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The effects of antiepileptic drugs on spatial learning and hippocampal protein kinase C gamma in immature rats.

机译:抗癫痫药对未成熟大鼠空间学习和海马蛋白激酶Cγ的影响。

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This study was conducted to determine if alterations in hippocampal protein kinase C (PKC) gamma is one of the cellular mechanisms by which conventional antiepileptic drugs affect learning and memory. Wistar Rats (21-day-old) were divided into five groups: (1) control (no training and drugs); (2) training group (no drugs); (3) phenobarbital (PB) group; (4) carbamazepine (CBZ) group; and (5) valproate (VPA) group. A hippocampus dependent learning task (spatial changing learning) was used in the latter four groups lasting a total of 10 days. Correct responding rate of training group was significantly higher (P<0.05) than in the PB, CBZ and VPA group. The PKC gamma staining intensity in hippocampal CA1-2 region of training group was significant greater than that of the control and PB group. There was no difference in staining intensities between the CBZ, VPA group or training group. The amount of PKC gamma located in plasma membrane of hippocampal neurons was significantly higher in the training group (P<0.05) than the control, PB and VPA groups. No differences were found between the training and CBZ group. Lastly, the amount of PKC gamma in cytosol of hippocampus did not significantly differ between any of the five groups. These results indicate that the three antiepileptic drugs used in this study all disturbed the spatial learning of immature rats. Spatial learning was concomitant with activation of PKC gamma in hippocampal neurons. PB and VPA likely adversely affect learning and memory by interfering with PKC gamma activation, whereas CBZ may act by a different mechanism, possibly in the post-translocation process or by a PKC gamma independent pathway.
机译:进行这项研究来确定海马蛋白激酶C(PKC)γ的改变是否是传统抗癫痫药影响学习和记忆的细胞机制之一。 Wistar大鼠(21日龄)分为五组:(1)对照组(不进行训练和药物治疗); (2)培训班(无毒品); (3)苯巴比妥(PB)组; (4)卡马西平(CBZ)组; (5)丙戊酸盐(VPA)组。后四组使用海马依赖性学习任务(空间变化学习),总共持续10天。训练组正确应答率明显高于PB,CBZ和VPA组(P <0.05)。训练组海马CA1-2区PKCγ染色强度明显高于对照组和PB组。 CBZ,VPA组或训练组之间的染色强度没有差异。训练组海马神经元质膜中PKCγ的含量明显高于对照组,PB和VPA组(P <0.05)。训练组和CBZ组之间没有发现差异。最后,在五组中的任何一组中,海马胞浆中PKCγ的量均无显着差异。这些结果表明,本研究中使用的三种抗癫痫药都干扰了未成熟大鼠的空间学习。空间学习与海马神经元中PKCγ的激活同时发生。 PB和VPA可能通过干扰PKCγ激活而对学习和记忆产生不利影响,而CBZ可能通过不同的机制起作用,可能是在转运后过程中或通过PKCγ独立途径。

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