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Hormones of thyroid gland in sera of rats treated with different dose of concentrated potassium iodine solutions

机译:不同剂量的浓碘化钾溶液对大鼠血清甲状腺激素的影响

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Introduction Potassium iodine (KI) is used as a drug therapy for treating numerous diseases such as small-vessel vasculitis, erythema nodosum, vasculitis nodularis, Sweet's syndrome, tuberculosis and granulomatosis, and for iodized salt. At the same time, KI can be harmful. Iodine intake may increase the frequency of thyroiditis in humans, and may induce the occurrence of experimental thyroiditis (ET) in animals. Investigations on an experimental model for the examination of thyroiditis in Wistar rats have clearly showed morphological changes in the rat thyroid evoked by KI administration. Objective The purpose of this study was to compare the effects of low and high doses of KI on the thyroid gland of Wistar rats and determine the effect on hormone status (T4, T3 and TSH) in this rat strain. Methods Two groups of rats from the Wistar strain were treated with a low iodine dose (225 μg/g BW) and with a high iodine dose (675 μg/g BW) of KI solutions. Untreated nonimmunized animals served as controls. The solution was administrated daily intraperitoneally during the period of 26 consecutive days. Results Monitoring hormone status (TSH, T3 and T4) and morphological changes it was found that therapeutic doses of KI applied in treatment induced the occurrence of experimental thyroiditis (chronic destructive Hashimoto's thyroiditis in humans) and cell necrosis in animals not carrying a genetic susceptibility. Significant inflammatory changes were observed in rats treated with a high iodine dose. Conclusion The early iodine induced cell necrosis and inflammation in the nonimmunized animals without genetic susceptibility is a new experimental model of thyroiditis. .
机译:简介碘化钾(KI)用于治疗多种疾病,例如小血管血管炎,结节性红斑,结节性血管炎,Sweet综合征,肺结核和肉芽肿病以及加碘盐。同时,KI可能有害。摄入碘可能会增加人类甲状腺炎的发病率,并可能诱发动物实验性甲状腺炎(ET)的发生。对Wistar大鼠甲状腺炎的实验模型进行的研究清楚地显示了KI给药诱发的大鼠甲状腺的形态变化。目的本研究的目的是比较低剂量和高剂量KI对Wistar大鼠甲状腺的影响,并确定其对激素状态(T4,T3和TSH)的影响。方法用低碘剂量(225μg/ g BW)和高碘剂量(675μg/ g BW)的KI溶液处理Wistar品系的两组大鼠。未经处理的非免疫动物用作对照。在连续26天的时间内每天腹膜内施用该溶液。结果监测激素状态(TSH,T3和T4)和形态变化,发现治疗剂量的KI会诱发实验性甲状腺炎(人为慢性破坏性桥本甲状腺炎)的发生和未携带遗传易感性的动物的细胞坏死。在用高碘剂量治疗的大鼠中观察到明显的炎症变化。结论无基因易感性的非免疫动物早期碘诱导的细胞坏死和炎症反应是甲状腺炎的新实验模型。 。

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