Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar

Detalhes bibliográficos
Autor(a) principal: Froeder, Amanda Luana Forbrig
Data de Publicação: 2015
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000wqnj
Texto Completo: http://repositorio.ufsm.br/handle/1/6043
Resumo: The Celtis iguanaea species is popularly known as esporão-de-galo and its leaves are used in folk medicine to treat body aches, rheumatism, asthma, colic, indigestion, ulcers, and as a diuretic, and roots for urinary tract infections. This study aimed to contribute to the phytochemical, antioxidant and antimicrobial study from plant roots, as well as investigated the acute and subacute toxicity of the leaves of C. Iguanaea. The leaves and roots of the plant were dried, triturated and macerated with ethanol (70%) for seven days, with renewal of the solvent. The material was filtered and concentrated in a rotary evaporator to obtain the aqueous extract (AE). Part of the AE roots was taken to complete dryness yielding the crude extract (CE) and the remainder was fractionated successively with dichloromethane (DCM), ethyl acetate (EA) and n-buthanol (BU). All EA leaves was taken to dryness to give EB. In the antioxidant and phytochemical analysis of roots, the EA fraction showed the highest amount of polyphenols (221.55 ± 0.28 mg gallic acid equivalents/g), flavonoids (28.80 ± 0.09 mg quercetin equivalents/g) and alkaloids (3.96 ± 0.32 mg/g) and the best antioxidant capacity by DPPH method (IC50 = 27.97 ± 0.35 μg/mL), TBARS (IC50 = 42.03 ± 4.55 μg/mL) and the reduction of power test (EC50 = 0.86 ± 0.13 mg/mL, but no statistical difference compared to other extracts). This fraction was also capable of removing free radicals significantly through testing of DCFH-DA and able to completely reverse the oxidative damage by protein carbonyl assay. As regards the assessment of the toxicity of the leaves, a single dose of 2000 mg/kg of crude extract administered to rats did not cause mortality or morbidity, so, the extract was classified in categoty 5 (LD50 entre 2000-5000 mg/kg) in accordance with OECD 423. The guide subacute experiment, the animals were divided into four groups: control and experimental (doses of 100, 200 and 400 mg/kg) for 28 days. There was in increase in blood sugar of the animals, indicating a possible pancreatic toxicity. Moreover, enzyme levels and histological analysis indicated that the extract does not hepatotoxic effect, even at the highest dose used. The findings contributed to reveal some phytochemicals and antioxidants characteristics of the species and show that C. iguanaea can be considered safe.
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spelling Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos WistarPhytochemical study and toxicity (acute and subacute) of Celtis iguanaea (Jacq.) Sarg. in Wistar ratsEsporão-de-galoAntioxidanteToxicidadeCannabaceaeAntioxidantsToxicityCannabaceaeCNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIAThe Celtis iguanaea species is popularly known as esporão-de-galo and its leaves are used in folk medicine to treat body aches, rheumatism, asthma, colic, indigestion, ulcers, and as a diuretic, and roots for urinary tract infections. This study aimed to contribute to the phytochemical, antioxidant and antimicrobial study from plant roots, as well as investigated the acute and subacute toxicity of the leaves of C. Iguanaea. The leaves and roots of the plant were dried, triturated and macerated with ethanol (70%) for seven days, with renewal of the solvent. The material was filtered and concentrated in a rotary evaporator to obtain the aqueous extract (AE). Part of the AE roots was taken to complete dryness yielding the crude extract (CE) and the remainder was fractionated successively with dichloromethane (DCM), ethyl acetate (EA) and n-buthanol (BU). All EA leaves was taken to dryness to give EB. In the antioxidant and phytochemical analysis of roots, the EA fraction showed the highest amount of polyphenols (221.55 ± 0.28 mg gallic acid equivalents/g), flavonoids (28.80 ± 0.09 mg quercetin equivalents/g) and alkaloids (3.96 ± 0.32 mg/g) and the best antioxidant capacity by DPPH method (IC50 = 27.97 ± 0.35 μg/mL), TBARS (IC50 = 42.03 ± 4.55 μg/mL) and the reduction of power test (EC50 = 0.86 ± 0.13 mg/mL, but no statistical difference compared to other extracts). This fraction was also capable of removing free radicals significantly through testing of DCFH-DA and able to completely reverse the oxidative damage by protein carbonyl assay. As regards the assessment of the toxicity of the leaves, a single dose of 2000 mg/kg of crude extract administered to rats did not cause mortality or morbidity, so, the extract was classified in categoty 5 (LD50 entre 2000-5000 mg/kg) in accordance with OECD 423. The guide subacute experiment, the animals were divided into four groups: control and experimental (doses of 100, 200 and 400 mg/kg) for 28 days. There was in increase in blood sugar of the animals, indicating a possible pancreatic toxicity. Moreover, enzyme levels and histological analysis indicated that the extract does not hepatotoxic effect, even at the highest dose used. The findings contributed to reveal some phytochemicals and antioxidants characteristics of the species and show that C. iguanaea can be considered safe.A espécie Celtis iguanaea é popularmente conhecida como esporão-de-galo, e suas folhas são utilizadas na medicina popular para o tratamento de dores no corpo, reumatismo, asma, cólicas, má digestão, úlceras e como diurético, e as raizes para infecções urinárias. O presente trabalho objetivou contribuir para o estudo fitoquímico, antioxidante e antimicrobiano das raízes da planta, assim como avaliar a toxicidade aguda e subaguda das folhas de C. iguanaea. As folhas e raízes da planta foram secas, trituradas e maceradas com etanol (70%) por sete dias, com renovação do solvente. O material foi filtrado e concentrado em evaporador rotatório a fim de obter o extrato aquoso (EA). Parte do EA das raízes foi levado a secura originando o extrato bruto (EB), e o restante foi fracionado sucessivamente com diclorometano (DCM), acetato de etila (AcOEt) e n-butanol (BuOH). Todo o EA das folhas foi levado a secura para obter EB. Na análise fitoquímica e antioxidante das raízes, a fração AcOEt apresentou a maior quantidade de polifenois (221,55 ± 0,28 mg equivalentes de ácido gálico/g), flavonoides (28,80 ± 0,09 mg equivalentes de quercetina/g) e alcaloides (3,96 ± 0,32 mg/g) e a melhor capacidade antioxidante através do método do DPPH (IC50 = 27,97 ± 0,35 μg/mL), TBARS (IC50 = 42,03 ± 4,55 μg/mL) e pelo teste de poder de redução (EC50 = 0,86 ± 0,13 mg/mL, mas sem diferença estatística em relação aos outros extratos). Esta fração também foi capaz de remover radicais livres de modo significativo, através do ensaio da DCFH-DA e capaz de reverter completamente o dano oxidativo através do ensaio da proteína carbonil. No que diz respeito a avaliação da toxicidade das folhas, uma única dose de 2000 mg/kg de extrato bruto administrada a ratos Wistar, não causou mortalidade ou morbidade, desta forma, o extrato foi classificado na categoria 5 (LD50 entre 2000-5000 mg/kg) de acordo com o Guia OECD 423. No ensaio subagudo, os animais foram divididos em quatro grupos: controle e os experimentais (doses de 100, 200 e 400 mg/kg) durante 28 dias. Observou-se um aumento na glicemia dos animais, indicando uma possível toxicidade pancreática. Por outro lado, alterações enzimáticas e a análise histológica indicaram que o extrato não possui efeito hepatotóxico, mesmo na maior dose de extrato utilizada. O resultados ajudam a elucidar algumas características fitoquímicas e antioxidantes da espécie e mostram que C. iguanaea pode ser considerado seguro.Universidade Federal de Santa MariaBRFarmacologiaUFSMPrograma de Pós-Graduação em Ciências FarmacêuticasAthayde, Margareth Lindehttp://lattes.cnpq.br/7866111734540735Boligon, Aline Augustihttp://lattes.cnpq.br/0251292056173520Bauermann, Liliane de Freitashttp://lattes.cnpq.br/5849925846135968Froeder, Amanda Luana Forbrig2016-11-012016-11-012015-03-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfFROEDER, Amanda Luana Forbrig. Phytochemical study and toxicity (acute and subacute) of Celtis iguanaea (Jacq.) Sarg. in Wistar rats. 2015. 105 f. Dissertação (Mestrado em Farmacologia) - Universidade Federal de Santa Maria, Santa Maria, 2015.http://repositorio.ufsm.br/handle/1/6043ark:/26339/001300000wqnjporinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-05-04T12:36:58Zoai:repositorio.ufsm.br:1/6043Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-05-04T12:36:58Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
Phytochemical study and toxicity (acute and subacute) of Celtis iguanaea (Jacq.) Sarg. in Wistar rats
title Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
spellingShingle Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
Froeder, Amanda Luana Forbrig
Esporão-de-galo
Antioxidante
Toxicidade
Cannabaceae
Antioxidants
Toxicity
Cannabaceae
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
title_short Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
title_full Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
title_fullStr Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
title_full_unstemmed Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
title_sort Estudo fitoquímico e de toxicidade (aguda e subaguda) de Celtis iguanaea (Jacq.) Sarg. em ratos Wistar
author Froeder, Amanda Luana Forbrig
author_facet Froeder, Amanda Luana Forbrig
author_role author
dc.contributor.none.fl_str_mv Athayde, Margareth Linde
http://lattes.cnpq.br/7866111734540735
Boligon, Aline Augusti
http://lattes.cnpq.br/0251292056173520
Bauermann, Liliane de Freitas
http://lattes.cnpq.br/5849925846135968
dc.contributor.author.fl_str_mv Froeder, Amanda Luana Forbrig
dc.subject.por.fl_str_mv Esporão-de-galo
Antioxidante
Toxicidade
Cannabaceae
Antioxidants
Toxicity
Cannabaceae
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
topic Esporão-de-galo
Antioxidante
Toxicidade
Cannabaceae
Antioxidants
Toxicity
Cannabaceae
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
description The Celtis iguanaea species is popularly known as esporão-de-galo and its leaves are used in folk medicine to treat body aches, rheumatism, asthma, colic, indigestion, ulcers, and as a diuretic, and roots for urinary tract infections. This study aimed to contribute to the phytochemical, antioxidant and antimicrobial study from plant roots, as well as investigated the acute and subacute toxicity of the leaves of C. Iguanaea. The leaves and roots of the plant were dried, triturated and macerated with ethanol (70%) for seven days, with renewal of the solvent. The material was filtered and concentrated in a rotary evaporator to obtain the aqueous extract (AE). Part of the AE roots was taken to complete dryness yielding the crude extract (CE) and the remainder was fractionated successively with dichloromethane (DCM), ethyl acetate (EA) and n-buthanol (BU). All EA leaves was taken to dryness to give EB. In the antioxidant and phytochemical analysis of roots, the EA fraction showed the highest amount of polyphenols (221.55 ± 0.28 mg gallic acid equivalents/g), flavonoids (28.80 ± 0.09 mg quercetin equivalents/g) and alkaloids (3.96 ± 0.32 mg/g) and the best antioxidant capacity by DPPH method (IC50 = 27.97 ± 0.35 μg/mL), TBARS (IC50 = 42.03 ± 4.55 μg/mL) and the reduction of power test (EC50 = 0.86 ± 0.13 mg/mL, but no statistical difference compared to other extracts). This fraction was also capable of removing free radicals significantly through testing of DCFH-DA and able to completely reverse the oxidative damage by protein carbonyl assay. As regards the assessment of the toxicity of the leaves, a single dose of 2000 mg/kg of crude extract administered to rats did not cause mortality or morbidity, so, the extract was classified in categoty 5 (LD50 entre 2000-5000 mg/kg) in accordance with OECD 423. The guide subacute experiment, the animals were divided into four groups: control and experimental (doses of 100, 200 and 400 mg/kg) for 28 days. There was in increase in blood sugar of the animals, indicating a possible pancreatic toxicity. Moreover, enzyme levels and histological analysis indicated that the extract does not hepatotoxic effect, even at the highest dose used. The findings contributed to reveal some phytochemicals and antioxidants characteristics of the species and show that C. iguanaea can be considered safe.
publishDate 2015
dc.date.none.fl_str_mv 2015-03-27
2016-11-01
2016-11-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv FROEDER, Amanda Luana Forbrig. Phytochemical study and toxicity (acute and subacute) of Celtis iguanaea (Jacq.) Sarg. in Wistar rats. 2015. 105 f. Dissertação (Mestrado em Farmacologia) - Universidade Federal de Santa Maria, Santa Maria, 2015.
http://repositorio.ufsm.br/handle/1/6043
dc.identifier.dark.fl_str_mv ark:/26339/001300000wqnj
identifier_str_mv FROEDER, Amanda Luana Forbrig. Phytochemical study and toxicity (acute and subacute) of Celtis iguanaea (Jacq.) Sarg. in Wistar rats. 2015. 105 f. Dissertação (Mestrado em Farmacologia) - Universidade Federal de Santa Maria, Santa Maria, 2015.
ark:/26339/001300000wqnj
url http://repositorio.ufsm.br/handle/1/6043
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
BR
Farmacologia
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade Federal de Santa Maria
BR
Farmacologia
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
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
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