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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
21

Coordination des actions et des habitudes : approche neurocomportementale chez le rat / Coordination of actions and habits : a neurobehavioural approach in rats

Tran-Tu-Yen, Delphine 10 December 2010 (has links)
: Mon travail de thèse a porté sur l’étude neurocomportementale des actions et des habitudes chez le Rat. En effet, lors d’un apprentissage opérant la réponse peut être acquise selon deux systèmes associatifs. Le premier dépend d’une représentation des conséquences de la réponse, le second d’une association plus « simple » entre le stimulus et la réponse. Un premier axe de recherche a consisté à étudier plusieurs paramètres du conditionnement, afin de déterminer leur influence sur le contrôle de la réponse instrumentale par un système plutôt que l’autre. Le deuxième axe de recherche a porté sur l’étude des substrats neuronaux impliqués dans l’acquisition et l’expression d’une action, par l’intermédiaire de techniques d’inactivation cérébrale et d’étude immuno-histochimique de l’expression génique de la protéine Fos. / Previous research has established that instrumental conditioning, in both primates and rats, is mediated by two concurrent associative systems. In early stages of training, instrumental response is thought to be mediated by an association between the action and the outcome (A-O). While training proceeds however, as the response becomes less sensible to the outcome value, it is conceived as being mediated by an association between thestimulus and the response (S-R). Recent evidences suggest that the both systems operate in tandem and/or competition from the beginning of training. This work aimed at studying the mechanisms that coordinate the control of the instrumental response by the goal-directedsystem or the habit system. A first batch of results indicates no effect of the amount of training sessions on the goal-directed nature of the conditioned instrumental response. Indeed,the outcome devaluations by CTA or selective satiety reduced the instrumental performances,independently of the training procedure applied. The instrumental responses resulting from our 3 training procedures depend of an actualized representation of their outcomes. A secondbatch of results indicates that information about the context of instrumental conditioning isincluded in the incentive representation of the outcome. Indeed, we observed no sensitivity tooutcome devaluation when devaluation occurred outside the training context. These results offer new original hypotheses about context encoding and the nature of instrumental responding. A third batch of experiments investigates the role of the prelimbic cortex in acquisition vs. expression of goal-directed instrumental behaviour, using reversible neuronal inactivation. The results show that the prelimbic cortex plays a transient but crucial role in theacquisition of goal-directed responding and that the A-O and S-R systems can operate in a competitive fashion early in training. Using ex-vivo imaging, a last batch of experiments aimed to study the temporal cerebral activation throughout instrumental training with a focuson prefrontal and striatal regions. Results show levels of Fos expression that vary with regions. At the beginning of conditioning, the density of Fos positive nuclei is high in the prefrontal regions. It decreases with training. Labelling is denser in the dorsomedial striatumthan in the dorsolateral striatum. The weak activation in the dorsolateral striatum appears consistent with the absence of habit. These data are in accordance with data of the literature concerning dynamics of activation in cortico-striatal circuits. Furthermore, they are in agreement with the suggestion that activity in the prelimbic cortex could promote the acquisition of goal-directed action by the induction of neuronal plasticity in the dorsal striatum.
22

Behavioral and muscular deficits induced by Muscimol injection into the primate primary motor cortex during a reach-to-grasp task

Serrano, Eleonore 12 1900 (has links)
Le contrôle moteur fin et précis des doigts est une habileté importante dans la vie quotidienne pour écrire ou manger par exemple. Ce contrôle moteur est pris en charge par le cortex moteur primaire (M1) qui transmet le signal neuronal à la moelle épinière via la voie corticospinale. Le macaque rhésus est un excellent modèle pour étudier ce système moteur car, comme chez l’humain, il possède cette voie cortico-motoneuronale directe. Bien que les déficits du contrôle moteur de la main suite à des inactivations de M1 aient été étudiés sur des modèles de singes, peu d’études ont décrit les changements musculaires sous-tendant ces déficits. Le but de cette étude était d’évaluer les effets d’une inactivation partielle de M1 sur le comportement et l’activation du patron musculaire du membre supérieur chez le macaque rhésus. Pour ce faire, nous avons effectué des injections intra-corticales de Muscimol, un agoniste du GABA, pour inactiver temporairement l’aire de représentation de la main de M1. Des singes ont été entrainés à réaliser une tâche d’atteinte et de préhension qui requière l’utilisation du pouce et de l’index pour attraper une pastille de nourriture. En parallèle, les activités électromyographiques (EMG) des muscles proximaux et distaux du membre supérieur contralatéral aux sites d’injections ont été enregistrées. L’inactivation partielle de M1 entraine différents déficits moteurs comme une diminution du taux de succès, une perte des mouvements indépendants des doigts, une première flexion de l’index plus lente, et l’apparition de nouvelles stratégies de préhension pour attraper la pastille. Dans le cas de trouble sévère, les singes ont présentés tous ces déficits comportementaux. Ces troubles moteurs étaient sous-tendus par des activités musculaires anormales. En effet, les analyses EMG ont mis en évidence des changements dans les latences et les patrons d’activations musculaires des muscles proximaux et distaux au cours de la phase d’atteinte, d’ajustement et de préhension. Dans le cas de trouble modéré, les patrons d’activations musculaires étaient préservés malgré certain déficits visibles. Cependant, les patrons d’activations musculaires étaient altérés si la tâche demandait une rotation de l’avant-bras et de la main. Ces résultats montrent que les déficits comportementaux et les changements musculaires dépendent de la sévérité des troubles moteurs et/ou de la difficulté de la tâche (i.e. une rotation de l’avant-bras). / Fine digit movements contribute to many different aspects of our daily life and require appropriate muscle coordination. The main pathway through which M1 sends motor commands to spinal motor neurons is via the corticospinal tract. The rhesus macaque, like humans, have this direct corticomotoneuronal pathway of M1, making it a useful model to study this system. Although the effect of M1 inactivation on the control of the hand in term of behavioral changes has been studied in monkeys, little is known of how muscle activation patterns of the upper limb during reaching and grasping in monkeys becomes altered. The goal of this study was to evaluate the effect of a partial inactivation of the primary motor cortex (M1) in rhesus macaques on both behavioral performance and muscle activations. To do so we performed intra-cortical injections of Muscimol, a GABA agonist, to inactivate the hand area of M1. Monkeys performed a reach-to-grasp task that required a precision grip to retrieve a food pellet from a well. Electromyographic (EMG) activity of the proximal and distal muscles of the contralateral upper limb were recorded and quantified relative to the behavioral performance. We found that depending on the severity of the impairment, the Muscimol injection could induce several different movement abnormalities, such as decrease in the success rate, loss of independent finger movements, longer duration of the first flexion of the index finger, and use of alternate types of grasp to retrieve the food pellet. In cases of severe impairment, monkeys displayed all these movement abnormalities concurrently. In addition, we observed that behavioral deficits were associated with muscle discoordination. Indeed, EMG analysis revealed that the latencies and the muscle activation patterns were altered during the reach, hand preshaping and the grasp phases of the movement. These inappropriate EMG activities were visible on both proximal and distal muscles of the upper limb. In cases of mild impairment, monkeys had fewer behavioral deficits, but still showed some changes in the temporal muscle activation patterns. In contrast to the severe cases, the muscle activation patterns were more preserved. Interestingly, in the mild cases, the muscle activation patterns were altered if a rotation of the forearm was required by the task. Thus, we found that behavioral and muscular activation changes were dependent on the severity of the impairment and/or the difficulty of the task (i.e. required a rotation of the forearm).
23

Inhibition of RVLM synaptic activation at peak hyperthermia reduces visceral sympathetic nerve discharge

Hosking, Kimberley Gowens January 1900 (has links)
Master of Science / Department of Anatomy and Physiology / Michael J. Kenney / Hyperthermia is an environmental stressor that produces marked increases in visceral sympathetic nerve discharge (SND) in young rats. The brainstem in rats contains the essential neural circuitry for mediating visceral sympathetic activation; however, specific brainstem sites involved remain virtually unknown. The rostral ventral lateral medulla (RVLM) is a key central nervous system region involved in the maintenance of basal SND and in mediating sympathetic nerve responses evoked from supraspinal sites. In the present study we tested the hypothesis that inhibition of RVLM synaptic activation at peak hyperthermia (internal body temperature, Tc, increased to 41.5°C) would affect heating-induced visceral sympathetic activation. Experiments were completed in chloralose-urethane anesthetized, baroreceptor-intact and sinoaortic-denervated, 3-6 month-old Sprague-Dawley rats. Bilateral inhibition of RVLM synaptic activation produced by muscimol microinjections (400 and 800 pmol) at 41.5°C resulted in immediate and significant reductions in peak heating-induced renal and splenic sympathoexcitation. Interruption of RVLM synaptic activation and axonal transmission by lidocaine microinjections (40 nmol) at 41.5°C produced significant reductions in hyperthermia-induced sympathetic activation to similar levels produced by RVLM muscimol microinjections. The total amount of SND inhibited by RVLM muscimol and lidocaine microinjections was significantly more during hyperthermia (41.5°C) than normothermia (38°C). These findings demonstrate that maintenance of sympathetic activation at peak hyperthermia is dependent on the integrity of RVLM neural circuits.
24

L'ANXIETE LIEE AU SEVRAGE A LA COCAINE : Etude comportementale et neuroanatomique

El Hage, Cynthia, El Hage, Cynthia 02 July 2012 (has links) (PDF)
L'anxiété est un symptôme prédominant au cours des périodes initiales de sevrage à la cocaïne et est considéré comme un facteur important de rechute. Le but de cette étude était de caractériser les dysfonctionnements cérébraux qui pourraient contribuer à l'expression de cet état pathologique chez le rat. Les rats sont traités avec de la cocaïne en chronique et le comportement anxieux est évalué au cours du sevrage dans différents paradigmes expérimentaux (tests du labyrinthe en croix surélevé, du confinement dans un bras ouvert surélevé et de l'enfouissement défensif). Nos résultats ont montré que le sevrage à la cocaïne induit un état anxieux élevé qui persiste pendant au moins 28 jours de sevrage. Nous avons ensuite utilisé l'immunohistochimie de Fos pour comparer les patterns d'activation cérébrale chez les rats sevrés et témoins après exposition au test de l'OA. Nos données ont montré que l'anxiété élevée des rats sevrés était accompagnée d'une altération de la réactivité des neurones glutamatergiques de la partie dorsale du cortex préfrontal médian (dCPFm) et de certaines régions sous-corticale (aires hypothalamiques latérale et antérieure et le noyau paraventriculaire du thalamus). Nous avons ensuite montré que l'inactivation pharmacologique du dCPFm avec du muscimol atténuait les comportements anxieux des rats sevrés suggérant ainsi une hyperréactivité de cette région corticale durant le traitement des informations de type anxieux. Notre étude amène des données nouvelles quant aux substrats neuronaux sous-tendant l'anxiété pathologique observée au cours du sevrage à la cocaïne et souligne l'importance du CPFm dans la régulation de cet état d'anxiété pathologique.
25

Papel do Estriado Dorsal e dos receptores D1 e D2 na modulação do sobressalto avaliado pela tarefa de Inibição Pré-pulso em ratos

Rodrigues, Samanta January 2014 (has links)
Orientadora: Profa. Dra. Tatiana Lima Ferreira / Dissertação (mestrado) - Universidade Federal do ABC, Programa de Pós-Graduação em Neurociência e Cognição, 2014.
26

Direct Connections between the Lateral Entorhinal Cortex and Hippocampus or Medial Prefrontal cortex: Their Role in the Retrieval of Associative Memories

Tanninen, Stephanie 27 November 2012 (has links)
Consolidation of associative memories may depend on communication between the lateral entorhinal cortex (LEC) and hippocampus (HPC) for recently learned memories and the LEC and medial prefrontal cortex (mPFC) for remote memories. To determine whether direct connections between these regions are necessary for the retrieval of a recently or remotely learned memory, rats acquired an associative memory through trace eyeblink conditioning and were tested for memory retention after inactivating the regions of interest with the GABAA agonist, muscimol. Inactivating the LEC-HPC connection did not impair memory retrieval. However, inactivating the LEC-mPFC connection impaired remote, but not recent, memory retrieval. Thus, the LEC and mPFC connection is necessary for the retrieval of a remotely, but not recently learned associative memory. Increased reliance on the entorhinal-prefrontal connection indicates the strengthening of functional connectivity between the two regions, which may be a biological correlate for the proposed reorganization during systems consolidation.
27

Direct Connections between the Lateral Entorhinal Cortex and Hippocampus or Medial Prefrontal cortex: Their Role in the Retrieval of Associative Memories

Tanninen, Stephanie 27 November 2012 (has links)
Consolidation of associative memories may depend on communication between the lateral entorhinal cortex (LEC) and hippocampus (HPC) for recently learned memories and the LEC and medial prefrontal cortex (mPFC) for remote memories. To determine whether direct connections between these regions are necessary for the retrieval of a recently or remotely learned memory, rats acquired an associative memory through trace eyeblink conditioning and were tested for memory retention after inactivating the regions of interest with the GABAA agonist, muscimol. Inactivating the LEC-HPC connection did not impair memory retrieval. However, inactivating the LEC-mPFC connection impaired remote, but not recent, memory retrieval. Thus, the LEC and mPFC connection is necessary for the retrieval of a remotely, but not recently learned associative memory. Increased reliance on the entorhinal-prefrontal connection indicates the strengthening of functional connectivity between the two regions, which may be a biological correlate for the proposed reorganization during systems consolidation.
28

Mecanismos prosencefálicos envolvidos na ingestão de sódio e água induzida pela ativação gabaérgica do núcleo parabraquial lateral /

Roncari, Camila Ferreira. January 2010 (has links)
Orientador: José Vanderlei Menani / Banca: Eduardo Colombari / Banca: Lisandra Brandino de Oliveira / Resumo: Estudos recentes mostraram a existência de importantes mecanismos de controle da ingestão de sódio e água no núcleo parabraquial lateral (NPBL), uma estrutura pontina localizada dorsolateralmente ao pedúnculo cerebelar superior. Lesões eletrolíticas ou neurotóxicas do NPBL aumentam a ingestão de água induzida por administração central ou periférica de angiotensina II (ANG II). O bloqueio dos receptores serotoninérgicos, colecistocinérgicos ou glutamatérgicos com injeções bilaterais no NPBL de metisergida, proglumide ou DNQX, respectivamente, aumentam a ingestão de solução hipertônica de NaCl induzida por tratamento com o diurético furosemida combinado com doses baixas do inibidor da enzima conversora de angiotensina captopril injetados subcutaneamente. Metisergida injetada no NPBL ainda aumenta a ingestão de NaCl induzida por ANG II administrada no ventrículo lateral (VL) ou no órgão subfornical (OSF) e por privação hídrica por 24 h, depleção de sódio ou DOCA. Além disso, a ativação de receptores adrenérgicos a2 com injeções de moxonidina ou noradrenalina no NPBL aumenta a ingestão de NaCl induzida por furosemida + captopril. Sendo assim, esses estudos mostram que o bloqueio dos mecanismos inibitórios do NPBL com injeções de antagonistas de receptores serotoninérgicos, colecistocinérgicos e glutamatérgicos ou agonistas de receptores adrenérgicos aumenta a ingestão de NaCl e água induzida por tratamentos prévios. No entanto, mais recentemente mostrou-se que a ativação gabaérgica do NPBL induz ingestão de NaCl e água em ratos saciados e normovolêmicos que não receberam nenhum tratamento prévio. Essa resposta é reduzida pelo bloqueio dos mecanismos colinérgicos centrais. No presente estudo, investigamos o efeito da desativação de mecanismos prosencefálicos facilitatórios na ingestão de NaCl e água induzida pela ativação gabaérgica...(Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Recent studies have shown important mechanisms for the control of sodium and water intake in the lateral parabrachial nucleus (LPBN), a pontine structure localized dorsolaterally to the superior cerebellar peduncle. Electrolytic or neurotoxic lesions of the LPBN increase water intake induced by central or peripheral administration of angiotensin II (ANG II). The blockade of serotonergic, cholecystokinergic or glutamatergic receptors with bilateral injections of methysergide, proglumide or DNQX, respectively, into the LPBN increases hypertonic NaCl intake induced by the treatment with subcutaneous injections of diuretic furosemide combined with low dose of angiotensin converting enzyme inhibitor captopril. LPBN injections of methysergide also increases NaCl intake induced by ANG II injected in the lateral ventricle (LV) or into the subfornical organ (SFO) and 24 h water deprivation, sodium depletion or DOCA. Moreover, activation of α2-adrenoceptors with injections of moxonidine or noradrenaline into the LPBN also increases NaCl intake induced by furosemide + captopril. Therefore theses studies have shown that blockade of LPBN inhibitory mechanisms with injections of serotonergic, cholecystokinergic or glutamatergic antagonists or adrenergic agonists increase NaCl and water intake induced by treatments that induce water and/or NaCl intake. However, recently it has been shown that GABAergic activation of the LPBN induces NaCl and water intake in satiated and normovolemic rats that received no previous treatment, a response reduced by the blockade of central cholinergic mechanisms. In the present study, we investigated the effects of deactivation of forebrain facilitatory mechanisms on NaCl and water intake induced by gabaergic activation of the LPBN. Rats with stainless steel cannulas implanted into the LV or SFO and bilaterally into the LPBN were used to test the effects of the blockade... (Complete abstract click electronic access below) / Mestre
29

Determination of Dissociation Constants for GABAA Receptor Antagonists using Spontaneously Active Neuronal Networks in vitro

Oli-Rijal, Sabnam 12 1900 (has links)
Changes in spontaneous spike activities recorded from murine frontal cortex networks grown on substrate-integrated microelectrodes were used to determine the dissociation constant (KB) of three GABAA antagonists. Neuronal networks were treated with fixed concentrations of GABAA antagonists and titrated with muscimol, a GABAA receptor agonist. Muscimol decreased spike activity in a concentration dependent manner with full efficacy (100% spike inhibition) and a 50% inhibitory concentration (IC50) of 0.14 ± 0.05 µM (mean ± SD, n=6). At 10, 20, 40 and 80 µM bicuculline, the muscimol IC50 values were shifted to 4.3 ± 1.8 µM (n=6), 6.8 ± 1.7 µM (n=6), 19.3 ± 3.54 µM (n=10) and 43.5 µM (n=2), respectively (mean ± SD). Muscimol titration in the presence of 10, 20, 40 µM of gabazine resulted in IC50s values of 20.1 (n=2), 37.17 (n=4), and 120.45 (n=2), respectively. In the presence of 20, 80, and 160 µM of TMPP (trimethylolpropane phosphate) the IC50s were 0.86 (n=2), 3.07 (n=3), 6.67 (n=2) µM, respectively. Increasing concentrations of GABAA antagonists shifted agonist log concentration-response curves to the right with identical efficacies, indicating direct competition for the GABAA receptor. A Schild plot analysis with linear regression resulted in slopes of 1.18 ± 0.18, 1.29 ± 0.23 and 1.05 ± 0.03 for bicuculline, gabazine and TMPP, respectively. The potency of antagonists was determined in terms of pA2 values. The pA2 values were 6.63 (gabazine), 6.21 (bicuculline), and 5.4 (TMPP). This suggests that gabazine has a higher binding affinity to the GABAA receptor than bicuculline and TMPP. Hence, using spike rate data obtained from population responses of spontaneously active neuronal networks, it is possible to determine key pharmacological properties of drug-receptor interactions.
30

Influence of Temporary Inactivation of the Prefrontal Cortex or Hippocampus during Stress on the Subsequent Expression of Anxiety and Memory

Halonen, Joshua D 04 March 2009 (has links)
The neural pathways underlying the symptoms of Post Traumatic Stress Disorder (PTSD) have not been fully elucidated. Intrusive memories, persistent anxiety and other cognitive deficits have been attributed to maladaptive or otherwise aberrant processing in specific brain regions, including the hippocampus, amygdala and prefrontal cortex. Our laboratory has developed an animal model of PTSD which results in the enhancement of memory for a place associated with exposure to a predator, anxiety-like behavior, increased startle and impaired memory in a non-aversive memory task. To better understand how the interaction of the hippocampus and prefrontal cortex contribute to the different symptoms of the disorder, we investigated the transient inactivation of each structure during an intense stressor. Our results show that long-term contextual fear associations involve activity in both the hippocampus and the prefrontal cortex, but only the prefrontal cortex is involved in cued fear memories as well.

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