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dc.contributor.authorSALAZAR, MARCOS
dc.contributor.authorCHÉRIGO, LILIA
dc.contributor.authorACOSTA, HILDAURA
dc.contributor.authorOTERO, RAFAEL
dc.contributor.authorMARTÍNEZ-LUIS, SERGIO
dc.date.accessioned2020-07-18T21:25:58Z
dc.date.available2020-07-18T21:25:58Z
dc.date.issued2014-06-20
dc.identifier.otherDOI: 10.2478/acph-2014-0033
dc.identifier.urihttp://repositorio-indicasat.org.pa/handle/123456789/208
dc.descriptionSignificant inhibition of the coagulant and hemorrhagic effects of Bothrops asper venom was demonstrated by ethanolic extract prepared from the leaves of Brownea rosademonte. In vitro experiments preincubating 5.5 mg of extract kg–1 b.m. for 30 min with a minimum hemorrhagic dose of venom (273.8 ± 16.1 µg of venom kg–1 b.m.) lowered the hemorrhagic activity of the venom alone in CD-1 mice by 51.5 ± 2.6 %. Additionally, 1.7 mg extract L–1 plasma prolonged 5.1 times the plasma coagulation time. Fractionation of the extract led to the isolation of two compounds: ononitol (1) and quercetrin (2). The structure of compounds 1 and 2 was established by spectroscopic analyses, including APCI-HRMS and NMR (1 H, 13C, HSQC, HMBC and COSY). A quercetrin concentration of 0.11 mmol L–1 prolonged the plasma coagulation time 2.6 times demonstrating that this compound was one of the active constituents of the Brownea rosademonte extract.en_US
dc.description.abstractSignificant inhibition of the coagulant and hemorrhagic effects of Bothrops asper venom was demonstrated by ethanolic extract prepared from the leaves of Brownea rosademonte. In vitro experiments preincubating 5.5 mg of extract kg–1 b.m. for 30 min with a minimum hemorrhagic dose of venom (273.8 ± 16.1 µg of venom kg–1 b.m.) lowered the hemorrhagic activity of the venom alone in CD-1 mice by 51.5 ± 2.6 %. Additionally, 1.7 mg extract L–1 plasma prolonged 5.1 times the plasma coagulation time. Fractionation of the extract led to the isolation of two compounds: ononitol (1) and quercetrin (2). The structure of compounds 1 and 2 was established by spectroscopic analyses, including APCI-HRMS and NMR (1 H, 13C, HSQC, HMBC and COSY). A quercetrin concentration of 0.11 mmol L–1 prolonged the plasma coagulation time 2.6 times demonstrating that this compound was one of the active constituents of the Brownea rosademonte extract.en_US
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dc.language.isoengen_US
dc.rightsInfo:eu-repo/semantics/openAccess
dc.rightshttps://creativecommons.org/licenses/by/4.0/deed.es
dc.subjectBothrops asper (Viperidae) venomen_US
dc.subjectBrownea rosademonte (Caesalpinaceae)en_US
dc.subjectquercetrinen_US
dc.subjectanticoagulanten_US
dc.subjectantihemorrhagicen_US
dc.subjectantiproteolyticen_US
dc.subjectantihemolyticen_US
dc.titleEvaluation of anti-Bothrops asper venom activity of ethanolic extract of Brownea rosademonte leavesen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeInfo:eu-repo/semantics/publishedversion


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