Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species

Detalhes bibliográficos
Autor(a) principal: Santos, Catarina dos [UNESP]
Data de Publicação: 2018
Outros Autores: Galaverna, Renan S., Angolini, Celio F. F, Nunes, Vania V. A. [UNESP], de Almeida, Luiz F. R. [UNESP], Ruiz, Ana L. T. G., de Carvalho, João E, Duarte, Regina M. T., Duarte, Marta C. T, Eberlin, Marcos N
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/molecules23050986
http://hdl.handle.net/11449/176240
Resumo: Myrcia bella Cambess., Myrcia fallax (Rich.) DC. and Myrcia guianensis (Aubl.) DC. (Myrtaceae) are trees found in Brazilian Cerrado. They have been widely used in folk medicine for the treatment of gastrointestinal disorders, hemorrhagic and infectious diseases. Few reports have been found in the literature connecting their phenolic composition and biological activities. In this regard, we have profiled the main phenolic constituents of Myrcia spp. leaves extracts by ESI(−)Q-TOF-MS. The main constituents found were ellagic acid (M. bella), galloyl glucose isomers (M. guianensis) and hexahydroxydiphenic (HHDP) acid derivatives (M. fallax). In addition, quercetin and myricetin derivatives were also found in all Myrcia spp. extracts. The most promising antioxidant activity, measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity, was found for M. fallax extracts (EC50 8.61 ± 0.22 µg·mL− 1), being slightly less active than quercetin and gallic acid (EC50 2.96 ± 0.17 and 2.03 ± 0.02 µg·mL− 1, respectively). For in vitro antiproliferative activity, M. guianensis showed good activity against leukemia (K562 TGI = 7.45 µg·mL− 1). The best antimicrobial activity was observed for M. bella and M. fallax to Escherichia coli (300 and 250 µg·mL− 1, respectively). In conclusion, the activities found are closely related to the phenolic composition of these plants.
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spelling Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia speciesBiological activitiesESI(−)Q-TOF-MSMyrcia spp.Phenolic compoundsMyrcia bella Cambess., Myrcia fallax (Rich.) DC. and Myrcia guianensis (Aubl.) DC. (Myrtaceae) are trees found in Brazilian Cerrado. They have been widely used in folk medicine for the treatment of gastrointestinal disorders, hemorrhagic and infectious diseases. Few reports have been found in the literature connecting their phenolic composition and biological activities. In this regard, we have profiled the main phenolic constituents of Myrcia spp. leaves extracts by ESI(−)Q-TOF-MS. The main constituents found were ellagic acid (M. bella), galloyl glucose isomers (M. guianensis) and hexahydroxydiphenic (HHDP) acid derivatives (M. fallax). In addition, quercetin and myricetin derivatives were also found in all Myrcia spp. extracts. The most promising antioxidant activity, measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity, was found for M. fallax extracts (EC50 8.61 ± 0.22 µg·mL− 1), being slightly less active than quercetin and gallic acid (EC50 2.96 ± 0.17 and 2.03 ± 0.02 µg·mL− 1, respectively). For in vitro antiproliferative activity, M. guianensis showed good activity against leukemia (K562 TGI = 7.45 µg·mL− 1). The best antimicrobial activity was observed for M. bella and M. fallax to Escherichia coli (300 and 250 µg·mL− 1, respectively). In conclusion, the activities found are closely related to the phenolic composition of these plants.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Biological Sciences Faculty of Sciences and Letters University of São Paulo State (UNESP)ThoMSon Mass Spectrometry Laboratory Institute of Chemistry University of Campinas (UNICAMP)Department of Botany Institute of Biosciences of Botucatu UNESP—Univ. Estadual PaulistaFaculty of Pharmaceutical Sciences University of Campinas (UNICAMP), P.O. Box 859CPQBA Microbiology Division University of Campinas, P.O. Box 6171Department of Biological Sciences Faculty of Sciences and Letters University of São Paulo State (UNESP)Department of Botany Institute of Biosciences of Botucatu UNESP—Univ. Estadual PaulistaFAPESP: 2017/15610-0Universidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Santos, Catarina dos [UNESP]Galaverna, Renan S.Angolini, Celio F. FNunes, Vania V. A. [UNESP]de Almeida, Luiz F. R. [UNESP]Ruiz, Ana L. T. G.de Carvalho, João EDuarte, Regina M. T.Duarte, Marta C. TEberlin, Marcos N2018-12-11T17:19:44Z2018-12-11T17:19:44Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.3390/molecules23050986Molecules, v. 23, n. 5, 2018.1420-3049http://hdl.handle.net/11449/17624010.3390/molecules230509862-s2.0-850461026312-s2.0-85046102631.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecules0,855info:eu-repo/semantics/openAccess2023-12-21T06:22:26Zoai:repositorio.unesp.br:11449/176240Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-21T06:22:26Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
title Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
spellingShingle Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
Santos, Catarina dos [UNESP]
Biological activities
ESI(−)Q-TOF-MS
Myrcia spp.
Phenolic compounds
title_short Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
title_full Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
title_fullStr Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
title_full_unstemmed Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
title_sort Antioxidative, antiproliferative and antimicrobial activities of phenolic compounds from three myrcia species
author Santos, Catarina dos [UNESP]
author_facet Santos, Catarina dos [UNESP]
Galaverna, Renan S.
Angolini, Celio F. F
Nunes, Vania V. A. [UNESP]
de Almeida, Luiz F. R. [UNESP]
Ruiz, Ana L. T. G.
de Carvalho, João E
Duarte, Regina M. T.
Duarte, Marta C. T
Eberlin, Marcos N
author_role author
author2 Galaverna, Renan S.
Angolini, Celio F. F
Nunes, Vania V. A. [UNESP]
de Almeida, Luiz F. R. [UNESP]
Ruiz, Ana L. T. G.
de Carvalho, João E
Duarte, Regina M. T.
Duarte, Marta C. T
Eberlin, Marcos N
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Campinas (UNICAMP)
dc.contributor.author.fl_str_mv Santos, Catarina dos [UNESP]
Galaverna, Renan S.
Angolini, Celio F. F
Nunes, Vania V. A. [UNESP]
de Almeida, Luiz F. R. [UNESP]
Ruiz, Ana L. T. G.
de Carvalho, João E
Duarte, Regina M. T.
Duarte, Marta C. T
Eberlin, Marcos N
dc.subject.por.fl_str_mv Biological activities
ESI(−)Q-TOF-MS
Myrcia spp.
Phenolic compounds
topic Biological activities
ESI(−)Q-TOF-MS
Myrcia spp.
Phenolic compounds
description Myrcia bella Cambess., Myrcia fallax (Rich.) DC. and Myrcia guianensis (Aubl.) DC. (Myrtaceae) are trees found in Brazilian Cerrado. They have been widely used in folk medicine for the treatment of gastrointestinal disorders, hemorrhagic and infectious diseases. Few reports have been found in the literature connecting their phenolic composition and biological activities. In this regard, we have profiled the main phenolic constituents of Myrcia spp. leaves extracts by ESI(−)Q-TOF-MS. The main constituents found were ellagic acid (M. bella), galloyl glucose isomers (M. guianensis) and hexahydroxydiphenic (HHDP) acid derivatives (M. fallax). In addition, quercetin and myricetin derivatives were also found in all Myrcia spp. extracts. The most promising antioxidant activity, measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity, was found for M. fallax extracts (EC50 8.61 ± 0.22 µg·mL− 1), being slightly less active than quercetin and gallic acid (EC50 2.96 ± 0.17 and 2.03 ± 0.02 µg·mL− 1, respectively). For in vitro antiproliferative activity, M. guianensis showed good activity against leukemia (K562 TGI = 7.45 µg·mL− 1). The best antimicrobial activity was observed for M. bella and M. fallax to Escherichia coli (300 and 250 µg·mL− 1, respectively). In conclusion, the activities found are closely related to the phenolic composition of these plants.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:19:44Z
2018-12-11T17:19:44Z
2018-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/molecules23050986
Molecules, v. 23, n. 5, 2018.
1420-3049
http://hdl.handle.net/11449/176240
10.3390/molecules23050986
2-s2.0-85046102631
2-s2.0-85046102631.pdf
url http://dx.doi.org/10.3390/molecules23050986
http://hdl.handle.net/11449/176240
identifier_str_mv Molecules, v. 23, n. 5, 2018.
1420-3049
10.3390/molecules23050986
2-s2.0-85046102631
2-s2.0-85046102631.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Molecules
0,855
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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