A ouabaína (OUA), um inibidor da Na+ ,K+-ATPase, foi identificada como uma substância endógena presente no plasma humano, e parece estar envolvida na resposta ao estresse agudo, em animais e seres humanos. O estresse crônico é um importante fator agravante de doenças psiquiátricas, incluindo depressão e ansiedade. Além disso, problemas cognitivos são cada vez mais reconhecidos como importantes componentes da ansiedade e depressão. Diante disto, o presente trabalho buscou investigar os efeitos da OUA (1,8 <font face = \"symbol\">mg/kg) na hiperatividade do eixo HPA, na neuroinflamação, na expressão de receptores e proteínas envolvidos na plasticidade sináptica, nos efeitos comportamentais (como déficit de memória de longa duração, depressão e ansiedade) e atividade da Na+,K+-ATPase induzidos pelo protocolo de estresse crônico imprevisível (CUS) realizado ao longo de 14 dias em ratos. Nossos resultados demonstraram que o tratamento intermitente com OUA é capaz de reverter a hiperatividade do eixo HPA induzido pelo CUS, por meio da redução de glicocorticoide, redução na expressão de CRH-CRHR1, bem como diminuir a neuroinflamação, e aumentar os níveis de BDNF e fazer o que na expressão dos receptores CRHR2. Essas alterações bioquímicas contribuíram para uma reversão nos prejuízos na memória de longo prazo induzida pelo CUS. Ademais os animais tratados apenas com OUA, bem como os submetidos ao CUS e tratados com OUA obtiveram uma melhora na memória emocional, averiguada no teste comportamental de condicionamento da memória ao medo. Os resultados encontrados sugerem que o protocolo de CUS por 14 dias promove uma adaptação neuronal facilitando a redesignação da memória ao medo, aqui configurado pelo choque, e o tratamento com a OUA abrevia esse processo. Em conclusão os nossos resultados sugerem que o tratamento intermitente com OUA suscita uma adaptação no eixo HPA, por meio de alterações na expressão dos receptores para CRH no hipocampo e hipotálamo, resultando em uma adaptação na memória emocional relacionada ao medo. / Ouabain (OUA), an inhibitor of Na+, K+ -ATPase, has been identified as an endogenous substance present in human plasma, and appears to be involved in the response to acute stress in animals and humans. Chronic stress is an important aggravating factor of psychiatric illness, including depression and anxiety. In addition, cognitive problems are increasingly recognized as important components of anxiety and depression. The present work aimed to investigate the effects of OUA (1.8 <font face = \"symbol\">mg/kg) on HPA axis hyperactivity, neuroinflammation, expression of receptors and proteins involved in synaptic plasticity, behavioral effects (such as long-term memory deficit duration, depression and anxiety) and Na+,K+-ATPase activity induced by the unpredictable chronic stress protocol (CUS) performed over 14 days in rats. Our results demonstrated that intermittent treatment with OUA was able of reversing CUS-induced HPA axis hyperactivity, by reducing glucocorticoid levels, CRH-CRHR1 expression, as well as reducing CUS-induced low-grade neuroinflammation, and increase BDNF levels and expression of CRHR2 receptors. These biochemical changes contributed to a reversal in CUS-induced long-term memory impairment. In addition, animals treated only with OUA, as well as those submitted to CUS, and also treated with OUA obtained an improvement in emotional memory, which was explored in the fear conditioning test. These results suggest that the CUS protocol of 14 days promotes a neural adaptation facilitating a reassignment of the memory to the fear, here configured by the shock, and the treatment with the OUA shortens that process. In conclusion, our results suggest that intermittent treatment with OUA induces an adaptation on the HPA axis, through alterations in the expression of receptors for CRH in the hippocampus and hypothalamus, resulting in an adjustment in fear-related emotional memory.

Lactato é o produto da redução do piruvato, reação fundamental para controle intracelular do pH e o estado redox da célula em que é produzido. Na corrente sanguínea, ele se difunde aos tecidos que expressam MCTs e é consumido como um importante substrato energético. No mestrado, observamos que o lactato promove elevação da síntese/secreção do GH. E nesse sentido, pretendemos identificar os potenciais hormônios hipotalâmicos que estariam implicados nessa regulação, bem como na sua possível mecanismo de ação direta sobre as células hipofisárias. Nossos resultados mostram que o lactato aumenta a atividade de neurônios em diferentes regiões hipotalâmicas, regulando a expressão gênica e proteica de Ghrh e Somatostatina (SST). Ainda, observamos que o mesmo promove regulações pós transcricionais sobre o mRNA de Gh, aumentando a sua cauda poli(A), o que pode refletir no aumento da estabilidade do transcrito. Nos experimentos com camundongos Lit/ Lit, observamos a importância de um tônus estimulatório do GHRH para a estimulação da expressão de GH. Em experimentos com camundongos KO MCT1+/- identificamos que o lactato é uma parte fundamental para o exercício ativar o eixo somatotrófico. Ainda, caracterizamos que as células GH3 apresentam a expressão do mRNA do receptor de lactato (Gpcr 81) e de 3 diferentes isoformas de transportadores de lactato (Mct1, 3, 4). Além disso, na mesma cultura celular observamos a elevação do conteúdo intra e extracelular de GH, bem como no aumento da concentração intracelular de Ca++ que explicaria a maior secreção do GH e que quando inibimos os MCTs, seu efeito sobre o aumento do mRNA de Gh não é mais reproduzido. Assim, nosso trabalho mostra diferentes abordagens experimentais que convergem para ações diretas do lactato via transportadores membrânicos sobre o aumento da atividade de somatotrofos, bem como o aumento da atividade do eixo somatotrófico em diferentes níveis do eixo. / Lactate is the product of pyruvate reduction, a fundamental reaction for intracellular pH control and the redox state of the cell in which it is produced. In the bloodstream, it diffuses into tissues expressing MCTs and is consumed as an important energy substrate. In the master\'s degree, we observed that lactate promotes elevation of GH synthesis / secretion. In this sense, we intend to identify the potential hypothalamic hormones that would be involved in this regulation, as well as in its possible mechanism of direct action on the pituitary cells. Our results show that lactate increases the activity of neurons in different hypothalamic regions, regulating the gene and protein expression of Ghrh and Somatostatin (SST). Furthermore, we observed that it promotes post-transcriptional regulation of the Gh mRNA, increasing its poly(A) tail length, which may reflect the increase in transcript stability. In experiments with Lit/ Lit mice, we observed the importance of stimulating GHRH tone for the stimulation of GH expression. In experiments with MCT1+/- KO mice we identified that lactate is a key part of exercise to activate the somatotrophic axis. Furthermore, we characterized that GH3 cells show lactate receptor mRNA expression (Gpcr 81) and 3 different isoforms of lactate transporters (Mct 1, 3, 4). In addition, in the same cell culture we observed the elevation of the intra and extracellular content of GH, as well as the increase of intracellular concentration of Ca++ that would explain the higher secretion of GH and that when we inhibited the MCTs, its effect on the increase of the Gh mRNA is no longer reproduced. Thus, our work shows direct lactate actions, via membrane transporters, on the increment of somatotrophic axis activity by different experimental approaches.

A partir do entendimento de que as transformações do espaço compõem um movimento único e totalizante, buscamos problematizar a questão na composição das transformações que se sucedem em Sorocaba. O recorte do Eixo Sudeste nos serve como base empírica da sustentação de nossa problemática. As transformações do espaço urbano deste Município estão diretamente ligadas aos interesses de diversas escalas e níveis da realidade. Para isto, a compreensão histórica da materialização deste setor do espaço urbano, assim como sua identidade no território sorocabano nos aproxima do movimento social em suas diversas instâncias, desta forma, exploramos a possibilidade da realização de um exercício teórico de aproximar as transformações no espaço urbano de Sorocaba à reprodução da sociedade como todo. / From the understanding that the transformations of space make up a unique and totalizing movement, we try to problematize this question in the composition of the transformations that succeed in Sorocaba. The cutting of the Southeast Hub serves as an empirical basis for sustaining our problematic. The transformations of the urban space of this Municipality are directly linked to interests of different scales and levels of reality. For this, the historical understanding of the materialization of this urban space industry, as well as its identity in Sorocaba territory approaches in the social movement in its various instances, therefore we explored the possibility of carrying out a theoretical exercise to bring the changes in the urban space Sorocaba to the reproduction of society as a whole.

Made available in DSpace on 2016-08-10T10:50:51Z (GMT). No. of bitstreams: 1 MARCOS BITTAR HADDAD.pdf: 8678763 bytes, checksum: dab73fe4557f6485149862aeba1ac89a (MD5) Previous issue date: 2011-04-11 / The paper aims to presenting an enough theoretical to explain the dynamics occurring in the region. For this purpose, it discusses about the concept of region and regional development. It revisits the classic theories regarding the location and agglomeration factors on recent regional economy production. At the end of the first chapter it weaves an explanation about the using of the Development Axis conception resuming the classic scientific literature. It deals with the federal government planning and the historical structuring of Goiânia-Anápolis-Brasília Axis, emphasizing the particular characteristics of each one of them. After, it examines the federal government regional planning as well as major problems resulting from its implementation. Notes that there was a gradual interruption from federal government planning for the Axis and that, only at present, there is a return to this planning. It indicates that the rupture was mentioned harmful in terms of economy and demographics for the Axis. And that the proposals in the political context of the New Republic have not been implemented or have become insufficient to promote regional development. At the end of the third chapter it deals with the proposals of the PAC considering the necessity of this project to ensure social and economic dynamics of the Goiânia- Anapolis-Brasilia Axis. / O trabalho faz um recorte teórico para explicar o dinamismo ocorrido na região. Para tanto, retoma discussões acerca dos conceitos de região e de desenvolvimento regional. Ainda, revisita teorias clássicas de localização, fatores de aglomeração e a produção recente sobre economia regional. No fim do primeiro capítulo, tece uma justificativa da utilização do conceito de Eixo de Desenvolvimento retomando a literatura cientifica clássica. Aborda o planejamento federal e a estruturação histórica do Eixo Goiânia- Anápolis-Brasília, dando ênfase para as características particulares de cada município. Em seguida, analisa o planejamento federal para a região, bem como os principais problemas decorrentes de sua implementação. Constata que houve interrupção gradual no planejamento estatal para o Eixo e que, somente na atualidade, ocorre a retomada no planejamento federal. Aponta que a mencionada ruptura foi prejudicial em termos econômicos e demográficos para o Eixo e que as propostas, no contexto político da Nova República, não foram implementadas ou tornaram-se insuficientes para alavancar o desenvolvimento regional. No final do terceiro capítulo, alinha as propostas do PAC e considera o projeto necessário para assegurar a dinâmica socioeconômica do Eixo Goiânia - Anápolis Brasília.

Há evidencias de interação bidirecional dos eixos HPA e HPG envolvendo diferentes estruturas, entretanto, os mecanismos envolvidos são pouco compreendidos. Situações de estresse podem alterar a função reprodutiva, e hormônios gonadais podem modificar a resposta de estresse. O objetivo deste trabalho foi verificar se estrógeno (E 2) e progesterona (P4) modificam a atividade basal do eixo hipotálamo-hipófise-adrenal (HPA), analisada pelas secreções de corticosterona (CORT) e de P4 e pelas expressões de receptores para corticosteróides (mineralocorticóides, MR e glicocorticóides, GR) em sítios cerebrais de retroalimentação do eixo HPA. Ratas Wistar adultas foram mantidas em ciclo claro-escuro de 12h e acesso livre à ração e água. O ciclo estral foi monitorado por esfregaço vaginal e a determinação da secreção de hormônio luteinizante (LH) foi realizada para confirmação do proestro. Seis amostras de sangue foram coletadas através de cateter na jugular, durante a tarde (13-18h), dos seguintes grupos de ratas: ovariectomizadas (OVX); controles em proestro; tratadas com antagonista de E 2 (tamoxifen) ou de P4 (RU486), ou ambos; tratadas com os respectivos veículos dos antagonistas. O plasma foi separado e estocado para dosagens hormonais por radioimunoensaio. Após a última coleta de sangue, os animais foram anestesiados e perfundidos para remoção dos cérebros, que foram manipulados para verificação por imunofluorescência, da expressão de MR e de GR na região CA1 e no subículo do hipocampo ventral, e de GR no núcleo paraventricular (PVN). Os resultados mostram que: a secreção de LH confirmou a fase de proestro; a secreção basal de CORT não foi alterada pelas manipulações de injeções nem pela remoção dos ovários; ocorreu pico de secreção de CORT e de P 4 às 14h em todos os grupos experimentais; os antagonistas de E 2 e de P 4 não alteraram a secreção total de CORT, porém o RU486 aumentou (às 13 e 15h) e o tamoxifen reduziu (às 15h) a concentração de CORT; um segundo pico de secreção de P 4 no final da tarde (17-18h) foi bloqueado pela ovariectomia e por Tamoxifen , e amplificado por RU486; o segundo pico de P 4 também não ocorreu em ratas tratadas com Tamoxifen e RU486 ; não houve alteração do número de neurônios com expressão de GR e MR na região CA 1 e no subículo do hipocampo ventral nem de GR no PVN. Em conclusão, nossos resultados indicam que: E2 e P 4 podem exercer efeitos antagônicos sobre a secreção basal de CORT, respectivamente estimulatório e inibitório; os picos de secreção de P 4 têm origens diferentes, o primeiro (14h) da adrenal e o segundo (17-18h) do ovário; E 2 estimula a secreção ovariana de P 4 na tarde de proestro; E2 e P 4 não alteram o número de neurônios que expressam GR e MR em sítios de retroalimentação do eixo HPA, mas não se pode descartar que alterem a atividade desses neurônios. / There is evidence for a bidirectional communication between HPA and HPG axis involving different structures, however the involved mechanisms are poorly known. Stress situations may alter the reproductive function, and gonadal steroids may modify the stress response. The aim of this study was verify if estrogen (E 2) and progesterone (P 4 ) can alter the basal activity of hypothalamic-pituitary-adrenal axis, analyzed by corticosterone (CORT) and P 4 secretions and by mineralocorticoid and glicocorticoid receptors (MR and GR, respectively) expression at HPA axis central feedback sites. Adult female Wistar rats were kept in 12h light-dark cycle and had free access to food and water. The estrous cycle was monitored by vaginal smears and the luteinizing hormone dosage was done to confirm proestrus. Six samples of blood were collected by jugular cannula, during the afternoon (13-18h), of the following groups: ovariectomized (OVX), proestrus controls, treated with E 2 or P 4 antagonists (tamoxifen or RU486, respectively), or with both, and treated with antagonists vehicle. The plasm was stored for hormonal dosages by radioimmunoassay. After the last blood sample, animals were anesthetized, perfused, and the brains were removed and processed for immunofluorescence to analyze MR and GR expression at ventral hippocampus CA 1 and subiculum, and GR expression at paraventricular nucleus (PVN). The results showed that: LH secretion confirmed the proestrus; CORT basal secretion was not altered by injections neither by ovariectomy; there was a CORT and a P4 secretion peak at 14h in all experimental groups, E 2 and P 4 antagonists did not modify the CORT total secretion, however RU486 increased (at 13 and 15h) and tamoxifen reduced (at 15h) CORT levels, another P4 secretion peak in the late afternoon (17-18h) was blocked by ovariectomy and tamoxifen, but enhanced by RU486, the P 4 second peak did not occur in rats treated with both tamoxifen and RU486, there were no changes in the number of neurons expressing GR and MR at ventral hippocampus CA 1 and subiculum neither of GR expressing neurons at PVN. In conclusion, our results indicate that: E2 and P 4 can have antagonistic effects over basal CORT secretion; stimulatory and inhibitory, respectively; the P 4 secretion peaks have different origins, the first (14h) is adrenals and the second (17-18h) is ovarian: E2 stimulates ovarian P 4 secretion in the proestrus afternoon; E 2 and P 4 do not alter the number of neurons that express MR and GR at HPA axis feedback sites, but one can not exclude the possibility that they alter the activity of these neurons.

Ethanol exposure during pregnancy is one of the leading causes of preventable birth defects, leading to a range of symptoms collectively known as fetal alcohol spectrum disorder (FASD). More moderate levels of prenatal ethanol exposure (PNE) lead to a range of behavioural deficits including aggression, poor social interaction, poor cognitive performance and increased likelihood of addiction in later life. Current theories suggest that adaptation in the hypothalamic-pituitaryadrenal (HPA) axis and neuroendocrine systems contributes to mood alterations underlying behavioural deficits and vulnerability to addiction. This has led to the suggestion that corticotrophin-releasing factor (CRF) antagonists and glucocorticoid (steroid) inhibitors may be potential therapeutics to address the deficits of PNE and for the treatment of addiction. The zebrafish (Danio rerio) has several advantages over mammalian models, such as low cost of maintenance, short life cycle, easy embryological manipulation and the possibility of large-scale genetic screening. By using this model, our aim is to determine whether developmental ethanol exposure provokes changes in the HPA axis (HPI axis in fish), as it does in mammalian models, therefore opening the possibilities of using zebrafish to elucidate the mechanisms involved, and to test novel therapeutics to alleviate deleterious symptoms. Thus this thesis focuses solely on the effect of developmental ethanol exposure on the functioning of the HPI axis in zebrafish. Stress-reactivity in zebrafish larvae ethanol-treated 1-9 days post 4 fertilisation (dpf) was assessed using thigmotaxis and thigmotaxis following airstress. In both tests, lower stress-related responses were obtained with ethanol treated animals, in that they spent less time at the edges of the apparatus (P<0.01, n=3). They also showed lower total body cortisol (P=0.04, n=14). Larvae also showed the same behaviour pattern two weeks after ethanol exposure, (23dpf) (P=0.04, n=3), again with reduced total cortisol (P=0.03, n=4). HPI-related gene transcription was also assessed in 9dpf ethanol treated zebrafish larvae, by qRT-PCR. Revealing up-regulation of CRH, CRHBP and CRHR2, normalized against β-Actin, Elav1 and Gap43 housekeeping genes. In situ hybridization revealed no spatial changes in CRH, CRH-BP and POMC with animals at the same stage. Behavioural stress-reactivity differences in 6-months old adults that had been exposed developmentally to ethanol were assessed using novel tank diving and thigmotaxis. Both assays indicated a decrease in stress-like behaviour due to early ethanol exposure compared to controls (P<0.05, n=5 both). Finally, cortisol levels were assayed from 9dpf larvae and 6-month-old adults that had been treated with ethanol during early development showed a significant reduction in cortisol output when air-exposed stressed compared to controls (P=0.04, n=5). Conclusion: Early ethanol exposure produced significant changes in cortisol, HPI gene mRNA expression and stress-reactive behaviour in 9dpf animals. Changes in cortisol and behaviour were still detected in 6-months old adults, developmentally treated with ethanol, indicating that early ethanol exposure has permanent effects on the HPI axis. 5 As our data contradicts the findings in mammalian literature where early ethanol exposure increases stress-like behaviour in later life, it is also possible that more permanent effects of PNE in mammals may arise through maternal-offspring interactions, during and post gestation, such as breastfeeding and maternal grooming of the offspring, which are absent in the zebrafish model.

O presente trabalho apresenta um estudo numérico e experimental sobre o desempenho aerodinâmico de turbinas eólicas de eixo vertical envolvendo rotores Savonius convencional de duplo-estágio e helicoidal. O estudo experimental é realizado no Túnel Aerodinâmico Professor Debi Pada Sadhu, do Laboratório de Mecânica dos Fluidos da UFRGS. As simulações numéricas são realizadas com o software Fluent/ANSYS utilizando o Método dos Volumes Finitos. São comparados os coeficientes de torque estático e dinâmico, o coeficiente de potência, além de uma análise aerodinâmica das duas turbinas. As medições são realizadas empregando Tubos de Pitot, um torquímetro estático digital e um torquímetro simples construído para a medição do torque dinâmico. As turbinas são fabricadas através da técnica de prototipagem 3D, com uma semelhança de dimensões e parâmetros. As soluções numéricas são resolvidas através da equação da continuidade, das equações de Navier-Stokes com médias de Reynolds (RANS) e pelo modelo de turbulência k-ω SST. A qualidade da malha utilizada é avaliada através do método de Índice de Convergência de Malha (GCI), para três diferentes tamanhos de malha. São feitas análises dos rotores na forma estática para diferentes ângulos de incidência e com a turbina em rotação são feitas análises para diferentes razões de velocidades de ponta de pá (λ). Resultados demonstram que a turbina helicoidal apresenta um coeficiente de torque positivo para todos os ângulos do rotor, assim como a turbina convencional de dois estágios. O coeficiente de torque dinâmico da turbina helicoidal é superior ao da turbina de duplo-estágio para a maioria dos casos, e também apresenta menor oscilação de torque ao longo de cada rotação. Por consequência, o coeficiente de potência do rotor helicoidal também se tornou superior, com um valor máximo encontrado na ordem de 11,8% para um λ de 0,65 no caso experimental, e de 8,4% para o mesmo λ no caso numérico, quando comparado com o rotor de duplo-estágio. Os erros relativos entre as simulações numéricas e os resultados experimentais estão entre 2,16% e 13,4%. Uma estimativa de potência gerada é feita para ambos os casos, para uma razão de velocidade de ponta de 0,65, onde a turbina helicoidal apresenta melhores resultados em relação ao rotor de duplo-estágio, na ordem de 13,6% para uma velocidade de 10,4 m/s. / This paper presents a numerical and experimental study of vertical axis wind turbine performance comparison involving two-stage and helical Savonius rotors. The experimental study is conducted in the Aerodynamic Tunnel Professor Debi Pada Sadhu at the Fluid Mechanics Laboratory of the UFRGS. The numerical simulations are performed with the Fluent/ANSYS software using the Finite Volumes Method. The static and dynamic torque coefficients, the power coefficients, and an aerodynamic analysis of the two turbines are compared. Measurements are made using Pitot tubes, a digital static torque wrench and a simple wrench constructed for the dynamic torque measurement. The aerodynamics rotors are manufactured by 3D prototyping technique with similar dimensions and parameters. Numerical solutions are solved by the continuity equation, the Reynolds Averaged Navier-Stokes (RANS) equations and the turbulence model k-ω SST. The quality of the mesh used is evaluated used the Grid Convergence Index (GCI) method, for three different mesh sizes. The rotors analyzes are made in static form for different angles of incidence and for the rotating turbine analyzes are made for differents tip speed ratio (λ). Results show that the helical turbine has a positive static torque coefficient for any rotor angles, as well as conventional two-stage turbine. The dynamic torque coefficient of the helical turbine is higher than the two-stage turbine for most cases and also shows less torque variation along each rotation. Consequently, the power coefficient of the helical rotor also become higher, with a maximum value found on the order of 11.8% for a λ of 0.65 in the experimental case, and 8.4% for the same λ number when compared with the two-stage rotor. The relative errors between the numerical simulations and the experimental results are between 2.16% and 13.4%. A generated power estimate is made for both cases, for a tip speed ratio of 0.65, where the helical turbine provides better results compared to two-stage rotor in order of 13.6% for a velocity of 10.4 m/s.

Introdução: o estresse psicológico aumenta a permeabilidade intestinal em roedores e humanos, potencialmente levando a inflamação de baixo grau e aos sintomas em distúrbios gastrintestinais funcionais. No entanto, o efeito do estresse agudo combinado ao estresse da vida crônica, que mimetiza potencialmente melhor a situação humana, é desconhecido. Além disso, há poucos dados disponíveis sobre os efeitos do estresse em intestino delgado versus cólon. Métodos: ratos Wistar foram alocados em quatro protocolos de estresse: 1/ controles; 2/ estresse agudo (isolamento e movimentos limitados); 3/ Crowding stress:crônico e 4/ estresse agudo + estresse crônico. Amostras de jejuno e cólon foram colhidas para estudar a permeabilidade em câmaras deUssing, a expressão gênica de moléculas de junção firmes e a densidade de mastócitos. Níveis de corticosterona no plasma foram medidos. Principais resultados:corticosterona plasmática foi avaliada nas três condições de estresse, teve níveis mais altos na condição de estresse combinado. Permeabilidade do jejuno foi aumentada em todas as condições de estresse e correlacionada com os níveis de corticosterona. O aumento da expressão das claudinas 1, 5 e 8, daocludina e da ZO-1 foi detectado no estado de estresse agudo no jejuno. Em contraste, a permeabilidade do cólon foi aumentada no protocolo de estresse combinado, e a expressão de moléculas das junção firmes permaneceu inalterada. O aumento da densidade de mastócitos foi observado no cólon nos ratos submetidos aos estresses crônico e combinado. Conclusão e inferências:os estresses agudo, crônico e combinado influenciam diferentemente a permeabilidade intestinal, a expressão de moléculas de junção firmes e a atividade dos mastócitos, no jejuno e no cólon. Estes resultados fornecem uma visão mais aprofundada dos mecanismos de hiperpermeabilidade intestinal relacionadas ao estresse. / Background: Psychological stress increases intestinal permeability in rodents and humans, potentially leading to low-grade inflammation and symptoms in functional gastrointestinal disorders through disturbances in brain-gut axis. However, the effect of acute stress on the background of Crhonic life stress, potentially better approaching the human situation, is unknown. Moreover, only limited information is available on the effects in small intestine versus colon in animal model. Methods: Wistar rats were allocated to 4 stress protocols: 1/ sham; 2/ acute stress (isolation and limited movement); 3/ Crhonic crowding stress and 4/ acute + Crhonic stress (n = 8 per group). Jejunum and colon were harvested to study permeability in Ussing chambers, gene expression of tight junction molecules and mast cell density. Plasma corticosterone levels were measured. Key Results: Plasma corticosterone was elevated in all three stress conditions, with the highest levels in the combined stress condition. Permeability of the jejunum was increased in all stress conditions and correlated with corticosterone levels. Increased expression of claudin 1, 5 and 8, occludin and ZO-1 was detected in the acute stress condition in the jejunum. In contrast, colonic permeability was increased in the acute on Crhonic stress protocol only and the expression of tight junction molecules was unaltered. Increased mast cell density was observed in the Crhonic and acute on Crhonic stress condition in the colon only. Conclusion and Inferences: Acute, Crhonic and combined stress differentially affect intestinal permeability, expression of tight junction molecules and mast cells in the jejunum and the colon. These findings provide further insight in the mechanisms of stress-related intestinal hyperpermeability and barrier.

Le développement des anticorps monoclonaux thérapeutiques est en plein essor notamment à cause de leur bénéfice important pour le traitement des cancers. Cependant, à l’heure actuelle, aucun anticorps monoclonal sur le marché ou en phase III ne cible de RCPGs, en dépit de l’implication grandissante de ces récepteurs dans la carcinogenèse. Parmi les RCPGs les plus pertinents pour l’oncologie, souvent cités dans la littérature et dont certains inhibiteurs chimiques sont en phase clinique avancée, on trouve les deux sous-types de récepteurs des endothélines ETAR et ETBR. Dans ce contexte, mon projet de thèse a consisté à produire des anticorps monoclonaux capables de lier spécifiquement les récepteurs des endothélines, puis à les caractériser dans le but d’évaluer leur potentiel antitumoral. Grâce à une stratégie d’immunisation génique, un ensemble de 27 anticorps monoclonaux, tous spécifiques de la forme native d’ETBR, a été obtenu. Un de ces anticorps, nommé rendomab-B1, a fait l’objet d’une caractérisation précise et s’est révélé être un puissant inhibiteur allostérique d’ETBR. De plus, cette propriété antagoniste a permis de bloquer l’action autocrine antiapoptotique de l’ET-1 sur des cellules endothéliales vasculaires, suggérant ainsi que le rendomab-B1 pourrait être utilisé comme agent thérapeutique afin d’inhiber les effets tumorigènes liés à la suractivation de l’axe ET1/ETBR au niveau de l’endothélium vasculaire tumoral. Par ailleurs, le rendomab-B1 a également été testé sur des lignées de mélanomes humains ; l’absence de fixation de l’anticorps malgré la présence de récepteurs ETB fonctionnels à la surface de ces cellules suggère l’existence d’une forme moléculaire atypique du récepteur, potentiellement spécifique aux mélanomes. A la lumière de ces résultats, le rendomab-B1 apparaît comme un outil prometteur, à la fois pour l’étude structurale et fonctionnelle d’ETBR, mais aussi pour une éventuelle thérapie anticancéreuse. Enfin, les 26 autres anticorps monoclonaux anti-ETBR, actuellement en cours de caractérisation, constituent également des molécules potentiellement intéressantes pour un usage fondamental ou thérapeutique impliquant ETBR. Pour conclure, ces travaux ont démontré l’intérêt de la méthode d’immunisation génique pour la production d’anticorps monoclonaux anti-RCPGs à visée thérapeutique. / For a decade, monoclonal antibodies have become increasingly important for the biotherapeutic management of cancer. However, none of the monoclonal antibodies currently on the market or in late stage clinical trial do target a G-protein coupled receptor in spite of the emerging role of these receptors in tumor progression. Among the therapeutically relevant GPCRs for oncology, the endothelin receptors (ETAR and ETBR) are particularly attractive considering their overexpression in a wide range of tumors and their involvement in various stages of tumorigenesis. In this context, my PhD project consisted in producing and characterizing monoclonal antibodies directed against endothelin receptors with a view to use them as anti-tumor agents. Using an original DNA immunization strategy, we produced a panel of 27 monoclonal antibodies which selectively recognized ETBR expressed at the surface of transfected cells. One of these antibodies, named rendomab-B1, was extensively characterized and proved to be a potent allosteric antagonist of ETBR. Moreover, rendomab-B1 was able to disrupt the autocrine ET1-mediated survival loop on vascular endothelial cells, suggesting that this antibody could be used to prevent the pro-tumorigenic effect due to ET-1 and ETBR upregulation in the tumor-surrounding endothelium. Furthermore, rendomab-B1 binding onto ETBR was also assessed on melanoma cell lines and revealed that a tumor-specific form of ETBR may exist, as illustrated by the poor fixation of rendomab-B1 on these cells in spite of the presence of functional ETB receptors. Together, these results present rendomab-B1 as promising agent, not only for the structural and functional study of ETBR, but also for its therapeutic modulation in the case of cancer for instance. Finally, the other 26 monoclonal antibodies, whose characterization is still ongoing, also constitute potential tools for fundamental or therapeutic applications involving ETBR. To conclude, this work has highlighted the relevance of the DNA immunization approach to generate monoclonal antibodies against the native form of GPCRs.

Il est admis que l’axe endothéline (endothélines ET-1, -2 et -3 et leurs RCPG ETAR et ETBR), participe à la progression tumorale. Alors qu’ETAR est par exemple surexprimé dans le cancer de l’ovaire, ETBR l’est dans le mélanome. Cette surexpression, ainsi que l’implication d’ETA/BR dans la carcinogenèse, font de ces RCPG une cible tumorale pertinente. En raison de leurs forte spécificité, actions cytotoxiques variées, possibilités de couplage, les anticorps monoclonaux (AcM) sont des outils de choix en diagnostic et thérapie anti-cancéreuse. Cependant, on déplore actuellement l’absence d’AcM ciblant des RCPG sur le marché. Par une technique d’immunisation génique, 4 AcM anti-ETAR et 24 anti-ETBR ont été produits. Les résultats préliminaires obtenus avec les anti-ETAR sont prometteurs puisque ces AcM lient avec une haute affinité ETAR surexprimé dans des cellules CHO, l’un d’eux inhibant fortement la liaison du ligand. Mon travail de thèse s’est cependant concentré sur la caractérisation d’un anti-ETBR. Cet AcM reconnaît de façon spécifique et avec une forte affinité la conformation native d’ETBR surexprimé à la surface de cellules de mélanomes, suggérant l’existence d’une forme tumorale du récepteur. Suite à sa liaison aux cellules UACC-257 (lignée de mélanome), l’AcM se trouve internalisé. Dans ces cellules, malgré son incapacité à inhiber la liaison de l’ET, cet AcM inhibe l’activation de la voie PLC induite par le ligand et est également un fort inhibiteur de la migration due à l’activation de l’axe endothéline. Ces travaux soulignent l’intérêt de cet AcM comme outil diagnostique et thérapeutique dans le cas du mélanome. / It has been admitted that endothelin axis (endothelins ET-1, -2 and -3 and related GPCRs ETAR and ETBR) is involved in tumor progression. For instance, while ETAR is overexpressed in ovarian cancer, ETBR is in melanoma. This overexpression, as well as ETA/BR involvement in carcinogenesis, make these GPCRs a relevant tumor target. Because of their high specificity, various cytotoxic actions, possibilities of coupling, the monoclonal antibodies (mAbs) are useful tools in diagnosis and anti-cancer therapy. However, the absence of mAbs targeting GPCRs on the market is regrettable. Thanks to DNA immunization, 4 anti-ETAR mAbs and 24 anti-ETBR mAbs were produced. Preliminary results obtained with anti-ETAR are promising since these mAbs bind ETAR overexpressed in CHO cells with high affinity, one of them being a potent inhibitor of ligand binding. However, the aim of my PhD research works focused on the characterization of one anti-ETBR. This mAb specifically recognizes with high affinity the native conformation of ETBR overexpressed on the surface of melanoma cells, suggesting the existence of a tumor-specific receptor. Following its binding on UACC-257 cells (melanoma cell line), the mAb is internalized. In these cells, despite its inability to inhibit ET binding, this mAb is able to inhibit the ligand-induced activation of PLC pathway and display a potent inhibition of endothelin axis-induced migration. This work highlights the interest of this mAb as a tool for diagnosis and therapy in melanoma.