Brazilian Medicinal Plant Acts on Prostaglandin Level and Helicobacter pylori
| Main Author: | |
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| Publication Date: | 2008 |
| Other Authors: | , , , , , , |
| 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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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 |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
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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 |
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eng |
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eng |
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Journal of Medicinal Food 1.954 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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701-708 application/pdf |
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Mary Ann Liebert, Inc. |
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Mary Ann Liebert, Inc. |
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Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
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