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dc.contributor.authorChin, Michael S.
dc.contributor.authorFreniere, Brian B.
dc.contributor.authorBonney, Caitlin F.
dc.contributor.authorLancerotto, Luca
dc.contributor.authorSaleeby, Jonathan H.
dc.contributor.authorLo, Yuan-Chyuan
dc.contributor.authorOrgill, Dennis P.
dc.contributor.authorFitzgerald, Thomas J.
dc.contributor.authorLalikos, Janice F.
dc.date2022-08-11T08:08:20.000
dc.date.accessioned2022-08-23T15:51:53Z
dc.date.available2022-08-23T15:51:53Z
dc.date.issued2013-04-01
dc.date.submitted2013-07-08
dc.identifier.citationPlast Reconstr Surg. 2013 Apr;131(4):707-16. doi: 10.1097/PRS.0b013e3182818b94. <a href="http://dx.doi.org/10.1097/PRS.0b013e3182818b94">Link to article on publisher's site</a>
dc.identifier.issn1529-4242 (Electronic)
dc.identifier.doi10.1097/PRS.0b013e3182818b94
dc.identifier.pmid23542244
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29011
dc.description<p>Medical student Brian Freniere participated in this study as part of the Senior Scholars research program at the University of Massachusetts Medical School.</p>
dc.description.abstractBACKGROUND: Ionizing radiation is known to have deleterious chronic effects on skin, including fibrosis and poor wound healing, hypothesized as mediated by ischemia and hypoxia. Past studies have been unable to simultaneously investigate changes in perfusion and oxygenation as separate parameters. Hyperspectral imaging has emerged as a tool with which to concurrently measure skin perfusion and oxygenation. The authors investigated the use of hyperspectral imaging in a novel murine model of chronic radiation injury. METHODS: Areas of flank skin (n = 20) on hairless mice were exposed to a 50-Gy dose of beta-radiation. Hyperspectral imaging acquisition was performed at select points through 8 weeks. Immunohistochemical staining and gene expression analysis were performed to evaluate cutaneous vascular density, epidermal cell hypoxia, and angiogenic factors. RESULTS: All irradiated areas developed a chronic-phase wound by day 28. Hyperspectral imaging demonstrated a 21 percent decline in perfusion on day 56 (p < 0.001), whereas oxygenation levels were unchanged. A 1.7-fold reduction in blood vessel density was measured in irradiated skin compared with control tissue (p < 0.001), but no difference in epidermal cell hypoxia was observed. Vascular endothelial growth factor and related receptor expression were significantly lower in irradiated tissue. CONCLUSIONS: The authors' analysis does not support the presence of hypoxia in chronic-phase irradiated skin but suggests that hypoperfusion may be a predominant characteristic. The concurrent states of hypoperfusion and normoxia may be explained by the lower metabolic demands of fibrosed tissue.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23542244&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1097/PRS.0b013e3182818b94
dc.subjectAnimals
dc.subjectFibrosis
dc.subjectMale
dc.subjectMice
dc.subjectMice, Hairless
dc.subjectOxygen
dc.subjectRadiation Injuries
dc.subject*Regional Blood Flow
dc.subjectSkin
dc.subjectOncology
dc.subjectPlastic Surgery
dc.subjectSkin and Connective Tissue Diseases
dc.titleSkin perfusion and oxygenation changes in radiation fibrosis
dc.typeJournal Article
dc.source.journaltitlePlastic and reconstructive surgery
dc.source.volume131
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/124
dc.identifier.contextkey4295142
html.description.abstract<p>BACKGROUND: Ionizing radiation is known to have deleterious chronic effects on skin, including fibrosis and poor wound healing, hypothesized as mediated by ischemia and hypoxia. Past studies have been unable to simultaneously investigate changes in perfusion and oxygenation as separate parameters. Hyperspectral imaging has emerged as a tool with which to concurrently measure skin perfusion and oxygenation. The authors investigated the use of hyperspectral imaging in a novel murine model of chronic radiation injury.</p> <p>METHODS: Areas of flank skin (n = 20) on hairless mice were exposed to a 50-Gy dose of beta-radiation. Hyperspectral imaging acquisition was performed at select points through 8 weeks. Immunohistochemical staining and gene expression analysis were performed to evaluate cutaneous vascular density, epidermal cell hypoxia, and angiogenic factors.</p> <p>RESULTS: All irradiated areas developed a chronic-phase wound by day 28. Hyperspectral imaging demonstrated a 21 percent decline in perfusion on day 56 (p < 0.001), whereas oxygenation levels were unchanged. A 1.7-fold reduction in blood vessel density was measured in irradiated skin compared with control tissue (p < 0.001), but no difference in epidermal cell hypoxia was observed. Vascular endothelial growth factor and related receptor expression were significantly lower in irradiated tissue.</p> <p>CONCLUSIONS: The authors' analysis does not support the presence of hypoxia in chronic-phase irradiated skin but suggests that hypoperfusion may be a predominant characteristic. The concurrent states of hypoperfusion and normoxia may be explained by the lower metabolic demands of fibrosed tissue.</p>
dc.identifier.submissionpathfaculty_pubs/124
dc.contributor.departmentDepartment of Surgery, Division of Plastic and Reconstructive Surgery
dc.contributor.departmentDepartment of Radiation Oncology
dc.source.pages707-16


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