dc.creatorSalazar, AM
dc.creatorVivas, J
dc.creatorSánchez, EE
dc.creatorRodríguez-Acosta, Alexis
dc.creatorGuerrero, B
dc.date2013-11-29T17:12:26Z
dc.date2013-11-29T17:12:26Z
dc.date2013-11-29
dc.date.accessioned2022-10-28T00:56:28Z
dc.date.available2022-10-28T00:56:28Z
dc.identifierhttp://hdl.handle.net/10872/5148
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4939374
dc.descriptionThe coral snake Micrurus tener tener (Mtt) from the Elapidae family inhabits the southwestern United States and produces severe cases of envenomations. Although the majority of Mtt venom components are neurotoxins and phospholipase A2s, this study demonstrated, by SDS-PAGE and molecular exclusion chromatography (MEC), that these venoms also contain high-molecular- weight proteins between 50 and 150 kDa that target the hemostatic system. The biological aspects of other Micrurus venoms were also studied, such as the LD50s of Micrurus isozonus (from 0.52 to 0.61 mg/kg). A pool from these venoms presented a LD50 of 0.57 mg/kg, Micrurus f. fulvius (Mff) and Mtt had LD50s of 0.32 and 0.78 mg/kg, respectively. These venoms contained fibrino(geno)lytic activity, they inhibited platelet aggregation, as well as factor Xa and/or plasmin- like activities. M. isozonus venoms from different Venezuelan geographical regions inhibited ADP-induced platelet aggregation (from 50 to 68%). Micrurus tener tener venom from the United States was the most active with a 95.2% inhibitory effect. This venom showed thrombin-like activity on fibrinogen and human plasma. Fractions of Mtt showed fibrino(geno)lytic activity and inhibition on plasmin amidolytic activity. Several fractions degraded the fibrinogen Aα chains, and fractions F2 and F7 completely degraded both fibrinogen Aα and Bβ chains. To our knowledge, this is the first report on thrombin-like and fibrino(geno)lytic activity and plasmin or factor Xa inhibitors described in Micrurus venoms. Further purification and characterization of these Micrurus venom components could be of therapeutic use in the treatment of hemostatic disorders.
dc.descriptionThis research was supported by FONACIT grant (G-2005000400), Caracas, Venezuela, and funds from Texas A&M University-Kingsville, Kingsville, Texas, U.S.A.
dc.languageen_US
dc.relationToxicon;58(1): 35–45. 2011
dc.subjectCoral snakes
dc.subjectFibrino(geno)lytic activity
dc.subjectHemostasis
dc.subjectMicrurus tener tener
dc.subjectPlasmin inhibitors
dc.subjectVenom
dc.titleHemostatic and toxinological diversities in venom of Micrurus tener tener, Micrurus fulvius fulvius and Micrurus isozonus coral snakes
dc.typeArticle


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