Título : In vitro activity of Erigeron bonariensis L. essential oil and its main polyacetylenic compound as neutralizers of bothropic venoms
Autor(es) : Minteguiaga, Manuel
Torres, Ana María
Umpiérrez, Noelia
Catalán, César A.N.
Dellacassa, Eduardo
Fecha de publicación : 22-ago-2025
Tipo de publicación: Documento de conferencia
Versión: Publicado
Publicado en: Simpósio Latino-Americano De Óleos Essenciais (SILOE). Viçosa, Brasil. 20 a 22 de agosto de 2025.
Areas del conocimiento : Ciencias Naturales y Exactas
Ciencias Químicas
Química Orgánica
Ciencias Biológicas
Zoología, Ornitología, Entomología, Etología
Otros descriptores : Bothrops alternatus
Bothrops diporus
Essential oil
Erigeron bonariensis
Resumen : INTRODUCTION: Erigeron bonariensis L. is an aromatic and medicinal plant native of South America but currently distributed worldwide given its weed character. The chemical composition of its essential oil (EBEO) has been deeply investigated, highlighting the presence of mono- and sesquiterpenes, and polyacetylenes (PAs). In particular, cis-lachnophyllum acid methyl ester (LAME) has been reported to be one of the major components of EBEOs, where it accounts for more than 20% of the oil. The in vitro role of EBEO and other extracts as inhibitors of the effects of snake venom (including bothropic venoms) has been reported, but isolated components have not been evaluated so far. OBJECTIVE: Perform a systematic evaluation of the in vitro activity of EBEO and LAME against Bothrops diporus venom. METHODOLOGY: E. bonariensis plant material was collected at the full-flowering stage from a wild population in Canelones, Uruguay. EBEO was obtained by hydro-distillation using a Clevenger apparatus, while its composition was studied by GC-MS applying previously published protocols. LAME was isolated from EBEO by column chromatography, and its identity was corroborated by NMR. Both EBEO and LAME were incubated with B. diporus venom and submitted to the following in vitro alexiteric tests: inhibition of proteolysis (with casein as a model), indirect inhibition of hemolysis (using agarose erythrocyte-egg yolk medium), inhibition of coagulation of normal plasma (assessed by a coagulometer COL1 Wiener) and alteration of the venom proteins bands (followed by SDS-PAGE). RESULTS, DISCUSSION AND CONCLUSIONS: Assessed by GC-MS, EBEO showed as main components LAME (32.8%), limonene (23.5%), germacrene D (8.2%), trans-β-ocimene (6.9%) and β-pinene (5.0%). LAME was isolated in 94% purity according to GC-MS. EBEO and LAME altered B. diporus venom protein bands and exerted inhibition of proteolysis in SDS-PAGE. Moreover, both inhibit indirect hemolysis (26.3% and 57.9% respectively), whereas only LAME inhibits coagulation (60.6%). A preliminary SDS-PAGE study using B. alternatus venom also suggested in vitro neutralizing activity. The obtained results confirm the potential of EBEO as a neutralizer of bothropic venom, highlighting the role of LAME and PAs.
URI / Handle: https://hdl.handle.net/20.500.12381/5349
Institución responsable del proyecto: Universidad de la República
Universidad Nacional de Tucumán
Universidad Nacional del Nordeste
Financiadores: Programa de Desarrollo de las Ciencias Básicas
Asociación de Universidades Grupo Montevideo
Nivel de Acceso: Acceso abierto
Licencia CC: Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND)
Aparece en las colecciones: Publicaciones de ANII

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