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Morphometric and functional changes of salivary gland dysfunction after radioactive iodine ablation in a murine model

DC Field Value Language
dc.contributor.author임재열-
dc.date.accessioned2018-05-10T06:44:16Z-
dc.date.available2018-05-10T06:44:16Z-
dc.date.issued2013-
dc.identifier.issn1050-7256-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/158540-
dc.description.abstractBACKGROUND: Ablation of the thyroid tissue using radioactive iodine (RAI) after the surgical removal of well-differentiated thyroid cancer can induce radiation-related salivary gland (SG) dysfunction. However, in vivo changes of SGs after RAI administration in appropriate animal models are not well described in the literature. This study was undertaken to document morphometric and functional changes during the 12 months after RAI administration in a murine model of RAI-induced SG dysfunction. METHODS: Four-week-old female C57BL/6 mice (n = 60) were divided into an RAI-treated group (n = 30) that received RAI orally (0.01 mCi/g body weight) and an unexposed control group (n = 30). Mice in both groups were divided into five subgroups (n = 6 per subgroup) and euthanized at 1, 2, 3, 6, and 12 months post-RAI administration. Salivary flow rates and salivary lag times were measured at 1, 2, 3, 6, and 12 months after RAI administration. Morphological and histological examinations and terminal deoxynucleotidyl transferase dUTP nick end labeling assays were performed. In addition, changes in salivary (99m)Tc pertechnetate uptake and excretion were observed by single-photon emission computed tomography. RESULTS: In RAI-treated mice, the SGs were significantly lighter than those of unexposed controls at all study time points. Lag times to salivation in the RAI-treated group were greater than in the unexposed controls, but mean salivary flow rates were lower. Histologic examinations of SGs in the RAI group showed pale cytoplasm, atypical ductal configuration, septal widening, cytoplasmic vacuolization with pleomorphism, lymphocyte infiltration, and increased fibrosis. Furthermore, more apoptotic cells were observed in acini and ducts in the RAI group. In addition, patterns of (99m)Tc pertechnetate uptake and excretion in the RAI group were quite different from those observed in controls at 1 and 12 months post-RAI. CONCLUSION: Various histological alterations were observed in mice exposed to RAI, that is, an increase in apoptotic acini and ductal cells and functional SG deterioration. The murine model of RAI-induced SG dysfunction used in the present study appears to be applicable to preclinical research on RAI-induced sialadenitis in patients with well-differentiated thyroid cancer.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMary Ann Liebert Publishers-
dc.relation.isPartOfTHYROID-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHApoptosis-
dc.subject.MESHBody Weight-
dc.subject.MESHFemale-
dc.subject.MESHIn Situ Nick-End Labeling-
dc.subject.MESHIodine Radioisotopes/pharmacology*-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred C57BL-
dc.subject.MESHSaliva/diagnostic imaging-
dc.subject.MESHSaliva/metabolism-
dc.subject.MESHSalivary Glands/diagnostic imaging*-
dc.subject.MESHSalivary Glands/physiopathology*-
dc.subject.MESHSalivary Glands/radiation effects-
dc.subject.MESHSialadenitis/diagnostic imaging*-
dc.subject.MESHSialadenitis/physiopathology-
dc.subject.MESHTechnetium/pharmacokinetics*-
dc.subject.MESHThyroid Gland/diagnostic imaging*-
dc.subject.MESHThyroid Gland/radiation effects-
dc.subject.MESHTime Factors-
dc.subject.MESHTomography, Emission-Computed, Single-Photon-
dc.titleMorphometric and functional changes of salivary gland dysfunction after radioactive iodine ablation in a murine model-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Otorhinolaryngology-
dc.contributor.googleauthorJeong-Seok Choi-
dc.contributor.googleauthorIn Suh Park-
dc.contributor.googleauthorSeok-Ki Kim-
dc.contributor.googleauthorJae-Yol Lim-
dc.contributor.googleauthorYoung-Mo Kim-
dc.identifier.doi10.1089/thy.2012.0243-
dc.contributor.localIdA03396-
dc.relation.journalcodeJ02729-
dc.identifier.eissn1557-9077-
dc.identifier.pmid23607283-
dc.contributor.alternativeNameLim, Jae Yol-
dc.contributor.affiliatedAuthorLim, Jae Yol-
dc.citation.volume23-
dc.citation.number11-
dc.citation.startPage1445-
dc.citation.endPage1451-
dc.identifier.bibliographicCitationTHYROID, Vol.23(11) : 1445-1451, 2013-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers

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