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作 者:刘志华[1] 汪惠丽[1] 吴圣[2] 刘阳[2] 陈向涛[2]
机构地区:[1]合肥工业大学生物与食品工程学院,安徽合肥230009 [2]安徽医科大学药学院,安徽合肥230032
出 处:《中国药理学与毒理学杂志》2014年第2期161-167,共7页Chinese Journal of Pharmacology and Toxicology
基 金:国家重点基础研究发展计划项目课题(973计划课题,2012CB525003);国家自然科学基金项目(31200851);国家自然科学基金项目(21307024);新世纪优秀人才支持计划(NCET-12-0835);高等学校博士学科点专项科研基金(20130111110024);中国博士后科学基金(2013M531500);合肥工业大学黄山青年学者基金(407-037030);中央高校基本科研业务费专项资金(2013HGCH0016);中央高校基本科研业务费专项资金(2013HGQC0033);中央高校基本科研业务费专项资金(2013HGBH0013);安徽医科大学七年制学生"早期接触科研"训练计划(2012-ZQKY-59)~~
摘 要:目的探讨发育关键期双酚A(BPA)暴露对海马齿状回(DG)区突触形成和树突棘的影响及其机制。方法出生7 d的SD大鼠,腹腔注射BPA 50,250和500μg·kg-1·d-1,连续7 d。Golgi-Cox染色分析海马DG区树突棘密度和树突棘头形态大小,Western blotting检测β联蛋白,Wnt7a及Wnt5a蛋白表达。结果 BPA 50,250和500μg·kg-1组海马DG区树突棘密度依次为9.67±0.17,8.97±0.13,(8.71±0.15)/10μm,相对于正常对照组的(10.21±0.17)/10μm,BPA 50,250和500μg·kg-1·d-1组树突棘密度显著下降(P<0.05)。正常对照组树突棘头为(0.67±0.03)μm2,BPA 50,250和500μg·kg-1组树突棘头依次为0.53±0.03,0.51±0.03和(0.50±0.03)μm2,显著低于正常对照组(P<0.05)。BPA 50,250和500μg·kg-1·d-1组磷酸化的β联蛋白占总体β联蛋白的百分比分别提高了18.28%,32.22%和57.01%,而Wnt7a表达显著降低(P<0.05),Wnt5a表达显著提高(P<0.05)。结论在BPA所引起的突触形成和树突棘的损伤中,Wnt信号通路可能起关键作用。OBJECTIVE To investigate the effects and its underlying mechanism of bisphenoI-A (BPA) exposure on spine and synapse formation in detate gyrus (DG) area of hippocampus during criti- cal developmental period. METHODS Sprague-Dawley(SD) rats were injected intraperitoneally with BPA (50,250 and 500 pg.kg-1 .d-1 -1) from postnatal day 7 (PND7) to PND14. Dendritic spine morphol- ogy in DG area was examined using Golgi-Cox staining method and determined with Image J software. Western blotting method was employed to test the Writ related proteins. RESULTS The spine density and the average spine head size in BPA exposed groups significantly decreased in a close-dependent manner when compared to control group( P 〈 0.05). Meanwhile, Wnt related proteins were affected dur- ing BPA exposure. Specifically, the percentage of phosphorylated β-catenin increased following BPA ex- posure (P 〈0.05), whereas Wnt7a expression level was significantly decreased and Wnt5a expression level increased (P〈0.05). CONCLUSION Wnt signaling pathway plays an important role in BPA-in- duced impairments in spine and synapse formation.
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