Caracterização farmacológica e avaliação da atividade gastroprotetora do extrato etanólico das folhas de Celtis iguanaea (JACQ.) Sargent (Ulmaceae) - Esporão-de-galo

Detalhes bibliográficos
Autor(a) principal: Sousa, Fábio Borges de
Data de Publicação: 2011
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFG
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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spelling 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/9841Celtis 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
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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
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.
url http://repositorio.bc.ufg.br/tede/handle/tede/9841
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language por
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dc.relation.confidence.fl_str_mv 600
600
600
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dc.relation.cnpq.fl_str_mv 6216025074656932336
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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
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