Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori

Bibliographic Details
Main Author: Lima, Z. P. [UNESP]
Publication Date: 2008
Other Authors: Calvo, Tamara Regina [UNESP], Silva, E. F., Pellizzon, C. H. [UNESP], Vilegas, Wagner [UNESP], Brito, A. R. M. S., Bauab, T. M. [UNESP], Hiruma-Lima, Clélia Akiko [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1089/jmf.2007.0676
http://hdl.handle.net/11449/17639
Summary: Among the current treatment strategies for the peptic ulcer patient with Helicobacter pylori infection, the method of choice is triple therapy based on the concurrent use of proton inhibitors and two antibiotics. Alchornea triplinervia is a medicinal plant commonly used by people living in the Cerrado region of Brazil to treat gastrointestinal ulcers. In the present work we proposed therapy based on this medicinal plant that presents effective gastroprotective action with antibiotic effects. Oral pretreatment with methanolic extract (ME) of A. triplinervia in rats and mice decreased the gastric injuries induced by ethanol and HCl/ethanol. Increasing the dose reduced the gastroprotective effects of ME on the gastric lesions induced by nonsteroidal anti-inflammatory drug. After pylorus ligature of mice, oral administration of ME induced a decrease not only in total acid but also in the ulcer index. We also observed that ME displayed antibacterial activity against H. pylori. Liquid-liquid separation of ME indicated that active constituents responsible for the gastroprotective action are concentrated in the ethyl acetate fraction (EAF) (50% protection) rather than in the aqueous fraction, which did not induce significant gastroprotection at the same dose (100 mg/kg). EAF induced an increase of gastric mucosa prostaglandin (PG) E(2) levels, which remained high even after previous administration of indomethacin. The phytochemical profile of ME revealed that EAF contains mainly flavonoids. In conclusion, all these results suggest that ME did not show acute toxicity, but exhibited an antisecretory property, anti-H. pylori effect, and gastroprotective action. The observed effect did not involve the participation of nitric oxide or endogenous sulfhydryl groups. However, EAF showed a more efficient gastroprotective effect than ME at a lower dose and protected the gastric mucosa by increasing PGE(2).
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spelling Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pyloriAlchornea triplinerviaflavonoidsgastroprotective actionHelicobacter pyloriprostaglandin E(2)Among the current treatment strategies for the peptic ulcer patient with Helicobacter pylori infection, the method of choice is triple therapy based on the concurrent use of proton inhibitors and two antibiotics. Alchornea triplinervia is a medicinal plant commonly used by people living in the Cerrado region of Brazil to treat gastrointestinal ulcers. In the present work we proposed therapy based on this medicinal plant that presents effective gastroprotective action with antibiotic effects. Oral pretreatment with methanolic extract (ME) of A. triplinervia in rats and mice decreased the gastric injuries induced by ethanol and HCl/ethanol. Increasing the dose reduced the gastroprotective effects of ME on the gastric lesions induced by nonsteroidal anti-inflammatory drug. After pylorus ligature of mice, oral administration of ME induced a decrease not only in total acid but also in the ulcer index. We also observed that ME displayed antibacterial activity against H. pylori. Liquid-liquid separation of ME indicated that active constituents responsible for the gastroprotective action are concentrated in the ethyl acetate fraction (EAF) (50% protection) rather than in the aqueous fraction, which did not induce significant gastroprotection at the same dose (100 mg/kg). EAF induced an increase of gastric mucosa prostaglandin (PG) E(2) levels, which remained high even after previous administration of indomethacin. The phytochemical profile of ME revealed that EAF contains mainly flavonoids. In conclusion, all these results suggest that ME did not show acute toxicity, but exhibited an antisecretory property, anti-H. pylori effect, and gastroprotective action. The observed effect did not involve the participation of nitric oxide or endogenous sulfhydryl groups. However, EAF showed a more efficient gastroprotective effect than ME at a lower dose and protected the gastric mucosa by increasing PGE(2).Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)São Paulo State Univ, Inst Biociencias, Dept Fisiol, Botucatu, SP, BrazilSão Paulo State Univ, Inst Biociencias, Dept Morfol, Botucatu, SP, BrazilSão Paulo State Univ, Inst Quim, Dept Quim Organ, Araraquara, BrazilSão Paulo State Univ, Dept Ciencias Biol, Araraquara, BrazilUniv Estadual Campinas, Inst Biol, Dept Fisiol & Biofis, São Paulo, BrazilSão Paulo State Univ, Inst Biociencias, Dept Fisiol, Botucatu, SP, BrazilSão Paulo State Univ, Inst Biociencias, Dept Morfol, Botucatu, SP, BrazilSão Paulo State Univ, Inst Quim, Dept Quim Organ, Araraquara, BrazilSão Paulo State Univ, Dept Ciencias Biol, Araraquara, BrazilMary Ann Liebert, Inc.Universidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Lima, Z. P. [UNESP]Calvo, Tamara Regina [UNESP]Silva, E. F.Pellizzon, C. H. [UNESP]Vilegas, Wagner [UNESP]Brito, A. R. M. S.Bauab, T. M. [UNESP]Hiruma-Lima, Clélia Akiko [UNESP]2014-05-20T13:49:29Z2014-05-20T13:49:29Z2008-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article701-708application/pdfhttp://dx.doi.org/10.1089/jmf.2007.0676Journal of Medicinal Food. New Rochelle: Mary Ann Liebert Inc., v. 11, n. 4, p. 701-708, 2008.1096-620Xhttp://hdl.handle.net/11449/1763910.1089/jmf.2007.0676WOS:000261384700016WOS000261384700016.pdf001939377980106938145049013868440000-0002-8645-37770000-0003-3032-25560000-0002-4494-4180Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Medicinal Food1.954info:eu-repo/semantics/openAccess2025-05-28T05:09:09Zoai:repositorio.unesp.br:11449/17639Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-28T05:09:09Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
title Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
spellingShingle Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
Lima, Z. P. [UNESP]
Alchornea triplinervia
flavonoids
gastroprotective action
Helicobacter pylori
prostaglandin E(2)
title_short Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
title_full Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
title_fullStr Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
title_full_unstemmed Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
title_sort Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
author Lima, Z. P. [UNESP]
author_facet Lima, Z. P. [UNESP]
Calvo, Tamara Regina [UNESP]
Silva, E. F.
Pellizzon, C. H. [UNESP]
Vilegas, Wagner [UNESP]
Brito, A. R. M. S.
Bauab, T. M. [UNESP]
Hiruma-Lima, Clélia Akiko [UNESP]
author_role author
author2 Calvo, Tamara Regina [UNESP]
Silva, E. F.
Pellizzon, C. H. [UNESP]
Vilegas, Wagner [UNESP]
Brito, A. R. M. S.
Bauab, T. M. [UNESP]
Hiruma-Lima, Clélia Akiko [UNESP]
author2_role 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 Lima, Z. P. [UNESP]
Calvo, Tamara Regina [UNESP]
Silva, E. F.
Pellizzon, C. H. [UNESP]
Vilegas, Wagner [UNESP]
Brito, A. R. M. S.
Bauab, T. M. [UNESP]
Hiruma-Lima, Clélia Akiko [UNESP]
dc.subject.por.fl_str_mv Alchornea triplinervia
flavonoids
gastroprotective action
Helicobacter pylori
prostaglandin E(2)
topic Alchornea triplinervia
flavonoids
gastroprotective action
Helicobacter pylori
prostaglandin E(2)
description Among the current treatment strategies for the peptic ulcer patient with Helicobacter pylori infection, the method of choice is triple therapy based on the concurrent use of proton inhibitors and two antibiotics. Alchornea triplinervia is a medicinal plant commonly used by people living in the Cerrado region of Brazil to treat gastrointestinal ulcers. In the present work we proposed therapy based on this medicinal plant that presents effective gastroprotective action with antibiotic effects. Oral pretreatment with methanolic extract (ME) of A. triplinervia in rats and mice decreased the gastric injuries induced by ethanol and HCl/ethanol. Increasing the dose reduced the gastroprotective effects of ME on the gastric lesions induced by nonsteroidal anti-inflammatory drug. After pylorus ligature of mice, oral administration of ME induced a decrease not only in total acid but also in the ulcer index. We also observed that ME displayed antibacterial activity against H. pylori. Liquid-liquid separation of ME indicated that active constituents responsible for the gastroprotective action are concentrated in the ethyl acetate fraction (EAF) (50% protection) rather than in the aqueous fraction, which did not induce significant gastroprotection at the same dose (100 mg/kg). EAF induced an increase of gastric mucosa prostaglandin (PG) E(2) levels, which remained high even after previous administration of indomethacin. The phytochemical profile of ME revealed that EAF contains mainly flavonoids. In conclusion, all these results suggest that ME did not show acute toxicity, but exhibited an antisecretory property, anti-H. pylori effect, and gastroprotective action. The observed effect did not involve the participation of nitric oxide or endogenous sulfhydryl groups. However, EAF showed a more efficient gastroprotective effect than ME at a lower dose and protected the gastric mucosa by increasing PGE(2).
publishDate 2008
dc.date.none.fl_str_mv 2008-12-01
2014-05-20T13:49:29Z
2014-05-20T13:49:29Z
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/10.1089/jmf.2007.0676
Journal of Medicinal Food. New Rochelle: Mary Ann Liebert Inc., v. 11, n. 4, p. 701-708, 2008.
1096-620X
http://hdl.handle.net/11449/17639
10.1089/jmf.2007.0676
WOS:000261384700016
WOS000261384700016.pdf
0019393779801069
3814504901386844
0000-0002-8645-3777
0000-0003-3032-2556
0000-0002-4494-4180
url http://dx.doi.org/10.1089/jmf.2007.0676
http://hdl.handle.net/11449/17639
identifier_str_mv Journal of Medicinal Food. New Rochelle: Mary Ann Liebert Inc., v. 11, n. 4, p. 701-708, 2008.
1096-620X
10.1089/jmf.2007.0676
WOS:000261384700016
WOS000261384700016.pdf
0019393779801069
3814504901386844
0000-0002-8645-3777
0000-0003-3032-2556
0000-0002-4494-4180
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Medicinal Food
1.954
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 701-708
application/pdf
dc.publisher.none.fl_str_mv Mary Ann Liebert, Inc.
publisher.none.fl_str_mv Mary Ann Liebert, Inc.
dc.source.none.fl_str_mv Web of Science
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 repositoriounesp@unesp.br
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