Submitted by Luciana Ferreira (lucgeral@gmail.com) on 2017-07-25T11:03:30Z No. of bitstreams: 2 Dissertação - Isis Gabrielli Barbieri de Oliveira - 2017.pdf: 1486050 bytes, checksum: fcc7f785120d547ad310a16b98732ea1 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2017-07-25T11:04:15Z (GMT) No. of bitstreams: 2 Dissertação - Isis Gabrielli Barbieri de Oliveira - 2017.pdf: 1486050 bytes, checksum: fcc7f785120d547ad310a16b98732ea1 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Made available in DSpace on 2017-07-25T11:04:15Z (GMT). No. of bitstreams: 2 Dissertação - Isis Gabrielli Barbieri de Oliveira - 2017.pdf: 1486050 bytes, checksum: fcc7f785120d547ad310a16b98732ea1 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2017-06-27 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / The presence of circadian rhythms in organisms is a biological event, indispensable to the process of adaptation to the environment and fundamental for the survival of the species. The loss of the phase relationship between the biological rhythms and the behavior leads impairment of the body function. Thus, the aim of this study was to evaluate the effects of the forced locomotor activity desynchronization on the cardiovascular and metabolic parameters. Male Wistar rats, aged approximately 60 days, were distributed into two experimental groups: control group (CTR) submitted to the light/dark cycle (LD) of 24h-T24 (n=12) and desynchronized group (DSC) submitted to the LD cycle of 22h -T22 (n = 18) for eight weeks. Records of the locomotor activity were made daily to both groups. Food ingestion, water intake and body weight were monitored weekly. Following of this period the animals were allocated into two experimental protocols. In the first protocol the CTR and DSC animals were submitted to records of mean arterial pressure (MAP) and heart rate (HR), as well as pharmacological tests of baroreceptor reflex function and cardiac autonomic control, such as intrinsic pacemaker heart rate (IPHR); vagal and sympathetic effects and sympathetic-vagal index (SVI). In the second protocol, CTR and DSC animals were fasted for at least 12 hours, anesthetized and euthanized by decapitation to collect blood, liver and adrenal glands for posterior analysis of plasma glucose, triglycerides, total cholesterol, VLDL, HDL, LDL; the expression of proteins involved in the insulin signaling cascade (IR-β; IRS-2; PI3K; AKT), the gluconeogenic enzyme - PEPCK, SOD-1 and CAT; and morphometry. Although there was no significant difference in feed and water intake between groups, a higher weight gain of DSC animals was observed from week 7 onwards. In relation to the pattern of locomotor activity, DSC animals presented lower levels on total locomotor activity with a predominance of its activity during the light phase of the LD cycle. Although we did not observe significant alterations in the basal MAP and HR levels between the groups, the DSC animals showed reduction of the baroreflex sensitivity by the bradycardic index, as well as a higher cardiac sympathetic effect. No differences were observed between the groups for the other parameters of cardiac autonomic control. Regarding the biochemical parameters, we observed in the DSC animals, a reduction in HDL cholesterol associated with an increase in LDL cholesterol, which promoted a high index of Castelli I and II, compared to the CTR. There were no differences in plasma levels of glucose, triglycerides, total cholesterol and VLDL. DSC animals also showed an increase in weight and in the total area of the adrenal glands. In addition, we observed decreased IRβ, IRS-2, PI3-K and Akt proteins, as well as increased expression of the gluconeogenic enzyme PEPCK in DSC animals, suggesting hepatic insulin resistance. Finally, we observed a reduction in the expression of the SOD-1 and CAT enzymes in the DSC animals in relation to the CTR animals. Summarizing, our results suggest that a 22h symmetrical photoperiod (T-22) promotes lower baroreflex sensitivityand increased sympathetic effect on the heart. In addition, metabolic disorders such as hepatic insulin resistance and increased hepatic oxidative stress were observed in the desynchronized rats. / A presença de ritmos circadianos nos organismos é um evento biológico, indispensável ao processo de adaptação ao meio e fundamental para a sobrevivência das espécies. A perda de relação de fase entre os ritmos biológicos e o comportamento promovem prejuízo às funções orgânicas. Diante disso, o objetivo deste estudo foi avaliar os efeitos de uma dessincronização forçada da atividade locomotora nos parâmetros cardiovasculares e metabólicos. Ratos Wistar machos, com idade aproximada de 60 dias, foram distribuídos em dois grupos experimentais: grupo controle (CTR) submetido ao ciclo claro/escuro (CE) de 24h - T24 (n=12) e grupo dessincronizado (DSC) submetido ao ciclo claro/escuro (CE) de 22h - T22 (n=18) por oito semanas. Registros da atividade locomotora foram feitos diariamente para ambos os grupos. O consumo alimentar, ingestão de água e o peso corporal foram monitorados semanalmente. Ao final deste período os animais foram alocados em dois protocolos experimentais. No primeiro protocolo os animais CTR e DSC foram submetidos a registros da pressão arterial média (PAM) e frequência cardíaca (FC), bem como testes farmacológicos da função do reflexo barorreceptor e controle autonômico cardíaco, tais como frequência cardíaca intrínseca de marcapasso (FCIM); efeitos vagal e simpático e índice simpático-vagal (ISV). No segundo protocolo os animais CTR e DSC foram deixados em jejum de no mínimo 12 horas, anestesiados e eutanasiados por decapitação para coleta de sangue, fígado e glândulas adrenais para posterior análise dos níveis plasmáticos de glicose, triglicerídios, colesterol total, VLDL, HDL, LDL; da expressão de proteínas envolvidas na cascata de sinalização da insulina (IR-β; IRS-2; PI3K; AKT), enzima gliconeogênica – PEPCK, SOD-1 e CAT; e da morfometria. Embora não houve diferença significativa no consumo de ração e água entre os grupos, observou-se maior ganho de peso dos animais DSC a partir da 7ª semana. Em relação ao padrão da atividade locomotora os animais DSC apresentaram menor atividade locomotora total e um predomínio da mesma durante a fase clara do ciclo CE. Apesar de não observamos alterações significativas nos níveis de PAM e FC basais entre os grupos, os animas DSC apresentaram redução da sensibilidade barorreflexa pelo índice bradicárdico, assim como maior efeito simpático cardíaco. Não foram observadas diferenças entre os grupos para os demais parâmetros de controle autonômico cardíaco. Quanto aos parâmetros bioquímicos, observamos, nos animais DSC, redução do colesterol HDL associado a uma elevação do colesterol LDL, o que promoveu elevados índice de Castelli I e II comparados aos CTR. Não houve diferenças nos níveis plasmáticos de glicose, triglicerídios, colesterol total e VLDL. Os animais DSC também apresentaram aumento no peso e na área total das glândulas adrenais. Além disso, observamos diminuição das proteínas IRβ, IRS-2, PI3-K e Akt, bem como aumento da expressão da enzima gliconeogênica PEPCK nos animais DSC, sugerindo resistência hepática à insulina. Por fim observamos redução na expressão das enzimas SOD-1 e CAT nos animais DSC em relação aos animais CTR. Sumarizando, nossos resultados sugerem que um fotoperíodo simétrico de 22h (T-22) promove menor sensibilidade barorreflexa, maior efeito simpático sobre o coração. Além disso, foram observados distúrbios metabólicos, como resistência à insulina hepática e aumento do estresse oxidativo hepático, nos ratos dessincronizados.

A exposição ambiental aos poluentes orgânicos persistentes tem recebido amplo destaque na literatura recentemente devido à extensa associação entre o desenvolvimento de doenças metabólicas, obesidade e/ou diabetes mellitus, e a presença destes poluentes, principalmente os organoclorados, como as bifenilas policloradas (PCBs), no organismo. Por outro lado, os mecanismos de ação destes poluentes é controverso devido à elevada quantidade de representantes destas classes, gerando diversidade de protocolos de exposição e escassez de estudos experimentais. Por isto, foi objetivo deste trabalho elucidar os mecanismos de ação tóxica do PCB126, nas doses de 0,1; 1 ou 10 µg/kg de massa corpórea, em ratos Wistar machos, durante quinze dias, expostos por instilação intranasal. O procotolo de exposição empregado foi caracterizado e considerado suficiente para causar toxicidade, uma vez que foram observadas alterações no sistema imune, metabolismo e em parâmetros relacionados à gênese do diabetes mellitus. A caracterização da exposição foi determinada pela quantificação da concentração de PCB126 no fígado e pulmão (CG/MS) e pelo aumento da expressão do receptor aril hidrocarboneto (AhR) no rim, fígado, pulmão e tecido adiposo (Western Blot). O efeito imunossupressor do PCB126 foi evidenciado pelo comprometimento da produção de células na medula óssea e, consequentemente, no número de células totais no sangue circulante. Adicionalmente, foi evidenciada a interferência do poluente na via de ativação mediada por receptores acoplados à proteína G (GPCRs), principalmente em neutrófilos, alterando importantes funções destas células, como a expressão de moléculas de adesão, geração de espécies reativas de oxigênio e migração. Entre as alterações metabólicas observadas, destacamos o aumento dos níveis de triglicerídeos e colesterol sérico, aumento da liberação de ácidos graxos livres; aumento da atividade da enzima hepática gama glutamil transferase; aumento da resistência à insulina e aumento da geração de óxido nítrico pelas ilhotas de Langerhans, dados estes, possivelmente relacionados ao comprometimento das células beta (β) pancreáticas, confirmados pelo aumento da expressão de GLUT4 no tecido adiposo, aumento da concentração de insulina sérica e aumento do estresse oxidativo nas ilhotas de Langerhans. Em conjunto, os dados obtidos destacam importantes alterações causadas pela exposição intranasal ao PCB126, evidenciando a participação do poluente na gênese do diabetes mellitus do tipo II. / The environmental exposure to persistent organic pollutants has been widely highlighted in recent literature due to the extensive association between the development of metabolic diseases, obesity and/or diabetes mellitus, and presence of these pollutants, especially organochlorines such as polychlorinated biphenyls (PCBs) in organism. Moreover, the mechanisms of action of these pollutants are controversial due to the high number of PCBs congeners, diversity of exposure protocols and lack of experimental studies. Therefore, the aim of this study was to elucidate the mechanisms of PCB126\'s toxic action at doses of 0.1; 1 or 10 µg/kg body weight in male Wistar rats exposed by intranasal instillation for 15 days. The established exposure procotol was characterized and considered sufficient to cause toxicity since changes were observed in the immune system, metabolism and in parameters related to the pathogenesis of diabetes mellitus. Characterization of exposure was determined by quantifying the concentration of PCB126 in liver and lung (GC-MS) and by the increased expression of aryl hydrocarbon receptor (AhR) in kidney, liver, lung, and adipose tissue (Western blot). The immunosuppressive effect of PCB126 was evidenced by impairment of cell production in the bone marrow and thus the total number of cells in the circulation. In addition, the interference of the pollutant in the activation pathway mediated by G-protein coupled receptors (GPCRs), in particular in neutrophils, was observed by changing important functions of these cells such as the expression of adhesion molecules, reactive oxygen species generation, and migration. Among the metabolic changes observed, we highlight the increased levels of triglycerides and serum cholesterol, increased release of free fatty acids; increased gamma glutamyl transferase hepatic enzyme activity; increased insulin resistance and increased generation of nitric oxide by the islets of Langerhans, these data possibly related to the impairment of beta cells (β) pancreatic function, suggested by the increased expression of GLUT4 in adipose tissue, increased serum insulin concentration and increased oxidative stress in the islets of Langerhans. Altogether, these results highlight important changes caused by intranasal exposure to PCB126, suggesting participation of the pollutant in the genesis of diabetes mellitus type II.

Introdução - A dieta hiperlipídica é uma das principais causas da obesidade, provocando importantes alterações metabólicas, como aumento de gordura corporal, dislipidemia e resistência à ação da insulina. Além disso, a obesidade gera um quadro inflamatório crônico e de baixa intensidade no tecido adiposo branco, que é caracterizado pela ativação de vias inflamatórias, como a via do fator de transcrição nuclear kappa B (NF-kB), que é responsável pela transcrição de genes com ação pró-inflamatória, como o fator de necrose tumoral (TNF)-alfa e a proteína quimiotática para monócitos (MCP)-1. A erva-mate (Ilex paraguariensis) contém compostos bioativos, como o ácido clorogênico, a quercetina e o kaempferol, os quais apresentam a capacidade de modular a expressão de genes envolvidos na resposta inflamatória. Objetivo - Investigar o efeito da ingestão do extrato aquoso de erva-mate sobre os parâmetros metabólicos e sobre a resposta inflamatória no tecido adiposo branco de ratos alimentados com ração hiperlipídica. Material e métodos - Ratos machos Wistar foram submetidos à ração controle ou hiperlipídica por 12 semanas. Após esse período, 12 animais de cada grupo foram eutanasiados, constituindo os grupos baseline. O restante dos animais foi distribuído em quatro grupos que receberam, por gavagem, o extrato aquoso de erva-mate (1 g/kg massa corporal/dia) ou água, durante quatro semanas. Após esse período, todos os animais foram eutanasiados. Durante a 12a e a 16a semana do protocolo experimental, os animais foram submetidos ao teste oral de tolerância à glicose e ao teste intraperitoneal de tolerância à insulina. A partir do sangue, foram determinadas as concentrações de glicose, de insulina e de biomarcadores inflamatórios, bem como o perfil lipídico. A composição corporal foi determinada por meio da análise química da carcaça. A partir do tecido adiposo periepididimal, foi avaliada a expressão das proteínas chaves envolvidas na inflamação crônica e na resistência à ação da insulina, por Western blot, bem como a expressão gênica de adipocinas por PCR em tempo real. Resultados - A ração hiperlipídica provocou aumento da adiposidade, alteração do perfil lipídico, intolerância à glicose e inflamação sistêmica. No tecido adiposo periepididimal, a ração hiperlipídica provocou redução da fosforilação da AKT nos animais estimulados agudamente com insulina. A ingestão do extrato aquoso de erva-mate, por quatro semanas, reduziu o ganho de peso corporal e melhorou o perfil lipídico nos animais alimentados com a ração hiperlipídica em relação ao correspondente grupo tratado com água. Contudo, o extrato aquoso de erva-mate não foi capaz de reverter as demais alterações metabólicas provocadas pela ingestão da ração hiperlipídica. Conclusão - A ingestão da ração hiperlipídica promoveu alterações metabólicas, todavia, não induziu inflamação crônica no tecido adiposo periepididimal. Por outro lado, a ingestão do extrato aquoso de ervamate foi capaz de reduzir o ganho de peso corporal e melhorar o perfil lipídico dos animais que consumiram a ração hiperlipídica / Introduction - High-fat diet is one of the main causes of obesity, inducing significant metabolic changes, such as increased fat mass, dyslipidemia and insulin resistance. Furthermore, obesity is associated with a chronic state of low-grade inflammation in white adipose tissue, which is characterized by activation of inflammatory pathways, like nuclear factor kappa B (NF-kB) pathway, implicated in the transcription of many genes with pro-inflammatory action, such as tumor necrosis factor (TNF)-alpha and monocyte chemotatic protein (MCP)-1. Yerba mate (Ilex paraguariensis) contains bioactive compounds, such as chlorogenic acid, quercetin and kaempferol that have the ability to modulate genes envolved in inflammatory response. Objective - To investigate the effect of yerba mate aqueous extract consumption on metabolic parameters and on inflammatory response in white adipose tissue of high-fat diet-fed rats. Material and methods - Male Wistar rats were submitted a control or a high-fat diet for 12 weeks. After this period, 12 rats of each group were euthanized, constituting the baseline groups. The remainder animals were distributed into four groups, which received by intragastric gavage the yerba mate aqueous extract or vehicle (1 g/kg body weight/day) for four weeks and then, all animals were euthanized. Oral glucose and intraperitoneal insulin tolerance tests were performed at 12 and 16 weeks of experimental protocol. Blood glucose, insulin, lipid profile and inflammatory markers were measured. Water, lipid, protein and ash content were analyzed by carcass chemical composition. Periepididymal adipose tissue were employed to evaluate key proteins involved in inflammatory and insulin signaling pathway by Western blot, and adipokines gene expression by real time PCR. Results - High-fat diet induced body adiposity, dyslipidemia, glucose intolerance and systemic inflammation. In periepididymal fat, high-fat diet decreased AKT phosphorylation in rats acutelly stimulated with insulin. The consumption of yerba mate aqueous extract for four weeks reduced body weight gain and improved lipid profile in high-fat diet group compared to non-treated group. However, yerba mate did not repair others dysfunctions induced by high-fat feeding. Conclusion - High-fat feeding produced some metabolic dysfunctions, but did not induce chronic inflammation in periepididymal adipose tissue. On the other hand, the yerba mate aqueous extract consumption reduced body weight gain and improved lipid profile of rats fed a high-fat diet

Introdução: O atual estilo de vida traz consequências negativas no que se refere aos padrões dietéticos, nível de atividade física (AF), uso de tabaco e estresse psicossocial, os quais predispõem ao aumento de doenças crônicas não-transmissíveis. Dieta rica em frutas, legumes e verduras (FLV) pode atenuar os efeitos sobre o risco cardiometabólico, havendo evidências consistentes de benefícios na prevenção da obesidade, dislipidemia e diabetes tipo 2. O consumo de FLV, fontes de vitaminas e minerais essenciais para a homeostase corporal está aquém do desejado. Estes alimentos contribuem para um perfil cardiometabólico favorável, atenuando o estresse oxidativo, inflamação e resistência à insulina. Objetivo: Este estudo analisou a associação entre o consumo FLV e de certos micronutrientes com marcadores do estado oxidativo, inflamatório e de resistência à insulina em indivíduos de risco cardiometabólico. Métodos:Nesta análise transversal foram incluídos 205 participantes (65 por cento mulheres; média de idade de 54,1 anos) do Estudo de Prevenção de Diabetes do CS-Escola da FSP-USP, com pré-diabetes ou de síndrome metabólica sem diabetes. Foram submetidos a questionários e coletas de sangue. Entre as dosagens, a superóxido dismutase (SOD) e a LDL oxidada (LDLox) serviram para indicar o estado anti/pró-oxidativo. O nível de AF foi medido pela versão longa do IPAQ. Três recordatórios alimentares de 24h foram empregados para cálculo da ingestão de micronutrientes e de FLV. Três categorias de consumo de FLV consumidas foram criadas considerando-se a recomendação internacional e a ingestão de micronutrientes estratificada segundo tercis de consumo, analisados por ANOVA. Coeficiente de Pearson e regressão linear múltipla foram também empregados. Resultados: Os participantes consumiram uma média de 1800 kcal/dia e 3,7 porções/1000 kcal de FLV. Ao longo das categorias de ingestão de FLV, os valores médios de circunferência da cintura (p=0,06) e pressão arterial diastólica (p=0,05) tenderam a diminuir e adiponectina (p=0,05) a aumentar. Indivíduos no tercil mais alto de ingestão de zinco apresentaram valores mais baixos de massa gorda e HOMA-IR, enquanto as concentrações de PCR foram marginalmente significantes (p=0,06). O HOMA-IR associou-se inversamente com ingestão de zinco e magnésio em todos os modelos. Associações diretas foram encontradas entre as concentrações de SOD com ingestão de FLV, bem como de magnésio em modelos ajustados. A concentração de LDLox se associou inversamente a ingestões de magnésio, vitaminas C e E em modelos ajustados. Resultados similares foram encontrados entre a concentração de LDLox e FLV, mas perdeu a significância após ajustes. Associação direta entre LDLox e ingestão de selênio manteve-se nos modelos ajustados. Conclusão: Nosso estudo sugere que a análise do consumo de FLV e/ou de certas vitaminas e minerais, ainda que estejam abaixo dos níveis recomendados, pode ser útil para identificar estresse oxidativo e resistência à insulina. / Introduction: Current lifestyle has deleterious consequences in dietary habits, physical activity, smoking and psychosocial stress, which have predisposed to non-communicable chronic diseases. A diet rich in fruits and vegetables can attenuate the effects on cardiometabolic risk, and there is consistent evidence of its benefit on the prevention of obesity, dyslipidemia and type 2 diabetes. Worldwide the consumption of fruits and vegetables, sources of vitamins and minerals, which are essential for body homeostasis, is low. These foods contribute to a favorable cardiometabolic profile, attenuating oxidative stress, inflammation and insulin resistance. Objective: Associations between the consumption of certain micronutrients and fruits and vegetables with markers of oxidative status, inflammation and insulin resistance were examined in individuals at cardiometabolic risk. Methods: This cross-sectional analysis included 205 participants (65 per cent women, mean age 54.1 years) with pre-diabetes or with metabolic syndrome without diabetes of the Diabetes Prevention Study of the FSP-USP Health Care Unit. They were submitted to questionaires blood collection. Superoxide dismutase (SOD) and oxidized LDL (oxLDL) were used to indicate the oxidative status. The physical activity level was measured by the long version of IPAQ. Three 24-hour dietary recalls were used to calculate intake of micronutrients and of fruits and vegetables. Three categories of fruits and vegetables consumption were created taking into consideration international recommendations, and micronutrient intake were grouped according tertiles of consumption, these categories analyzed by ANOVA. Pearsons correlation coefficient and multiple linear regression were used. Results: Participants consumed a mean of 1,800 kcal per day and 3.7/1000 kcal servings of fruit and vegetables. Mean values of waist circumference (p=0.06) and diastolic blood pressure (p=0.05) tended to decrease, and adiponectin (p=0.05) to increase across the categories of fruits and vegetables intake. Individuals in the highest tertile of zinc intake showed lower values of fat mass and HOMA-IR, while CRP concentrations were marginally significant (p=0.06). HOMA-IR was inversely associated with zinc and magnesium intakes in all the models. Direct associations were found between SOD concentrations and fruits and vegetables as well as magnesium intakes in adjusted models, while oxLDL concentration was inversely associated with magnesium, vitamin C and E intakes. Similar results were found between oxLDL concentration and fruits and vegetables intake but significance disappeared after adjustments. A direct association between oxLDL and selenium intake was detected after multiple adjustments. Conclusion: Our study suggest that fruits and vegetables and/or selected vitamins and minerals intakes albeit below recommended levels may be useful to identifying oxidative stress and insulin resistance.

Obesity-associated metabolic disorders are amongst the most prevalent causes of death worldwide. Understanding how obesity leads to the development of the Metabolic Syndrome (MetS) and cardiovascular disease (CVD) will enable the development of novel therapies that dissociate obesity from its cardiometabolic complications. Our laboratory views the functional capacity of white adipose tissue (WAT), the organ designed for safe lipid storage, as a key factor in the development of MetS and CVD. At a genetically-defined stage of the aberrant WAT expansion that occurs during obesity, adipocytes undergo a functional failure, resulting in an impaired control of serum free fatty acid (FFA) concentration. In such setting, FFAs and their metabolic derivatives accumulate in other organs, where they cause lipotoxicity, leading to the development of insulin resistance and CVD. We therefore aim to understand the pathophysiological mechanisms that induce adipocyte dysfunction. The past two decades of research have established the immune system as an important regulator of WAT function. The number of adipose tissue macrophages (ATMs), the most abundant immune cell type in WAT, increases during obesity, resulting in WAT inflammation. Multiple genetic and pharmacological intervention studies of murine models of obesity have assigned a causal link between ATM pro-inflammatory activation and WAT dysfunction. However, while the propagation of inflammation in ATMs during obesity has been extensively studied, factors triggering ATM inflammatory activation are less clear. Recently, our lab has observed lipid accumulation in the ATMs isolated from obese mice. Lipid-laden ATMs were pro-inflammatory, leading us to hypothesise that aberrant lipid build-up in macrophages triggers WAT inflammation during obesity. This thesis expands on the initial findings from our lab and describes two novel mechanisms that potentially contribute to lipid-induced inflammatory activation of ATMs. In chapter 3, the role of de novo phosphatidylcholine (PC) synthesis pathway during lipotoxicity in macrophages is addressed. The first part of the chapter demonstrates that lipotoxic environment increased de novo PC synthesis rate in bone marrow-derived macrophages (BMDMs) and ATMs, and that loss of rate-limiting enzyme in de novo PC synthesis pathway, CTP:phosphocholine cytidylyltransferase a (CCTa) diminished saturated FFA-induced inflammation in BMDMs. In the second part, I show that macrophage-specific CCTa deletion did not impact on the development of WAT inflammation or systemic insulin resistance, but had a minor benefitial effect on hepatic gene transcription during obesity. Chapter 4 develops on recent observations of interactions between sympathetic nerves and macrophages in WAT. In the first part of the chapter, I demonstrate that stimulating B2-adrenergic receptor (B2AR), the main receptor for sympathetic neurotransmitter norepinephrine in macrophages, enhanced intracellular triglyceride storage by up-regulating diacylglycerol O-acyltransferase 1 (Dgat1) gene expression in BMDMs. The second part of the chapter shows that macrophage-specific B2AR deletion did not modulate systemic glucose and lipid metabolism during obesity, but mice lacking B2ARs in macrophages demonstrated augmented hepatic glucose production on a chow diet. Furthermore, systemic B2AR blockade or macrophage-specific B2AR deletion in mice did not affect the thermogenic response to cold exposure. Chapter 5 includes the characterisation of B2AR stimulation-induced changes to the global cellular proteome of BMDMs, and a subsequent validation of the role of candidate transcription factors in regulating B2AR agonism-induced gene expression in BMDMs.

Introdução - A dieta hiperlipídica é uma das principais causas da obesidade, provocando importantes alterações metabólicas, como aumento de gordura corporal, dislipidemia e resistência à ação da insulina. Além disso, a obesidade gera um quadro inflamatório crônico e de baixa intensidade no tecido adiposo branco, que é caracterizado pela ativação de vias inflamatórias, como a via do fator de transcrição nuclear kappa B (NF-kB), que é responsável pela transcrição de genes com ação pró-inflamatória, como o fator de necrose tumoral (TNF)-alfa e a proteína quimiotática para monócitos (MCP)-1. A erva-mate (Ilex paraguariensis) contém compostos bioativos, como o ácido clorogênico, a quercetina e o kaempferol, os quais apresentam a capacidade de modular a expressão de genes envolvidos na resposta inflamatória. Objetivo - Investigar o efeito da ingestão do extrato aquoso de erva-mate sobre os parâmetros metabólicos e sobre a resposta inflamatória no tecido adiposo branco de ratos alimentados com ração hiperlipídica. Material e métodos - Ratos machos Wistar foram submetidos à ração controle ou hiperlipídica por 12 semanas. Após esse período, 12 animais de cada grupo foram eutanasiados, constituindo os grupos baseline. O restante dos animais foi distribuído em quatro grupos que receberam, por gavagem, o extrato aquoso de erva-mate (1 g/kg massa corporal/dia) ou água, durante quatro semanas. Após esse período, todos os animais foram eutanasiados. Durante a 12a e a 16a semana do protocolo experimental, os animais foram submetidos ao teste oral de tolerância à glicose e ao teste intraperitoneal de tolerância à insulina. A partir do sangue, foram determinadas as concentrações de glicose, de insulina e de biomarcadores inflamatórios, bem como o perfil lipídico. A composição corporal foi determinada por meio da análise química da carcaça. A partir do tecido adiposo periepididimal, foi avaliada a expressão das proteínas chaves envolvidas na inflamação crônica e na resistência à ação da insulina, por Western blot, bem como a expressão gênica de adipocinas por PCR em tempo real. Resultados - A ração hiperlipídica provocou aumento da adiposidade, alteração do perfil lipídico, intolerância à glicose e inflamação sistêmica. No tecido adiposo periepididimal, a ração hiperlipídica provocou redução da fosforilação da AKT nos animais estimulados agudamente com insulina. A ingestão do extrato aquoso de erva-mate, por quatro semanas, reduziu o ganho de peso corporal e melhorou o perfil lipídico nos animais alimentados com a ração hiperlipídica em relação ao correspondente grupo tratado com água. Contudo, o extrato aquoso de erva-mate não foi capaz de reverter as demais alterações metabólicas provocadas pela ingestão da ração hiperlipídica. Conclusão - A ingestão da ração hiperlipídica promoveu alterações metabólicas, todavia, não induziu inflamação crônica no tecido adiposo periepididimal. Por outro lado, a ingestão do extrato aquoso de ervamate foi capaz de reduzir o ganho de peso corporal e melhorar o perfil lipídico dos animais que consumiram a ração hiperlipídica / Introduction - High-fat diet is one of the main causes of obesity, inducing significant metabolic changes, such as increased fat mass, dyslipidemia and insulin resistance. Furthermore, obesity is associated with a chronic state of low-grade inflammation in white adipose tissue, which is characterized by activation of inflammatory pathways, like nuclear factor kappa B (NF-kB) pathway, implicated in the transcription of many genes with pro-inflammatory action, such as tumor necrosis factor (TNF)-alpha and monocyte chemotatic protein (MCP)-1. Yerba mate (Ilex paraguariensis) contains bioactive compounds, such as chlorogenic acid, quercetin and kaempferol that have the ability to modulate genes envolved in inflammatory response. Objective - To investigate the effect of yerba mate aqueous extract consumption on metabolic parameters and on inflammatory response in white adipose tissue of high-fat diet-fed rats. Material and methods - Male Wistar rats were submitted a control or a high-fat diet for 12 weeks. After this period, 12 rats of each group were euthanized, constituting the baseline groups. The remainder animals were distributed into four groups, which received by intragastric gavage the yerba mate aqueous extract or vehicle (1 g/kg body weight/day) for four weeks and then, all animals were euthanized. Oral glucose and intraperitoneal insulin tolerance tests were performed at 12 and 16 weeks of experimental protocol. Blood glucose, insulin, lipid profile and inflammatory markers were measured. Water, lipid, protein and ash content were analyzed by carcass chemical composition. Periepididymal adipose tissue were employed to evaluate key proteins involved in inflammatory and insulin signaling pathway by Western blot, and adipokines gene expression by real time PCR. Results - High-fat diet induced body adiposity, dyslipidemia, glucose intolerance and systemic inflammation. In periepididymal fat, high-fat diet decreased AKT phosphorylation in rats acutelly stimulated with insulin. The consumption of yerba mate aqueous extract for four weeks reduced body weight gain and improved lipid profile in high-fat diet group compared to non-treated group. However, yerba mate did not repair others dysfunctions induced by high-fat feeding. Conclusion - High-fat feeding produced some metabolic dysfunctions, but did not induce chronic inflammation in periepididymal adipose tissue. On the other hand, the yerba mate aqueous extract consumption reduced body weight gain and improved lipid profile of rats fed a high-fat diet

Metabolic Syndrome Insulin Resistance Is Associated with Discordant Distribution of GLUT4 and the Insulin Receptor in Fast-Twitch and Slow-Twitch Muscle Fiber Types We have previously shown that We have previously shown that strength training alone improved insulin responsiveness in sedentary controls but not in metabolic syndrome subjects. Immunoblots of metabolic syndrome subjects[apos] muscle homogenates showed training-related increases in GLUT4 and mitochondrial enzymes was half that seen in the controls. To determine if this was due to changes primarily in fast-twitch fibers (strength fibers), we performed immunohistochemical (IHC) studies on muscle sections from these subjects to quantify fiber-specific changes in GLUT4, phospho-AMPK, phospho-mTOR, ATP synthase, and the insulin receptor. Signal intensity in confocal microscopic images was digitally quantified and the amount in each fiber type was adjusted by the fiber composition and the average size of each fiber type. Fiber type was classified using monoclonal antibodies against slow-twitch (type 1 fibers) and fast-twitch (type 2a and 2b fibers) myosin heavy chains. At baseline, both groups had slightly more insulin receptor in slow-twitch fibers, and most of the ATP synthase (mitochondrial marker) was in fast-twitch fibers. In controls, 55% of GLUT4 was in slow-twitch fibers, whereas metabolic syndrome subjects had only 33% of their GLUT4 in slow-twitch fibers. The IHC data showed modest increases in GLUT4 (9-25%), and substantial increases of ATP synthase (55-95%), and insulin receptors (44-104%) in both fiber types in both groups. Training-related increases were seen in phospho-AMPK (25% in slow-twitch, 15% in fast-twitch) only in the control subjects but no change in phospho-mTOR in either subject group. At baseline, metabolic syndrome subjects[apos] muscle had 56% of insulin receptors expressed in slow-twitch fibers, but only 33% of the GLUT4 was in these fibers. Thus, the untrained muscle composition of the metabolic syndrome subjects exhibited a mismatch between insulin receptors and GLUT4 in their fiber-specific distributions. This mismatch may contribute to the insulin resistance seen in the metabolic syndrome and may be involved in the diminished insulin sensitivity response to strength training in these subjects.

Resistance training of healthy young men typically results in muscle hypertrophy and a shift in vastus lateralis composition away from type IIx fibers to an increase in IIa fiber content. Our previous studies of 8 wk of resistance training found that many metabolic syndrome men and women paradoxically increased IIx fibers with a decrease in IIa fibers. To confirm the hypothesis that obese subjects might have muscle remodeling after resistance training very different from healthy lean subjects, we subjected a group of nine obese male volunteers to progressive resistance training for a total of 16 wk. In these studies, weight loss was discouraged so that muscle changes would be attributed to the training alone. Detailed assessments included comparisons of histological examinations of needle biopsies of vastus lateralis muscle pretraining and at 8 and 16 wk. Prolonging the training from 8 to 16 wk resulted in increased strength, improved body composition, and more muscle fiber hypertrophy, but euglycemic clamp-quantified insulin responsiveness did not improve. Similar to prior studies, muscle fiber composition shifted toward more fast-twitch type IIx fibers (23 to 42%). Eight weeks of resistance training increased the muscle expression of phosphorylated Akt2 and mTOR. Muscle GLUT4 expression increased, although insulin receptor and IRS-1 expression did not change. We conclude that resistance training of prediabetic obese subjects is effective at changing muscle, resulting in fiber hypertrophy and increased type IIx fiber content, and these changes continue up to 16 wk of training.

Orientador: Doris Hissako Matsushita / Banca: Maria Aparecida Visconti / Banca: Flávia Lombardi Lopes / Banca: Joel Claudio Heimann / Banca: Fernando Yamamoto Chiba / Resumo: Atualmente, está bem estabelecido que o ambiente fetal está ligado à saúde materna, e estímulos ou agressões anormais durante a vida intra-uterina podem resultar em mudanças na fisiologia e metabolismo da prole, aumentando o risco de doenças na vida adulta, este fenômeno é conhecido como programação fetal. Alterações na metilação do DNA e expressão gênica são consideradas mecanismos moleculares responsáveis por esta programação. Estudos anteriores demonstraram que a doença periodontal (DP) materna promove resistência insulínica, aumento nas concentrações plasmáticas de citocinas, redução do conteúdo de GLUT4 e do seu índice de translocação para membrana plasmática em sua prole adulta. E citocinas, como por exemplo, o TNF-α, têm sido relacionadas com a redução da expressão de GLUT4 por meio da ativação do fator de transcrição nuclear κappa B (NF-κB). Além disso, esta citocina pode estimular algumas serinas quinases, incluindo IκB quinase (IKK), c-Jun amino-terminal kinase (JNK) e quinases reguladas por sinais extracelulares (ERKs) que estão envolvidas na resistência insulínica. Tais achados evidenciam a necessidade de realizar mais estudos para verificar os mecanismos envolvidos nestas alterações. Portanto, os objetivos do presente estudo foram avaliar em ratos adultos, proles de ratas com DP: 1) glicemia e insulinemia; 2) expressão do RNAm da proteína transportadora de glicose GLUT4 e do IRS1 em muscular esquelético gastrocnêmio (MG); 3) o grau de metilação do DNA na região p... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: It is well establishedthat the fetal environment is linked to maternal health, and abnormal stimuli or aggressions during intrauterine life can result in changes in the physiology and metabolism of offspring, increasing the risk of disease in adult life, this phenomenon is known as fetal programming. Changes in DNA methylation and gene expression are considered molecular mechanisms responsible for this programming. Previous studies have demonstrated that maternal periodontaldisease (PD) promotes insulin resistance, increased plasma concentrations of cytokines, reduced GLUT4 content and its plasma membrane translocation index in its adult offspring. And cytokines, such as TNF-α, have been linked to reduced GLUT4 expressionthrough the activation of nuclear transcription factor kappa B (NF-κB). In addition, this cytokine can stimulate some serine kinases including IκB kinase (IKK), c-Jun amino-terminal kinase (JNK) and extracellular signal-regulated kinases (ERKs)that are involved in insulin resistance. These findings evidenced the need for further studies to verify the mechanisms involved in these changes. Therefore, the objectives of the present study were to evaluate in adult rats, offspring of rats with PD: 1) birth weight and during the75 days of age;2) glycemia and insulinemia; 3) GLUT4 and IRS1mRNA expression in skeletal muscle gastrocnemius (MG); 4) the degree of DNA methylation in the promoter region of the GLUT4 gene in MG; 5) phosphorylation of JNK, IKKα/β, ERK 1/2, N... (Complete abstract click electronic access below) / Doutor

<p>Skeletal muscle accounts for the largest part of insulin-mediated glucose uptake. Insulin resistance (IR) is the main component of insulin resistance syndrome (IRS) and is an essential cause of a number of cardiovascular risk factors. This thesis investigates the relationships between muscle morphological characteristics and IRS because skeletal muscle is responsible for the majority of glucose uptake.</p><p>In this population-based sample of 70-year-old men, higher proportion of type I fibers as well as higher capillarization were related to higher insulin sensitivity and higher self-reported physical activity, which were related to a lower prevalence of type IIB fibers. Serum triglycerides, HDL cholesterol and plasminogen activator inhibitor-1 (PAI-1) activity were significantly related to fiber distribution and muscle capillarization and muscle morphology, in part, explained the association between these metabolic risk factors with physical activity level. BMI, glucose intolerance, PAI-1 activity, serum FFA concentration, proportion of type IIB fibers, HDL cholesterol level, drug treatment, physical activity level, and W/H ratio together explained 55% of the variation in the insulin sensitivity index. In addition, almost a twofold improvement of the correlations was seen after correcting for intraindividual variation. Glucose tolerant hypertensive subjects showed a lower capillary supply when compared to controls. Capillary density was negatively correlated to the increase in mean arterial pressure over two decades as well as to supine heart rate 20 years before. Interestingly, supine heart rate showed an independent inverse association to the percentage of type I fibers and a positive correlation to the percentage of type IIB muscle fibers. Capillary density and elevated serum free fatty (FFA) acid values were inversely associated with insulin-mediated blood flow and thus to endothelial dysfunction, which has been linked to IR. In fact, capillary density and serum FFA level together explained 71% of the variation in insulin-mediated leg blood flow changes.</p><p>In conclusion, these population-based findings support the observations that muscle morphological features and insulin sensitivity are related to each other. Muscle morphology might explain some of the beneficial impact of physical activity on the components of IRS. Accordingly, we suggest that alterations in muscle morphology should be considered as an essential part of the IRS.</p>