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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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. |
format | Online Article Text |
id | pubmed-7322210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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