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Combined Extracts of Artemisia and Green Tea, Mitigated Alcoholic Gastritis Via Enhanced Heat-shock Protein 27

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dc.contributor.authorKim, Yong Seok-
dc.contributor.authorJeong, Migyeong-
dc.contributor.authorHan, Young Min-
dc.contributor.authorPark, Jong Min-
dc.contributor.authorKwon, Sang Oh-
dc.contributor.authorHong, Seong Pyo-
dc.contributor.authorHahm, Ki Baik-
dc.date.accessioned2022-07-12T07:37:48Z-
dc.date.available2022-07-12T07:37:48Z-
dc.date.issued2018-03-
dc.identifier.issn1598-9992-
dc.identifier.issn2233-6869-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150413-
dc.description.abstractBackground/Aims: Several lines of evidence from epidemiologic and laboratory studies have shown that the consumption of Artemisia or green tea extracts (MPGT) is inversely associated with the risk of alcohol-induced damage and other chronic diseases. Supported by previous studies showing that the combined extract of Artemisia and green tea, MPGT, exerted significantly either antioxidative or anti-inflammatory actions against Helicobacter pylori-associated gastric diseases, it was hypothesized that MPGT can offer protection against alcoholic gastritis. Methods: Ethanol was administered to induce gastric damage in Wistar rats, which had been pretreated with various doses of MPGT, to measure the rescuing action of a MPGT pretreatment against ethanol-induced gastric damage. In addition, the molecular mechanisms for the preventive effects were examined. Results: The MPGT pretreatment (100, 300, and 500 mg/kg) alleviated the ethanol-induced gastric damage, which was evidenced by the significant decrease in calcium-dependent phospholipase A2, MAPKs, and NF-κB levels compared to ethanol alone. Furthermore, the MPGT pretreatment preserved 15-prostaglandin dehydrogenase, whereas cyclooxygenase-2 was decreased significantly. All of these biochemical changes led to the significant alleviation of alcohol-associated gastric mucosal damage. Ethanol significantly increased the TUNEL positivity in the stomach, but MPGT decreased the apoptotic index significantly, which was associated with significantly lower pathological scores of ethanol-induced mucosal ulcerations. The significant protective changes observed alcoholic gastritis with MPGT were related to the increased expression of cytoprotective genes, such as heat-shock protein (HSP)27, HSP60, and PDGF. Conclusions: The efficient anti-inflammatory, anti-apoptotic, and regenerative actions of MPGT make it a potential nutrient phytoceutical to rescue the stomach from alcoholic gastritis.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisher대한소화기학회-
dc.titleCombined Extracts of Artemisia and Green Tea, Mitigated Alcoholic Gastritis Via Enhanced Heat-shock Protein 27-
dc.title.alternativeArtemisia와 Green Tea 추출 복합물의 Heat-shock Protein 27 발현 증가를 통한 알코올성 위염 억제 효과-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4166/kjg.2018.71.3.132-
dc.identifier.scopusid2-s2.0-85059798351-
dc.identifier.bibliographicCitation대한소화기학회지, v.71, no.3, pp 132 - 142-
dc.citation.title대한소화기학회지-
dc.citation.volume71-
dc.citation.number3-
dc.citation.startPage132-
dc.citation.endPage142-
dc.type.docTypeArticle-
dc.identifier.kciidART002325317-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlusalcohol-
dc.subject.keywordPluscyclooxygenase 2-
dc.subject.keywordPlusheat shock protein 27-
dc.subject.keywordPlusimmunoglobulin enhancer binding protein-
dc.subject.keywordPlusphospholipase A2-
dc.subject.keywordPlusplant extract-
dc.subject.keywordPlusplatelet derived growth factor-
dc.subject.keywordPlusanimal-
dc.subject.keywordPlusArtemisia-
dc.subject.keywordPluschemically induced-
dc.subject.keywordPluschemistry-
dc.subject.keywordPlusdrug effect-
dc.subject.keywordPlusgastritis-
dc.subject.keywordPlusgenetics-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmetabolism-
dc.subject.keywordPluspathology-
dc.subject.keywordPlusrat-
dc.subject.keywordPlusstomach mucosa-
dc.subject.keywordPlustea-
dc.subject.keywordPlusupregulation-
dc.subject.keywordPlusveterinary medicine-
dc.subject.keywordPlusWistar rat-
dc.subject.keywordPlusAnimals-
dc.subject.keywordPlusArtemisia-
dc.subject.keywordPlusCyclooxygenase 2-
dc.subject.keywordPlusEthanol-
dc.subject.keywordPlusGastric Mucosa-
dc.subject.keywordPlusGastritis-
dc.subject.keywordPlusHSP27 Heat-Shock Proteins-
dc.subject.keywordPlusMale-
dc.subject.keywordPlusNF-kappa B-
dc.subject.keywordPlusPhospholipases A2-
dc.subject.keywordPlusPlant Extracts-
dc.subject.keywordPlusPlatelet-Derived Growth Factor-
dc.subject.keywordPlusRats-
dc.subject.keywordPlusRats, Wistar-
dc.subject.keywordPlusTea-
dc.subject.keywordPlusUp-Regulation-
dc.subject.keywordAuthorEthanol-
dc.subject.keywordAuthorGastric damages-
dc.subject.keywordAuthorArtemisia extracts-
dc.subject.keywordAuthorGreen tea extracts-
dc.subject.keywordAuthorHSP27-
dc.identifier.urlhttps://synapse.koreamed.org/articles/1100123-
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서울 의과대학 > 서울 생화학·분자생물학교실 > 1. Journal Articles

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