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dc.contributor.authorKim, Dong-Eog-
dc.contributor.authorKim, Jeong-Yeon-
dc.contributor.authorNahrendorf, Matthias-
dc.contributor.authorLee, Su-Kyoung-
dc.contributor.authorRyu, Ju Hee-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorSchellingerhout, Dawid-
dc.date.accessioned2024-01-20T16:01:03Z-
dc.date.available2024-01-20T16:01:03Z-
dc.date.created2021-09-05-
dc.date.issued2011-12-
dc.identifier.issn0039-2499-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/129768-
dc.description.abstractBackground and Purpose-High experimental variability in mouse embolic stroke models could mask the effects of experimental treatments. We hypothesized that imaging thrombus directly would allow this variability to be controlled. Methods-We optically labeled thrombi with a near-infrared fluorescent (NIRF) probe C15 that is covalently linked to fibrin by factor-XIIIa. Labeled thrombus was injected into the left distal internal carotid artery (ICA) of C57/BL6 mice (n=47), near its bifurcation, and laser-Doppler cerebral-blood-flow (CBF) was assessed for 30 minutes. NIRF thrombus imaging was done ex vivo at 24 hours. Results-CBF variably decreased to 43.9 +/- 17.3% at 5 minutes (rCBF; 11.2 similar to 80.4%). NIRF thrombus imaging at 24 hours showed variability in distribution (ICA bifurcation, adjacent and/or remote areas) and burden (2279 +/- 1270 pixels; 0 similar to 5940 pixels). Final infarct size was also variable (21.0 +/- 10.3%; 4.7 similar to 60.3% of the bihemispheric volume). Despite this heterogeneity, a strong thrombus-infarct correlation was maintained. The left hemispheric target infarct size (% of the hemisphere) correlated with thrombus burden, as a stronger predictor of infarct volume (P<0.001, r=0.50) than rCBF (P=0.02, r=-0.34). The infarct size was best predicted by a combination of thrombus imaging and CBF: left-hemispheric big-thrombi (>1865 pixels)/low-rCBF (<= 42%) had an infarct volume of 56.9 +/- 10.4% (n=12), big-thrombi/high-rCBF had 45.9 +/- 23.5% (n=11), small-thrombi/low-rCBF 35.7 +/- 17.3% (n=11) and small-thrombi/ high-rCBF 27.3 +/- 16.4% (n=12). Conclusions-This is the first study to demonstrate that the highly heterogeneous nature of the mouse embolic stroke model can be characterized and managed by using near-infrared fluorescent thrombus imaging combined with CBF monitoring to stratify animals into useful subgroups. (Stroke. 2011;42:3566-3573.)-
dc.languageEnglish-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.subjectACTIVATED FACTOR-XIII-
dc.subjectFIBRINOLYTIC RESISTANCE-
dc.subjectCEREBRAL-ISCHEMIA-
dc.subjectSTROKE-
dc.subjectOCCLUSION-
dc.titleDirect Thrombus Imaging as a Means to Control the Variability of Mouse Embolic Infarct Models The Role of Optical Molecular Imaging-
dc.typeArticle-
dc.identifier.doi10.1161/STROKEAHA.111.629428-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSTROKE, v.42, no.12, pp.3566 - 3573-
dc.citation.titleSTROKE-
dc.citation.volume42-
dc.citation.number12-
dc.citation.startPage3566-
dc.citation.endPage3573-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000297941500048-
dc.identifier.scopusid2-s2.0-84856220510-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryPeripheral Vascular Disease-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaCardiovascular System & Cardiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusACTIVATED FACTOR-XIII-
dc.subject.keywordPlusFIBRINOLYTIC RESISTANCE-
dc.subject.keywordPlusCEREBRAL-ISCHEMIA-
dc.subject.keywordPlusSTROKE-
dc.subject.keywordPlusOCCLUSION-
dc.subject.keywordAuthorthrombus imaging-
dc.subject.keywordAuthorembolic cerebral infarction-
dc.subject.keywordAuthormolecular imaging-
dc.subject.keywordAuthoroptical imaging-
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