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Antioxidant activity of pomegranate juice reduces acute lung injury secondary to hyperoxia in an animal model

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dc.contributor.author Husari A.
dc.contributor.author Khayat A.
dc.contributor.author Bitar H.
dc.contributor.author Hashem Y.
dc.contributor.author Rizkallah A.
dc.contributor.author Zaatari G.
dc.contributor.author El Sabban M.
dc.contributor.editor
dc.date 2014
dc.date.accessioned 2017-10-05T15:59:41Z
dc.date.available 2017-10-05T15:59:41Z
dc.date.issued 2014
dc.identifier 10.1186/1756-0500-7-664
dc.identifier.isbn
dc.identifier.issn 17560500
dc.identifier.uri http://hdl.handle.net/10938/19165
dc.description.abstract Background: Hyperoxia triggers the release of toxic reactive oxygen species (ROS). Pomegranate Juice (PJ) is a rich source of potent antioxidants. We assessed the effects of PJ supplementation on Acute Lung Injury (ALI) in adult rats exposed to hyperoxia for 5 days. Methods. Adult rats were divided into four different groups: control, hyperoxia, hyperoxia + PJ and PJ. Animals were placed in chambers containing either room air or oxygen above 95percent for a total of 5 days. Two different PJ concentrations were utilized and the control group received placebo water. Animals were euthanized and their lungs were excised. Assessment of lung injury was accomplished by: a) wet to dry ratio (W-D) method, b) measurement of albumin concentration in the bronchoalveolar lavage fluid (BALF), c) oxidative stress, d) histological evaluation of the lung e) apoptosis and f) transcriptional expression levels of the inflammatory mediators IL-1β, IL-6 and TNF-alpha. Results: An increase in the W-D and albumin leak was noted in Hyperoxia (p 0.05). Those findings were attenuated by the higher dose of PJ supplementation. Hyperoxia increased ROS production. Again PJ significantly reduced oxidative stress. Lung sections showed significant reduction in inflammation, edema, and infiltrating neutrophils in Hyperoxia + 80 μmol-kg when compared with Hyperoxia. TUNEL demonstrated significant apoptosis in the Hyperoxia, which was diminished in the Hyperoxia + 80 μmol-kg. Furthermore, increase in IL-1β and IL-6 was noted in Hyperoxia. Again, 80 μmol-kg of PJ significantly reduced the expression of inflammatory mediators. Conclusion: In this animal model, PJ supplementation attenuated ALI associated with hyperoxia.
dc.format.extent
dc.language English
dc.publisher BioMed Central Ltd.;
dc.relation.ispartof Publication Name: BMC Research Notes; Publication Year: 2014; Volume: 7; no. 1;
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Antioxidant activity of pomegranate juice reduces acute lung injury secondary to hyperoxia in an animal model
dc.type Article
dc.contributor.affiliation Husari, A., Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, American University of Beirut, P.O. Box 11-236Riad El Solh, Beirut, Lebanon
dc.contributor.affiliation Khayat, A., Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, American University of Beirut, P.O. Box 11-236Riad El Solh, Beirut, Lebanon
dc.contributor.affiliation Bitar, H., Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, American University of Beirut, P.O. Box 11-236Riad El Solh, Beirut, Lebanon
dc.contributor.affiliation Hashem, Y., Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, American University of Beirut, P.O. Box 11-236Riad El Solh, Beirut, Lebanon
dc.contributor.affiliation Rizkallah, A., Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, American University of Beirut, P.O. Box 11-236Riad El Solh, Beirut, Lebanon
dc.contributor.affiliation Zaatari, G., Department of Pathology and Laboratory Medicine, American University of BeirutBeirut, Lebanon
dc.contributor.affiliation El Sabban, M., Department of Biochemistry, American University of BeirutBeirut, Lebanon
dc.contributor.authorAddress Husari, A.; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, American University of Beirut, P.O. Box 11-236, Lebanon
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Pathology and Laboratory Medicine;
dc.contributor.authorDepartment Pathology and Laboratory Medicine
dc.contributor.authorDivision
dc.contributor.authorEmail
dc.contributor.faculty Faculty of Medicine
dc.contributor.authorInitials empty
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited
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dc.identifier.articleNo 664
dc.identifier.coden
dc.identifier.pubmedID
dc.identifier.scopusID 84907437017
dc.identifier.url
dc.publisher.address
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dc.relation.ispartofConferenceCode
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dc.relation.ispartofConferenceHosting
dc.relation.ispartofConferenceLoc
dc.relation.ispartofConferenceSponsor
dc.relation.ispartofConferenceTitle
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dc.relation.ispartOfISOAbbr
dc.relation.ispartOfIssue 1
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle BMC Research Notes
dc.relation.ispartofPubTitleAbbr BMC Res. Notes
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 7
dc.source.ID
dc.type.publication Journal
dc.subject.otherAuthKeyword Acute lung injury
dc.subject.otherAuthKeyword Antioxidants
dc.subject.otherAuthKeyword Hyperoxia
dc.subject.otherAuthKeyword Inflammatory mediators
dc.subject.otherAuthKeyword Reactive oxygen species
dc.subject.otherChemCAS
dc.subject.otherIndex
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