Caracterização bioquímica e funcional de uma metaloprotease isolada da peçonha da serpente Bothrops moojeni

CHAPTER II: Bothrops snake venoms contain proteins that contribute to the local and systemic effects seen after envenoming, such as edema, myonecrosis, coagulation disorders and hemorrhage. These effects can be triggered by the toxic action of metalloproteinases present in the bothropic venom. This...

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Detalles Bibliográficos
Autor: Mamede, Carla Cristine Neves
Tipo de recurso: tesis de maestría
Estado:Versión publicada
Fecha de publicación:2011
País:Brasil
Institución:Universidade Federal de Uberlândia (UFU)
Repositorio:Repositório Institucional da UFU
Idioma:portugués
OAI Identifier:oai:repositorio.ufu.br:123456789/15833
Acceso en línea:https://repositorio.ufu.br/handle/123456789/15833
Access Level:acceso abierto
Palabra clave:Bothrops moojeni, metaloprotease, fibrinogenases, mionecrose
Bothrops
Enzimas proteolíticas
Jararaca (Cobra) Veneno
Cobra venenosa - Veneno
Metalloprotease
Fibrinogenases
Myonecrosis
CNPQ::CIENCIAS BIOLOGICAS::GENETICA
Descripción
Sumario:CHAPTER II: Bothrops snake venoms contain proteins that contribute to the local and systemic effects seen after envenoming, such as edema, myonecrosis, coagulation disorders and hemorrhage. These effects can be triggered by the toxic action of metalloproteinases present in the bothropic venom. This study aimed to perform the purification, biochemical and functional characterization of a metalloproteinase called Moozincin, from Bothrops moojeni snake venom. Moozincin has approximate molecular mass of 28 kDa, displays relevant fibrinogenolytic activity and can be classified as a non-hemorrhagic fibrinogenolytic metalloprotease, in the class P-I. Moozincin was also able to induce edema, myonecrosis and hyperalgesia in experimental animals. Morphological analysis of the evolution of muscle injury revealed the occurrence of degenerative events and leukocyte infiltration already at three hours after application of Moozincin. These effects dominate until 48 hours after administration of the metalloprotease, when hemorrhagic effect was also demonstrated later in skeletal muscle, probably triggered by the action characteristic of metalloproteinases on vascular components and / or indirect action resulting from muscle injury.