Hemorrhagic, coagulant and fibrino(geno)lytic activities of crude venom and fractions from mapanare (Bothrops colombiensis) snakes

被引:26
作者
Giron, Maria E. [2 ]
Salazar, Ana M. [1 ]
Aguilar, Irma [2 ]
Perez, John C. [3 ]
Sanchez, Elda E. [3 ]
Arocha-Pinango, Carmen L. [1 ]
Rodriguez-Acosta, Alexis [2 ]
Guerrero, Belsy [1 ]
机构
[1] Inst Venezolano Invest Cient, Ctr Med Expt, Lab Fisiopatol, Caracas 1020A, Venezuela
[2] Cent Univ Venezuela, Secc Inmunoquim, Inst Trop Med, Caracas, Venezuela
[3] Texas A&M Univ, NTRC, Kingsville, TX 78363 USA
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 2008年 / 147卷 / 01期
关键词
Bothrops colombiensis; coagulation; fibrinolysis; intra-population venom variability; snake venom;
D O I
10.1016/j.cbpc.2007.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bothrops colonibiensis venom from two similar geographical locations were tested for their hemostatic functions and characterized by gelfiltration 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 mu g 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 alpha chains and a slower degradation of p chains, which could possibly be due to a higher content of alpha 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 fibrinzymography 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. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:113 / 121
页数:9
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