Brasil | masterThesis
dc.contributorUchoa, Adriana Ferreira
dc.contributorhttp://lattes.cnpq.br/2448189217304566
dc.contributorhttp://lattes.cnpq.br/6644671747055211
dc.contributorSantos, Elizeu Antunes dos
dc.contributor41305655400
dc.contributorhttp://lattes.cnpq.br/6762251930590306
dc.contributorMedeiros, Caroline Addison Carvalho Xavier de
dc.contributorhttp://lattes.cnpq.br/2982271986555450
dc.contributorRabêlo, Luciana Maria Araújo
dc.contributorhttp://lattes.cnpq.br/2165223941043909
dc.creatorCruz, Joelton Igor Oliveira da
dc.date.accessioned2022-02-04T22:47:41Z
dc.date.accessioned2022-10-06T12:54:23Z
dc.date.available2022-02-04T22:47:41Z
dc.date.available2022-10-06T12:54:23Z
dc.date.created2022-02-04T22:47:41Z
dc.date.issued2017-09-28
dc.identifierCRUZ, Joelton Igor Oliveira da. Avaliação da atividade anticoagulante e bloqueadora de elastase de um inibidor de tripsina isolado de Caesalpinea pyramidalis Tul. 2017. 69f. Dissertação (Mestrado em Ciências Biológicas) - Centro de Biociências, Universidade Federal do Rio Grande do Norte, Natal, 2017.
dc.identifierhttps://repositorio.ufrn.br/handle/123456789/45819
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3960919
dc.description.abstractPlants are subject to a diversity of unfavorable biotic and abiotic conditions, undergoing constantly some evolutionary adaptation, that can contribute to its reproduction and survival. The development of sophisticated defense strategies against pests and pathogens such as the synthesis of several natural bioactive compounds stands out as part of this adaptive biological arsenal. A key group of bioactive molecules in this context are the protease inhibitors, which compromise the activity of digestive enzymes of herbivores, as well as an action of pathogens, contributing to the balance of biological interactions. Protease inhibitors, are important molecules because of their heterologous potential in other biological systems, and may have in vitro and in vivo effects on several biological models, as well as therapeutic properties in a range of disorders that compromise human health. In this work an inhibitor of serinoprotease (CpTI), was isolated from the Caesalpinia pyramidalis Tul. seeds by fractionation of the crude extract with 30- 60% ammonium sulfate, followed by separation in affinity chromatography on TrypsinSepharose 4B-CNBr-actived column, the retained peak was enriched in inhibitory activity for trypsin, chymotrypsin and elastase serine protease type. The thermostability test showed that CpTI was able to maintain its functionality up to 80 °C and the concentrations required to inhibit 50% of the activity of the trypsin, human neutrophil elastase and chymotrypsin enzymes were 17, 21 and 156 μg/mL, respectively. CpTI also prolonged the coagulation time by the intrinsic pathway (TPPa) in more than 80 seconds at a concentration of 36.2 μg / mL. It was also observed that CpTI has no cytotoxic activity to red blood cells at any of the concentrations tested (0,03 , 0,125 e 0,5 mg/mL). These results demonstrate the potential therapeutic use of CpTI in processes involving inflammation and coagulation.
dc.publisherUniversidade Federal do Rio Grande do Norte
dc.publisherBrasil
dc.publisherUFRN
dc.publisherPROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS BIOLÓGICAS
dc.rightsAcesso Aberto
dc.subjectCoagulação
dc.subjectElastase neutrofílica humana
dc.subjectCatingueira
dc.subjectInflamação
dc.titleAvaliação da atividade anticoagulante e bloqueadora de elastase de um inibidor de tripsina isolado de Caesalpinea pyramidalis Tul.
dc.typemasterThesis


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