Submitted by Cláudia Bueno (claudiamoura18@gmail.com) on 2015-11-18T18:39:05Z No. of bitstreams: 2 Dissertação - Cândida Dias Soares - 2010.pdf: 1198463 bytes, checksum: acc22e0252670b4f6969e526efca18eb (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2015-11-19T14:26:37Z (GMT) No. of bitstreams: 2 Dissertação - Cândida Dias Soares - 2010.pdf: 1198463 bytes, checksum: acc22e0252670b4f6969e526efca18eb (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) / Made available in DSpace on 2015-11-19T14:26:37Z (GMT). No. of bitstreams: 2 Dissertação - Cândida Dias Soares - 2010.pdf: 1198463 bytes, checksum: acc22e0252670b4f6969e526efca18eb (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) Previous issue date: 2010-09-14 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / The national surveys of dementia and its implications for language, although in small numbers, line up with the international literature in the early trends of research. The articles presented were intended to draw a profile comparison between the differential Neurolinguistics degenerative dementia of Alzheimer type and non-Alzheimer's and dementia compare the two groups with a control group. The study was conducted from March 2008 to December 2009 were evaluated in 90 participants in the Dementia Clinic of the Hospital das Clinicas, Federal University of Goias The sample consisted of 30 patients with frontotemporal lobar degeneration (DLF), 30 patients with AD and 30 subjects with no dementia. We applied the following tests neurolinguistic: Boston Diagnostic Aphasia Examination (BDAE), Boston Naming Test (Boston Naming Test - BNT), Verbal Fluency Category for Semantics and Semantic and Phonemic Fluency (FAS), Token Test, subtest of Vocabulary / WAIS-R Similarities subtest of and / WAIS-R. To compare the performance of the group used the Mann-Whitney. All groups showed substantial linguistic differences. The APP group stood out from the other groups when compared to DA, showing that fluency, vocabulary, abstraction of ideas, understanding, reading and writing are more impaired. The FTD group reinforced the presence of dysfunction in semantic and phonemic verbal fluency DS group showed a statistically significant abstractive capacity with respect to the AD group. The DLF group is the group where the oral expression was shown to be noticeably compromised compared to the AD group. The language is therefore an indispensable tool to aid in the differential diagnosis of dementia. / As investigações nacionais das demências e suas implicações na linguagem, embora ainda em pequeno número, alinham-se com a literatura internacional, nas primeiras tendências de investigação. Os artigos apresentados tiveram como objetivo traçar um perfil diferencial neurolinguístico comparativo entre as demências degenerativas do tipo Alzheimer e não Alzheimer e comparar os dois grupos demenciais com um grupo controle. Foi realizado o estudo no período de março de 2008 a dezembro de 2009 em que foram avaliados 90 participantes do Ambulatório de Demências do Hospital das Clínicas da Universidade Federal de Goiás. A amostra foi constituída por 30 pacientes com Degenerações Lobares Frontotemporais (DLF); 30 pacientes com DA e 30 indivíduos com ausência de demência. Foram aplicados os seguintes testes neurolinguísticos: Teste de Boston para Diagnóstico da Afasia (BDAE), Teste de Nomeação de Boston (Boston Naming Test – BNT), Fluência Verbal por Categoria Semântica e Fluência Fonêmica e Semântica (F.A.S.),Token Test, Subteste de Vocabulário / WAIS-R e Subteste de Semelhanças / WAIS-R. Para comparar o desempenho dos grupo utilizou-se o teste de Mann-Whitney. Todos os grupos avaliados mostraram diferenças lingüísticas significativas. O grupo APP destacou-se dos demais grupos quando comparado ao grupo DA, demonstrando que a fluência, o vocabulário, a abstração de idéias, a compreensão, a leitura e a escrita encontram-se mais comprometidas. O grupo DFT reforçou a presença da disfunção na fluência verbal fonêmica semântica e o grupo DS demonstrou significância estatística na capacidade abstrativa com relação ao grupo DA. O grupo DLF foi o grupo em que a expressão oral mostrou-se visivelmente mais comprometida comparada ao grupo DA. A linguagem é, portanto, um instrumento indispensável para auxiliar no diagnóstico diferencial das demências.

This thesis is one of the first works in the Czech language dealing with the personality and work of Marcus Cornelius Fronto, Roman rhetor of 2. century A. D. and teacher of Marcus Aurelius. After the palimpsest with the correspondence of Fronto was found in early 19th century, the reputation of this man suffered greatly. The man had been seen for many decades as superficial and flat archaisator, whose letters have no or only very little value for us. The aim of this tesis is to examinate the most problematical questions connected with Fronto, firstly his attitude to philosophy and the opinion, that archaism is the main and ubiquitous characteristic of his style. This theoretical treatise is accompanied with translation of several selected texts.

La sclérose latérale amyotrophique (SLA) et la démence fronto-temporale (DFT) sont des maladies neurodégénératives fatales, actuellement sans traitement. Ces maladies entrainent la dégénérescence des neurones moteurs et corticaux, engendrant des troubles moteurs et cognitifs et ultimement menant à la mort des patients souvent par détresse respiratoire trois à cinq ans après l’apparition des premiers symptômes. À l’échelle d’une vie, le risque de développer ces pathologies est de 1 pour 300-400 pour la SLA et 1 pour 742 pour la DFT, faisant de ces pathologies un risque majeur. Avec le vieillissement de la population que nous connaissons actuellement, il est évident que l’incidence de ces maladies deviendra de plus en plus élevée. Ainsi il est essentiel de comprendre les mécanismes moléculaires sous-jacents à ces pathologies dans le but de développer des thérapies effectives et prévenir l’impact de ces pathologies dans notre société. À ce jour, l’étiologie de la SLA-DFT est encore débattue, cependant la communauté scientifique s’accorde sur le fait que l’interaction entre la génétique et l’environnement joue un rôle essentiel dans le développement de ces maladies. La caractéristique moléculaire principale de ces pathologies est la localisation cytoplasmique de la protéine, normalement, nucléaire TDP-43. TDP-43 est un régulateur clef de l’homéostasie des ARNs. Parmi ces nombreuses fonctions, TDP-43 régule la formation des granules de stress, en régulant leur protéine régulatrice G3BP1. Ces granules formés d’ARN et de protéines se forment pour protéger les cellules durant une période de stress. Récemment, ces granules ont fait l’objet de nombreuses études et leurs dysfonctions ont été associées à la SLA-DFT. Dans cette thèse, nous avons approfondi l’étude de la régulation de TDP-43 sur G3BP1. Nous avons défini que TDP-43 stabilise les transcrits de G3BP1 de par une liaison forte à une séquence conservée à travers l’évolution se situant dans le 3’UTR de G3BP1. La perte de localisation nucléaire, la présence de mutations ou de TDP-35, une isoforme pathologique de TDP-43, sont associées à une diminution des niveaux de G3BP1. Également, d’un point de vue histopathologique, dans le cortex orbitofrontal des patients atteints de SLA-DFT, les neurones présentant une localisation cytoplasmique de TDP-43 ont une perte des niveaux transcriptionnels de G3BP1, associant alors directement G3BP1 à la maladie. Par la suite, nous avons défini que la perte de fonction en tant que stabilisateur, permet la liaison de microARNs sur les transcrits de G3BP1, engendrant leur dégradation. Le blocage de la liaison de microARNs sur G3BP1 empêche la dégradation des transcrits et restaure les fonctions de la protéine. Ainsi, nous avons déterminé un moyen de contrer la perte de fonction de TDP-43 sur G3BP1. De façon intéressante, en plus de la formation des granules de stress, G3BP1 est essentielle pour l’homéostasie neuronale et la survie neuronale post-stress. Par conséquent, la restauration de la protéine est potentiellement une avenue thérapeutique multi-approche pour le traitement de ces maladies. / Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two fatal neurodegenerative diseases, currently without cure. These diseases lead to the degeneration of motor and cortical neurons, causing motor and cognitive disorders and ultimately leading to death, often from respiratory distress three to five years after the onset. Over a lifetime, the risk of developing these conditions is 1 in 300-400 for ALS and 1 in 742 for FTD, making these conditions a major risk. With the current aging of the population, it is evident that the incidence of these diseases will become increasingly high. It is therefore essential to understand the molecular mechanisms underlying these pathologies in order to develop effective therapies. To this day, the etiology of ALS-FTD is still debated. However, the scientific community agrees that the interaction between genetics and the environment play an essential role in the development of these diseases. The main molecular characteristic of these pathologies is the cytoplasmic localization of the normally nuclear protein TDP-43. TDP-43 is a key regulator of RNA homoeostasis. Among these many functions, TDP-43 regulates the formation of stress granules, by regulating their nucleator protein G3BP1. These granules of RNA and protein form to protect cells during times of stress. Recently these granules have been the subject of several studies and their dysfunction has been associated with ALS-FTD. In this thesis, we have deepened the study of the regulation of TDP-43 on G3BP1. We have defined that TDP-43 stabilizes G3BP1 transcripts by strong binding to a sequence conserved through evolution located in the 3'UTR of G3BP1. Loss of nuclear localization, the presence of mutations or of TDP-35, a pathological isoform of TDP-43, are associated with decreased levels of G3BP1. Also, histopathologically, in the orbitofrontal cortex of patients with ALS-DFT, neurons with cytoplasmic localization of TDP-43 have a loss of transcriptional levels of G3BP1, directly associating G3BP1 with the disease. Subsequently, we defined that TDP-43 loss of function as a stabilizer allows the binding of two microRNAs on the G3BP1 transcripts, causing their degradation. Blocking the binding of these microRNAs to G3BP1 prevents the degradation of the transcripts and restores the functions of the protein. Thus, we have determined a way to counter the loss of function of TDP-43 on G3BP1. Interestingly, in addition to the formation of stress granules, G3BP1 is essential for neuronal homoeostasis and post-stress neuronal survival. Therefore, the restoration of the protein is potentially a multi-approach therapeutic avenue for the treatment of these diseases.

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Existing neurocomputational and empirical data link deficient neuromodulation of the fronto-parietal and hippocampal-striatal circuitries with aging-related increase in processing noise and declines in various cognitive functions. Specifically, the theory of aging neuronal gain control postulates that aging-related suboptimal neuromodulation may attenuate neuronal gain control, which yields computational consequences on reducing the signal-to-noise-ratio of synaptic signal transmission and hampering information processing within and between cortical networks. Intervention methods such as cognitive training and non-invasive brain stimulation, e.g., transcranial direct current stimulation (tDCS), have been considered as means to buffer cognitive functions or delay cognitive decline in old age. However, to date the reported effect sizes of immediate training gains and maintenance effects of a variety of cognitive trainings are small to moderate at best; moreover, training-related transfer effects to non-trained but closely related (i.e., near-transfer) or other (i.e., far-transfer) cognitive functions are inconsistent or lacking. Similarly, although applying different tDCS protocols to reduce aging-related cognitive impairments by inducing temporary changes in cortical excitability seem somewhat promising, evidence of effects on short- and long-term plasticity is still equivocal. In this article, we will review and critically discuss existing findings of cognitive training- and stimulation-related behavioral and neural plasticity effects in the context of cognitive aging, focusing specifically on working memory and episodic memory functions, which are subserved by the fronto-parietal and hippocampal-striatal networks, respectively. Furthermore, in line with the theory of aging neuronal gain control we will highlight that developing age-specific brain stimulation protocols and the concurrent applications of tDCS during cognitive training may potentially facilitate short- and long-term cognitive and brain plasticity in old age.

Existing neurocomputational and empirical data link deficient neuromodulation of the fronto-parietal and hippocampal-striatal circuitries with aging-related increase in processing noise and declines in various cognitive functions. Specifically, the theory of aging neuronal gain control postulates that aging-related suboptimal neuromodulation may attenuate neuronal gain control, which yields computational consequences on reducing the signal-to-noise-ratio of synaptic signal transmission and hampering information processing within and between cortical networks. Intervention methods such as cognitive training and non-invasive brain stimulation, e.g., transcranial direct current stimulation (tDCS), have been considered as means to buffer cognitive functions or delay cognitive decline in old age. However, to date the reported effect sizes of immediate training gains and maintenance effects of a variety of cognitive trainings are small to moderate at best; moreover, training-related transfer effects to non-trained but closely related (i.e., near-transfer) or other (i.e., far-transfer) cognitive functions are inconsistent or lacking. Similarly, although applying different tDCS protocols to reduce aging-related cognitive impairments by inducing temporary changes in cortical excitability seem somewhat promising, evidence of effects on short- and long-term plasticity is still equivocal. In this article, we will review and critically discuss existing findings of cognitive training- and stimulation-related behavioral and neural plasticity effects in the context of cognitive aging, focusing specifically on working memory and episodic memory functions, which are subserved by the fronto-parietal and hippocampal-striatal networks, respectively. Furthermore, in line with the theory of aging neuronal gain control we will highlight that developing age-specific brain stimulation protocols and the concurrent applications of tDCS during cognitive training may potentially facilitate short- and long-term cognitive and brain plasticity in old age.

Il est de plus en plus reconnu que les connexions du cerveau jouent un rôle important sur la fonction cérébrale, en particulier les fonctions cognitives supérieures comme le langage. Cependant l’imperfection des techniques traitant les connexions macroscopiques humaines a empêché l’avancement de nos connaissances sur l'anatomie des faisceaux. Nous nous appuyons ainsi aujourd’hui essentiellement sur la littérature du XIXème siècle. Les définitions des trajets et des connexions anatomiques de nombreux faisceaux sont constamment débattues. En utilisant l'imagerie de diffusion, nous réévaluons les anatomies des faisceaux clés dans une grande cohorte saine. Nous utilisons une nouvelle approche de segmentation des faisceaux qui vise à reproduire la méthode introduite par les dissectionistes. Celle-ci définit un tract comme l’ensemble des fibres passant par une même tige, minimisant ainsi l’a priori sur leurs terminaisons. Nous nous concentrons sur les faisceaux d'association des capsules externe et extrême, notamment les faisceaux occipito-frontal inférieur (FOFI) et unciné (FU) impliqués dans le circuit du langage ventral. Nous passons en revue la littérature sur ces tracts, fournissons des descriptions détaillées de leurs connectivités anatomiques et donnons un nouvel éclairage sur leur asymétrie et organisation interne. Dans une première étude, nous confirmons que les deux faisceaux ont de plus vastes projections dans le cortex qu'on ne le pensait, et nous présentons de nouveaux résultats concernant les branches asymétriques des faisceaux. Dans une deuxième étude, nous étudions en profondeur le FU et ses sous composantes. Nous résolvons un débat d’un siècle en exhibant clairement sa frontière avec le FOFI et nous identifions pour chaque sous composante des caractéristiques anatomiques distinctives y compris des asymétries. Ces résultats apportent un éclairage nouveau sur le FOFI et le FU qui sera crucial pour démêler leurs rôles multifonctionnels. / The importance of the brain’s connections for cerebral function is increasingly emphasized especially for higher cognitive functions like language. But the imperfection of the techniques used to address the human macroscopic connections has prevented the advancement of our knowledge on the anatomy of fibre pathways. Thus we rely heavily on XIXth century literature. Controversy surrounding the anatomical course and connections of many fibre pathways persists. Using diffusion imaging, we reevaluate the anatomies of key pathways in a large healthy cohort. We use a novel tract segmentation approach that aims to reproduce the method introduced by dissectionists – defining a tract as all fibers passing through a stem, thus minimizing a priori on their terminations. We focus on the association pathways of the external and extreme capsules, namely the inferior fronto-occipital (IFOF) and uncinate fasciculi (UF), implicated in the ventral language circuitry. We review the literature on these tracts, provide detailed descriptions of their connectional anatomies and present new insights regarding their asymmetry and internal organization. In a first study, we confirm that both tracts have more extensive projections within the cortex than previously thought and present new results regarding asymmetrical tract branches. In a second study we further investigate the UF including its subcomponents. We resolve a century old debate by clarifying its elusive boundary with the IFOF and reveal the distinctive anatomical features including asymmetry patterns of each subcomponent. These results shed new light on the IFOF and UF and will be crucial for disentangling their multifunctional roles.

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