Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
dARK ID: | ark:/38995/00130000084d7 |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/9841 |
Resumo: | Celtis iguanaea (Jacq.) Sargent is a small postage plant, it has very flexible branches, armed with spines. The tea obtained through it leaves is popularly used for body pain, rheumatism, chest pain, asthma, cramps, poor digestion and as diuretic. In this study, we evaluated the leaves of Celtis iguanaea, which were collected in Hidrolândia-GO, dried in an ethanolic extract of esporão-de-galo (EEEG). The EEEG was dissolved in water and fractionated by successive liquid-liquid partition with hexane (FH), dichloromethane (FD), ethyl acetate (FAcE) and the aqueous phase (EA). The animals used were Swiss Mice (male, adults, weighing 35–40 mg/kg). After the pharmacological screening, the animals were subjected to analysis of treatment effects with EEEG (100, 300 and 1000 mg/kg p.o.) on the central nervous system (CNS) through the open-field test, “rota-rod” test, and sleep induction by pentobarbital. To evaluate the effects on the gastrointestinal tract, the animals were orally pre-treated with ethanolic extract of esporão-de-galo (EEEG 100, 300 and 1000 mg/kg), vehicle (10 mL/kg) or ranitidine (50 mg/kg) before induction of gastric lesions by indomethacin (30 mg/kg - s. c.), ethanol 75 % (v/v), and stress by contention and hypothermia, and treated intraduodenally in the model of gastric lesions induced by pyloric ligation. The effects of the extract on the volume, pH and total acidity of gastric secretion were evaluated by pyloric ligation method. We also tested if the EEEG and fractions affected the intestinal transit and gastric emptying by the methods of activated charcoal and phenol-red respectively. The hexane fraction (FH 180 mg/kg), dichloromethane fraction (FD 9 mg/kg), ethyl acetate fraction (FAcE 16 mg/kg) and aqueous fraction (FA 360 mg/kg), administered orally, were tested in model of induction of lesions by indomethacin (30 mg/kg s.c.), to elucidate the active fractions of the extract. After determining the active fraction, it was tested in different doses to establish the dose-dependent relationship. A possible action on the intestinal transit was also evaluated. In the evaluation of the EEEG on CNS, we didn’t found any evidence of activity on this system. In models of lesion induction by different ulcerogenic agents (indomethacin, ethanol, stress and pyloric ligation) using EEEG at doses of 100, 300 and 1000 mg/kg, was observed a significant reduction in both the number of ulcers and in the lesions rate caused by these agents. By intraduodenal administration in the model of pyloric ligation, we evaluated volume, free acidity and total acidity, and the animals treated with the EEEG had a reduction in volume, free acidity and total acidity. Only the hexane fraction (FH) showed gastroprotective activity, being effective reducing the number of ulcers and the lesions rate. When we evaluated the parameters of gastric secretion with this fraction (FH), we observed a decrease in volume, increase in pH and decrease in total acidity. Both EEEG and its hexane fraction didn’t alter intestinal motility or gastric emptying. The results of this study suggest that the EEEG has a gastroprotective activity, and this activity involves the active ingredients of the plant with systemic activity, which may justify the popular use of Celtis iguanaea for the treatment of gastritis and gastric ulcers. |
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Costa, Elson Alveshttp://lattes.cnpq.br/2607893423583912Costa, Elson AlvesPaula, José Realino deSilveira, Nusa de Almeidahttp://lattes.cnpq.br/2112285517698102Sousa, Fábio Borges de2019-07-17T13:52:15Z2011-06-30SOUSA, Fábio Borges de. Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo. 2011. 79 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2011.http://repositorio.bc.ufg.br/tede/handle/tede/9841ark:/38995/00130000084d7Celtis iguanaea (Jacq.) Sargent is a small postage plant, it has very flexible branches, armed with spines. The tea obtained through it leaves is popularly used for body pain, rheumatism, chest pain, asthma, cramps, poor digestion and as diuretic. In this study, we evaluated the leaves of Celtis iguanaea, which were collected in Hidrolândia-GO, dried in an ethanolic extract of esporão-de-galo (EEEG). The EEEG was dissolved in water and fractionated by successive liquid-liquid partition with hexane (FH), dichloromethane (FD), ethyl acetate (FAcE) and the aqueous phase (EA). The animals used were Swiss Mice (male, adults, weighing 35–40 mg/kg). After the pharmacological screening, the animals were subjected to analysis of treatment effects with EEEG (100, 300 and 1000 mg/kg p.o.) on the central nervous system (CNS) through the open-field test, “rota-rod” test, and sleep induction by pentobarbital. To evaluate the effects on the gastrointestinal tract, the animals were orally pre-treated with ethanolic extract of esporão-de-galo (EEEG 100, 300 and 1000 mg/kg), vehicle (10 mL/kg) or ranitidine (50 mg/kg) before induction of gastric lesions by indomethacin (30 mg/kg - s. c.), ethanol 75 % (v/v), and stress by contention and hypothermia, and treated intraduodenally in the model of gastric lesions induced by pyloric ligation. The effects of the extract on the volume, pH and total acidity of gastric secretion were evaluated by pyloric ligation method. We also tested if the EEEG and fractions affected the intestinal transit and gastric emptying by the methods of activated charcoal and phenol-red respectively. The hexane fraction (FH 180 mg/kg), dichloromethane fraction (FD 9 mg/kg), ethyl acetate fraction (FAcE 16 mg/kg) and aqueous fraction (FA 360 mg/kg), administered orally, were tested in model of induction of lesions by indomethacin (30 mg/kg s.c.), to elucidate the active fractions of the extract. After determining the active fraction, it was tested in different doses to establish the dose-dependent relationship. A possible action on the intestinal transit was also evaluated. In the evaluation of the EEEG on CNS, we didn’t found any evidence of activity on this system. In models of lesion induction by different ulcerogenic agents (indomethacin, ethanol, stress and pyloric ligation) using EEEG at doses of 100, 300 and 1000 mg/kg, was observed a significant reduction in both the number of ulcers and in the lesions rate caused by these agents. By intraduodenal administration in the model of pyloric ligation, we evaluated volume, free acidity and total acidity, and the animals treated with the EEEG had a reduction in volume, free acidity and total acidity. Only the hexane fraction (FH) showed gastroprotective activity, being effective reducing the number of ulcers and the lesions rate. When we evaluated the parameters of gastric secretion with this fraction (FH), we observed a decrease in volume, increase in pH and decrease in total acidity. Both EEEG and its hexane fraction didn’t alter intestinal motility or gastric emptying. The results of this study suggest that the EEEG has a gastroprotective activity, and this activity involves the active ingredients of the plant with systemic activity, which may justify the popular use of Celtis iguanaea for the treatment of gastritis and gastric ulcers.Celtis iguanaea (Jacq.) Sargent é uma planta de pequeno porte, dotada de ramos flexíveis e armados de espinhos. O chá das folhas desta planta é usado popularmente para dores no corpo, reumatismo, dores no peito, asma, cólicas, má-digestão e como diurético. Neste trabalho, avaliou-se as folhas de Celtis iguanaea, que foram coletadas em Hidrolândia- GO, dessecadas em estufa com circulação de ar a 40ºC, trituradas e extraídas por maceração com etanol 96ºGL, obtendo-se assim o extrato etanólico de esporão-de-galo (EEEG). O EEEG foi solubilizado em água e fracionado por partição líquido-líquido sucessiva com hexano (FH), diclorometano (FD), acetato de etila (FAcE) e a fase aquosa (FA). Os animais utilizados foram camundongos albinos Swiss (machos, adultos, pesando entre 35–40g). Após determinação das doses na triagem farmacológica geral, foram avaliados os efeitos dos tratamentos com o EEEG nas doses de 100, 300 e 1000 mg/kg v.o., sobre o Sistema Nervoso Central (SNC) através dos testes de campo-aberto, “rota-rod” e indução de sono por pentobarbital. Para a avaliação dos efeitos sobre o trato gastrointestinal (TGI), os animais foram pré-tratados pela via oral com EEEG (100, 300 e 1000 mg/kg), veículo (10 mL/kg) ou ranitidina (50 mg/kg), antes da indução das lesões gástricas por indometacina (30 mg/kg s.c.), etanol 75 % (v/v), estresse por contenção e hipotermia, e tratados intraduodenalmente no modelo de indução de lesões por ligadura de piloro. Os efeitos do extrato sobre o volume, pH e acidez total da secreção gástrica foram avaliados pelo método da ligadura pilórica. Também foi avaliado se o EEEG e suas frações afetavam o trânsito intestinal e o esvaziamento gástrico pelos métodos do carvão ativado e vermelho de fenol, respectivamente. As frações hexânica (FH 180 mg/kg), diclorometano (FD 9 mg/kg), acetato de etila (FAcE 16 mg/kg) e aquosa (FA 360 mg/kg) administradas oralmente foram testadas em modelo de indução de lesões por indometacina (30 mg/kg s.c.), visando determinar a(s) fração(ões) ativa(s) do extrato. Após determinação da fração ativa, a mesma foi testada em diferentes doses para verificar se havia uma relação dose-efeito. Uma possível ação sobre o trânsito intestinal também foi avaliada. Na avaliação do EEEG no SNC, não foi encontrada nenhuma evidência de atividade sobre este sistema. Nos modelos de indução de lesões pelos diferentes agentes ulcerogênicos (indometacina, etanol, estresse e ligadura pilórica), utilizando o EEEG nas doses de 100, 300 e 1000 mg/kg, foi observada uma redução tanto no número de úlceras quanto no índice de lesões provocadas por esses agentes. Através da administração intraduodenal no modelo de ligadura pilórica, avaliou-se o volume, acidez livre e acidez total, em que os animais tratados com o EEEG tiveram uma redução no volume, acidez livre e acidez total. Dentre as frações testadas somente a FH mostrou atividade gastroprotetora, sendo eficaz na redução do número de úlceras e no índice de lesões. Quando foram avaliados os parâmetros da secreção gástrica com esta fração hexânica, observamos uma redução no volume, aumento do pH e redução da acidez total. Tanto o EEEG quanto a fração hexânica mostraram efeitos dose dependente nos modelos de úlceras e secreção gástrica, porém não alteraram a motilidade gastrointestinal. Os resultados encontrados neste trabalho permitem sugerir que o EEEG possui uma atividade gastroprotetora, e que nesta atividade estão envolvidos os princípios ativos da planta com atividade sistêmica, que podem justificar o uso popular de Celtis iguanaea para o tratamento de gastrites e úlceras gástricas.Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2019-07-16T18:33:24Z No. of bitstreams: 2 Dissertação - Fábio Borges de Sousa - 2011.pdf: 1528392 bytes, checksum: fa88cb02a6948ff8da86cc364a5f02b9 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2019-07-17T13:52:15Z (GMT) No. of bitstreams: 2 Dissertação - Fábio Borges de Sousa - 2011.pdf: 1528392 bytes, checksum: fa88cb02a6948ff8da86cc364a5f02b9 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Made available in DSpace on 2019-07-17T13:52:15Z (GMT). No. of bitstreams: 2 Dissertação - Fábio Borges de Sousa - 2011.pdf: 1528392 bytes, checksum: fa88cb02a6948ff8da86cc364a5f02b9 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2011-06-30application/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Ciências Farmacêuticas (FF)UFGBrasilFaculdade Farmácia - FF (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessEsporão-de-galoCeltis iguanaeaPlantas medicinaisGastritesÚlceras gástricasGastroproteçãoCeltis iguanaeaMedicinal plantsGastritisGastric ulcersGastroprotection.FARMACIA::ANALISE E CONTROLE E MEDICAMENTOSCaracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galoPharmacological characterization and evaluation of gastroprotective activity of the ethanolic extract of leaves of Celtis iguanaea (JACQ.) 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dc.title.eng.fl_str_mv |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
dc.title.alternative.eng.fl_str_mv |
Pharmacological characterization and evaluation of gastroprotective activity of the ethanolic extract of leaves of Celtis iguanaea (JACQ.) Sargent (Ulmaceae)- Esporão-de-galot |
title |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
spellingShingle |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo Sousa, Fábio Borges de Esporão-de-galo Celtis iguanaea Plantas medicinais Gastrites Úlceras gástricas Gastroproteção Celtis iguanaea Medicinal plants Gastritis Gastric ulcers Gastroprotection. FARMACIA::ANALISE E CONTROLE E MEDICAMENTOS |
title_short |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
title_full |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
title_fullStr |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
title_full_unstemmed |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
title_sort |
Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo |
author |
Sousa, Fábio Borges de |
author_facet |
Sousa, Fábio Borges de |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Costa, Elson Alves |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/2607893423583912 |
dc.contributor.referee1.fl_str_mv |
Costa, Elson Alves |
dc.contributor.referee2.fl_str_mv |
Paula, José Realino de |
dc.contributor.referee3.fl_str_mv |
Silveira, Nusa de Almeida |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/2112285517698102 |
dc.contributor.author.fl_str_mv |
Sousa, Fábio Borges de |
contributor_str_mv |
Costa, Elson Alves Costa, Elson Alves Paula, José Realino de Silveira, Nusa de Almeida |
dc.subject.por.fl_str_mv |
Esporão-de-galo Celtis iguanaea Plantas medicinais Gastrites Úlceras gástricas Gastroproteção |
topic |
Esporão-de-galo Celtis iguanaea Plantas medicinais Gastrites Úlceras gástricas Gastroproteção Celtis iguanaea Medicinal plants Gastritis Gastric ulcers Gastroprotection. FARMACIA::ANALISE E CONTROLE E MEDICAMENTOS |
dc.subject.eng.fl_str_mv |
Celtis iguanaea Medicinal plants Gastritis Gastric ulcers Gastroprotection. |
dc.subject.cnpq.fl_str_mv |
FARMACIA::ANALISE E CONTROLE E MEDICAMENTOS |
description |
Celtis iguanaea (Jacq.) Sargent is a small postage plant, it has very flexible branches, armed with spines. The tea obtained through it leaves is popularly used for body pain, rheumatism, chest pain, asthma, cramps, poor digestion and as diuretic. In this study, we evaluated the leaves of Celtis iguanaea, which were collected in Hidrolândia-GO, dried in an ethanolic extract of esporão-de-galo (EEEG). The EEEG was dissolved in water and fractionated by successive liquid-liquid partition with hexane (FH), dichloromethane (FD), ethyl acetate (FAcE) and the aqueous phase (EA). The animals used were Swiss Mice (male, adults, weighing 35–40 mg/kg). After the pharmacological screening, the animals were subjected to analysis of treatment effects with EEEG (100, 300 and 1000 mg/kg p.o.) on the central nervous system (CNS) through the open-field test, “rota-rod” test, and sleep induction by pentobarbital. To evaluate the effects on the gastrointestinal tract, the animals were orally pre-treated with ethanolic extract of esporão-de-galo (EEEG 100, 300 and 1000 mg/kg), vehicle (10 mL/kg) or ranitidine (50 mg/kg) before induction of gastric lesions by indomethacin (30 mg/kg - s. c.), ethanol 75 % (v/v), and stress by contention and hypothermia, and treated intraduodenally in the model of gastric lesions induced by pyloric ligation. The effects of the extract on the volume, pH and total acidity of gastric secretion were evaluated by pyloric ligation method. We also tested if the EEEG and fractions affected the intestinal transit and gastric emptying by the methods of activated charcoal and phenol-red respectively. The hexane fraction (FH 180 mg/kg), dichloromethane fraction (FD 9 mg/kg), ethyl acetate fraction (FAcE 16 mg/kg) and aqueous fraction (FA 360 mg/kg), administered orally, were tested in model of induction of lesions by indomethacin (30 mg/kg s.c.), to elucidate the active fractions of the extract. After determining the active fraction, it was tested in different doses to establish the dose-dependent relationship. A possible action on the intestinal transit was also evaluated. In the evaluation of the EEEG on CNS, we didn’t found any evidence of activity on this system. In models of lesion induction by different ulcerogenic agents (indomethacin, ethanol, stress and pyloric ligation) using EEEG at doses of 100, 300 and 1000 mg/kg, was observed a significant reduction in both the number of ulcers and in the lesions rate caused by these agents. By intraduodenal administration in the model of pyloric ligation, we evaluated volume, free acidity and total acidity, and the animals treated with the EEEG had a reduction in volume, free acidity and total acidity. Only the hexane fraction (FH) showed gastroprotective activity, being effective reducing the number of ulcers and the lesions rate. When we evaluated the parameters of gastric secretion with this fraction (FH), we observed a decrease in volume, increase in pH and decrease in total acidity. Both EEEG and its hexane fraction didn’t alter intestinal motility or gastric emptying. The results of this study suggest that the EEEG has a gastroprotective activity, and this activity involves the active ingredients of the plant with systemic activity, which may justify the popular use of Celtis iguanaea for the treatment of gastritis and gastric ulcers. |
publishDate |
2011 |
dc.date.issued.fl_str_mv |
2011-06-30 |
dc.date.accessioned.fl_str_mv |
2019-07-17T13:52:15Z |
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.citation.fl_str_mv |
SOUSA, Fábio Borges de. Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo. 2011. 79 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2011. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/9841 |
dc.identifier.dark.fl_str_mv |
ark:/38995/00130000084d7 |
identifier_str_mv |
SOUSA, Fábio Borges de. Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo. 2011. 79 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2011. ark:/38995/00130000084d7 |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/9841 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.program.fl_str_mv |
824936988196152412 |
dc.relation.confidence.fl_str_mv |
600 600 600 |
dc.relation.department.fl_str_mv |
6010281161524209375 |
dc.relation.cnpq.fl_str_mv |
6216025074656932336 |
dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
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 Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Ciências Farmacêuticas (FF) |
dc.publisher.initials.fl_str_mv |
UFG |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Faculdade Farmácia - FF (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFG instname:Universidade Federal de Goiás (UFG) instacron:UFG |
instname_str |
Universidade Federal de Goiás (UFG) |
instacron_str |
UFG |
institution |
UFG |
reponame_str |
Repositório Institucional da UFG |
collection |
Repositório Institucional da UFG |
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Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
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tasesdissertacoes.bc@ufg.br |
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1815172596518354944 |