Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2016-04-05T15:03:43Z No. of bitstreams: 2 Dissertação - Ariany Rafaella Neto Silva - 2015.pdf: 893987 bytes, checksum: 388b303a349c43a6a3fe0cc14e611756 (MD5) license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2016-04-05T15:26:45Z (GMT) No. of bitstreams: 2 Dissertação - Ariany Rafaella Neto Silva - 2015.pdf: 893987 bytes, checksum: 388b303a349c43a6a3fe0cc14e611756 (MD5) license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) / Made available in DSpace on 2016-04-05T15:26:45Z (GMT). No. of bitstreams: 2 Dissertação - Ariany Rafaella Neto Silva - 2015.pdf: 893987 bytes, checksum: 388b303a349c43a6a3fe0cc14e611756 (MD5) license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) Previous issue date: 2015-08-04 / Fundação de Amparo à Pesquisa do Estado de Goiás - FAPEG / This study was developed with the objective of evaluating the response of bovine embryos produced in vitro (PIV) the addition of resveratrol (Resv) to recultivo to embryos vitrified (Experiment 1-E1) and medium Holding for fresh embryos (Experiment 2-E2) to check the maintenance or improvement in the quality of these embryos. In E1 PIV vitrified bovine embryos were heated and recultivados in the medium containing 0.5 μM of resveratrol, evaluating the re-expansion rates, hatching and cell quality by analysis of TUNEL. In E1, the hatching rate of recultivo more than 24 hours after (P < 0.05) in the Resv Group (37,7 vs. 19,1%). The rate of embryos according to the stage of development did not show difference between treatments. Even in E1, for fresh embryos PIV the total number of cells (NTC) was superior to that found in the vitrified embryos (131,6 vs 88,8 and 82,7%) , as well as the NCA (number of apoptotic cells) was lower (6,3 ± 0,8) compared with control groups and resveratrol (15,8 ± 1.2 and 13,5 ± 1,0), which did not differ among themselves in these variables. No difference was observed in embryos degenerates and reactive oxygen species (ROS) and Glutathione (GSH). In E2 bovine embryos were fresh bottled PIV in 0,25 ml straws with a holding in the presence (TR6 and TR10) or absence (TH6 and TH10) of resveratrol and kept on warming plate to 36° C in different times, six and 10 hours, followed by the unloading spouts and recultivo until 24 hours. Hatching rates at 24 hours of embryos treated with antioxidant tended to be greater than in the control. Bx TR10 rates was higher (51,2%) the TR6 (30,8%) (P < 0.05), the other stages of development were similar, the NTC was lower in TH10. The index of EROS was superior in TH10 (23,4126 ± 1,5661). The values of the GSH TR6 (95,2208) were larger than TH6 (30,7594) (P < 0.05), the TR10 issuing GSH (49,5330 ± 6,5332) did not differ from TH10 group (47,2044) (P > 0,05). / Esse estudo foi desenvolvido com os objetivos de avaliar a resposta de embriões bovinos produzidos in vitro (PIV) à adição de resveratrol (Resv) aos meios de recultivo para embriões vitrificados (Experimento 1 - E1) e Holding para embriões frescos (Experimento 2 - E2) para verificar a manutenção ou melhora na qualidade desses embriões. No E1 embriões bovinos PIV vitrificados foram aquecidos e recultivados em meio contendo 0,5 μM de resveratrol, avaliando-se as taxas de reexpansão, eclosão e qualidade celular através da análise de TUNEL. No E1, a taxa de eclosão após 24 horas de recultivo foi superior (P < 0.05) no grupo Resv (37,7 vs 19,1%). Na taxa de embriões de acordo com o estágio de desenvolvimento não apresentaram diferença entre tratamentos. Ainda no E1, para os embriões PIV frescos o número total de células (NTC) foi superior ao encontrado nos embriões vitrificados (131,6 vs 88,8 e 82,7%), assim como o NCA (número de células apoptóticas) foi menor (6,3 ± 0,8) em relação aos grupos controle e resveratrol (15,8 ± 1,2 e 13,5 ± 1,0), que não diferiram entre si nessas variáveis. Não foi observada diferença nas taxas de embriões degenerados e emissão de espécies reativas ao oxigênio (EROS) e glutationa (GSH). No E2 embriões bovinos PIV frescos foram envasados em palhetas de 0,25mL com meio holding na presença (TR6 e TR10) ou ausência (TH6 e TH10) de resveratrol e mantidos sobre placa aquecedora a 36°C em diferentes tempos, seis e 10 horas, seguido do desenvase e recultivo até 24 horas. As taxas de eclosão às 24hs dos embriões tratados com antioxidante tenderam a ser maior que no controle. As taxas de Bx TR10 foi superior (51,2%) ao TR6 (30,8%) (P < 0,05), os demais estágios de desenvolvimento apresentaram-se semelhantes. O NTC foi menor no TH10, assim como a MCI. O índice de EROS foi superior no TH10 (23,4126 ± 1,5661). Os valores de GSH do TR6 (95,2208) foram maiores que TH6 (30,7594) (P < 0,05), no TR10 a emissão de GSH (49,5330 ± 6,5332) não diferiu do grupo TH10 (47,2044) (P > 0,05).

>Magister Scientiae - MSc / The production of reactive oxygen species (ROS) is prominent in all aerobic metabolisms including plants. For this reason, the redox homeostasis of the production and scavenging of these intermediates is imperative for growth, development and survival during unfavourable conditions. In this study, a putative glutathione peroxidase gene (Glyma17g34110) from Glycine max (soybean) was identified and analyzed. The successful characterisation of Glyma17g34110 provided evidence of it being a glutathione peroxidase using glutathione as its preferred electron donor and substrate. Furthermore, it is known that antioxidant enzymes such as GPX exist in various tissues, performing a diverse set of functions. By a bioinformatic analysis of Glyma17g34110 and its promoter region, it was indicated that Glyma17g34110 could be a putative chloroplast protein that could play an important role in photosynthesis.One of the major factors affecting plant growth and development worldwide is abiotic stresses such as salinity. In the presence of salinity the production of harmful ROS is increased, resulting in detrimental reactions with important biological features (DNA, protein and lipid membranes), leading to cell death. The analysis of Glyma17g34110 under salt stress revealed that it is a salt sensitive gene and thus, the down-regulation of Glyma17g34110 could be due to the lack of known defence and response cis-acting elements present in the promoter region. Furthermore, it was proven in previous studies that the application of exogenous nitric oxide (NO) increases the activity of antioxidant enzymes. In this thesis it was observed that the presence of exogenously applied NO increased the expression of Glyma17g34110 tremendously in all soybean tissues (leaves, roots and nodules) investigated.Studies have found numerous cis-acting elements to be NO responsive, however, none of these elements were found in the promoter region upstream of glyma17g34110. This suggests that novel cis-acting elements could be present in the promoter region of Glyma17g34110.Thus, increasing the expression of Glyma17g34110 during salinity in the presence of NO, as well as the identification of these novel cis-acting elements, could lead to the enhancement of the defence mechanisms against ROS, which could lead to increasing plant tolerance to stress.

Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Botany Candidate: Ingrid Salanciová Supervisor: PharmDr. Jana Karlíčková, Ph.D. Title of Thesis: Interactions of reduced and oxidized glutathione with copper, iron and zinc Copper (Cu), iron (Fe) and zinc (Zn) are important trace elements that are necessary for proper function of the body. Excess but also the lack of these metals may lead to pathological conditions. Glutathione is the main antioxidant in the human body so it is expected to protect the organism against concequences of metal excess. Glutathione occurs in the reduced (GSH) and oxidized state as glutathione disulfide (GSSG) in the organism, both states forming an important redox system. On the other hand, glutathione can reduce these metals so that could participate in the formation of free radicals (metal based Fenton reaction). In this diploma thesis, was tested the ability of reduced and oxidized glutathione to interact with Fe, Cu and Zn in various (patho) physiological pH conditions was tested by using in vitro spectrophotometric competitive methods. Interactions include not only the chelation of Cu, Fe and Zn ions, but also their reductive activity toward Cu2+ and Fe3+ cations. Hematoxylin, bathocuproinedisulfonic acid disodium salt, ferrozine...

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Backround: Oxidative stress (OS) has been implicated in pathogenesis of human disorders such as depressive disorder, sepsis, cardiovascular disease, acute and chronic pancreatitis, and cancer. Increased OS is result of imbalance between increased reactive oxygen and nitrogen species (RONS) production and / or insufficient activity of antioxidant defence system. Antioxidant system, which is composed of antioxidant enzymes such as superoxide dismutase, catalase, glutathione peroxidases (GPX), glutathione reductase (GR) and non- enzymatic antioxidant reduced glutathione (GSH) plays an important role in the protection of cells against enhanced OS. The aim of this study was to assess the OS markers and antioxidant enzymes in different pathophysiological states. Materials and methods: Activities of erythrocyte glutathione peroxidase (GPX1), GR and concentration of GSH as well as levels of OS markers were analysed in six different pathophysiologic states. These parameters were measured in 35 women with depressive disorder (DD), 40 patients with metabolic syndrome (MetS), 30 septic patients (S) followed up in the course of sepsis; 15 non-septic critically ill patients (NC), 13 patients with acute pancreatitis (AP), 50 with chronic pancreatitis (CP) and 50 patients with pancreatic cancer (PC), compared to...

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Plus de 50 % des handicaps neurodéveloppementaux sont dus à une exposition périnatale à des stress toxiques ou oxydants. Comprendre comment le cerveau est protégé au cours du développement périnatal et pourquoi ses mécanismes de défense sont dépassés lorsque l’enfant est soumis à un stress important est donc crucial. La barrière sang – liquide céphalorachidien (LCR), localisée au niveau des plexus choroïdes, présente une capacité de détoxification élevée et pourrait donc avoir un rôle prépondérant dans la protection du cerveau au stade périnatal. Nous avons étudié la capacité de plusieurs enzymes choroïdiennes à protéger l'environnement liquidien cérébral pendant la période postnatale chez le rat, et évalué si leurs activités pouvaient être induites par la voie du nuclear factor erythroid-2-related factor 2 (Nrf2). Le facteur Nrf2 peut en effet moduler l’expression de différents gènes codant pour des enzymes de détoxification. Nous avons montré que les glutathion transférases (Gst) et les glutathion peroxydases (Gpx), intervenant respectivement dans l’inactivation des molécules toxiques et dans la régulation du stress oxydant, présentaient des activités choroïdiennes élevées pendant la période postnatale, et avons caractérisé fonctionnellement leur capacités de neuroprotection. Le traitement des ratons avec du diméthylfumarate (DMF), inducteur de la voie Nrf2, induit la migration nucléaire de Nrf2, augmente l’activité choroïdienne Gst, et réduit de 40 % le passage cérébral de toxiques substrats des Gst. Ces données montrent la capacité neuroprotectrice précoce des plexus choroïdes, et indique qu’elle peut être induite pharmacologiquement / More than 50 % of intellectual or sensory-motor deficits in children are due to perinatal exposure to oxidative stress or toxicants. Understanding brain protection mechanisms during development is crucial to design therapeutic strategies to address these disabilitating disorders. The choroid plexuses, forming an interface between the blood and the cerebrospinal fluid (CSF), have a high detoxifying capacity, suggesting their involvement in neuroprotection. The nuclear factor erythroid-2-related factor 2 (Nrf2) pathway can modulate the expression of several genes encoding for antioxidant proteins and detoxifying enzymes. We studied the ability of several choroidal enzyme families to protect the brain fluid environment during the postnatal period in rat and explored whether this protection can be enhanced by Nrf2 pathway. We focused on glutathione transferases (Gsts), which conjugate toxic compounds to glutathione, and glutathione peroxidases (Gpxs), which detoxify reactive oxygen species. Gst and Gpx specific activities were high during the postnatal period in choroid plexuses compared to the cerebral cortex, and their neuroprotective functions were efficient. The Nrf2 factor is expressed in choroid plexuses during the perinatal period. Treatment of rat pups with Nrf2 activator dimethylfumarate induced Nrf2 nuclear translocation and increased Gst activities in choroid plexus tissues. The dimethylfumarate treatment resulted in a large decrease of the blood-to-CSF permeability of a prototypical Gst substrate. These data substantiate the early neuroprotective functions of choroid plexuses, which can be enhanced upon treatment with clinically used pharmacological compounds

Foi estudado o efeito da lactona sesquiterpênica licnofolido sobre o \"burst\" respiratório de leucócitos polimorfonucleares inflamatórios (PMN) estimulados por forbol (PMA), pelo peptídeo quimiotático fMLP ou zimozan opsonizado (OZ). O licnofolido inibiu de forma dose-dependente a liberação de O2&#8226;- pelos PMN, sem alteração do período \"Iag\" do complexo NADPH. oxidase. O efeito foi mais acentuado quando os PMN foram estimulados diretamente pela via de proteína quinase C. A adição de ditiotreitol ou glutationa reduzida (GSH) às suspensões celulares antes da incubação com licnofolido preveniu parcialmente o efeito inibitório. O tratamento dos PMN com a lactona determinou uma queda drástica dos níveis celulares de GSH livre, sem incremento de glutationa oxidada (GSSG). A reação direta entre GSH e licnofolido foi confirmada com a detecção de um aduto glutationil-licnofolido através de identificação por espectrometria de massa (ESI-MS/MS). A S-tiolação protéica induzida pelo PMA foi reduzida em PMN tratados com Iicnofo/ido, como detectado através de determinação de incorporação de [35S], sendo que 80% desses tióis foram identificados como GSH. Uma série de proteínas S-glutationadas foi detectada através de autoradiografias, sendo que aquelas correspondentes a 38 e 24 kDa tiveram essa modificação póstraducional suprimida pelo tratamento com dose de licnofolido capaz de suprimir o \"burst\" respiratório dos PMN. Estes resultados indicam que a depleção celular de GSH causada pelo licnofolido impede a sustentação do \"burst\" respiratório pelos PMN, em correlação direta com a diminuição de S-glutationação protéica. / An investigation was made into the action of the sesquiterpene lactone lychnopholide on the respiratory burst of inflammatory polymorphonuclear leukocytes. Lychnopholide determined concentration-related inhibition of the generation of phorbol 12-myristate 13-acetate-, chemotatic peptide-, and opsonized zymozan-induced superoxide anion with no effect on the lag time of the assembly of the NADPH oxidase complex, such action was greater on the protein kinase C pathway that on both membrane receptor dependent stimuli via. Subsequent additions of D-glucose, Ca2+, Mg2+, dithiothreitol ar reduced glutathione (GSH) did not reverse the inhibitory action. The addition of both thiols prior to the lychnopholide treatment partially hindered the inhibition rate. The endogenous level of GSH in leukocytes was drastically depleted under the lychnopholide treatment, without corresponding increases occurring in the oxidized form (GSSG). A direct reaction between glutathione and lychnopholide was confirmed from a glutathionyl-lychnopholide adduct detected by electrospray mass spectrometry analysis and identified by tandem mass analysis in cellular extracts. Protein S-thiolation induced by PMA stimulation was decreased in lactone-treated PMN as detected by [35S] scintillation count, which indicated that about 80% of the thiols were glutathione. A subset of S-glutathionylated proteins was identified through gel electrophoresis, which revealed that the modification of the phorbol-triggered protein sulfhydryl in the protein bands corresponding to 38 and 24 kDa was precluded by the lychnopholide treatment correlated with respiratory burst inhibition. These results show that GSH depletion determined by lychnopholide treatment renders PMN to sustain respiratory burst, whose action is proportional to protein S-glutahionylation decrease.

O enxofre é um dos elementos essenciais para as plantas e as exigências nutricionais nesse nutriente variam com a espécie e a taxa de crescimento das plantas. Com o objetivo geral de avaliar o efeito da nutrição em enxofre no crescimento e no metabolismo do capimtanzânia (Panicum maximum cv. Tanzânia) e do estilosante (Stylosanthes guianensis cv. Mineirão) desenvolveu-se a presente pesquisa com os objetivos específicos de avaliar os efeitos do fornecimento de enxofre em: i) modificações morfológicas, produtivas e nutricionais ocorridas na parte aérea e nas raízes; ii) metabolismo do nitrogênio e as consequentes alterações na composição e concentrações de aminoácidos; iii) concentrações de enxofre total, enxofre-sulfato e glutationa e na atividade das enzimas glutationa redutase e glutationa sulfo-transferase nas folhas recém-expandidas e raízes; iv) crescimento, metabolismo da glutationa e atividade das enzimas envolvidas no ciclo ascorbato-glutationa e v) absorção de sulfato e a expressão de genes de transportadores de sulfato. Os experimentos foram conduzidos em casa de vegetação e camara de crescimento, empregando-se soluções nutritivas. As doses de enxofre aplicadas foram ajustadas de modo a permitir nutrição baixa, intermediária e alta em enxofre para cada espécie. O enxofre afetou diretamente na emissão de folhas e de perfilhos, área foliar, comprimento e superfície radicular do capim-tanzânia e do estilosante Mineirão, aumentando a produção de massa seca da parte aérea e das raízes. A baixa disponibilidade de enxofre ocasionou o desequilíbrio nutricional com o nitrogênio nas plantas, evidenciado por alta relação nitrogênio:enxofre e altas concentrações de nitrato e aminoácidos livres no tecido vegetal. Sob limitação de enxofre, o capim apresentou predomínio de asparagina na composição aminoacídica, enquanto no estilosante ocorreu a predominância de arginina. A aplicação de enxofre aumentou as concentrações de enxofre total, enxofre-sulfato e glutationa nas folhas diagnósticas e raízes para ambas as espécies forrageiras. As plantas crescidas sob limitação de enxofre apresentaram alta atividade da enzima glutationa redutase visando regenerar a glutationa reduzida, que atua protegendo as células contra danos oxidativos decorrentes do estresse da deficiência nutricional. O fornecimento de enxofre aumentou a atividade da glutationa sulfo-transferase incrementando a capacidade do vegetal de suportar estresses ambientais. A baixa disponibilidade de enxofre induziu o aumento da atividade de enzimas antioxidantes que atuam na regeneração da glutationa e do ascorbato na forma reduzida. As plantas crescidas em baixa disponibilidade de enxofre apresentaram aumento da concentração de glutationa e maior alocação desse composto nas raízes. A distribuição de glutationa das folhas para as raízes em condição de limitação de enxofre regula a absorção de sulfato no capim e no estilosante de modo diferenciado. Para o capim com alta concentração de glutationa nas raízes decresce o influxo total de 34S, enquanto para o estilosante não ocasiona a redução da absorção de sulfato. / Sulfur is an essential element required by plants and the nutritional requirements in this nutrient vary according to species and plant growth rate. This research had the main objective of evaluating the effect of sulfur nutrition on growth and metabolism of Guinea grass (Panicum maximum cv. Tanzânia) and stylo (Stylosanthes guianensis cv. Mineirão) and was developed with the specific objectives to determine the effects on i) morphological, productive and nutritional changes in plant shoots and roots, ii) nitrogen metabolism and the changes in the composition and concentrations of amino acids, iii) concentrations of total sulfur, sulfur-sulfate and glutathione and the activity of the enzymes glutathione reductase and glutathione sulfo-transferase in recently expanded leaves and roots, iv) growth, glutathione metabolism and activity of enzymes involved in ascorbate-glutathione cycle and v) sulfate uptake and expression of sulfur transporters genes. The experiments were carried out in greenhouse and growth chamber, by using nutrient solutions. Sulfur supply were adjusted to low, intermediate and high S nutrition for each species. Sulfur supply influences the emission of leaves, tillering, leaf area, root length and surface of Guinea grass and stylo increasing production of dry mass of aboveground and roots. Sulfur limitation alters the distribution of photosynthates between aboveground and roots of Guinea grass and stylo providing reduction in dry matter production of roots. The plants of Guinea grass increase root surface as a mechanism for adaptation to limited S in the culture medium. The relative chlorophyll index (RCI) in the recently expanded leaves relates to the production of dry mass of aboveground and can be used to assess S nutritional status in Guinea grass and stylo. The application of S proves necessary to increase production of dry mass in Guinea grass and stylo. Low S availability caused nutritional imbalance with N in Guinea grass and stylo plants, as shown by a high N:S ratio and high concentrations of N-nitrate and free amino acids in plant tissues. Among amino acids, asparagine predominated in S-limited guineagrass and arginine in Slimited stylo. Increased S supply regulates N:S ratio at values close to 20:1, which provides N and S concentrations that are more suitable for protein synthesis and forage production in plants of both species. Adding S increased concentrations of total S, S-sulfate, and glutathione in diagnostic leaves and roots of both species collected at the two harvests. Plants grown under S limitation showed high levels of GR activity, related to the regeneration of GSH, which acts to protect cells against oxidative damage caused by the stress of nutritional deficiency. S supply increased GST activity, and consequently plants\' capacity to withstand environmental stresses. Low S availability increased activity of the antioxidant enzymes that act in the regeneration of GSH and AsA. Plants grown with low S availability showed higher concentration of glutathione and greater allocation of glutathione to roots. For Guinea grass, high glutathione concentrations in roots decrease the 34S uptake. For stylo not cause reduction of 34S uptake.

<p>A number of active site mutants of human Alpha class glutathione transferase A1-1 (hGST A1-1) were made and characterized to determine the structural determinants for alkenal activity. The choice of mutations was based on primary structure alignments of hGST A1-1 and the Alpha class enzyme with the highest alkenal activity, hGST A4-4, from three different species and crystal structure comparisons between the human enzymes. The result was an enzyme with a 3000-fold change in substrate specificity for nonenal over 1-chloro-2,4-dinitrobenzene (CDNB).</p><p>The C-terminus of the Alpha class enzymes is an α-helix that folds over the active site upon substrate binding. The rate-determining step is product release, which is influenced by the movements of the C-terminus, thereby opening the active site. Phenylalanine 220, near the end of the C-terminus, forms an aromatic cluster with tyrosine 9 and phenylalanine 10, positioning the β-carbon of the cysteinyl moiety of glutathione. The effects of phenylalanine 220 mutations on the mobility of the C-terminus were studied by the viscosity dependence of k_cat and k_cat/K_m with glutathione and CDNB as the varied substrates. </p><p>The compatibility of slightly different subunit interfaces within the Alpha class has been studied by heterodimerization between monomers from hGST A1-1 and hGST A4-4. The heterodimer was temperature sensitive, and rehybridized into homodimers at 40 ˚C. The heterodimers did not show strictly additive activities with alkenals and CDNB. This result combined with further studies indicates that there are factors at the subunit interface influencing the catalytic properties of hGST A1-1.</p>