No description available.

No description available.

No description available.

Les récepteurs de type Toll (TLR) sont des récepteurs cellulaires jouant un rôle pivot dans le déclenchement de la réponse immunitaire après une infection ou une blessure, c'est-à-dire une inflammation. L'activation de la signalisation TLR a été associée à l’épilepsie. Dans ce projet, j'utilisai trois modèles distincts pour étudier comment le déclenchement des TLR contribue à l'épileptogenèse. Il existe une corrélation entre les malformations corticales développementales telle la dysplasie corticale focale (FCD) et convulsions fébriles dans les enfants de bas âge. Récemment, une réponse neuro-inflammatoire fut identifiée dans les lésions FCD. Nous postulâmes que l'inflammation induite par le FCD peut augmenter la sensibilité aux crises (chapitre 2). Nous modélisâmes FCD en induisant une congélation-lésion corticale chez le rat néonatal. La lésion corticale déclencha des effecteurs en aval de TLR4, spécifiquement le précurseur de la cytokine Caspase-1, dans l'hippocampe ipsilatéral à la lésion. Les rats lésés développèrent des crises fébriles expérimentales nettement plus rapidement que les rats témoins. Le blocage de l'activité de la Caspase-1 prolongea significativement la latence des crises chez les rats lésés. Nos résultats impliquent l'inflammation médiée par la Caspase-1 en tant que déclencheur des crises fébriles chez les enfants avec FCD préexistante. Des études antérieures déterminèrent que l'activation systémique de la cascade TLR4 abaisse le seuil de crise. Nous étudiâmes si la pénétration des cellules immunitaires périphériques dans le cerveau pendant la stimulation TLR4 favorise l'activité ictal en stimulant la voie TLR4 dans les leucocytes prélevés sur la rate de rat (splénocytes). Ensuite, nous co-cultivâmes des splénocytes avec des coupes organotypiques dérivées du cerveau in vitro (chapitre 3). L'ajout de splénocytes stimulés par TLR4 donna lieu à une neuro-inflammation et à une excitation neuronale accrue. L’ajout de splénocytes non-stimulés n’eut aucun effet pro-inflammatoire ou pro-excitateur dans les coupes organotypiques. De plus, l'inhibition de la Caspase-1 dans des coupes organotypiques co-cultivées avec des splénocytes stimulés diminua la neuro-inflammation et l'hyperexcitabilité neuronale. Nos résultats suggèrent que l'infiltration de leucocytes activés par TLR4 dans le cerveau augmente la prédisposition aux crises via les mécanismes médiés par la Caspase-1. Précédemment, des rapports montrèrent que l'activation de la signalisation TLR3 facilite l'évolution des crises. L'introduction d'un agoniste synthétique TLR3 chez la souris in vivo et des coupes organotypiques hippocampiques in vitro produisirent des mécanismes anti-inflammatoires dépendants de la dose et du temps (chapitre 4). La stimulation TLR3 supprimait les crises d'hippocampe in vivo et réduisait l'excitabilité synaptique dans le réseau hippocampique à la fois in vivo et in vitro. Nous avons déterminé que les effets anticonvulsivants médiés par TLR3 étaient principalement provoqués par les cascades en aval IRF3 / IFN-β. Ainsi, nos données suggèrent que l'activation de TLR3 peut protéger le cerveau contre les crises par la production d'IFN-β. Nos résultats donnent un aperçu des nouveaux mécanismes cellulaires sous-jacents à la modulation inflammatoire de l'excitabilité neurale. Notre découverte des rôles de la Caspase-1 et de l'IFN-β dans l'influence du seuil de crise améliorera notre compréhension des fondements moléculaires de la génération de crises ce qui pourraient améliorer le traitement de l'épilepsie. / Toll-like receptors (TLRs) are cellular receptors that play a pivotal role in initiating immune response following infection or injury, i.e. inflammation. Nevertheless, activation of TLR signaling has been associated with seizure manifestation. In this research, I employed three distinct models to study how triggering TLRs contributes to ictogenesis. There is a correlation between developmental cortical malformations, e.g. focal cortical dysplasia (FCD), and fever-provoked, i.e. febrile, seizures in young children. Recently, neuroinflammation was reported in FCD lesions. Therefore, we posited that FCD-induced inflammation may increase seizure susceptibility (Chapter 2). To recapitulate FCD pathology, we induced a cortical freeze-lesion in neonatal rats. Lesioning the cortex triggered TLR4 downstream effectors, specifically the cytokine precursor Caspase-1, in the hippocampus ipsilateral to the lesion. Further, lesioned rats developed experimental febrile seizures markedly faster than sham control rats. Strikingly, blocking Caspase-1 activity prior to seizure induction significantly prolonged seizure latency in lesioned rats. Our results implicate Caspase-1-mediated inflammation as a main driver of febrile seizures in children with pre-existing brain malformations. In addition, previous reports determined that systemic activation of TLR4 cascade lowers seizure threshold. Hence, we developed an in vitro model to investigate whether penetration of peripheral immune cells into the brain during TLR4 stimulation promotes ictogenic activity (Chapter 3). First, we stimulated TLR4 pathway in leukocytes harvested from rat spleen, i.e. splenocytes. Thereafter, we co-cultured splenocytes with brain-derived organotypic slices in vitro. Adding TLR4-stimulated splenocytes gave rise to neuroinflammation and enhanced neuronal excitation, whereas adding unstimulated splenocytes failed to evoke pro-inflammatory or proexcitatory effects in organotypic slices. Moreover, Caspase-1 inhibition in organotypic slices cocultured with stimulated splenocytes diminished neuroinflammation and neuronal hyperexcitability. Our findings suggest that infiltration of TLR4-activated leukocytes into the brain elevate seizure predisposition via Caspase-1-mediated mechanisms. Beside TLR4 pathway, it was previously shown that activation of TLR3 signaling facilitates seizure evolution. In chapter 4, introducing a synthetic TLR3 agonist to mice in vivo and to hippocampal organotypic slices in vitro yielded anti-inflammatory mechanisms in a dose- and time-dependent manner. Also, we found that TLR3 stimulation suppressed hippocampal seizures in vivo and reduced synaptic excitability in the hippocampal network both in vivo and in vitro. Finally, we determined that TLR3-mediated anticonvulsive effects were chiefly driven by IRF3/IFN-β downstream cascades. Thus, our data suggests that TLR3 activation may protect the brain from seizures through production of IFN-β. Altogether, our findings provide insight into novel cellular mechanisms underlying inflammatory modulation of neural excitability. Furthermore, our discovery of the roles of Caspase-1 and IFN-β in influencing seizure threshold will improve our understanding of the molecular underpinnings of seizure generation, which may ultimately have therapeutic benefits for epilepsy treatment.

Text in Afrikaans / "Free people expect much from their police. In such societies the police stand at the point of balance on the one hand securing human rights on the other exercising their lawful powers given to them by Governments in the name of the people, to protect people and their institutions" (J Alderson Human Rights and Police Rights. Publication of the Council of Europe.) This is no small expectation. It means that the police are expected to maintain and secure the principles of democracy and human rights, the principles upon which our Constitution is based. At the same time it is the duty of a police service to maintain law and order which sometimes require the exercise of power and the use of force which on the face of it may appear to violate human dignity and certain rights and freedoms which a police force is expected to maintain in a democratic society. The manner of exercising that power has an impact on the credibility and effectiveness of the police. Human rights law internationally accepts that a police service needs to be given the power to, at times restrict certain individual freedoms in the interests of the security of the community at large. These restrictions may take place only in a constitutional way. If it takes place in an unconstitutional way the courts must have the right to exclude evidence which is unconstitutionally obtained. At this stage the courts have to formulate such a qualified exclusionary rule, but the ultimate goal must be to include such an exclusionary rule in a future Constitution. / Department of Criminal & Procedural Law / LL.M.

Alkohol har funnits sedan urminnes tider och är något som de flesta ungdomar och vuxna är bekanta med. Flertalet vet också att för mycket alkohol på lång sikt kan orsaka skador, framförallt på lever (fettlever) och njurar. Men inte alla vet att alkohol skadar hjärnan och kan ge kramper samt epilepsi. Alkohol har olika effekter på kroppen. Akut kan det öka den inhiberande och minska den excitatoriska signaleringen i hjärnan. Långvarigt kan det öka den excitatoriska signaleringen, minska den inhibitoriska samt öka alkoholtoleransen. I hjärnan är balansen mellan den inhibitoriska och excitatoriska signaleringen mycket betydelsefull och rubbningar kan orsaka skador som i sin tur kan orsaka krampanfall. Dessa krampanfall kan bli allvarliga och ibland dödliga. Studier kring sambandet mellan alkohol och epilepsi utförda av Samokhvalov et al. (2010), Devetag et al. (1983), Bråthen et al. (1999), Tartara et al. (1983), Bartolomei et al. (1997), Victor och Brausch (1967) och Hillbom (1980) har visat på olika resultat, men trots skillnaden i resultaten har korrelationen mellan alkohol och epilepsi varit tydlig. I studien av Devetag et al. (1983) hade 58 % av 153 alkoholister anfall icke relaterade till abstinens, alkoholinducering eller sjukdom/skada. Av 60 patienter med krampanfall var 30 stycken (50 %) icke relaterade till abstinens, alkoholinducering eller sjukdom/skada i studien utförd av Bartolomei et al. (1997). Bråthen et al. (1999)  utförde en studie på 142 alkoholister med krampanfall där 16 stycken (36 %) var icke-relaterade till abstinens, alkoholinducering eller sjukdom/skada. Vidare påvisade Tartara et al. (1983) i sin studie 30 patienter med krampanfall där 3 stycken (10 %) inte var relaterade till abstinens, alkohlinducering eller sjukdom/skada. Krampanfall som inte är relaterade till abstinens, akoholinducering eller sjukdom/skada är kluriga och svåra att utreda. Många forskare har försökt få insikt i och reda ut frågan om alkohols influens över utvecklingen av epilepsi och hur det skulle tänkas gå till. När kan alkoholrelaterade krampanfall klassificeras som epilepsi, vad innebär ett alkoholrelaterat krampanfall och vilka orsaker existerar som leder till att sådanan krampanfall uppstår. I den här litteraturstudien utreds kopplingen mellan alkoholism och epilepsi för att bättre förstå sambandet. Till studien har 20 vetenskapliga artiklar använts för att förstå vilka effekter alkohol har på kroppen, vad det innebär att ha epilepsi och hur de båda är kopplade. För att komma fram till ett svar på den framförda frågeställningen i studien, om långvarigt bruk av alkohol ger kramper och epilepsi, användes 7 studier vars undersökingar huvudsakligen fokuserat på alkoholister inlagda med krampanfall. Resultaten från de 7 studierna indikerar sammantaget att alkohol sannolikt kan orsaka epilepsi. Ingen av studierna har visat motsatsen. Långvarigt bruk av alkohol ger kramper och kan även ge epilepsi, men hur det går till är inte klarlagt. Samtidigt finns det många individer som missbrukar alkohol och som inte får epilepsi eller aldrig ens upplever ett enda krampanfall. / Alcohol has been used for drinking for many years and is a substance that is well known to most teenagers and adults. Most people also know that alcohol, when misused, can cause damage to both the liver and the kidneys but not as many people know about the damage alcohol can cause the brain. The damage that alcohol causes in the brain can lead to conditions where the patient can experience seizures, whitch can further devlop into epilepsy. Alcohol has different effects on the body. An immidiate response to alcohol is that the inhibitory signaling in the brain increases and the excitatory signaling decreases. When it comes to a prolonged misuse of alcohol the effects on the brain are the opposite and it can also increase the tolerance for alcohol. Inhibitory and excitatory signaling in the brain are essential and disturbance of those signals can be very damaging to the brain. The damages can develop and become permanent and it can also trigger different kinds of seizures. The seizures can in turn become very serious and fatal. Studies on the connection between alcohol and epilepsy has been conducted by Samokhvalov et al. (2010), Devetag et al. (1983), Bråthen et al. (1999), Tartara et al. (1983), Bartolomei et al. (1997), Victor och Brausch (1967) och Hillbom (1980) and have shown different results. The results however have shown a clear correlation between alcohol and epilepsi. In the study performed by Devetag et al. (1983) 58 % of 153 patients experienced seizures not related to alcohol withdrawl, alcohol induction or injury/disease. Of 60 patients who presented seizures in the study conducted by Bartolomei et al. (1997), 30 (50 %) had seizures not related to alcohol withdrawl, alcohol induction or injury/disease. A study performed by Bråthen et al. (1999) showed  16 patients (36 %) of 142 with seizures not related to alcohol withdrawl, alcohol indiction or injury/disease. Furthermore, a study conducted by Tartara et al. (1983) showed 30 patients with seizures, where 3 (10 %) of them were not related to alcohol withdrawl, alcohol induction or injury/disease. Seizures not related to alcohol withdrawl, alcohol abuse or injury/disease are difficult to investigate. Many scientists have tried to get insight in as to how alcohol can influence the ethiopathogenesis of epilepsy. What is alcohol-related seizures, what is the cause behind the seizures and how does one decide if the seizures can be defines as epilepsy. This literature review investigates the link between alcoholism and epilepsy to better understand this connection. The question of issue was ”if prolonged misuse of alcohol can lead to epilepsy” and to unravel the question, 7 studies were used. The studies main focus was alcoholism and seizures. The results from the studies indicated in total that alcohol prabably can cause epilepsy since none of the studies showed the opposite. A prolonged misuse of alcohol can lead to seizures and even epilepsy, but how this comes to be is not clear and needs to be properly investigated. Not to forget, some people who misuse alcohol do not get epilepsy and some never experience even a single seizure.

Les neurones des couches superficielles du collicule supérieur et du cortex visuel primaire du rat adulte sont sensibles à de basses fréquences spatiales de haut contraste défilant à des vitesses élevées. Entre les jours post-nataux 27-30 et l’âge adulte, les fréquences temporelles optimales des neurones du cortex visuel primaire augmentent, tandis que leurs seuils de contraste diminuent. Cependant, les fréquences spatiales optimales, les valeurs de résolution spatiale et les bandes passantes spatiales de ces neurones sont, dès l’ouverture des paupières, similaires à celles observées chez le rat adulte. Ces profils de réponse neuronale suggèrent que les projections rétino-colliculaires et rétino-géniculo-corticales sont essentiellement issues de neurones ganglionnaires rétinofuges magnocellulaires et koniocellulaires. Les neurones du cortex visuel primaire du rat ayant subi des convulsions hyperthermiques présentent, dès l’ouverture des paupières, de basses fréquences spatiales optimales, de larges bandes passantes directionnelles et temporelles ainsi que des seuils de contraste élevés par rapport aux neurones du rat normal. À l’âge adulte, de basses fréquences temporelles optimales et de larges bandes passantes spatiales sont également observées chez le rat ayant subi des convulsions hyperthermiques. L’altération des profils de réponse des neurones du cortex visuel primaire du rat ayant subi de convulsions hyperthermiques suggère un déséquilibre entre les mécanismes neuronaux excitateurs et inhibiteurs de cette aire corticale. Ces résultats suggèrent également qu’un épisode unique de convulsions fébriles infantiles suffit à altérer le développement des propriétés spatio-temporelles des champs récepteurs des neurones du cortex visuel primaire. / Neurons in superficial layers of the rat superior colliculus and primary visual cortex are sensitive to highly contrasted low spatial frequencies drifting at fast speeds. Between post-natal days 27-30 and adulthood, the optimal temporal frequencies of neurons in the primary visual cortex increase, whereas their contrast thresholds decrease. However, the optimal spatial frequencies, spatial resolution values and spatial bandwidths of these neurons are, soon after eyelid opening, similar to those observed in the adult rat. These neuronal response profiles suggest that the retino-collicular and retino-geniculo-cortical projections are mainly innervated by magnocellular and koniocellular retinal ganglion cells. Neurons in the primary visual cortex of rats having experienced hyperthermic seizures are, soon after eyelid opening, sensitive to low optimal spatial frequencies and show broad directional and temporal bandwidths, as well as elevated contrast thresholds when compared to neurons of normal rats. At adulthood, low optimal temporal frequencies and broad spatial bandwidths are also observed in rats having experienced hyperthermic seizures. The alteration of response profiles of neurons in the primary visual cortex of rats having experienced hyperthermic seizures suggests an unbalance between excitatory and inhibitory mechanisms in this cortical structure. These results also suggest that a single episode of febrile seizures could be sufficient to impede the development of the spatio-temporal receptive field properties of neurons in the primary visual cortex.

A doença de Unverricht-Lundborg (DUL) é considerada uma doença rara, autossômica recessiva, sendo também denominada de Epilepsia Mioclônica Progressiva do tipo1 (emp1), causada por mutações no gene codificador (CSTB) da proteína cistatina B. A cistatina B é uma proteína essencial para a regulação dos processos fisiológicos do ser humano, e sua expressão reduzida parece ser a causa primária da EMP1. A doença em geral se inicia entre os seis e dezesseis anos, manifestando-se tanto como crises mioclônicas como por crises tônicoclônicas generalizadas. Trata-se de uma doença grave e limitante, cujo diagnóstico preciso é extremamente importante para as condutas apropriadas, incluindo aconselhamento genético. Este estudo tem como objetivo o estudo molecular e caracterização da expansão instável de repetição dodecamérica (CCCCGCCCCGCG) da região promotora 5\' não traduzida do gene CSTB entre pacientes com suspeita de EMP1 na população brasileira. No presente estudo, selecionamos 64 pacientes entre eles 54 casos índices do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto (HCFMRP-USP) com suspeita de EMP1. Os restantes 10 casos eram parentes dos casos índices. Os 54 pacientes foram seguidos no setor de Epilepsia com diagnostico clinico e eletrofisiológico de EMP1, e foram encaminhados para o setor de Neurogenética para diagnostico molecular. Destes 54 casos índices, apenas 5 foram diagnosticados através da biologia molecular com expansão dodecamera acima de 30 repetições, sugestivo de DUL. Espera-se, com este estudo, identificar a população de pacientes com EPM1 que tenham mutação no gene CSTB e com os resultados de este projeto possibilitar assim um melhor entendimento da etiopatogenia e proporcionar um diagnóstico preciso dos casos de DUL. / Unverricht-Lundborg disease (ULD) is considered a rare autosomal recessive disease, also known as Progressive Myoclonic Epilepsy Type 1 (EMP1), caused by mutations in the CSTB gene, which provides instructions for making a protein called Cystatin B. Such protein is essential for regulating a person\'s physiological processes, and its reduced expression seems to be the first cause of EMP1. Affected individuals usually begin showing signs and symptoms of the disorder between the ages of 6 and 16, which manifests both as myoclonus or as generalized tonic-clonic crises. It is a grave and limiting condition whose precise diagnosis is extremely important for appropriate conducts, including genetic counseling. This study has as a goal the molecular evaluation and characterization of the unstable expansion of the decametric repetition (CCCCGCCCCGCG) from the non-translated CSTB\'s 5\' gene promoter region among Brazilian patients with suspected EMP1. In this study, 64 patients were selected, among them 54 key figures from Hospital das Clínicas of Faculdade de Medicina de Ribeirão Preto (HCFMRP-USP) with suspected EMP1. The other 10 figures were related to the key figures. The 54 patients were followed in the Epilepsy sector with EMP1 clinical and electrophysiological diagnostics and were forwarded to the neurogenetics sector for a molecular diagnostic. From such 54 key figures, only 5 were diagnosed through molecular biology with decametric expansion above 30 repetitions, suggestive of ULD. This study is aimed to identify the EPM1 patients with CSTB genetic mutation and hopefully the results of this identification will enable a better understanding of the etiopathogeny and provide with a exact diagnosis of ULD cases.

Apresentamos dados e argumentos que indicam que: a) as crises epilépticas apresentadas por Trinomys yonenagae em campo e em cativeiro são espontâneas e idiopáticas; e b) elas podem ser decorrentes de processos evolutivos. A epilepsia nesta espécie foi caracterizada em cativeiro a partir de um cadastro iniciado há 16 anos, formado por progenitores e descendentes de seis colônias de T. yonenagae, coletados na Caatinga de Ibiraba (BA), e adultos (129,90 ± 5,92g) e filhotes nascidos em cativeiro num total de 295 indivíduos. A prevalência e a incidência em indivíduos epilépticos (EE) foram estimadas e as crises epilépticas foram analisadas por meio das manifestações comportamentais, baseando-se na escala de Racine. Aspectos da procriação (n=11), a locomoção, a ansiedade (testes de arena, n= 35) e índices fisiológicos (balanço hídrico-alimentar, n=6), importantes ao fitness, foram mensurados. Somente duas colônias apresentaram EE representando 9% e 28% dos nascimentos. Do total de indivíduos (165 e 130) 9,8% são EE (n=29; 14 e 15), sendo que as representam 52% e os 48%. A prevalência é de 20 a 30% e a incidência variou de 2 a 10 casos/ano, nos últimos cinco anos. As crises são observadas somente em adultos (n=24) a menor latência é de 13m e a frequência é variável (1 a 24 em seis anos). A maioria iniciou-se por congelamento e 50% atingiram o estágio 5 da escala de Racine. Em todos os casais, de 5 a 50% dos filhotes são EE e ocorreu estro pós-parto, como esperado para a espécie. Os filhotes são saudáveis e tanto a média de filhotes por ninhada (1,9±0,3), como a média do número de ninhadas por casal (6,5±5,0) é igual à de casais não epilépticos (NE). O teste de arena indica que descendentes de EE (DE) e as EE são menos ansiosas que as NE. Não há diferença entre os grupos dos índices fisiológicos estimados. A diferença no número de EE nas colônias, a alta prevalência e % de filhotes EE, e a diferença de comportamento das fêmeas DE indicam a base genética desta epilepsia. Neste contexto, consideramos que em Trinomys yonenagae, a epilepsia límbica não compromete o fitness, o que abre possibilidades de ser decorrente de processos evolutivos envolvendo o escalonamento de respostas de anti-predação / We present data and discuss the possibility that: a) the seizures presented by Trinomys yonenagae in the wild and in captivity are spontaneous and idiopathic, and b) they may be due to evolutionary processes. Epilepsy was characterized in this species in captivity from a survey started 16 years ago, made up of parents and descendants from six colonies of T. yonenagae collected in the Caatinga of Ibiraba (BA), and adults (129.90 ± 5.92 g) and pups born in captivity in a total of 295 individuals. The prevalence and incidence in individuals with epilepsy (EE) were estimated and seizures were analyzed by behavioral manifestations, based on Racine´s scale. Locomotion and anxiety indexes (open-field test, n = 35), as well as aspects of breeding (n = 11) and physiological indicators (balance food and water, n = 6), important to fitness were measured. Only two colonies showed EE, representing 9% and 28% of births. Approximately 10% of total individuals (165 and 130 ) are EE (n = 29, 14 and 15 ), and the represent 52 and 48%. In the last five years prevalence is 20-30%, and incidence ranged from 2 to 10 cases/ year. Seizures are only observed in adults (n = 24), the lowest latency is 13 months and the frequency is variable (1 to 24 in six years). The first stage is freezing and 50% reached stage 5 of Racine´s scale. In all couples, 5-50% of puppies are EE and occurred postpartum estrus, as expected for the species. The puppies are healthy and both the average offspring per litter (1.9 ± 0.3), as well as the average number of litters per couple (6.5 ± 5.0) is equal to values presented by non-epileptic couples (NE). The open-field test indicates that descendants of EE (DE) and EE are less anxious than NE. There is no difference between EE and NE regarding food and water intake. The difference in the number of EE in the colonies, the high percentage of EE pups, and the difference in the behavior of DE indicate the genetic basis of this epilepsy. In this context, we consider that in Trinomys yonenagae the limbic epilepsy seems to not compromise the fitness, which opens possibilities to be the result of evolutionary processes involving the escalation of antipredator responses

O presente estudo comparou o fluxo sanguíneo cerebral regional avaliado através da tomografia por emissão de fóton simples (SPECT) de pacientes com crises epilépticas temporais com pacientes com crises não epilépticas psicogênicas (CNEP). Todos os SPECT foram realizado no período ictal, tendo as CNEP sido induzidas por métodos sugestivos e de hipnose. Os grupos de pacientes com epilepsia e CNEP foram ainda comparados com um terceiro grupo, denominado grupo de sujeitos saudáveis. As comparações dos SPECT foram feitas através da análise visual (radiologista cego ao estudo) e semiquantitativa pelo programa Statistical Parametric Mapping (SPM). Os objetivos do estudo foram: (1) estabelecer a sensibilidade e a especificidade do SPECT ictal para o diagnóstico diferencial entre CNEP e crises epilépticas parciais complexas em pacientes com epilepsia do lobo temporal, em comparação com o VEEG associado a técnicas de hipnose; (2) avaliar através da análise quantitativa voxel a voxel do SPECT as alterações de perfusão cerebral dos pacientes com CNEP em relação aos pacientes com epilepsia, dos pacientes com CNEP em relação a um grupo controle de sujeitos normais e dos pacientes com epilepsia em relação a um grupo controle de sujeitos saudáveis. Foram estudados 30 pacientes no grupo com CNEP, 22 pacientes no grupo com epilepsia e 29 sujeitos saudáveis. Os resultados mostram que os SPECT ictais dos pacientes do grupo CNEP foram diferentes dos SPECT ictais dos pacientes com epilepsia. Na análise visual o SPECT ictal apresentou sensibilidade de 50% e especificidade de 91% para o diagnóstico de CNEP . Na análise comparativa voxel a voxel entre os grupos os resultados revelaram que: (a) houve aumento de perfusão cerebral em lobo temporal esquerdo e tronco cerebral nos pacientes do grupo epilepsia em relação ao grupo controle normal; (b) houve diminuição de perfusão cerebral no lobo frontal esquerdo e córtex anterior do cíngulo nos pacientes do grupo epilepsia em relação ao grupo controle normal; (c) houve aumento de perfusão cerebral no giro do cíngulo e precuneus á direita nos pacientes do grupo CNEP em relação ao grupo epilepsia; (d) houve diminuição perfusão cerebral em amígdala direita nos pacientes do grupo CNEP em relação ao grupo epilepsia; (e) houve aumento de perfusão cerebral na cauda do núcleo caudado esquerdo, giro précentral esquerdo e tálamo direito nos pacientes do grupo CNEP em relação ao grupo controle normal. Desta forma, após a análise estatística dos resultados concluímos que na análise visual, um SPECT ictal positivo em um paciente com suspeita de CNEP não confirma nem afasta tal suspeita, já que a sensibilidade do método foi baixa (50%). Na análise visual, um SPECT ictal negativo em um paciente com suspeita de CNEP afasta a possibilidade de epilepsia do lobo temporal com 91% de acerto (especificidade do método). O resultado da análise visual do SPECT ictal de CNEP revelou valor de sensibilidade abaixo do encontrado na literatura, e valor de especificidade superior ao encontrado na literatura. A análise quantitativa dos SPECT de crise epiléptica em comparação com os de sujeitos saudáveis em repouso, mostrou concordância com a análise visual em relação à lateralidade. Tal comparação revelou ainda ativação de áreas compatíveis com o que se encontra na literatura. A análise quantitativa dos SPECT ictais do grupo CNEP em comparação com os do grupo epilepsia revelou ativação de estruturas cerebrais posteriores (precuneus e giro cíngulo), não havendo comparação semelhante na literatura. A análise quantitativa dos SPECT ictais do grupo CNEP em comparação com os de sujeitos saudáveis em repouso, mostrou ativação do sistema estriatotalamocortical, achado em concordância com a literatura. A ativação do sistema estriatotalamocortical nos pacientes com CNEP mostrou ser um correlato neuroanatômico clinicamente relevante, com forte associação estatística. / The study compared regional cerebral blood flow assessed by positron emission tomography single photon (SPECT) in patients with temporal lobe epilepsy and patients with psychogenic nonepileptic seizures (PNES). All SPECT were performed in the ictal period, PNES having been induced by and suggestive methods of hypnosis. The groups of patients with epilepsy and PNES were compared with a third group, called group of healthy subjects. SPECT comparisons were made by visual analysis (radiologist blinded to the study) and semiquantitative analysis by Statistical Parametric Mapping (SPM). The study objectives were: (1) to establish the sensitivity and specificity of ictal SPECT for the differential diagnosis between PNES and complex partial seizures in patients with temporal lobe epilepsy, compared with VEEG associated with hypnosis techniques, (2) to assess by quantitative analysis of SPECT voxel to voxel changes in cerebral perfusion of patients with PNES compared to patients with epilepsy, patients with PNES compared to a control group of normal subjects and patients with epilepsy compared to a control group of healthy subjects. We studied 30 patients in the PNES group, 22 patients in the group with epilepsy and 29 healthy subjects. The results show that ictal SPECT of patients in the PNES group were different from the ictal SPECT of patients with epilepsy. The visual analysis of ictal SPECT had a sensitivity of 50% and specificity of 91% for the diagnosis of PNES. In the voxel voxel comparative analysis between the groups the results showed that: (a) increased cerebral perfusion in the left temporal lobe and brain stem in patients of epilepsy group compared to normal control group, (b) a decrease in cerebral perfusion in the left frontal lobe and anterior cingulate cortex in patients of epilepsy group compared to normal control group, (c) increased cerebral perfusion in the cingulate gyrus and precuneus in the right group of PNES patients compared to epilepsy group, (d) decreased cerebral perfusion in the right amygdala in patients PNES group compared to the epilepsy group, (e) increased cerebral perfusion in the left tail of the caudate nucleus, left pre-central gyrus and right thalamus in patients in the PNES group compared to group normal control. Therefore, after statistical analysis of the results we conclude that in visual analysis, a positive ictal SPECT in a patient with suspected PNES neither confirms nor removes the suspicion, since the sensitivity was low (50%). In visual analysis, a negative ictal SPECT in a patient with suspected PNES rules out the possibility of temporal lobe epilepsy with 91% accuracy (specificity of the method). The result of visual analysis of ictal SPECT of PNES revealed sensitivity value below that found in the literature and specificity value higher than that found in the literature. The quantitative analysis of SPECT of seizures compared with those of healthy subjects at rest, showed agreement with visual analysis in relation to laterality. This comparison also revealed activation in areas consistent with that found in the literature. The quantitative analysis of SPECT ictal PNES group compared with the epilepsy group showed activation of posterior brain structures (cingulate gyrus and precuneus), with no similar comparison in the literature. The quantitative analysis of SPECT ictal PNES group compared to healthy subjects at rest, showed activation of the estriatotalamocortical, a finding in agreement with the literature. The activation of the estriatotalamocortical circuit in patients with PNES proved to be a neuroanatomical correlate clinically relevant, with strong statistical association