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帖利军, 潘建平, 胡晓, 张瑞娟, 葛玲. 甲减及高碘大鼠海马组织神经生长相关蛋白的表达[J]. 中国公共卫生, 2002, 18(12): 1433-1436. DOI: 10.11847/zgggws2002-18-12-14
引用本文: 帖利军, 潘建平, 胡晓, 张瑞娟, 葛玲. 甲减及高碘大鼠海马组织神经生长相关蛋白的表达[J]. 中国公共卫生, 2002, 18(12): 1433-1436. DOI: 10.11847/zgggws2002-18-12-14
TIE Li-jun, PAN Jian-ping, HU Xiao, . Expression of GAP-43 in Hippocampal Formation During Brain Developmental Critical Period of both Hypothyroid and Excessive Iodine Rats[J]. Chinese Journal of Public Health, 2002, 18(12): 1433-1436. DOI: 10.11847/zgggws2002-18-12-14
Citation: TIE Li-jun, PAN Jian-ping, HU Xiao, . Expression of GAP-43 in Hippocampal Formation During Brain Developmental Critical Period of both Hypothyroid and Excessive Iodine Rats[J]. Chinese Journal of Public Health, 2002, 18(12): 1433-1436. DOI: 10.11847/zgggws2002-18-12-14

甲减及高碘大鼠海马组织神经生长相关蛋白的表达

Expression of GAP-43 in Hippocampal Formation During Brain Developmental Critical Period of both Hypothyroid and Excessive Iodine Rats

  • 摘要: 目的 研究高碘对甲状腺激素以及甲减、高碘对脑发育临界期大鼠海马组织神经生长相关蛋白表达的影响.方法 分别选用他巴唑及碘化油诱导建立的甲减及高碘大鼠动物模型,用免疫细胞化学方法结合图像分析对正常、高碘及甲减大鼠脑发育临界期海马组织神经生长相关蛋白的变化进行定性、定量研究.结果 (1)甲减及高碘脑发育临界期大鼠海马结构内神经生长相关蛋白的分布趋势与正常对照组相似.表现为腔隙层、放射层及始层梯度染色,神经元胞体一般不染色.图像分析显示:甲减鼠海马CA1区GAP-43灰度值与对照组比明显升高(P<0.01);高碘鼠同一脑区其灰度值虽低于正常对照组,但经统计学分析无显着性差异(P>0.05).(2)高碘可引起血清甲状腺激素紊乱(T3↓、T4↑、T3/T4↓).结论 (1)高碘可引起甲状腺机能紊乱.(2)高碘及甲减在脑发育临界期可直接或间接影响神经生长相关蛋白的表达,进而影响Go蛋白信号转导系统及第二信号系统,导致学习、记忆障碍.

     

    Abstract: Objective To study the expression of GAP-43 hippocampal formation during brain developmental critical period of both hypothyroid and excessive iodine rats.Methods The model of hypothyroid and excessive iodine rats were established by pre-treatment with Thiamazole and Injection of iodine respectively,analysis of thyroid hormones,immunocytochemical method combining with image analysis were used to observe changes of GAP-43 in hippocampal formation of both normal and hypothroid as well as excessive iodine neonatal rats.Results The distribution tendency of GAP-43 in hippocampal formation was similarity in experimental pups as compared to age-matched controls.The grey values of GAP-43 were decreased in hypothyroidism(P<0.01),there were no statistical difference between excessive iodine pups and control(P> 0.05)of CA1 hippocampal formation during critical period of brain development.Conclusion (1)Excessive iodine could lead to thyroid hormones imbalance;(2)GAP-43 may be a molecular that thyroid hormones regulated directly or indirectly.By regulating GAP-43,thyroid hormones had an effect on Go protein signal transduction system,as occured in the wake of the second signal process and may affect the abilities of learning and memory.

     

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