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Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity

A bioactive compound isolated from the stem extract of Aristolochia sprucei through High Performance Liquid Chromatography (HPLC) was identified via Nuclear Magnetic Resonance (NMR) as the aristolochic acid (AA). This compound showed an inhibitory effect over the myotoxic activity of Bothrops jarara...

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Autores principales: González Rodríguez, Isela I., Francisco, Aleff F., Moreira-Dill, Leandro S., Quintero, Aristides, Guimarães, César L.S., Fernandes, Carlos A.H., Takeda, Agnes A.S., Zanchi, Fernando B., Caldeira, Cléopatra A.S., Pereira, Paulo S., Fontes, Marcos R.M., Zuliani, Juliana P., Soares, Andreimar M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322210/
https://www.ncbi.nlm.nih.gov/pubmed/32613196
http://dx.doi.org/10.1016/j.toxcx.2020.100049
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author González Rodríguez, Isela I.
Francisco, Aleff F.
Moreira-Dill, Leandro S.
Quintero, Aristides
Guimarães, César L.S.
Fernandes, Carlos A.H.
Takeda, Agnes A.S.
Zanchi, Fernando B.
Caldeira, Cléopatra A.S.
Pereira, Paulo S.
Fontes, Marcos R.M.
Zuliani, Juliana P.
Soares, Andreimar M.
author_facet González Rodríguez, Isela I.
Francisco, Aleff F.
Moreira-Dill, Leandro S.
Quintero, Aristides
Guimarães, César L.S.
Fernandes, Carlos A.H.
Takeda, Agnes A.S.
Zanchi, Fernando B.
Caldeira, Cléopatra A.S.
Pereira, Paulo S.
Fontes, Marcos R.M.
Zuliani, Juliana P.
Soares, Andreimar M.
author_sort González Rodríguez, Isela I.
collection PubMed
description A bioactive compound isolated from the stem extract of Aristolochia sprucei through High Performance Liquid Chromatography (HPLC) was identified via Nuclear Magnetic Resonance (NMR) as the aristolochic acid (AA). This compound showed an inhibitory effect over the myotoxic activity of Bothrops jararacussu and Bothrops asper venoms, being also effective against the indirect hemolytic activity of B. asper venom. Besides, AA also inhibited the myotoxic activity of BthTX-I and MTX-II with an efficiency greater than 60% against both myotoxins. Docking predictions revealed an interesting mechanism, through which the AA displays an interaction profile consistent with its inhibiting abilities, binding to both active and putative sites of svPLA(2). Overall, the present findings indicate that AA may bind to critical regions of myotoxic Asp 49 and Lys49-PLA(2)s from snake venoms, highlighting the relevance of domains comprising the active and putative sites to inhibit these toxins.
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spelling pubmed-73222102020-06-30 Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity González Rodríguez, Isela I. Francisco, Aleff F. Moreira-Dill, Leandro S. Quintero, Aristides Guimarães, César L.S. Fernandes, Carlos A.H. Takeda, Agnes A.S. Zanchi, Fernando B. Caldeira, Cléopatra A.S. Pereira, Paulo S. Fontes, Marcos R.M. Zuliani, Juliana P. Soares, Andreimar M. Toxicon X Venomics at the crossroads between ecological and clinical toxinology, Edited by: Dr. Juan Calvete, Dr.Jose Maria Gutiérrez and Dr. Cleópatra A.S. Caldeira A bioactive compound isolated from the stem extract of Aristolochia sprucei through High Performance Liquid Chromatography (HPLC) was identified via Nuclear Magnetic Resonance (NMR) as the aristolochic acid (AA). This compound showed an inhibitory effect over the myotoxic activity of Bothrops jararacussu and Bothrops asper venoms, being also effective against the indirect hemolytic activity of B. asper venom. Besides, AA also inhibited the myotoxic activity of BthTX-I and MTX-II with an efficiency greater than 60% against both myotoxins. Docking predictions revealed an interesting mechanism, through which the AA displays an interaction profile consistent with its inhibiting abilities, binding to both active and putative sites of svPLA(2). Overall, the present findings indicate that AA may bind to critical regions of myotoxic Asp 49 and Lys49-PLA(2)s from snake venoms, highlighting the relevance of domains comprising the active and putative sites to inhibit these toxins. Elsevier 2020-06-20 /pmc/articles/PMC7322210/ /pubmed/32613196 http://dx.doi.org/10.1016/j.toxcx.2020.100049 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Venomics at the crossroads between ecological and clinical toxinology, Edited by: Dr. Juan Calvete, Dr.Jose Maria Gutiérrez and Dr. Cleópatra A.S. Caldeira
González Rodríguez, Isela I.
Francisco, Aleff F.
Moreira-Dill, Leandro S.
Quintero, Aristides
Guimarães, César L.S.
Fernandes, Carlos A.H.
Takeda, Agnes A.S.
Zanchi, Fernando B.
Caldeira, Cléopatra A.S.
Pereira, Paulo S.
Fontes, Marcos R.M.
Zuliani, Juliana P.
Soares, Andreimar M.
Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity
title Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity
title_full Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity
title_fullStr Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity
title_full_unstemmed Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity
title_short Isolation and structural characterization of bioactive compound from Aristolochia sprucei aqueous extract with anti-myotoxic activity
title_sort isolation and structural characterization of bioactive compound from aristolochia sprucei aqueous extract with anti-myotoxic activity
topic Venomics at the crossroads between ecological and clinical toxinology, Edited by: Dr. Juan Calvete, Dr.Jose Maria Gutiérrez and Dr. Cleópatra A.S. Caldeira
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322210/
https://www.ncbi.nlm.nih.gov/pubmed/32613196
http://dx.doi.org/10.1016/j.toxcx.2020.100049
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