Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add filters








Year range
1.
Braz. j. med. biol. res ; 41(1): 12-17, Jan. 2008. graf
Article in English | LILACS | ID: lil-469981

ABSTRACT

A serine proteinase with thrombin-like activity was isolated from the venom of the Central American pit viper Bothrops asper. Isolation was performed by a combination of affinity chromatography on aminobenzamidine-Sepharose and ion-exchange chromatography on DEAE-Sepharose. The enzyme accounts for approximately 0.13 percent of the venom dry weight and has a molecular mass of 32 kDa as determined by SDS-PAGE, and of 27 kDa as determined by MALDI-TOF mass spectrometry. Its partial amino acid sequence shows high identity with snake venom serine proteinases and a complete identity with a cDNA clone previously sequenced from this species. The N-terminal sequence of the enzyme is VIGGDECNINEHRSLVVLFXSSGFL CAGTLVQDEWVLTAANCDSKNFQ. The enzyme induces clotting of plasma (minimum coagulant dose = 4.1 µg) and fibrinogen (minimum coagulant dose = 4.2 µg) in vitro, and promotes defibrin(ogen)ation in vivo (minimum defibrin(ogen)ating dose = 1.0 µg). In addition, when injected intravenously in mice at doses of 5 and 10 µg, it induces a series of behavioral changes, i.e., loss of the righting reflex, opisthotonus, and intermittent rotations over the long axis of the body, which closely resemble the `gyroxin-like' effect induced by other thrombin-like enzymes from snake venoms.


Subject(s)
Animals , Mice , Blood Coagulation , Bothrops , Coagulants/isolation & purification , Crotalid Venoms/enzymology , Serine Endopeptidases/isolation & purification , Amino Acid Sequence , Antivenins/therapeutic use , Blood Coagulation/drug effects , Chromatography, Agarose , Chromatography, Ion Exchange , Costa Rica , Coagulants/administration & dosage , Coagulants/pharmacology , Drug Evaluation, Preclinical , Fibrinogen/metabolism , Serine Endopeptidases/chemistry , Serine Endopeptidases/genetics , Serine Endopeptidases/pharmacology , Snake Bites/physiopathology , Thrombin/chemistry
2.
Medicina (B.Aires) ; 64(6): 509-517, 2005. graf, ilus
Article in English | LILACS | ID: lil-444262

ABSTRACT

Due to variability of venom components from the same species of snakes that inhabit different regions, particular properties of the venom of Crotalus durissus terrificus that inhabits the North-East of Argentina were studied. Gyroxin, a thrombin-like enzyme, was isolated from this venom by gel filtration and affinity chromatography, it was found to be homogeneous according to SDS-PAGE, with a molecular weight of 33 kDa. [quot ]Gyroxin syndrome[quot ] in mice was tested and it showed changes in the animal behavior, confirming that the isolated thrombin-like enzyme is gyroxin. Effects of this enzyme and the crude venom on mice plasmatic fibrinogen levels were determined. The mice plasma fibrinogen decreased rapidly until incoagulability during the first hour after thrombin-like enzyme injection, then reaching its normal level 10 hours after injection; whereas crude venom resulted in a 60% decrease of the mice plasma fibrinogen, reaching its normal level after the same period of time. After 1 hour of gyroxin inoculation, intravascular coagulation was observed in histological cuttings of lung, cardiac muscle and liver. The isolated enzyme showed strong hydrolyzing activity on fibrinogen and fibrin in vitro, whereas the crude venom exhibited weak hydrolyzing activity on both substrates. It is probable that this very low activity is due to the low percentage of the enzyme in the crude venom. Decreasing of plasmatic fibrinogen levels may be due to either the coagulant or hydrolyzing actions of the enzyme.


Teniendo en cuenta la variabilidadde los componentes del veneno de serpientes de una misma especie que habitan regiones diferentes, se decidióestudiar las propiedades particulares del veneno de Crotalus durissus terrificus que habita el nordeste de Argentina, Giroxina, una enzima con actividad trombínica, fue aislada del veneno por cromatografía de filtración por gel y de afinidad; se comprobó su homogeneidad y se determinó su peso molecular, 33 kDa, por SDSPAGE. Se ensayó el síndrome giroxina en ratones, los que mostraron cambios en el comportamiento, confirmandoque la enzima tipo trombina aislada es giroxina. Se evaluó la acción de esta enzima sobre los niveles de fibrinógeno plasmático en ratones, comparándola con la del veneno crudo. Se comprobó que la enzima provoca una disminución de los niveles plasmáticos de fibrinógeno hasta la incoagulabilidad, durante la primer hora de inoculación, mientras que el veneno entero produjo una reducción del nivel plasmático en un 60%; sin embargo, en ambos casos, se evidenció una rápida reposición de fibrinógeno plasmático, alcanzando sus valores normales en un plazo de 10 horas. Se observó coagulación intravascular con la administración de giroxina una hora después de la inoculación, evidenciados en estudios histológicos de tejido pulmonar, cardíaco y hepático. En ensayos realizados in vitro, la enzima aislada mostró capacidad de degradar fibrinógeno como así también coágulos de fibrina, mientras que el veneno exhibió débil actividad hidrolítica sobre ambos sustratos. Es probable que esta baja actividad sea debida a la baja concentración de la enzima en el veneno. La disminución de los niveles de fibrinógeno plasmático observado en ratones se debería a la acción coagulante de la enzima, sin embargo no se descarta que también contribuya a este proceso una acción hidrolítica sobrefibrinógeno y fibrina por parte de la enzima.


Subject(s)
Animals , Female , Male , Mice , Crotalus , Fibrinogen/metabolism , Thrombin/metabolism , Crotalid Venoms/enzymology , Argentina , Coagulants/pharmacology , Liver/pathology , Lung/pathology , Crotalid Venoms/isolation & purification , Crotalid Venoms/metabolism , Crotalid Venoms/pharmacology
3.
Rev. bras. neurol ; 40(3): 33-39, jul.-set. 2004. ilus, tab
Article in Portuguese | LILACS | ID: lil-426215

ABSTRACT

As hemorragias intracranianas constituem-se num grave distúrbio, geralmente de origem vascular, que acomete a inexpansível caixa craniana. Acometimentos cerebrais envolvem a formação de uma área perilesional denominada zona de penumbra adicionada a edemas e efeitos de massa com elevação da pressão intracraniana. Muito se discute sobre o comportamento desta zona de penumbra nas situações de acidentes vasculares cerebrais isquêmicos. Hoje em dia, estudos mostram que esta mesma zona de penumbra está presente também nos acidentes vasculares hemorrágicos e, sendo assim, o neurocirurgião deve a qualquer custo evitar a expansão dos hematomas intracranianos que sabidamente crescem devido a hemorragias secundárias com posteriores déficits neurológicos. Numa meta-análise envolvendo 58 pacientes, várias foram as indicações para uso de rFVIIa, mostrando-se sempre eficácia na melhora dos parâmetros hematimétricos. Dentre as indicações para sangramentos em SNC, pode ser uma arma de utilidade na redução da disseminação da lesão inicial, protegendo a zona de penumbra e minimizando as seqüelas.


Subject(s)
Humans , Coagulants/pharmacology , Factor VIIa/therapeutic use , Cerebral Hemorrhage/blood , Cerebral Hemorrhage/therapy , Internal Medicine/methods , Recombinant Proteins/therapeutic use
4.
Indian J Exp Biol ; 1990 Jan; 28(1): 43-5
Article in English | IMSEAR | ID: sea-58812

ABSTRACT

As blood coagulation is a prelude for wound healing, a systemic haemocoagulant (Botropase) and local procoagulants (thrombin and fibrin) were evaluated on physical (wound breaking strength, wound half-closure time and period of epithelization), biochemical (granuloma-hydroxyproline and hexosamine) and histological attributes of healing wounds in albino rats. Botropase prompted all phases of tissue repair. Thrombin delayed wound contraction whereas fibrin had no discernable action. The findings that procoagulants modify healing process has bearing on their surgical use.


Subject(s)
Animals , Coagulants/pharmacology , Enzymes/pharmacology , Female , Fibrin/pharmacology , Male , Rats , Rats, Inbred Strains , Thrombin/pharmacology , Wound Healing/drug effects
SELECTION OF CITATIONS
SEARCH DETAIL