Anti-inflammatory effect of gallic acid-eluting stent in a porcine coronary restenosis model

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dc.contributor.authorKyungseob Lim-
dc.contributor.authorJ K Park-
dc.contributor.authorM H Jeong-
dc.contributor.authorI H Bae-
dc.contributor.authorD S Park-
dc.contributor.authorJ W Shim-
dc.contributor.authorJ H Kim-
dc.contributor.authorH K Kim-
dc.contributor.authorS S Kim-
dc.contributor.authorD S Sim-
dc.contributor.authorY J Hong-
dc.contributor.authorJ H Kim-
dc.contributor.authorY Ahn-
dc.date.accessioned2018-07-19T16:30:29Z-
dc.date.available2018-07-19T16:30:29Z-
dc.date.issued2018-
dc.identifier.issn1011-6842-
dc.identifier.uri10.6515/ACS.201805_34(3).20171204Ako
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17895-
dc.description.abstractBackground: Gallic acid (3,4,5-trihydroxybenzoic acid) is a natural polyphenol and strong natural antioxidant found abundantly in red wine and green tea. The aim of this study was to examine the anti-inflammatory effect of a novel gallic acid-eluting stent in a porcine coronary restenosis model. Methods: Fifteen pigs were randomized into three groups; in which a total of 30 coronary arteries (10 in each group) were implanted with gallic acid-eluting stents (GESs, n = 10), gallic acid and sirolimus-eluting stents (GSESs, n = 10), or sirolimus-eluting stents (SESs, n = 10). Histopathologic analysis was performed 28 days after stenting. Results: There were no significant differences in injury score and fibrin score among the groups, however there were significant differences in the internal elastic lamina (4.0 ± 0.83mm2 in GES vs. 3.0 ± 0.53mm2 in GSES vs. 4.6 ± 1.43 mm2 in SES, p < 0.0001), lumen area (2.3 ± 0.49 mm2 in GES vs. 1.9 ± 0.67 mm2 in GSES vs. 2.9 ± 0.56 mm2 in SES, p < 0.0001), neointimal area (1.7 ± 0.63 mm2 in GES vs. 1.1 ± 0.28 mm2 in GSES vs. 1.7 ± 1.17 mm2 in SES, p < 0.05), and percent area of stenosis (42.4% ± 9.22% in GES vs. 38.2% ± 12.77% in GSES vs. 33.9% ± 15.64% in SES, p < 0.05). The inflammation score was significantly lower in the GES and GSES groups compared to that in the SES group [1.0 (range: 1.0 to 2.0) in GES vs. 1.0 (range: 1.0 to 1.0) in GSES vs. 1.5 (range: 1.0 to 3.0) in SES, p < 0.05]. Conclusions: The GES group had a greater percent area of stenosis than the SES group. Although gallic acid in the GES and GSES groups did not show a synergistic effect in suppressing neointimal hyperplasia, it resulted in greater inhibition of the inflammatory reaction in the porcine coronary restenosis model than in the SES group.-
dc.publisherTaiwan Soc Cardiology-
dc.titleAnti-inflammatory effect of gallic acid-eluting stent in a porcine coronary restenosis model-
dc.title.alternativeAnti-inflammatory effect of gallic acid-eluting stent in a porcine coronary restenosis model-
dc.typeArticle-
dc.citation.titleActa Cardiologica Sinica-
dc.citation.number3-
dc.citation.endPage232-
dc.citation.startPage224-
dc.citation.volume34-
dc.contributor.affiliatedAuthorKyungseob Lim-
dc.contributor.alternativeName임경섭-
dc.contributor.alternativeName박준규-
dc.contributor.alternativeName정명호-
dc.contributor.alternativeName배인호-
dc.contributor.alternativeName박대성-
dc.contributor.alternativeName심재원-
dc.contributor.alternativeName김정하-
dc.contributor.alternativeName김현국-
dc.contributor.alternativeName김성수-
dc.contributor.alternativeName심두선-
dc.contributor.alternativeName홍영준-
dc.contributor.alternativeName김주한-
dc.contributor.alternativeName안영근-
dc.identifier.bibliographicCitationActa Cardiologica Sinica, vol. 34, no. 3, pp. 224-232-
dc.identifier.doi10.6515/ACS.201805_34(3).20171204A-
dc.subject.keywordInflammation-
dc.subject.keywordPercutaneous coronary intervention-
dc.subject.keywordRestenosis-
dc.subject.keywordStent-
dc.subject.localInflammation-
dc.subject.localinflammation-
dc.subject.localnflammation-
dc.subject.localPercutaneous coronary intervention-
dc.subject.localpercutaneous coronary intervention-
dc.subject.localRestenosis-
dc.subject.localrestenosis-
dc.subject.localStent-
dc.subject.localStents-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
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