Posttraumatic stress disorder (PTSD) is triggered after exposure to a traumatic event (experienced or witnessed) and its main symptomatology is composed of groups of avoidant, intrusive and hyperexcitability symptoms. It is estimated that 60.7% of men and 51.2% of women will experience at least one traumatic event during life and 8% of men and 20% of women will develop the disease. PTSD is associated with personal and economic costs, poor quality of life and about 1/3 of individuals will develop chronic symptoms despite adequate treatment. In January 2013, a fire of great proportions in a nightclub in Santa Maria-RS, known as KISS Nightclub, killed 242 young people and left hundreds with physical and psychological sequels. The great impact of this event caused an increase in the prevalence of several psychiatric disorders, among them PTSD. Given this, and the lack of effectiveness of standard treatment, other treatment strategies are necessary. Noninvasive neuromodulation techniques, such as Transcranial Direct Current Stimulation (tDCS), have been shown to be promising in the treatment of neuropsychiatric disorders. tDCS consists of the passage of small intensity electric current through the brain through electrodes, in order to modulate cortical excitability. It is an open experimental study with 8 patients whose primary objective was to evaluate the tDCS effect on PTSD symptoms, with exploratory analyzes to evaluate the effects on cognition and depressive and anxious symptoms. After treatment, there was improvement in PTSD symptoms, depression and anxiety, and these effects were maintained throughout the first month after treatment. The positive effects on cognition started slowly and progressively and were significant when assessed after 30 days of treatment. / O Transtorno do Estresse pós-Traumático (TEPT) é desencadeado após a exposição a um evento traumático (vivenciado ou testemunhado) e sua principal sintomatologia é composta por grupos de sintomas evitativos, intrusivos e de hiperexcitabilidade. Estima-se que 60,7% dos homens e 51,2% das mulheres experienciarão pelo menos um evento traumático durante a vida e que 8% dos homens e 20% das mulheres desenvolverão a doença. O TEPT está associado a custos pessoais e econômicos, qualidade de vida pobre e cerca de 1/3 dos indivíduos desenvolverão sintomas crônicos apesar do tratamento adequado. Em janeiro de 2013, um incêndio de grandes proporções em uma casa noturna em Santa Maria-RS, conhecida como Boate KISS, matou 242 jovens e deixou outras centenas com sequelas físicas e psicológicas. O grande impacto desse evento ocasionou aumento da prevalência de diversas patologias psiquiátricas, entre elas o TEPT. Diante disso, e da pouca efetividade do tratamento padrão, outras estratégias de tratamento se fazem necessárias. As técnicas de neuromodulação não invasiva, entre elas a Estimulação Transcraniana por Corrente Contínua (ETCC) têm se mostrado promissoras no tratamento de transtornos neuropsiquiátricos. A ETCC consiste na passagem de corrente elétrica de pequena intensidade pelo cérebro, através de eletrodos, com a finalidade de modular a excitabilidade cortical. Trata-se de um estudo experimental aberto com 8 pacientes cujo objetivo primário foi avaliar o efeito da ETCC nos sintomas de TEPT, com análises exploratórias para avaliar os efeitos em cognição e sintomas depressivos e ansiosos. Após o tratamento, houve melhora dos sintomas de TEPT, de depressão e de ansiedade, e esses efeitos se mantiveram durante todo o 1º mês após o tratamento. Os efeitos positivos na cognição iniciaram-se lenta e progressivamente e foram significativos quando avaliados após 30 dias do tratamento.

Introdução: Níveis elevados de ansiedade têm sido associados com intensidade e comportamento da dor em pacientes com dores aguda e crônica. Foi observado, em indíviduos com síndrome dolorosa miofascial (SDM), que o estresse e a ansiedade aumentam a predisposição para o desenvolvimento de pontos-gatilhos miofasciais. Adicionalmente a isto, existe a tendência do indivíduo experimentar emoções negativas em situações de estresse (neuroticismo), característica de personalidade associada ao traço de personalidade, que pode influenciar negativamente na experiência de dor. Indivíduos com alta ansiedade-traço são geralmente hipersensíveis a estímulos e psicologicamente mais reativos. É concebível supôr a coexistência de alteração na excitabilidade cortical, entre dor crônica e ansiedade nestes pacientes. Para melhorar a compreensão dos mecanismos centrais relacionados à ansiedade e à dor crônica, avaliou-se os parâmetros de excitabilidade cortical, usando estimulação magnética transcraniana (EMT), pulso único e pareado. Nossa hipótese é que a excitabilidade corticoespinhal seja modulada pela ansiedade favorecendo a perda de influxo inibitório descendente. Objetivos: O presente estudo teve como objetivo responder a três perguntas relacionadas à síndrome dolorosa miofascial (SDM): 1) A excitabilidade do córtex motor está relacionada com a ansiedade-traço? 2) A ansiedade-traço modula alterações da excitabilidade corticoespinhal, após dor evocada pelo Quantitative Sensory Testing (QST)? 3) A ansiedade-traço prevê resposta à dor evocada pelo QST, se receber simultaneamente um estímulo heterotópico [Conditioned Pain Modulation (CPM)]? Pacientes e métodos: Foram incluídas mulheres com SDM (n = 47) e controles saudáveis (n = 11), com idade entre 19 e 65 anos. A excitabilidade do córtex motor foi avaliada pela EMT, e a ansiedade foi avaliada com base no Inventário de Ansiedade Traço-Estado (IDATE). A incapacidade relacionada à dor foi avaliada pelo perfil da escala de dor crônica para a população brasileira (B:PCP:S), e as medidas psicofísicas da dor foram medidas pelo QST e CPM. Resultados: Nas pacientes, a ansiedade-traço foi positivamente correlacionada com a facilitação intracortical (FIC) no baseline e após a dor evocada pelo QST (β = 0,05 e β = 0,04, respectivamente) e negativamente relacionada com o período de silêncio cortical (PSC) no baseline e após a dor evocada pelo QST (β = -1,17 e β = -1,23, respectivamente) (P <0,05 para todas as comparações). Após dor evocada pelo QST, a incapacidade relacionada à dor crônica foi positivamente correlacionada com a FIC (β = 0,02) (P <0,05). Os escores de dor durante o CPM foram positivamente correlacionados com a ansiedadetraço, quando a incapacidade relacionada à dor crônica foi igualmente alta (β = 0,39, P = 0,02). A excitabilidade cortical das controles saudáveis permaneceu inalterada após o QST. Conclusões: Estes resultados sugerem que, na SDM, o desequilíbrio entre os sistemas excitatórios e inibitórios descendentes do trato corticoespinhal está associado concomitantemente a maiores níveis de ansiedade-traço e maiores níveis de incapacidade funcional ocasionados pela dor crônica. / Background: High levels of anxiety have been associated with the intensity and pain behavior in patients with acute and chronic pain. It was observed that in subjects with myofascial pain (SDM), stress and anxiety syndrome increase the predisposition for the development of myofascial trigger points. In addition to this, there is a tendency of individuals to experience negative emotions in stressful situations (neuroticism), personality characteristic associated with trait personality that may negatively influence in the experience of pain. Individuals with higher trait anxiety are usually hypersensitive to stimuli and more psychologically reactive. It is conceivable to assume the co-existence of change in cortical excitability, chronic pain and anxiety, in these patients. To improve the understanding of the central mechanisms related to anxiety and chronic pain, we assessed cortical excitability parameters by single and paired pulse transcranial magnetic stimulation (TMS). We hypothesize that corticospinal excitability is modulated by anxiety favoring loss of descendent inhibitory influx. Objectives: This study aimed to answer three questions related to chronic myofascial pain syndrome (MPS): 1) Is the motor cortex excitability, as assessed by transcranial magnetic stimulation parameters (TMS), related to state-trait anxiety? 2) Does anxiety modulate corticospinal excitability changes after evoked pain by Quantitative Sensory Testing (QST)? 3) Does the state-trait anxiety predict the response to pain evoked by QST if simultaneously receiving a heterotopic stimulus [Conditional Pain Modulation (CPM)]? Patient and methods: We included females with chronic MPS (n=47) and healthy controls (n=11), aged from 19 to 65 years. Motor cortex excitability was assessed by TMS, and anxiety was assessed based on the State-Trait Anxiety Inventory. The disability related to pain (DRP) was assessed by the Profile of Chronic Pain scale for the Brazilian population (B:PCP:S), and the psychophysical pain measurements were measured by the QST and CPM. Results: In patients, trait-anxiety was positively correlated to intracortical facilitation (ICF) at baseline and after QST evoked pain (β= 0.05 and β= 0.04, respectively) and negatively correlated to the cortical silent period (CSP) (β= -1.17 and β= -1.23, respectively) (P <0.05 for all comparisons). After QST evoked pain, the DRP was positively correlated to ICF (β= 0.02) (P<0.05). Pain scores during CPM were positively correlated with trait-anxiety when it was concurrently with high DRP (β= 0.39; P= 0.02). Controls’cortical excitability remained unchanged after QST. Conclusions: These findings suggest that, in chronic MPS, the imbalance between excitatory and inhibitory descending systems of the corticospinal tract is associated with higher trait-anxiety concurrent with higher DRP.

Introdução: Níveis elevados de ansiedade têm sido associados com intensidade e comportamento da dor em pacientes com dores aguda e crônica. Foi observado, em indíviduos com síndrome dolorosa miofascial (SDM), que o estresse e a ansiedade aumentam a predisposição para o desenvolvimento de pontos-gatilhos miofasciais. Adicionalmente a isto, existe a tendência do indivíduo experimentar emoções negativas em situações de estresse (neuroticismo), característica de personalidade associada ao traço de personalidade, que pode influenciar negativamente na experiência de dor. Indivíduos com alta ansiedade-traço são geralmente hipersensíveis a estímulos e psicologicamente mais reativos. É concebível supôr a coexistência de alteração na excitabilidade cortical, entre dor crônica e ansiedade nestes pacientes. Para melhorar a compreensão dos mecanismos centrais relacionados à ansiedade e à dor crônica, avaliou-se os parâmetros de excitabilidade cortical, usando estimulação magnética transcraniana (EMT), pulso único e pareado. Nossa hipótese é que a excitabilidade corticoespinhal seja modulada pela ansiedade favorecendo a perda de influxo inibitório descendente. Objetivos: O presente estudo teve como objetivo responder a três perguntas relacionadas à síndrome dolorosa miofascial (SDM): 1) A excitabilidade do córtex motor está relacionada com a ansiedade-traço? 2) A ansiedade-traço modula alterações da excitabilidade corticoespinhal, após dor evocada pelo Quantitative Sensory Testing (QST)? 3) A ansiedade-traço prevê resposta à dor evocada pelo QST, se receber simultaneamente um estímulo heterotópico [Conditioned Pain Modulation (CPM)]? Pacientes e métodos: Foram incluídas mulheres com SDM (n = 47) e controles saudáveis (n = 11), com idade entre 19 e 65 anos. A excitabilidade do córtex motor foi avaliada pela EMT, e a ansiedade foi avaliada com base no Inventário de Ansiedade Traço-Estado (IDATE). A incapacidade relacionada à dor foi avaliada pelo perfil da escala de dor crônica para a população brasileira (B:PCP:S), e as medidas psicofísicas da dor foram medidas pelo QST e CPM. Resultados: Nas pacientes, a ansiedade-traço foi positivamente correlacionada com a facilitação intracortical (FIC) no baseline e após a dor evocada pelo QST (β = 0,05 e β = 0,04, respectivamente) e negativamente relacionada com o período de silêncio cortical (PSC) no baseline e após a dor evocada pelo QST (β = -1,17 e β = -1,23, respectivamente) (P <0,05 para todas as comparações). Após dor evocada pelo QST, a incapacidade relacionada à dor crônica foi positivamente correlacionada com a FIC (β = 0,02) (P <0,05). Os escores de dor durante o CPM foram positivamente correlacionados com a ansiedadetraço, quando a incapacidade relacionada à dor crônica foi igualmente alta (β = 0,39, P = 0,02). A excitabilidade cortical das controles saudáveis permaneceu inalterada após o QST. Conclusões: Estes resultados sugerem que, na SDM, o desequilíbrio entre os sistemas excitatórios e inibitórios descendentes do trato corticoespinhal está associado concomitantemente a maiores níveis de ansiedade-traço e maiores níveis de incapacidade funcional ocasionados pela dor crônica. / Background: High levels of anxiety have been associated with the intensity and pain behavior in patients with acute and chronic pain. It was observed that in subjects with myofascial pain (SDM), stress and anxiety syndrome increase the predisposition for the development of myofascial trigger points. In addition to this, there is a tendency of individuals to experience negative emotions in stressful situations (neuroticism), personality characteristic associated with trait personality that may negatively influence in the experience of pain. Individuals with higher trait anxiety are usually hypersensitive to stimuli and more psychologically reactive. It is conceivable to assume the co-existence of change in cortical excitability, chronic pain and anxiety, in these patients. To improve the understanding of the central mechanisms related to anxiety and chronic pain, we assessed cortical excitability parameters by single and paired pulse transcranial magnetic stimulation (TMS). We hypothesize that corticospinal excitability is modulated by anxiety favoring loss of descendent inhibitory influx. Objectives: This study aimed to answer three questions related to chronic myofascial pain syndrome (MPS): 1) Is the motor cortex excitability, as assessed by transcranial magnetic stimulation parameters (TMS), related to state-trait anxiety? 2) Does anxiety modulate corticospinal excitability changes after evoked pain by Quantitative Sensory Testing (QST)? 3) Does the state-trait anxiety predict the response to pain evoked by QST if simultaneously receiving a heterotopic stimulus [Conditional Pain Modulation (CPM)]? Patient and methods: We included females with chronic MPS (n=47) and healthy controls (n=11), aged from 19 to 65 years. Motor cortex excitability was assessed by TMS, and anxiety was assessed based on the State-Trait Anxiety Inventory. The disability related to pain (DRP) was assessed by the Profile of Chronic Pain scale for the Brazilian population (B:PCP:S), and the psychophysical pain measurements were measured by the QST and CPM. Results: In patients, trait-anxiety was positively correlated to intracortical facilitation (ICF) at baseline and after QST evoked pain (β= 0.05 and β= 0.04, respectively) and negatively correlated to the cortical silent period (CSP) (β= -1.17 and β= -1.23, respectively) (P <0.05 for all comparisons). After QST evoked pain, the DRP was positively correlated to ICF (β= 0.02) (P<0.05). Pain scores during CPM were positively correlated with trait-anxiety when it was concurrently with high DRP (β= 0.39; P= 0.02). Controls’cortical excitability remained unchanged after QST. Conclusions: These findings suggest that, in chronic MPS, the imbalance between excitatory and inhibitory descending systems of the corticospinal tract is associated with higher trait-anxiety concurrent with higher DRP.

This dissertation is particularly focused on a novel approach of a wirelessly powered neuromodulation system for chronic patients. The inductively coupled transmitter (TX) and receiver (RX) coils are designed through optimization to achieve maximum efficiency. A power management unit (PMU) consisting of a voltage rectifier, voltage regulator along with a stimulation circuitry is also designed to provide pulse stimulation to genetically modified neurons. For continuous health monitoring purposes, the response from the brain due to stimulation needs to be recorded and transmitted wirelessly outside the brain for analysis. A low-power high-data duty-cycled impulse-radio ultra-wideband (IR-UWB) transmitter is designed and implemented using the standard CMOS process. Another focus of this dissertation is the design of a reverse electrowetting-on-dielectric (REWOD) based energy harvesting circuit for wearable sensor applications which is capable of generating a very low-frequency signal from motion activity such a walking, running, jogging, etc. A commercial off-the-shelf (COTS) based and on-chip based energy harvesting circuit is designed for very low-frequency signals. The experimental results show promising progress towards the advancement in the wirelessly powered neuromodulation system and building the self-powered wearable sensor.

No description available.

Objectif: Cette thèse vise à étudier si l’inhibition de la douleur par l’activation de la mémoire de travail (MT) peut être rehaussée par la Stimulation Transcranienne à Courant Direct (tDCS) chez des volontaires jeunes et des personnes âgées en bonne santé. La MT permet de sélectionner l’information pertinente à une tâche et de diriger l’attention vers l’exécution de cette tâche, permettant ainsi de limiter la capture de l'attention par des distracteurs, incluant la douleur. Cependant, cette inhibition de la capture attentionnelle par la douleur puisqu’il s’agit d’un processus descendant (top-down), peut être diminuée chez les personnes âgées en raison de la réduction des capacités de la MT. La tDCS est une méthode prometteuse à cet égard puisque la stimulation anodale du cortex préfrontal dorsolatéral (DLPFC) gauche permet d’améliorer les capacités de la MT. Méthodes: Cette thèse comporte deux expériences menées sur quarante jeunes adultes (première étude) et quinze personnes âgées (deuxième étude). Les expériences comportent deux séances de tDCS (tDCS anodale et simulée), pendant lesquelles de la douleur et le réflexe nociceptif de flexion étaient évoqués par une stimulation électrique à la cheville, alors que les participants exécutaient une tâche n-back (0-back et 2-back). Le protocole expérimental comportait cinq conditions dont l'ordre a été contrebalancé (0-back, 2- back, douleur, 0-back avec douleur et 2-back avec douleur), et qui ont été réalisées deux fois chacune (avant tDCS et pendant tDCS). Résultats: Les résultats indiquent que la neuromodulation du DLPFC gauche permet d’améliorer l’inhibition de la douleur par la MT, autant chez les jeunes adultes que chez les personnes âgées. Cependant, le réflexe nociceptif de flexion n’a pas été modulé par l’activation de la MT, suggérant que les effets bénéfiques de la tDCS reposent sur des mécanismes supraspinaux indépendants des voies inhibitrices descendantes. Ces études ont permis l'avancement des connaissances sur les interactions entre la cognition, la douleur et l'âge et montrent comment la neuromodulation peut changer ces interactions pour améliorer l'inhibition de la douleur. Ces résultats permettront le développement de protocoles de neuromodulation pour la gestion de la douleur chez les personnes âgées. / Objective: This thesis aimed to examine whether pain inhibition by working memory (WM) engagement can be enhanced by Transcranial Direct Current Stimulation (tDCS) in young and older healthy volunteers. Directing attention away from painful stimuli is under the control of WM that allows the selection of task-relevant information and directing attention towards task execution. However, top-down inhibition of nociceptive activity and pain may be altered in normal aging due to decreased WM. tDCS is a promising method in this regard since anodal tDCS of the left dorsolateral prefrontal cortex (DLPFC) was shown to improve WM performance. Methods: Two experiments were conducted on forty healthy (first study) and fifteen older volunteers (second study). They participated in two tDCS sessions (sham and anodal tDCS), in which the pain was evoked by electrical stimulation at the ankle. Participants performed an n-back task (0-back and 2-back) while they received random electrical stimulation to produce pain and the nociceptive flexion reflex, an index of spinal nociception. The experimental protocol comprised five counterbalanced conditions (0-back, 2-back, pain, 0-back with pain and 2-back with pain) that were performed twice (pre-tDCS baseline and during tDCS). Results: In both studies, neuromodulation of left DLPFC enhanced pain inhibition by WM. However, the nociceptive flexion reflex was not modulated by WM enhancement suggesting that improvement of pain inhibition by WM using tDCS is supraspinal and independent of descending inhibitory pathways. These studies improve our understanding of the interactions between cognition, pain and age and show how neuromodulation may change these interactions to improve pain inhibition. Findings support the development of neuromodulation protocols for pain management in older persons.

No description available.

No description available.

No description available.

Die Alkoholsucht ist ein global verbreitetes Phänomen und kennzeichnet sich durch eine Transition von kontrolliertem zu zwanghaftem Alkoholkonsum.Die Tendenz, einem neutralen Reiz eine Anreizwirkung zuzuschreiben, ist individuell unterschiedlich und stellt einen Risikofaktor für die Entwicklung einer Abhängigkeit dar.Zur Entwicklung spezifischer Präventionsstrategien ist ein besseres Verständnis der Zusammenhänge zwischen der Anreizsalienz und Alkoholabhängigkeit erforderlich.Der Übergang von mäßigem zu zwanghaftem Alkoholkonsum wurde durch das Modell des Alkoholentzugseffekts simuliert, das den menschlichen Alkoholrückfall nachahmt.Die Ratten erhielten freiwilligen Zugang zu verschieden Alkohollösungen mit wiederholten Deprivations- und Alkoholphasen.Die Ratten durchliefen zusätzlich den Pavlovian Conditioned Approach getestet, welcher die individuellen Tendenzen auf einen bedingten Reiz/Belohnung quantifiziert.Während des letzten ADE-Zyklus wurde mit Geschmacksverfälschung zwanghaftes Trinken ermittelt.Nach der Identifizierung zuverlässiger Prädiktoren für Suchtverhalten wurde präventive Neurostimulation durchgeführt, um die Tendenz der Tiere alkoholbezogenen Reizen eine motivationale Bedeutung beizumessen, zu beeinflussen, und die Manifestation eines Abhängigkeitsverhaltens zu verhindern. Weibchen tranken mehr Alkohol als Männchen und zeigten ST Verhalten im PavCA, während Männchen GT aufwiesen.Die Anwendung von transkranieller Gleichstromstimulation während PavCA führte zu mehr GT-Verhalten bei stimulierten Ratten.Frühe tDCS während des Trinkens hatte keinen Einfluss auf das akute und das Langzeit-Trinken. Die Ergebnisse zeigen eine komplexere Beziehung zwischen Anreizsalienz und Alkoholsucht und unterstreichen,individuelle Unterschiede und beide Geschlechter in der präklinischen Forschung zu berücksichtigen. / The consequences of alcohol dependence cause the global deaths of million people yearly.The ability of the environment can trigger dependent behavior and promote drinking.The tendency to attribute incentive salience to cues differs between subjects.By forming a cue-alcohol association, neutral cues receive motivational value,thereby predicting the likelihood of alcohol reward occurrence,known as Pavlovian learning.Understanding the relationship between incentive salience and alcohol addiction help inform treatment strategies.We study the relationship between incentive salience and alcohol addiction.The transition from moderate to compulsive alcohol intake can be captured by the alcohol deprivation effect rat model (mimics alcohol relapse in humans).Rats were given voluntary access to alcohol solutions with repeated abstinence/reintroduction phases.Further,rats were tested in the PavCA,which quantifies individual tendency toward a conditional cue and the reward, thus allowing to trace the process of attributing incentive salience to rewardcues.During the final ADE cycle,rats underwent a bitter taste adulteration test to assess for compulsive-like behavior.After identifying reliable predictors of addictive behavior,preventive tDCS was performed to influence the tendency of animals to attach motivational importance to alcohol-related stimuli,and to prevent the manifestation of alcohol addictive behavior.Females drank more alcohol than males and exhibited more ST behavior in the PavCA, whereas males showed GT behavior.PavCA phenotypes emerged early and remained stable.The application of tDCS during PavCA results in high GT numbers in stimulated rats.Early tDCS on drinking does not affect acute or long-term drinking.Our findings indicate a complex relationship between incentive salience and alcohol addiction and emphasize the importance of considering individual differences and both sexes in preclinical research.