Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica

Detalhes bibliográficos
Autor(a) principal: Dolwitsch, Carolina Bolssoni
Data de Publicação: 2020
Tipo de documento: Tese
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/22141
Resumo: Hesperozygis ringens (Benth.) Epling (Lamiaceae), is an aromatic plant, endemic to southern Brazil, it is popularly used as an insecticide, but it is not properly studied in the literature. In view of this gap, the objective of this work was to evaluate the antioxidant, antimicrobial, cytotoxic, genotoxic, trypanocidal and nematicide activity of Hesperozygis ringens extracts obtained by supercritical fluid extraction using carbon dioxide (SFE-CO2) and ultrasoundassisted extractions with ethanol (UAE-EtOH) in addition to obtaining an overview of the chemical composition of the species. In the SFE-CO2 extract were found major compounds: pulegone, limonene, linalool, ρ-mentone, neo-menthol, transcariophylene and β-Sitosterol. In the UAE-EtOH extract, rosmarinic acid, chlorogenic acid, caffeic acid, ferulic acid, rutin, ρ- cumaric acid, vanylic acid, resveratrol, luteolin, quercetin, apigenin and canferol were detected. Both extracts showed antioxidant activity against the DPPH radical (IC50 172,38 μg mL−1 and 9516 μg mL−1) for UAE-EtOH and SFE-CO2 extracts, respectively.). The UAEEtOH extract did not show antimicrobial activity against the tested microrganisms. The SFECO2 extract showed an inhibition halo in the diffusion disk assay against the Pseudomoas aeruginosa bacteria and the fungus Candidaa albincans, with lowest inhibiting concentration of 1.46 mg mL−1 in the microdilution assay. Well diffusion assay, demonstrated that SFECO2 extract in 10 mg mL−1 inhibited the bacteria Sthaphylococcus aureus ATCC33591, Sthaphylococcus aureus ATCC29213 and Sthaphylococcus epidermidis ATCC35984. Neither extract presented cytotoxicity or genotoxicity against human mononuclear blood cells at the concentrations 625-10000 μg mL-1 and 31.25-250 μg mL‾1, for SFE-CO2 and UAEEtOH respectively. Both extracts eliminated 100% of Trypanosoma evansi at the end of the time evaluated in the experiment (9h) in concentrations 2500 μg mL‾1, 1250 μg mL‾1, 625 μg mL‾1 (SFE-CO2) and 250 μg mL‾1, 62.5 μg mL‾1, 31.25 μg mL‾1 (UAE-EtOH). The SFE-CO2 extract at 10 mg mL‾1and the UAE-EtOH extract in 80 mg mL‾1and in their dilutions eliminated 80% of Meloidogyne javanica J2 larvae. Thus, the extractions proved to be adequate for the chemical composition analysis of H. ringens, which showed antioxidant, antimicrobial, trypanocidal, nematicide activity without showing cytotoxicity and genotoxicity. Therefore, of H. ringens can be an alternative for the development of new drugs
id UFSM_05102ab073c8d513e1bf25c4d3b1717b
oai_identifier_str oai:repositorio.ufsm.br:1/22141
network_acronym_str UFSM
network_name_str Manancial - Repositório Digital da UFSM
repository_id_str
spelling Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológicaHesperozygis ringens (Lamiaceae): chemical characterization and biological activitiesHesperozygis ringensAntioxidanteToxicidadeTripanocidaNematicidaAntimicrobianaAntioxidantToxicityTrypanocidalNematicideAntimicrobialCNPQ::CIENCIAS DA SAUDE::FARMACIAHesperozygis ringens (Benth.) Epling (Lamiaceae), is an aromatic plant, endemic to southern Brazil, it is popularly used as an insecticide, but it is not properly studied in the literature. In view of this gap, the objective of this work was to evaluate the antioxidant, antimicrobial, cytotoxic, genotoxic, trypanocidal and nematicide activity of Hesperozygis ringens extracts obtained by supercritical fluid extraction using carbon dioxide (SFE-CO2) and ultrasoundassisted extractions with ethanol (UAE-EtOH) in addition to obtaining an overview of the chemical composition of the species. In the SFE-CO2 extract were found major compounds: pulegone, limonene, linalool, ρ-mentone, neo-menthol, transcariophylene and β-Sitosterol. In the UAE-EtOH extract, rosmarinic acid, chlorogenic acid, caffeic acid, ferulic acid, rutin, ρ- cumaric acid, vanylic acid, resveratrol, luteolin, quercetin, apigenin and canferol were detected. Both extracts showed antioxidant activity against the DPPH radical (IC50 172,38 μg mL−1 and 9516 μg mL−1) for UAE-EtOH and SFE-CO2 extracts, respectively.). The UAEEtOH extract did not show antimicrobial activity against the tested microrganisms. The SFECO2 extract showed an inhibition halo in the diffusion disk assay against the Pseudomoas aeruginosa bacteria and the fungus Candidaa albincans, with lowest inhibiting concentration of 1.46 mg mL−1 in the microdilution assay. Well diffusion assay, demonstrated that SFECO2 extract in 10 mg mL−1 inhibited the bacteria Sthaphylococcus aureus ATCC33591, Sthaphylococcus aureus ATCC29213 and Sthaphylococcus epidermidis ATCC35984. Neither extract presented cytotoxicity or genotoxicity against human mononuclear blood cells at the concentrations 625-10000 μg mL-1 and 31.25-250 μg mL‾1, for SFE-CO2 and UAEEtOH respectively. Both extracts eliminated 100% of Trypanosoma evansi at the end of the time evaluated in the experiment (9h) in concentrations 2500 μg mL‾1, 1250 μg mL‾1, 625 μg mL‾1 (SFE-CO2) and 250 μg mL‾1, 62.5 μg mL‾1, 31.25 μg mL‾1 (UAE-EtOH). The SFE-CO2 extract at 10 mg mL‾1and the UAE-EtOH extract in 80 mg mL‾1and in their dilutions eliminated 80% of Meloidogyne javanica J2 larvae. Thus, the extractions proved to be adequate for the chemical composition analysis of H. ringens, which showed antioxidant, antimicrobial, trypanocidal, nematicide activity without showing cytotoxicity and genotoxicity. Therefore, of H. ringens can be an alternative for the development of new drugsHesperozygis ringens (Benth.) Epling (Lamiaceae) é uma planta aromática, endêmica do Sul do Brasil, é usada popularmente como inseticida, mas seu conhecimento é muito limitado. Em vista dessa lacuna, o objetivo desse trabalho foi avaliar a atividade antioxidante, antimicrobiana, citotóxica, genotóxica, tripanocida e nematicida de extratos de H. ringens obtidos por extração com fluido supercrítico usando dióxido de carbono (SFE-CO2) e sonda de ultrassom com etanol (UAE-EtOH), além de obter um panorama sobre a composição química da espécie. No extrato SFE-CO2 foram encontrados como compostos majoritários pulegona, limoneno, linalol, ρ-mentona, neo-mentol, transcariofileno e β-Sitosterol. O extrato UAE-EtOH apresentou ácido rosmarínico, ácido clorogênico, ácido caféico, ácido ferúlico, rutina, ácido ρ-cumárico, ácido vanílico, resveratrol, luteolina, quercetina, apigenina e canferol. Os dois extratos apresentaram atividade antioxidante frente ao radical DPPH, sendo que o extrato UAE-EtOH apresentou melhor atividade (IC50 172,38 μg/mL) do que o extrato SFE-CO2 (IC50 9516 μg/mL). O extrato UAE-EtOH não mostrou atividade antimicrobiana frente aos micro-organismos testados. O extrato SFE-CO2 apresentou halo de inibição no ensaio de disco difusão contra as bactérias Pseudomonas aeruginosa e ao fungo Candida albincans, e a menor concentração capaz de inibir o crescimento para ambos microorganismos no ensaio de microdiluição em placa foi de 1,46 mg/mL. Já no teste de perfuração em ágar o extrato SFE-CO2 em 10 mg mL-1 inibiu as bactérias S. aureus ATCC33591, S. aureus ATCC29213 e S. epidermidis ATCC35984. Tanto o extrato SFE-CO2 como o UAEEtOH não apresentaram citotoxidade pelo teste de MTT, nem genotoxicidade no ensaio cometa, nas concentrações 625-10000 μg mL-1 e 31.25-250 μg mL‾1, respectivamente. Ambos extratos eliminaram 100% de Trypanosoma evansi no final do tempo avaliado no experimento (9h), nas concentrações 2500 μg mL‾1; 1250 μg mL‾1; 625 μg mL‾1 (SFE-CO2) e 250 μg mL‾1; 62.5 μg mL‾1; 31.25 μg mL‾1 (UAE-EtOH). O extrato SFE-CO2 a 10 mg mL-1 e o extrato UAE-EtOH em 80 mg mL-1 e nas suas diluições eliminaram 80% de larvas J2 de Meloidogyne javanica. Dessa forma, as extrações mostaram-se adequadas para a análise da composição química de H. ringens, a qual apresentou atividade antioxidante, antimicrobiana, tripanocida, nematicida sem apresentar citotoxicidade e genotoxicidade. Sendo assim, H. ringens, pode ser uma alternativa para o desenvolvimento de novos medicamentos.Universidade Federal de Santa MariaBrasilAnálises Clínicas e ToxicológicasUFSMPrograma de Pós-Graduação em Ciências FarmacêuticasCentro de Ciências da SaúdeRosa, Marcelo Barcellos dahttp://lattes.cnpq.br/0308293154958870Carvalho, Camilo Amaro deSagrillo, Michele RoratoEssi, LilianaCardoso, Carmem DickowDolwitsch, Carolina Bolssoni2021-09-02T17:53:54Z2021-09-02T17:53:54Z2020-03-26info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/22141porAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2021-09-03T06:03:10Zoai:repositorio.ufsm.br:1/22141Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2021-09-03T06:03:10Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
Hesperozygis ringens (Lamiaceae): chemical characterization and biological activities
title Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
spellingShingle Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
Dolwitsch, Carolina Bolssoni
Hesperozygis ringens
Antioxidante
Toxicidade
Tripanocida
Nematicida
Antimicrobiana
Antioxidant
Toxicity
Trypanocidal
Nematicide
Antimicrobial
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
title_full Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
title_fullStr Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
title_full_unstemmed Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
title_sort Hesperozygis ringens (Benth). Epling: caracterização química e atividade biológica
author Dolwitsch, Carolina Bolssoni
author_facet Dolwitsch, Carolina Bolssoni
author_role author
dc.contributor.none.fl_str_mv Rosa, Marcelo Barcellos da
http://lattes.cnpq.br/0308293154958870
Carvalho, Camilo Amaro de
Sagrillo, Michele Rorato
Essi, Liliana
Cardoso, Carmem Dickow
dc.contributor.author.fl_str_mv Dolwitsch, Carolina Bolssoni
dc.subject.por.fl_str_mv Hesperozygis ringens
Antioxidante
Toxicidade
Tripanocida
Nematicida
Antimicrobiana
Antioxidant
Toxicity
Trypanocidal
Nematicide
Antimicrobial
CNPQ::CIENCIAS DA SAUDE::FARMACIA
topic Hesperozygis ringens
Antioxidante
Toxicidade
Tripanocida
Nematicida
Antimicrobiana
Antioxidant
Toxicity
Trypanocidal
Nematicide
Antimicrobial
CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Hesperozygis ringens (Benth.) Epling (Lamiaceae), is an aromatic plant, endemic to southern Brazil, it is popularly used as an insecticide, but it is not properly studied in the literature. In view of this gap, the objective of this work was to evaluate the antioxidant, antimicrobial, cytotoxic, genotoxic, trypanocidal and nematicide activity of Hesperozygis ringens extracts obtained by supercritical fluid extraction using carbon dioxide (SFE-CO2) and ultrasoundassisted extractions with ethanol (UAE-EtOH) in addition to obtaining an overview of the chemical composition of the species. In the SFE-CO2 extract were found major compounds: pulegone, limonene, linalool, ρ-mentone, neo-menthol, transcariophylene and β-Sitosterol. In the UAE-EtOH extract, rosmarinic acid, chlorogenic acid, caffeic acid, ferulic acid, rutin, ρ- cumaric acid, vanylic acid, resveratrol, luteolin, quercetin, apigenin and canferol were detected. Both extracts showed antioxidant activity against the DPPH radical (IC50 172,38 μg mL−1 and 9516 μg mL−1) for UAE-EtOH and SFE-CO2 extracts, respectively.). The UAEEtOH extract did not show antimicrobial activity against the tested microrganisms. The SFECO2 extract showed an inhibition halo in the diffusion disk assay against the Pseudomoas aeruginosa bacteria and the fungus Candidaa albincans, with lowest inhibiting concentration of 1.46 mg mL−1 in the microdilution assay. Well diffusion assay, demonstrated that SFECO2 extract in 10 mg mL−1 inhibited the bacteria Sthaphylococcus aureus ATCC33591, Sthaphylococcus aureus ATCC29213 and Sthaphylococcus epidermidis ATCC35984. Neither extract presented cytotoxicity or genotoxicity against human mononuclear blood cells at the concentrations 625-10000 μg mL-1 and 31.25-250 μg mL‾1, for SFE-CO2 and UAEEtOH respectively. Both extracts eliminated 100% of Trypanosoma evansi at the end of the time evaluated in the experiment (9h) in concentrations 2500 μg mL‾1, 1250 μg mL‾1, 625 μg mL‾1 (SFE-CO2) and 250 μg mL‾1, 62.5 μg mL‾1, 31.25 μg mL‾1 (UAE-EtOH). The SFE-CO2 extract at 10 mg mL‾1and the UAE-EtOH extract in 80 mg mL‾1and in their dilutions eliminated 80% of Meloidogyne javanica J2 larvae. Thus, the extractions proved to be adequate for the chemical composition analysis of H. ringens, which showed antioxidant, antimicrobial, trypanocidal, nematicide activity without showing cytotoxicity and genotoxicity. Therefore, of H. ringens can be an alternative for the development of new drugs
publishDate 2020
dc.date.none.fl_str_mv 2020-03-26
2021-09-02T17:53:54Z
2021-09-02T17:53:54Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/22141
url http://repositorio.ufsm.br/handle/1/22141
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Análises Clínicas e Toxicológicas
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Análises Clínicas e Toxicológicas
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
_version_ 1805922073982271488