Right parietal lesions often lead to neglect, in which patients fail to attend to leftward stimuli. Recent models of neglect suggest that, in addition to attentional impairments, patients demonstrate impairments of spatial remapping and/or spatial working memory (SWM). Although spatial remapping could be considered a kind of spatial memory process itself (i.e., updating remembered locations based on anticipated saccade outcomes), the two processes operate on very different time scales (milliseconds versus seconds). In the present study, the influence of saccadic and spatial remapping on SWM was examined in healthy individuals. An initial control condition, in which participants had to respond to a probe stimulus (i.e., “is the probe in the location previously occupied by the target?”) following a 1500 ms delay, was contrasted with conditions in which the fixation point moved (left, right, up, or down) at the onset of the delay. In a second version of the task, participants made covert shifts of attention at delay onset requiring covert spatial, rather than saccadic, remapping. In both tasks SWM performance was best when no remapping was required. Decrements in SWM were largest overall in the spatial remapping task, whereas for both saccadic and spatial remapping, a consistent cost was observed for remapping the target array into right visual space. Results are discussed in terms of hemispheric biases in attention and differences in performance for peripersonal versus extrapersonal space.

Introduction: Premenstrual Dysphoric Disorder (PMDD) is a condition that affects about 2-6% of women of reproductive age. The relation to ovarian steroids is apparent as symptoms are absent during anovulatory cycles. Neuroactive steroids like allopregnanolone have effect in the brain and on brain function and have been proposed to play an important role for the symptomatology of premenstrual symptoms and in the interaction between the GABAA receptor and alcohol. High doses of alcohol elevate allopregnanolone levels both in rats and humans. Allopregnanolone is a positive modulator of the GABAA receptor with sedative, anxiolytic and anticonvulsant effect in both human and animals. Aims: The aim was to investigate if a low dose (100μg) of GnRH agonist (buserelin) is effective for the treatment of PMDD and if allopregnanolone serum levels during treatment are associated to symptom severity. Furthermore, the studies aimed at investigating the effect of a low dose of alcohol upon saccadic eye movements in women with PMDD, and control subjects in different phases of the menstrual cycle, and to evaluate if there was a difference in response to alcohol between men and healthy women. We also wanted to see if this low dose of alcohol could have an effect on serum allopregnanolone levels in women with PMDD and control subjects in the follicular and luteal phases of the menstrual cycle. Methods: The effect of low dose (100μg) of GnRH agonist (buserelin) on premenstrual symptoms was evaluated in a randomized, placebo controlled, double-blinded cross-over trial. 27 PMDD patients were randomized to either GnRH agonist intranasally once a day or placebo for two months before the crossover. The main outcome measure was the daily symptom ratings for mood and physical symptoms made by the patients. In a subgroup of 12 women, grouped as buserelin responders and placebo responders, luteal phase serum progesterone, allopregnanolone, and pregnanolone was measured together with daily ratings for mood and physical symptoms. Alcohol responsiveness was measured in PMDD patients, female control subjects and men by comparing the effect of a low dose (0.2g/kg) of intravenous alcohol or placebo infusion upon saccadic eye movements. Blood samples for measurement of allopregnanolone and cortisol were taken throughout the alcohol/placebo challenges. Results: Low dose GnRH agonist was effective as treatment of premenstrual irritability and depression. Anovulatory cycles were confirmed in 56% of the subjects, particularly in older women. Buserelin as well as placebo responders displayed decreased allopregnanolone and progesterone levels in parallel with symptom improvement. PMDD patients displayed blunted saccadic eye movement response to alcohol infusion, especially in the luteal phase. Control subjects did not change their response to alcohol between cycle phases. We found no difference in saccadic eye movement sensitivity to alcohol between males and females. Allopregnanolone levels significantly decreased in the luteal phase following the alcohol infusion. Conclusions: Low dose GnRH agonist is effective in treatment of premenstrual depression and irritability but is likely to induce anovulation with increasing age. Independent of whether buserelin or placebo treatment was given decreased levels of allopregnanolone appear to be related to symptom improvement. Women with PMDD have altered saccadic eye movement sensitivity in response to alcohol, particularly in the luteal phase. The low dose of alcohol did not induce any difference in saccade measurements between males and females. Low dose of alcohol does not result in increased peripheral levels of allopregnanolone.

Describing human eye movement behavior as an alternating sequence of saccades and fixations turns out to be an oversimplification because the eyes continue to move during fixation. Small-amplitude saccades (e.g., microsaccades) are typically observed 1-2 times per second during fixation. Research on microsaccades came in two waves. Early studies on microsaccades were dominated by the question whether microsaccades affect visual perception, and by studies on the role of microsaccades in the process of fixation control. The lack of evidence for a unique role of microsaccades led to a very critical view on the importance of microsaccades. Over the last years, microsaccades moved into focus again, revealing many interactions with perception, oculomotor control and cognition, as well as intriguing new insights into the neurophysiological implementation of microsaccades. In contrast to early studies on microsaccades, recent findings on microsaccades were accompanied by the development of models of microsaccade generation. While the exact generating mechanisms vary between the models, they still share the assumption that microsaccades are generated in a topographically organized saccade motor map that includes a representation for small-amplitude saccades in the center of the map (with its neurophysiological implementation in the rostral pole of the superior colliculus). In the present thesis I criticize that models of microsaccade generation are exclusively based on results obtained during prolonged presaccadic fixation. I argue that microsaccades should also be studied in a more natural situation, namely the fixation following large saccadic eye movements. Studying postsaccadic fixation offers a new window to falsify models that aim to account for the generation of small eye movements. I demonstrate that error signals (visual and extra-retinal), as well as non-error signals like target eccentricity influence the characteristics of small-amplitude eye movements. These findings require a modification of a model introduced by Rolfs, Kliegl and Engbert (2008) in order to account for the generation of small-amplitude saccades during postsaccadic fixation. Moreover, I present a promising type of survival analysis that allowed me to examine time-dependent influences on postsaccadic eye movements. In addition, I examined the interplay of postsaccadic eye movements and postsaccadic location judgments, highlighting the need to include postsaccadic eye movements as covariate in the analyses of location judgments in the presented paradigm. In a second goal, I tested model predictions concerning preparatory influences on microsaccade generation during presaccadic fixation. The observation, that the preparatory set significantly influenced microsaccade rate, supports the critical model assumption that increased fixation-related activity results in a larger number of microsaccades. In the present thesis I present important influences on the generation of small-amplitude saccades during fixation. These eye movements constitute a rich oculomotor behavior which still poses many research questions. Certainly, small-amplitude saccades represent an interesting source of information and will continue to influence future studies on perception and cognition. / Die Beschreibung des Blickbewegungsverhaltens als eine sich abwechselnde Folge von Sakkaden und Fixationen stellt eine starke Vereinfachung dar, denn auch während einer Fixation bewegen sich die Augen. Typischerweise treten Bewegungen von kleiner Amplitude (z.B. Mikrosakkaden), 1-2 mal pro Sekunde während einer Fixation auf. Frühe Studien zu Mikrosakkaden wurden von Fragen bezüglich des Einflusses von Mikrosakkaden auf die visuelle Wahrnehmung, und Studien zu der Rolle von Mikrosakkaden bei der Fixationskontrolle dominiert. Fehlende Evidenz für eine Rolle, die ausschließlich Mikrosakkaden zufällt, führten zu einer sehr kritischen Betrachtung von Mikrosakkaden. In den letzten Jahren rückten Mikrosakkaden wieder mehr in den Fokus. Vielerlei Zusammenhänge mit Wahrnehmung, okulomotorischer Kontrolle und Kognition, sowie neue Erkenntnisse bezüglich der neurophysiologischen Implementierung von Mikrosakkaden konnten aufgedeckt werden. In den letzten Jahren wurden verschiedene Modelle der Mikrosakkadengenerierung vorgestellt. Auch wenn sich diese in ihren exakten Mechanismen unterscheiden, so teilen sie doch die Annahme, dass Mikrosakkaden in einer topographisch organisierten motorischen Karte für Sakkaden ausgelöst werden. Diese Karten beinhalten eine Repräsentation für klein-amplitudige Sakkaden im Zentrum der Karte (mit dem rostralen Pol der colliculi superiores als neurophysiologische Implementierung). In der vorliegenden Arbeit kritisiere ich, dass Modelle der Mikrosakkadengenerierung ausschließlich auf Resultaten langanhaltender präsakkadischer Fixation beruhen. Ich führe an, dass Mikrosakkaden in einer natürlicheren Situation untersucht werden sollten, nämlich während der Fixation nach einer großen Sakkade. Die Untersuchung postsakkadischer Fixation bietet eine neue Möglichkeit Modelle der Mikrosakkadengenerierung zu falsifizieren. In den Studien zeige ich, dass Signale über den Fehler in der Sakkadenlandeposition (visuelle und extra-retinale), sowie fehler-unabhängige Signale, wie die Zielreiz-Exzentrizität, einen entscheidenden Einfluss auf kleine Sakkaden haben. Diese Resultate erfordern Modifikationen an dem kürzlich eingeführten Modell von Rolfs, Kliegl und Engbert (2008), um die Generierung von kleinen Sakkaden auch während der postsakkadischen Fixation erklären zu können. Darüber hinaus präsentiere ich eine viel versprechende Ereigniszeitanalyse, die uns erlaubt zeitabhängige Einflüsse auf das postsakkadische Blickbewegungsverhalten zu untersuchen. Außerdem untersuche ich das Zusammenspiel von postsakkadischen Augenbewegungen und postsakkadischen Positionsurteilen. Dabei wird die Bedeutung von postsakkadischen Augenbewegungen als Kovariate in den statistischen Analysen betont. Ein zweites Ziel dieser Arbeit besteht darin Modellvorhersagen bezüglich vorbereitender Einflüsse auf die Mikrosakkadengenerierung zu untersuchen. Die Ergebnisse, hinsichtlich eines signifikanten Einflusses des preparatory set auf die Mikrosakkadenrate unterstützt die wesentliche Modellannahme, dass erhöhte fixationsbezogene Aktivität zu einer größeren Anzahl an Mikrosakkaden führt. In der vorliegenden Arbeit präsentiere ich wichtige Einflüsse auf die Generierung von kleinen Sakkaden während der Fixation. Diese Augenbewegungen stellen ein vielseitiges okulomorisches Verhalten dar, welche weiterhin zahlreiche Fragen mit sich bringen und sicherlich zukünftige Studien zu Wahrnehmung und Kognition beeinflussen werden.

Background: Premenstrual dysphoric disorder (PMDD) affects 3–8% of women in fertile ages. Combined oral contraceptives (OCs) are widely used and some users experience adverse mood effects. The cyclicity of PMDD symptoms coincides with increased endogenous levels of allopregnanolone after ovulation. Allopregnanolone enhances the effect of γ-aminobutyric acid (GABA) on the GABAA receptor, the principal inhibitory transmitter system in the brain. The sensitivity to other GABAA receptor agonists than allopregnanolone (i.e. benzodiazepines, alcohol and the 5 β epimer to allopregnanolone, pregnanolone) has been reported to depend on menstrual cycle phase and/or PMDD diagnosis. Isoallopregnanolone, the 3 β epimer to allopregnanolone, has previously been used to verify specific allopregnanolone GABAA receptor effects. Saccadic eye velocity (SEV) is a sensitive and objective measurement of GABAA receptor function. Aims: To study the pharmacological effects, and any effect on gonadotropin release, of intravenous allopregnanolone in healthy women. A second aim was to explore whether allopregnanolone sensitivity differs over the menstrual cycle or during OC use in healthy women, and thirdly in PMDD patients. Methods: Ten women were challenged with a cumulative dose of intravenous allopregnanolone in the follicular phase of the menstrual cycle. The effect on FSH and LH was compared to women exposed to isoallopregnanolone. A single dose of allopregnanolone was administered once in the follicular phase and once in the luteal phase in another ten healthy women and in ten PMDD patients, and additionally in ten women using OCs. Repeated measurements of SEV, subjectively rated sedation and serum concentrations after allopregnanolone injections were performed in all studies. Results: Allopregnanolone dose-dependently reduced SEV and increased subjectively rated sedation. Healthy women had a decreased SEV response in the luteal phase compared to the follicular phase. By contrast, PMDD patients had a decreased SEV response and subjectively rated sedation response to allopregnanolone in the follicular phase compared to the luteal phase. There was no difference in the SEV response to allopregnanolone between women using oral contraceptives and healthy naturally cycling women. Allopregnanolone decreased serum levels of FSH and LH whereas isoallopregnanolone did not affect FSH and LH levels. Conclusion: Intravenous allopregnanolone was safely given and produced a sedative response in terms of SEV and subjectively rated sedation in women. The sensitivity to allopregnanolone was associated with menstrual cycle phase, but in the opposite direction in healthy women compared to PMDD patients. The results suggest mechanisms of physiological tolerance to allopregnanolone across the menstrual cycle in healthy women and support that PMDD patients have a disturbed GABAA receptor function. In addition, one of our studies suggests that allopregnanolone might be involved in the mechanism behind hypothalamic amenorrhea.

Thesis (Ph. D.)--University of California, San Diego, 2005. / Vita. Includes bibliographical references.

Thesis (Ph. D.)--University of Oregon, 2006. / Typescript. Includes vita and abstract. "These investigations were supported in part by the National Institute on Deafness and Communication Disorders ... and the National Institute of General Medical Sciences"--P. viii. Includes bibliographical references (leaves 142-152). Also available for download via the World Wide Web; free to University of Oregon users.

Made available in DSpace on 2016-03-15T19:40:37Z (GMT). No. of bitstreams: 1 Alexandre Tadeu Fae Rosa.pdf: 3127122 bytes, checksum: 7cc2fee5f67c75093575447bd7628184 (MD5) Previous issue date: 2009-01-22 / Fundo Mackenzie de Pesquisa / Transcranial Direct Current Stimulation (tDCS) is a technique which is able to modulate cortical excitability in a safe, painless and non-invasive way. The effects of increasing and reduction of the excitability obtained after application of tDCS depend on the polarity which has been used (anodal or cathodal). This dissertation aims at investigating the effects of tDCS on the preparation of saccadic movements in reading. In the experiment, healthy volunteers performed a word-reading task after being exposed to anodal, cathodal or sham tDCS over the right frontal eye field (FEF). The results show that anodal tDCS applied over the right FEF has a delay effect on the performance of the subjects while making the first saccadic movement during reading. Besides, the results show a significant increase of the condition of cathodal stimulation when compared to sham and anodal stimulation related to time in which the subject looks at a fixation mark at the left side after the words appear on the screen. Also, concerning the average reading time of the whole set of words, there was not any significant difference on the main effects or interaction. / A estimulação transcraniana por corrente contínua (ETCC) é uma técnica capaz de modular a excitabilidade cortical de maneira segura, indolor e não-invasiva. Os efeitos de aumento ou diminuição da excitabilidade obtidos após a aplicação da ETCC dependem da polaridade utilizada (anódica ou catódica). Esta dissertação tem como objetivo investigar os efeitos produzidos pela ETCC na preparação de movimentos sacádicos durante a leitura. No experimento realizado, voluntários saudáveis realizaram uma tarefa de leitura de palavras após terem recebido ETCC anódica, catódica ou placebo em campo visual frontal (CVF) direito. Os resultados mostram que a ETCC catódica em CVF direito piora o desempenho dos sujeitos na realização do primeiro movimento sacádico durante a leitura. Além disso, os resultados revelaram aumento significativo da condição de estimulação catódica em comparação com o placebo e da estimulação catódica em comparação com a anódica com relação ao tempo em que o sujeito fixa o olhar no ponto de referência à esquerda depois do aparecimento dos itens a serem lidos. Ainda, com relação ao tempo médio de leitura de todo o conjunto de palavras, não houve nenhuma diferença significativa para os efeitos principais ou interação.

O presente estudo teve como objetivo avaliar o efeito da incerteza a respeito da direção do deslocamento de um alvo na estratégia visual e controle motor em uma tarefa de interceptação. Participaram do Experimento I 17 voluntários, executando movimentos manuais interceptativos de um alvo virtual projetado em uma tela de LCD. A tarefa interceptativa foi executada com um mouse sem fio. Os participantes foram submetidos a três condições experimentais em duas velocidades: (1) certeza de descolamento com direção inicial do alvo inalterada, (2) 50% de incerteza de mudança na direção de deslocamento do alvo, e (3) certeza de mudança na direção de deslocamento do alvo. Participaram do Experimento II 20 voluntários destros diferentes dos do experimento anterior, que executaram a mesma tarefa descrita no Experimento I. Dez voluntários integraram o grupo que recebeu informação prévia sobre a probabilidade de deslocamento do alvo antes de cada série de tentativas (INF), e os demais integraram o grupo que não recebeu informação prévia (SI). Ambos os grupos foram submetidos a três condições de avaliação: (1) 25% de certeza de mudança na direção do alvo, (2) 50% de certeza de mudança na direção do alvo, e (3) 75% de certeza de mudança na direção do alvo. Os resultados revelaram que o comportamento visual é modulado pela velocidade e incerteza sobre o deslocamento do alvo. Foi encontrado também que o conhecimento prévio sobre a probabilidade de deslocamento do alvo influenciou a estratégia visual utilizada e o desempenho da interceptação. Comportamentos preditivos foram evidenciados tanto no comportamento visual quanto no motor / The present study aimed to evaluate the effect of uncertainty about direction of target displacement on the visual strategy and motor control in an interception task. Seventeen volunteers participated of Experiment I. They performed interceptive manual movements of a virtual target projected on a LCD screen. The task was performed with a wireless mouse. Participants were submitted to three experimental conditions in two speeds: (1) certainty about unchanged initial target displacement direction, (2) 50% of uncertainty about change of target displacement direction, and (3) certainty about change of initial target displacement direction. Twenty volunteers different from Experiment I participated of Experiment II. Participants performed the same task described in the first experiment. Ten volunteers were assigned to a group which received prior information about the probability of displacement of the target before each condition (INF), and the others were assigned to a group that received no prior information (SI). The groups were evaluated in three conditions: 25%, 50% and 75% of uncertainty about change of target direction. Results of this study revealed that visual behavior is modulated by target speed and uncertainty about the target\'s motion. We also found that prior knowledge about the probability of the target\'s movement influenced the visual strategy used and the performance of the interception. Predictive behaviors were evidenced in both the visual and motor behavior

Active movements are a key feature of human behavior. Even when we do not move our limbs we almost never stop guiding our eyes. As a minimal but omnipresent form of behavior, fast eye movements, called saccades, sample the visual world and determine to a large extent what we perceive. Despite being an integral part of visual perception, prevalent research practice treats the human subject as a passive observer who fixates a spot on the screen and is not allowed to move. Yet, learning sensorimotor interactions by active exploration in order to predict future changes and guide actions seems to be a fundamental principle of neural organization. This results in neural patterns of active behavior that can be fundamentally different from the neural processes revealed in movement-restricted laboratory settings questioning the transferability of results from experimental paradigms demanding fixation to real-world free viewing behavior. In this thesis, we aim at studying the neural mechanisms underlying free viewing behavior. In order to assess the fast, flexible and possibly distributed neural dynamics of active vision, we established a procedure for studying eye movements in magnetoencephalography (MEG) and investigated oscillatory signatures associated with sensorimotor processes of eye movements and saccade target selection, two fundamental processes of active vision. Electroencephalography (EEG) and MEG can non-invasively measure fast neural dynamics and hence seem ideally suited for studying active vision in humans. However, artifacts related to eye movements confound both EEG and MEG signals, and a thorough handling of these artifacts is crucial for investigating neural activities during active movements. Mostly, cleaning of ocular artifacts has been performed for occasional eye movements and blinks in fixation paradigms in EEG. Less is known about the impact of ocular artifacts and especially the saccadic spike on MEG. As a first step to enable active vision studies in MEG, we investigated ocular artifacts and possible ways of their separation from neural signals in MEG. We show that the saccadic spike seriously distorts the spatial and spectral characteristics of the MEG signal (Study 2). We further tested if electrooculogram (EOG) based regression is feasible for corneo-retinal artifact removal (Study 1). Due to an often-raised concern, we addressed if EOG regression eliminates neural activity when applied for MEG. Our results do not indicate such susceptibility and we conclude that EOG regression for removing the corneo-retinal artifact in MEG is suitable. Based on insights from both studies, we established an artifact handling procedure including EOG regression and independent component analysis (ICA) to assess the neural dynamics of active vision. In Study 3, we investigated spectral signatures of neuronal activity across cortex underlying saccade preparation, execution and re-fixation in a delayed saccade task. During preparation and execution, we found a dichotomic signature of gamma power increases and beta power decreases in widespread cortical areas related to saccadic control, including fronto-parietal structures. Saccade direction specific signatures resided in hemisphere lateralized changes in low gamma and alpha power in posterior parietal cortex during preparation extending to extrastriate areas during re-fixation. Real-world behavior implies the constant need to flexibly select actions between competing behavioral alternatives depending on both sensory input and internal states. In order to assess internally motivated viewing behavior, we compared neuronal activity of externally cued saccades with saccades to freely chosen, equally valuable targets. We found gamma band specific power increases in fronto-parietal areas that are likely to reflect a fast transient process of action guidance for sensory-guided saccades and a sustained process for internally selecting between competing behavioral alternatives. The sustained signature of internal action selection suggests that a decision between spatially oriented movements is mediated within sensorimotor structures by neural competition between assemblies encoding parallel evolving movement plans. Since our observations support the assumption that a decision emerges through the distributed consensus of neural activities within effector specific areas rather than in a distinct decision module, they argue for the importance of studying mental processes within their ecologically valid and active context. This thesis shows the feasibility of studying neural mechanisms of active vision in MEG and provides important steps for studying neurophysiological correlates of free viewing in the future. The observed spectrally specific, distributed signatures highlight the importance of assessing fast oscillatory dynamics across the cortex for understanding neural mechanisms mediating real-world active behavior.

Le système visuel a évolué de manière à prendre en compte les conséquences de nos mouvements sur notre perception. L’évolution nous a particulièrement doté de la capacité à percevoir notre environnement visuel comme stable et continu malgré les importants déplacements de ses projections sur nos rétines à chaque fois que nous déplaçons nos yeux, notre tête ou notre corps. Des études chez l’animal ont récemment montré que dans certaines aires corticales et sous-corticales, impliquées dans le contrôle attentionnel et dans l’élaboration des mouvements oculaires, des neurones sont capables d’anticiper les conséquences des futurs mouvements volontaires des yeux sur leurs entrées visuelles. Ces neurones prédisent ce à quoi ressemblera notre environnement visuel en re-cartographiant la position des objets d’importance à l’endroit qu’ils occuperont après l’exécution d’une saccade. Dans une série d’études, nous avons tout d’abord démontré que cette re- cartographie pouvait être évaluée de manière non invasive chez l’Homme avec de simples cibles en mouvement apparent. En utilisant l’enregistrement des mouvements des yeux combinés à des méthodes psychophysiques, nous avons déterminé la distribution des erreurs de re-cartographie à travers le champ visuel et ainsi découvert que la compensation des saccades oculomotrices se faisait de manière relativement précise. D’autre part, les patterns d’erreurs observés soutiennent un modèle de la constance spatiale basé sur la re-cartographie de pointeurs attentionnels et excluent d’autres modèles issus de la littérature. Par la suite, en utilisant des objets en mouvement continu et l’exécution de saccades au travers de leurs trajectoires, nous avons mis à jour une visualisation directe des processus de re-cartographie. Avec ce nouveau procédé nous avons à nouveau démontré l’existence d’erreurs systématiques de correction pour les saccades, qui s’expliquent par une re-cartographie imprécise de la position attendue des objets en mouvement. Nous avons par la suite étendu notre modèle à d’autres types de mouvements du corps et notamment étudié les contributions de récepteurs sous-corticaux (otoliths et canaux semi-circulaires) dans le maintien de la constance spatiale à travers des mouvements de la tête. Contrairement à des études décrivant une compensation presque parfaite des mouvements de la tête, nous avons observé une rupture de la constance spatiale pour des mouvements de roulis et de translation de la tête. Enfin, nous avons testé cette re-cartographie de la position des objets compensant un déplacement oculaire avec des cibles présentées à la limite du champ visuel, une re-cartographie censée placer la position attendue de l’objet à l’extérieur du champ visuel. Nos résultats suggèrent que les aires visuelles cérébrales impliquées dans ce processus de re-cartographie construisent une représentation globale de l’espace allant au-delà du traditionnel champ visuel. Pour finir, nous avons conduit deux expériences pour déterminer le déploiement de l’attention à travers l’exécution de saccades. Nous avons alors démontré que l’attention capturée par la présentation brève d’un stimuli est re-cartographiée à sa position spatiale correcte après l’exécution d’une saccade, et que cet effet peut être observé avant même l’initiation d’une saccade. L’ensemble de ces résultats démontre le rôle des pointeurs attentionnels dans la gestion du rétablissement des positions d’un objet dans l’espace ainsi que l’apport des mesures comportementales à un champ de recherche initialement restreint à l’électrophysiologie / The visual system has evolved to deal with the consequences of our own movements onour perception. In particular, evolution has given us the ability to perceive our visual world as stableand continuous despite large shift of the image on our retinas when we move our eyes, head orbody. Animal studies have recently shown that in some cortical and sub-cortical areas involved inattention and saccade control, neurons are able to anticipate the consequences of voluntary eyemovements on their visual input. These neurons predict how the world will look like after a saccadeby remapping the location of each attended object to the place it will occupy following a saccade.In a series of studies, we first showed that remapping could be evaluated in a non-invasive fashion in human with simple apparent motion targets. Using eye movement recordingsand psychophysical methods, we evaluated the distribution of remapping errors across the visualfield and found that saccade compensation was fairly accurate. The pattern of errors observedsupport a model of space constancy based on a remapping of attention pointers and excluded otherknown models. Then using targets that moved continuously while a saccade was made across themotion path, we were able to directly visualize the remapping processes. With this novel method wedemonstrated again the existence of systematic errors of correction for the saccade, best explainedby an inaccurate remapping of expected moving target locations. We then extended our model toother body movements, and studied the contribution of sub-cortical receptors (otoliths and semi-circular canals) in the maintenance of space constancy across head movements. Contrary tostudies reporting almost perfect compensations for head movements, we observed breakdowns ofspace constancy for head tilt as well as for head translation. Then, we tested remapping of targetlocations to correct for saccades at the very edge of the visual field, remapping that would place theexpected target location outside the visual field. Our results suggest that visual areas involved inremapping construct a global representation of space extending out beyond the traditional visualfield. Finally, we conducted experiments to determine the allocation of attention across saccades.We demonstrated that the attention captured by a brief transient was remapped to the correctspatial location after the eye movement and that this shift can be observed even before thesaccade.Taken together these results demonstrate the management of attention pointers to therecovery of target locations in space as well as the ability of behavioral measurements to address atopic pioneered by eletrophysiologists.