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Effect of Korean pear (Pyruspyrifolia cv. Shingo) juice on hangover severity following alcohol consumption

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dc.contributor.authorLee, Ho-Sun-
dc.contributor.authorIsse, Toyohi-
dc.contributor.authorKawamoto, Toshihiro-
dc.contributor.authorBaik, Hyun Wook-
dc.contributor.authorPark, Jong Y.-
dc.contributor.authorYang, Mihi-
dc.date.available2021-02-22T12:15:45Z-
dc.date.issued2013-08-
dc.identifier.issn0278-6915-
dc.identifier.issn1873-6351-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11247-
dc.description.abstractKorean pear has been used as a traditional prophylactic agent for alcohol hangover. However, its mechanism was not investigated in human yet. Therefore, we performed a randomized single blind crossover trial with 14 healthy young men to examine effects of Korean pear juice on alcohol hangover. All subjects consumed 540 ml of spirits (alcohol conc. 20.1 v/v%) after 30 min from the intervention, i.e. placebo or Korean pear juice treatment. Blood and urine specimens were collected in time-courses (9 time-points for 15 h after alcohol consumption). The total and average of hangover severity were alleviated to 16% and 21% by Korean pear juice at 15 h after the alcohol consumption, respectively (ps < 0.05). Particularly, 'trouble concentrating' was significantly improved by the pear juice treatment (p < 0.05). Impaired memory, and sensitivity to light and sound were significantly improved by Korean pear juice among the subjects with ALDH2*1/*1 or ALDH2*1/*2 genotypes (ps < 0.05) but not in the subjects with ALDH2*2/*2 genotype. In addition, the pear juice treatment lowered levels of blood alcohol (p < 0.01). Therefore, Korean pear juice may alleviate alcohol-hangover and its detoxification of alcohol seems to be modified by the genetic variation of ALDH2. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleEffect of Korean pear (Pyruspyrifolia cv. Shingo) juice on hangover severity following alcohol consumption-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.fct.2013.04.007-
dc.identifier.scopusid2-s2.0-84877828663-
dc.identifier.wosid000322099100014-
dc.identifier.bibliographicCitationFOOD AND CHEMICAL TOXICOLOGY, v.58, pp 101 - 106-
dc.citation.titleFOOD AND CHEMICAL TOXICOLOGY-
dc.citation.volume58-
dc.citation.startPage101-
dc.citation.endPage106-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusPLASMA-LIPIDS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusEXPOSURE-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusPOLYMORPHISM-
dc.subject.keywordPlusSYMPTOMS-
dc.subject.keywordPlusENZYMES-
dc.subject.keywordPlusTOLUENE-
dc.subject.keywordPlusAPPLE-
dc.subject.keywordAuthorAlcohol-
dc.subject.keywordAuthorHangover-
dc.subject.keywordAuthorKorean pear-
dc.subject.keywordAuthorALDH2-
dc.subject.keywordAuthorPharmacokinetics-
dc.subject.keywordAuthorPharmacodynamics-
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