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Propofol has delayed myocardial protective effects after a regional ischemia/reperfusion injury in an in vivo rat heart model

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dc.contributor.authorShin, I.W.-
dc.contributor.authorJang, I.S.-
dc.contributor.authorLee, S.-H.-
dc.contributor.authorBaik, J.-S.-
dc.contributor.authorPark, K.-E.-
dc.contributor.authorSohn, J.-T.-
dc.contributor.authorLee, H.K.-
dc.contributor.authorChung, Y.K.-
dc.date.accessioned2022-12-27T04:54:25Z-
dc.date.available2022-12-27T04:54:25Z-
dc.date.issued2010-
dc.identifier.issn2005-6419-
dc.identifier.issn2005-7563-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/25993-
dc.description.abstractBackground: It is well known that propofol protects myocardium against myocardial ischemia/reperfusion injury in the rat heart model. The aim of this study was to investigate whether propofol provides a protective effect against a regional myocardial ischemia/reperfusion injury in an in vivo rat heart model after 48 h of reperfusion. Methods: Rats were subjected to 25 min of left coronary artery occlusion followed by 48 h of reperfusion. The sham group received profopol without ischemic injury. The control group received normal saline with ischemia/reperfusion injury. The propofol group received profopol with ischemia/reperfusion injury. The intralipid group received intralipid with ischemia/reperfusion injury. A microcatheter was advanced into the left ventricle and the hemodynamic function was evaluated. The infarct size was determined by triphenyltetrazolium staining. The serum level of cardiac troponin-I (cTn-I) was determined by ELISA (enzyme-linked immunosorbent assay). Results: Propofol demonstrated protective effects on hemodynamic function and infarct size reduction. In the propofol group, the +dP/dtmax (P = 0.002) was significantly improved compared to the control group. The infarct size was 49.8% of the area at risk in the control group, and was reduced markedly by administration of propofol to 32.6% in the propofol group (P = 0.014). The ischemia/reperfusion-induced serum level of cTn-I was reduced by propofol infusion during the peri-ischemic period (P = 0.0001). Conclusions: Propofol, which infused at clinically relevant concentration during the peri-ischemic period, has delayed myocardial protective effect after regional myocardial ischemia/reperfusion injury in an in vivo rat heart model after 48 h of reperfusion. Copyright ? Korean Society of Anesthesiologists, 2010.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.titlePropofol has delayed myocardial protective effects after a regional ischemia/reperfusion injury in an in vivo rat heart model-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4097/kjae.2010.58.4.378-
dc.identifier.scopusid2-s2.0-77953466625-
dc.identifier.bibliographicCitationKorean Journal of Anesthesiology, v.58, no.4, pp 378 - 382-
dc.citation.titleKorean Journal of Anesthesiology-
dc.citation.volume58-
dc.citation.number4-
dc.citation.startPage378-
dc.citation.endPage382-
dc.type.docTypeArticle-
dc.identifier.kciidART001439036-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorIschemia/reperfusion injury-
dc.subject.keywordAuthorMyocardium-
dc.subject.keywordAuthorPropofol-
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