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首页> 外文期刊>International journal of developmental neuroscience: the official journal of the International Society for Developmental Neuroscience >Hypothyroidism following developmental iodine deficiency reduces hippocampal neurogranin, CaMK II and calmodulin and elevates calcineurin in lactational rats.
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Hypothyroidism following developmental iodine deficiency reduces hippocampal neurogranin, CaMK II and calmodulin and elevates calcineurin in lactational rats.

机译:发育碘缺乏后的甲状腺功能减退症会减少哺乳期大鼠的海马神经颗粒蛋白,CaMK II和钙调蛋白,并升高钙调神经磷酸酶。

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Developmental iodine deficiency (ID) leads to inadequate thyroid hormone that impairs learning and memory with an unclear mechanism. Here, we show that hippocampal neurogranin, calcium/calmodulin dependent protein kinase II (CaMKII), calmodulin (CaM) and calcineurin (CaN) are implicated in the brain impairment in lactational rat hippocampus following developmental ID and hypothyroidism. Three developmental rat models were created by administrating dam rats with either iodine-deficient diet or propylthiouracil (PTU, 5 ppm or 15 ppm)-added drinking water from gestational day (GD) 6 till postnatal day (PN) 21. Then, the neurogranin, CaMKII, CaM and CaN in the hippocampus were detected with immunohistochemistry and western blotting on PN14 and PN21. The iodine-deficient and hypothyroid pups showed significantly lower level of neurogranin, CaMKII and CaM and significantly increased CaN in hippocampal CA1 and CA3 regions than the controls on PN14 and PN21 (P<0.05, respectively). Data indicate that, in lactational rats, hippocampal neurogranin, CaMKII, CaM and CaN are involved in the brain impairment by developmental ID and hypothyroidism.
机译:发育碘缺乏症(ID)会导致甲状腺激素不足,从而以不清楚的机制损害学习和记忆。在这里,我们显示海马神经颗粒蛋白,钙/钙调蛋白依赖性蛋白激酶II(CaMKII),钙调蛋白(CaM)和钙调神经磷酸酶(CaN)与发育性ID和甲状腺功能减退后的哺乳期大鼠海马脑损伤有关。通过从妊娠第6天(GD)到出生后第21天(PN),给缺碘饮食或添加丙硫氧嘧啶(PTU,5 ppm或15 ppm)的饮用水的水坝大鼠给药,建立了三种发育中的大鼠模型。通过免疫组织化学和PN14和PN21的Western印迹检测海马中的CaMKII,CaM和CaN。缺碘和甲状腺功能减退的幼犬比PN14和PN21的对照组显示海马CA1和CA3区的神经颗粒素,CaMKII和CaM含量显着降低,而CaN显着升高(分别为P <0.05)。数据表明,在哺乳期大鼠中,海马神经颗粒蛋白,CaMKII,CaM和CaN参与了发育ID和甲状腺功能减退所致的脑损伤。

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