee huomioida arvioitaessa ohimolohkoepilepsiaa sairastavien lasten oppimiskykyä jo epilepsian alkuvaiheessa.

Abstract Autonomic dysfunction in epilepsy is widely recognized. Both partial and generalized epilepsies affect autonomic functions during interictal, ictal and postictal states. Interestingly, there is increasing evidence of interictal autonomic nervous system dysfunction as evidenced by reduced heart rate (HR) variability in patients with epilepsy. Reduced HR variation has also been detected in many other chronic diseases and it has been shown to be associated with unfavourable prognosis with an increased risk of mortality in various heart diseases. Recently, more attention has also been paid to possible association of decreased HR variability with sudden unexpected death in epilepsy (SUDEP). However, the clinical significance of the observed changes in cardiovascular regulation in patients with epilepsy is still poorly outlined and there are no long-term studies about changes in HR variation in relation to epilepsy. This study was designed to evaluate long-term changes in autonomic cardiovascular regulation in patients with temporal lobe epilepsy (TLE) and also to evaluate HR variation during vagus nerve stimulation (VNS) treatment in patients with refractory epilepsy, using 24-hour ambulatory ECG recordings. Special attention was paid to changes in HR variation and to circadian HR fluctuation over time. The results of this study show that autonomic cardiovascular regulation is affected both in patients with well-controlled TLE and in patients with refractory TLE, and that the cardiovascular dysregulation also presents itself with changes in circadian HR variability, with more pronounced alterations observed during the night time. HR variability was also found to decrease progressively with time in patients with chronic refractory TLE with uncontrolled seizures. VNS treatment was not observed to alter HR variation. / Tiivistelmä Epilepsiapotilailla esiintyy autonomisen hermoston toiminnan häiriöitä. Näitä häiriöitä voidaan todeta epilepsiakohtausten aikana, heti kohtausten jälkeen ja kohtausten välillä sekä paikallisalkuisissa että yleistyneissä epilepsioissa. Viimeaikaisissa tutkimuksissa on osoitettu kardiovaskulaarisen säätelyjärjestelmän häiriöiden voivan ilmentyä alentuneena sydämen sykevaihteluna epilepsiakohtausten väliaikoina. Sydänsairauksien yhteydessä sykevaihtelun vähenemisen on osoitettu liittyvän kohonneeseen kuolemanriskiin. Epilepsiapotilailla alentuneen sydämen sykevaihtelun on epäilty liittyvän epilepsiapotilailla ilmenevien odottamattomien ja ilman selkeää syytä tapahtuvien äkkikuolemien (SUDEP) lisääntyneeseen riskiin. Kertyneestä tiedosta huolimatta alentuneen sykevaihtelun kliininen merkitys epilepsiapotilailla on edelleen epäselvä. Pitkäaikaisseurantatutkimuksia sydämen sykevaihtelun muutoksista epilepsiapotilailla ei ole julkaistu. Tämän tutkimuksen tarkoituksena oli selvittää ohimolohkoepilepsiaan liittyviä pitkäaikaisia interiktaalisia (kohtausten välillä esiintyviä) kardiovaskulaarisia ilmentymiä. Lisäksi haluttiin tutkia vaikeahoitoisessa epilepsiassa käytetyn hoitomuodon, vagushermostimulaation, mahdollisia vaikutuksia sydämen toimintaan. Erityisesti haluttiin analysoida sykevaihtelun vuorokausirytmiä. Tulokset osoittavat autonomisen hermoston kardiovaskulaarisen säätelyjärjestelmän toiminnan olevan häiriintyneen sekä vaikeahoitoisilla että hyvähoitoisilla ohimolohkoalkuista epilepsiaa sairastavilla potilailla. Sydämen sykevariaatio on alentunut erityisesti yöaikaan. Lisäksi sydämen sykevaihtelu alenee pitkäaikaisseurannassa vaikeahoitoista epilepsiaa sairastavilla potilailla, joilla ilmenee toistuvia epileptisiä kohtauksia. Vagusstimulaatio ei aiheuttanut muutoksia syketaajuuden vaihteluun.

Chez les patients souffrants d’épilepsie du lobe temporal (ELT), des troubles cognitifs sont fréquemment décrits. Toutefois, certaines capacités cognitives restent à ce jour peu explorées dans le domaine de la recherche en épileptologie et non évaluées en pratique clinique, telles que les capacités de cognition sociale. Pourtant, des difficultés psychosociales et psychocomportementales ainsi qu’une altération de la qualité de vie (notamment dans sa dimension sociale) sont relevées chez les patients ELT et elles pourraient être en relation avec des perturbations de la cognition sociale. Par ailleurs, les anomalies cérébrales retrouvées chez ces patients, situées à proximité mais également plus à distance du foyer épileptique, comprenent des structures sous-tendant les capacités de cognition sociale. Dans ce contexte, l’objectif général de cette thèse était la caractérisation des capacités de cognition sociale des patients ELT d’un point de vue comportemental et en neuroimagerie. Les études comportementales menées ont permis de préciser l’impact d’une ELT unilatérale sur les capacités de cognition sociale. Il est notamment mis en évidence chez les patients ELT : (i) des troubles de reconnaissance émotionnelle en modalité visuelle et auditive associés à la présence de biais émotionnels, (ii) une modification de l’expérience émotionnelle, et (iii) des déficits de théorie de l’esprit (TdE) plus particulièrement prononcés sur le versant affectif de cette capacité. Certaines caractéristiques cliniques (âge de début, durée, latéralité de l’épilepsie, présence d’une sclérose hippocampique) peuvent moduler la sévérité de ces troubles. Par ailleurs, ces troubles sont associés à certaines perturbations psychocomportementales (anhédonie, apathie, modifications de l’affectivité et de l’empathie) et à une altération de la qualité de vie des patients. Sur base de ces études comportementales, nous avons identifié que les troubles de TdE apparaissent fréquents, affectant plus de 80% des patients ELT. Une étude en neuroimagerie fonctionnelle et l’analyse de données d’imagerie structurelle préliminaires ont permis de préciser l’impact d’une ELT sur le réseau cérébral sous-tendant les capacités de TdE. Nous relevons notamment que chez les patients ELT mésial avec sclérose hippocampique, les troubles de TdE semblent liées à des anomalies cérébrales situées principalement à distance du foyer épileptique, dépendantes de la latéralité de l’ELT et modulées par l’âge de début et la durée de l’épilepsie. En conclusion, dans une perspective de compréhension et de prise en charge globale des patients ELT, il convient de ne pas négliger l’étude des troubles de cognition sociale chez ces patients, et leur évaluation en pratique clinique devrait être plus systématique. / In patients suffering from temporal lobe epilepsy (TLE), cognitive disorders are frequently described. However, until now some cognitive capacities remain poorly explored in the field of epileptology research and not evaluated in clinical practice, such as social cognition capacities. However, psychosocial and psychobehavioral difficulties and an impaired quality of life (particularly in its social dimension) are raised in TLE patients and could be related to social cognition disorders. Furthermore, the cerebral abnormalities found in TLE patients, located close to the epileptic focus and also in more distant regions, include structures that support social cognition capacities. In this context, the general objective of this thesis was the characterization of social cognition capacities in TLE patients from a behavioral and neuroimaging point of view. Behavioral studies have allowed to specify the impact of unilateral TLE on social cognition capacities. It is notably identified in TLE patients: (i) emotion recognition disorders in both visual and auditory modality associated with emotional biases, (ii) changes in emotional experience, and (iii) theory of mind (ToM) disorders especially affecting the affective dimension of this capacity. Some clinical characteristics (age at onset, duration, laterality of epilepsy and presence of hippocampal sclerosis) can modulate the severity of these disorders. Furthermore, these disorders are associated with several psychobehavioral disorders (anhedonia, apathy, modified affectivity and empathy) and a worse quality of life for patients. On the basis of behavioral studies, it is identified that ToM impairments appear common, affecting more than 80% of TLE patients. A functional neuroimaging study and preliminary structural imaging data analysis have allowed to specify the TLE impact on the cerebral network underlying the ToM capacities. It is notably identified that in mesial TLE patients with hippocampal sclerosis, ToM disorders mainly reflect cerebral abnormalities located in distant cerebral regions from the epileptic focus, dependent of the laterality of epilepsy and modulated by the age at onset and the duration of epilepsy. In conclusion, in order to improve the understanding and the overall care of TLE patients, the investigation of social cognition disorders in these patients should not be neglected, and their assessment in clinical practice should be more regular.

L'épilepsie du lobe temporal est fréquente et souvent pharmacorésistante. L'épileptogenèse est imputée à la mort neuronale, l'inflammation ou au déséquilibre de la neurotransmission. Récemment, la perméabilité vasculaire a été reconnue comme une cause de crises d'épilepsie. Dans un modèle d'épilepsie chronique, nous avons montré une angiogenèse associant vascularisation, surexpression de VEGF, perte de protéines des jonctions serrées et perméabilité de la BHE. L'observation des immunoglobulines G (IgGs) comme marqueurs de perméabilité vasculaire nous a permis de découvrir que les IgGs s'accumulent dans les neurones. Nous avons alors étudié le rôle de ces protéines dans l'épileptogenèse. Ensuite, afin de corréler la perméabilité de la BHE à l'épileptogenèse, nous avons étudié le kindling, un modèle dans lequel les crises sont induites mais pas spontanées. Nous n'avons observé aucun remaniement vasculaire, si ce n'est une dérégulation transitoire de deux protéines de jonctions serrées. La comparaison de ces deux modèles confirme la contribution de la dérégulation de la BHE dans la genèse des crises et la désigne comme une nouvelle cible thérapeutique. / Temporal lobe epilepsy is the most frequent form of pharmacoresistant epilepsies. Epileptogenesis is commonly imputed to neuronal loss, inflammation and an imbalance in neurotransmission. Now, vascular permeability was shown to participate in epileptic seizures generation. In a model of chronic epilepsy, we showed a neo-vascularisation associated with VEGF over expression, loss of tight junction proteins and BBB permeability. The use of immunoglobulins G (IgGs) as markers of permeability vascular allowed us to discover that the IgGs accumulates in neurones. We then studied the role of these proteins in epileptogenesis. Then, to correlate BBB permeability to epileptogenesis, we studied the kindling, a model in which seizures are induced but never spontaneous. We observed no vascular remodeling, except for a transient deregulation of tight junctions proteins. The comparison of these models confirms the contribution of BBB deregulation and points it as new therapeutic target.