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Artemisia asiatica extracts protect against ethanol-induced injury in gastric mucosa of rats

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dc.contributor.authorPark, Sang Woon-
dc.contributor.authorOh, Tae Young-
dc.contributor.authorKim, Yong Seok-
dc.contributor.authorSim, Hyejin-
dc.contributor.authorPark, Sang Jong-
dc.contributor.authorJang, Eun Jung-
dc.contributor.authorPark, Joo Sang-
dc.contributor.authorBaik, Hyun Wook-
dc.contributor.authorHahm, Ki Baik-
dc.date.accessioned2022-12-21T02:51:44Z-
dc.date.available2022-12-21T02:51:44Z-
dc.date.issued2008-06-
dc.identifier.issn0815-9319-
dc.identifier.issn1440-1746-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/178563-
dc.description.abstractBackground and Aim: Based on our previous studies that Artemisia asiatica extracts exert either antioxidative or cytoprotective actions against non-steroidal anti-inflammatory drugs or Helicobacter pylori-induced gastric mucosal injury, or imposes qualified ulcer healing in an acetic acid-induced gastric ulcer model, we investigated the protective effects of Artemisia asiatica extracts against ethanol-induced gastric mucosal injury. Methods: Sprague-Dawley rats received 4 g/kg body weight (BW) of absolute ethanol intragastrically, which produced visible hemorrhagic gastric lesions 60 min later. Results: In this animal setting, the pretreatment of Artemisia extracts (30 or 100 mg/kg BW), 1 h before ethanol administration, significantly attenuated the source of gastric injury, which was assessed with gross and microscopic analysis (P < 0.01). Protection from alcohol-induced damage with Artemisia pretreatment was associated with significantly decreased lipid peroxidation, protecting gastric mucosa from glutathione depletion, as well as the inhibition of the cytochrome 2E1 ethanol-metabolizing enzyme. It attenuated the expressions of ethanol-induced pro-inflammatory cytokines, including interleukin (IL)-1 beta and interferon-gamma, a weak activation of IL-10, the inhibition of the alcohol-induced overexpression of intercellular adhesion molecule-1, and the considerable induction of heat shock protein-72 expression in gastric mucosal homogenates. Conclusion: The data suggest that the ethanol extracts of Artemisia asiatica exerted significant protection from alcohol-induced gastric mucosal injury through bioregulation, which is essential for cytoprotection and anti-inflammation.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherBlackwell Publishing Inc.-
dc.titleArtemisia asiatica extracts protect against ethanol-induced injury in gastric mucosa of rats-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/j.1440-1746.2008.05333.x-
dc.identifier.scopusid2-s2.0-44949133340-
dc.identifier.wosid000256540200027-
dc.identifier.bibliographicCitationJournal of Gastroenterology and Hepatology, v.23, no.6, pp 976 - 984-
dc.citation.titleJournal of Gastroenterology and Hepatology-
dc.citation.volume23-
dc.citation.number6-
dc.citation.startPage976-
dc.citation.endPage984-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusALCOHOL-CONSUMPTION-
dc.subject.keywordPlusLIPID-PEROXIDATION-
dc.subject.keywordPlusGLUTATHIONE-
dc.subject.keywordPlusDAMAGE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusDA-9601-
dc.subject.keywordPlusWOGONIN-
dc.subject.keywordPlusIL-10-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorArtemisia asiatica-
dc.subject.keywordAuthorDA-9601-
dc.subject.keywordAuthorethanol-
dc.subject.keywordAuthorgastric injury-
dc.subject.keywordAuthorglutathione-
dc.subject.keywordAuthorlipid peroxide-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/j.1440-1746.2008.05333.x-
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