1 Department of Otorhinolaryngology-Head and Neck Surgery, Inha University School of Medicine , Incheon, Republic of Korea.
Thyroid. 2013 Nov;23(11):1445-51. doi: 10.1089/thy.2012.0243. Epub 2013 Jul 25.
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.
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.
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.
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.
甲状腺组织的放射性碘(RAI)消融术在分化型甲状腺癌手术后,可以引起与辐射相关的唾液腺(SG)功能障碍。然而,在适当的动物模型中,RAI 给药后 SG 的体内变化在文献中描述得并不充分。本研究旨在描述 RAI 诱导的 SG 功能障碍的小鼠模型中,RAI 给药后 12 个月内的形态和功能变化。
将 4 周龄雌性 C57BL/6 小鼠(n=60)分为 RAI 治疗组(n=30),口服 RAI(0.01mCi/g 体重)和未暴露对照组(n=30)。两组小鼠再分为 5 个亚组(n=6 只/亚组),分别在 RAI 给药后 1、2、3、6 和 12 个月时安乐死。在 RAI 给药后 1、2、3、6 和 12 个月时测量唾液流量和唾液延迟时间。进行形态学和组织学检查以及末端脱氧核苷酸转移酶 dUTP 缺口末端标记测定。此外,通过单光子发射计算机断层扫描观察唾液(99m)Tc 放射性碘摄取和排泄的变化。
在 RAI 治疗组的小鼠中,SG 明显比未暴露对照组轻,所有研究时间点均如此。RAI 治疗组的唾液延迟时间大于未暴露对照组,但平均唾液流量较低。RAI 组 SG 的组织学检查显示细胞质苍白、导管结构不典型、隔增宽、细胞质空泡化伴多形性、淋巴细胞浸润和纤维化增加。此外,在 RAI 组的腺泡和导管中观察到更多的凋亡细胞。此外,在 RAI 给药后 1 和 12 个月,RAI 组的(99m)Tc 放射性碘摄取和排泄模式与对照组有很大不同。
在接受 RAI 暴露的小鼠中观察到各种组织学改变,即腺泡和导管细胞凋亡增加以及 SG 功能恶化。本研究中使用的 RAI 诱导的 SG 功能障碍的小鼠模型似乎适用于分化型甲状腺癌患者的 RAI 诱导唾液腺炎的临床前研究。