Dyslexic and control first-grade school children were compared in a Symbol-to-Sound matching test based on a non-linguistic audiovisual training which is known to have a remediating effect on dyslexia. Visual symbol patterns had to be matched with predicted sound patterns. Sounds incongruent with the corresponding visual symbol (thus not matching the prediction) elicited the N2b and P3a event-related potential (ERP) components relative to congruent sounds in control children. Their ERPs resembled the ERP effects previously reported for healthy adults with this paradigm. In dyslexic children, N2b onset latency was delayed and its amplitude significantly reduced over left hemisphere whereas P3a was absent. Moreover, N2b amplitudes significantly correlated with the reading skills. ERPs to sound changes in a control condition were unaffected. In addition, correctly predicted sounds, that is, sounds that are congruent with the visual symbol, elicited an early induced auditory gamma band response (GBR) reflecting synchronization of brain activity in normal-reading children as previously observed in healthy adults. However, dyslexic children showed no GBR. This indicates that visual symbolic and auditory sensory information are not integrated into a unitary audiovisual object representation in them. Finally, incongruent sounds were followed by a later desynchronization of brain activity in the gamma band in both groups. This desynchronization was significantly larger in dyslexic children. Although both groups accomplished the task successfully remarkable group differences in brain responses suggest that normal-reading children and dyslexic children recruit (partly) different brain mechanisms when solving the task. We propose that abnormal ERPs and GBRs in dyslexic readers indicate a deficit resulting in a widespread impairment in processing and integrating auditory and visual information and contributing to the reading impairment in dyslexia.

Cette thèse avait pour but d’étudier dans quelle mesure l’enrichissement des conditions d’hébergement jusqu’à- ou à partir d’-un âge auquel les déficits cognitifs sont déjà présents contribue au maintien de la mémoire spatiale observé chez des rats âgés hébergés toute leur vie en environnement enrichi (EE), et d’étudier certains mécanismes neurobiologiques susceptibles de contribuer à cette préservation. Nous avons montré que l’hébergement en EE n’a pas besoin d’être maintenu jusqu’à la fin de la vie pour permettre la préservation des fonctions cognitives chez le Rat âgé. De plus, un enrichissement tardif ne permet pas de récupérer des capacités déjà altérées mais permet la préservation de certaines fonctions d’altérations subséquentes. Ce maintien de la mémoire spatiale ne semble pas être dû à la modification par l’enrichissement du cycle veille-sommeil. Par contre, cet enrichissement induit une modification de l’activité oscillatoire hippocampique, et pourrait, en favorisant une synchronisation neuronale locale, promouvoir un traitement de l’information au sein de réseaux plus spécialisés. Enfin, l’exposition à un EE pendant toute la vie permet la préservation de l’innervation cholinergique de différentes aires cérébrales, un effet pouvant contribuer au maintien des fonctions cognitives chez les animaux âgés hébergés toute leur vie en EE. / This thesis aimed to investigate in which extent environmental enrichment (EE) until or from an age at which cognitive decline is already apparent contributes to the maintenance of spatial memory observed in aged rats housed all their life in EE, and to study some neurobiological mechanisms likely underlying this preservation. We showed that housing in EE does not need to be maintained until the end of life to allow the preservation of cognitive function in aged rats. Moreover, late EE does not permit the recovery from already altered capabilities, but enables the preservation of some functions of subsequent alterations. The maintenance of spatial memory does not seem to be due to EE-related modification of sleep-wake cycle. But, exposure to EE induces a modification of hippocampal oscillatory activity, and could, by supporting local neuronal synchronization, promote information processing in more specialized networks. Finally, EE preserves the cholinergic system from age-related alteration in different cerebral areas, a mechanism that could participate to the maintenance of cognitive function in aged rats housed all their life in EE.

No description available.

Comment le cerveau intègre-t-il toutes les informations sensorielles qu'il reçoit en une perception cohérente de l'environnement ? Cette intrigante et importante question en neuroscience n’est pas élucidée et a inspiré ce travail de thèse. Plus précisément, mon objectif a été d’étudier les modifications cérébrales induites par l’apprentissage d’une association entre un son et une odeur. Inhabituelle chez l’homme, hormis dans l’alimentation, cette association est pourtant fréquente chez l’animal, pour la détection de prédateurs par exemple. Mais sons et odeurs permettent surtout d'étudier les mécanismes cérébraux nécessaires à l'association entre deux sens très différents : le système auditif traite l’information en temps réel tandis que le système olfactif est lent et rythmé par la respiration. Ce travail de thèse était centré autour de la question suivante : comment le cerveau traite-t-il les interactions multisensorielles audio-olfactives ? En enregistrant l’activité de potentiel de champs local de plusieurs structures cérébrales chez des rats en train d’apprendre cette association, nous avons pu mettre en évidence un potentiel rôle des oscillations neuronales béta (15-35 Hz), dans le traitement et la mise en mémoire des différentes informations sensorielles. Ces oscillations représenteraient un lien fonctionnel entre aires cérébrales distantes, permettant l’intégration et l’association d'informations de natures très différentes. / Multisensory interactions are constantly present in our everyday life and allow a unified representation of environment. Cross modal integration is often studied in multisensory associative brain regions, but recent findings suggest that most of the brain could be multisensory. But at this time, we still don’t know how the brain deals with information from different sensory systems. In this project, we want to understand whether the establishment of neuronal oscillations can functionally connect sensory regions and take part of the multisensory integration, and how this connection is built up by learning. For this, we examine changes in the cortical network involved in the acquisition of a multisensory association between a sound and an odor in rats through the analysis of the local field potentials’ oscillations The originality of the project is to sample a large network of brain structures including primary sensory cortex (primary auditory cortex, olfactory bulb) and multimodal areas towards which converge these two senses: the piriform and perirhinal cortices. We have developed a behavioral GO/NO GO test in which the rat must combine simultaneous auditory and olfactory informations to succeed. Data and brain signals obtained in this task suggest that the power of oscillations in beta frequency band within the olfactory areas and the coherences of oscillations between these areas are modified by the multisensory learning.

The present study intended to examine the neural basis of audiovisual integration, hypothetically achieved by synchronized gamma-band oscillations (30--80 Hz) that have been suggested to integrate stimulus features and top--down information. To that end, we studied the impact of visual symbolic information on early auditory sensory processing of upcoming sounds. In particular, we used a symbol-to-sound--matching paradigm in which simple score-like patterns predict corresponding sound patterns. Occasionally, a single sound is incongruent with the corresponding element of the visual pattern. In response to expected sounds congruent with the corresponding visual symbol, a power increase of phase-locked (evoked) activity in the 40-Hz band was observed peaking 42-ms poststimulus onset. Thus, for the first time, we demonstrated that the comparison process between a neural model, the expectation, and the current sensory input is implemented at very early levels of auditory processing. Subsequently, expected congruent sounds elicited a broadband power increase of non--phase-locked (induced)activity peaking 152-ms poststimulus onset, which might reflect the formation of a unitary event representation including both visual and auditory aspects of the stimulation. Gamma-band responses were not present for unexpected incongruent sounds. A model explaining the anticipatory activation of cortical auditory representations and the match of experience against expectation is presented

La maladie d’Alzheimer (MA) est une pathologie neurodégénérative communément caractérisée par une perte progressive de la mémoire. L’étiologie de la MA demeure incertaine à ce jour ce qui complique l’élaboration de stratégies thérapeutiques permettant de l’éradiquer. L’accumulation des échecs thérapeutiques pourrait en partie s’expliquer par le fait que l’hypothèse amyloïde, qui met en avant l’implication prépondérante du peptide bêta-amyloïde (Aβ) dans la physiopathologie de la MA, serait incomplète. En utilisant un modèle murin transgénique de la MA, la souris TgCRND8, j’ai pu compléter l’hypothèse amyloïde en proposant l’implication, en plus de l’Aβ, du fragment carboxy-terminal bêta (β-CTF). Ces deux métabolites amyloïdogéniques de l’APP seraient responsables de l’altération de formes différentes de mémoire. Le dosage de ces métabolites dans l’hippocampe, suite au traitement chronique des souris avec un inhibiteur de β ou de γ-secrétase, a mis en évidence que le β-CTF serait responsable de l’atteinte de la mémoire impliquée dans la détection du remplacement d’un objet, alors que l’Aβ perturberait la mémoire permettant la détection du déplacement d’un objet. Ces travaux suggèrent qu’il serait judicieux de développer de nouvelles stratégies thérapeutiques qui diminuent à la fois les niveaux cérébraux des deux fragments amyloïdogéniques, le β-CTF et l’Aβ. / Alzheimer’s disease (AD) is a neurodegenerative pathology commonly characterized by a progressive memory loss. To these days, AD’s etiology has remained unclear which complicates the development of therapeutic strategies enabling to eradicate the pathology. The accumulation of therapeutic failures could partly be explained by the fact that the amyloid hypothesis, which highlights the leading involvement of the amyloid beta peptide (Aβ) in the physiopathology of AD, could be incomplete. Using a transgenic mouse model of AD, the TgCRND8 mice strain, I expanded the amyloid hypothesis, suggesting the involvement of the beta carboxy-terminal fragment (β-CTF), in addition to Aβ. These two amyloidogenic metabolites could be responsible for the alteration of different forms of memory. The dosage of these metabolites, after mice chronic treatment with either a β- or a γ-secretase inhibitor, highlighted the fact that β-CTF could be responsible for the deterioration of the memory involved in the detection of the replacement of an object. As for Aβ, it could disrupt the memory allowing the detection of the displacement of an object. This work suggests that it would be judicious to develop therapeutic strategies reducing brain levels of both amyloid fragments, β-CTF and Aβ.