Hemorrhagic, coagulant and fibrino(geno)lytic activities of crude venom and fractions from mapanare (Bothrops colombiensis) snakes
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- 作者：Marí ; a E. Giró ; n ; Ana M. Salazar ; Irma Aguilar ; John C. Pé ; rez ; Elda E. Sá ; nchez ; Carmen L. Arocha-Piñ ; ango ; Alexis Rodrí ; guez-Acosta ; Belsy Guerrero
- 关键词：Bothrops colombiensis ; Coagulation ; Fibrinolysis ; Intra-population venom variability ; Snake venom
- 刊名：Comparative Biochemistry and Physiology, Part C
- 出版年：2008
- 出版时间：January 2008
- 年：2008
- 卷：147
- 期：1
- 页码：113-121
- 全文大小：508 K
文摘
Bothrops colombiensis venom from two similar geographical locations were tested for their hemostatic functions and characterized by gel-filtration chromatography and SDS-PAGE electrophoresis. The snakes were from Caucagua and El Guapo towns of the Venezuelan state of Miranda. Fibrino(geno)lytic, procoagulant, hemorrhagic, lethal activities, gel-filtration chromatography and SDS-PAGE profiles were analyzed and compared for both venoms. The highest hemorrhagic activity of 5.3 μg was seen in El Guapo venom while Caucagua venom had the lowest LD50 of 5.8 mg/kg. Both venoms presented similar thrombin-like activity. El Guapo showed a factor Xa-like activity two times higher than Caucagua. Differences were observed in kallikrein-like and t-PA activities, being highest in El Guapo. Caucagua venom showed the maximum fibrin lysis. Both crude venom runs on Sephadex G-100 chromatography gave fraction SII with the high fibrinolytic activity. Proteases presented in SII fractions and eluted from Benzamidine-Sepharose (not bound to the column) provoked a fast degradation of fibrinogen α chains and a slower degradation of β chains, which could possibly be due to a higher content of α fibrinogenases in these venoms. The fibrinogenolytic activity was decreased by metalloprotease inhibitors. The results suggested that metalloproteases in SII fractions were responsible for the fibrinolytic activity. The analysis of samples for fibrin-zymography of SII fractions showed an active band with a molecular mass of approximately 30 kDa. These results reiterate the importance of using pools of venoms for antivenom immunization, to facilitate the neutralization of the maximum potential number of toxins.