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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products.
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Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products.

机译:缺乏肌营养不良蛋白基因产物的mdx和mdx3cv小鼠的空间分辨学习和CA1海马突触可塑性。

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Duchenne muscular dystrophy is frequently associated with a non-progressive cognitive deficit attributed to the absence of 427,000 mol. wt brain dystrophin, or to altered expression of other C-terminal products of this protein, Dp71 and/or Dp140. To further explore the role of these membrane cytoskeleton-associated proteins in brain function, we studied spatial learning and ex vivo synaptic plasticity in the mdx mouse, which lacks 427,000 mol. wt dystrophin, and in the mdx3cv mutant, which shows a dramatically reduced expression of all the dystrophin gene products known so far. We show that reference and working memories are largely unimpaired in the two mutant mice performing a spatial discrimination task in a radial maze. However, mdx3cv mice showed enhanced emotional reactivity and developed different strategies in learning the task, as compared to control mice. We also showed that both mutants display apparently normal levels of long-term potentiation and paired-pulse facilitation in the CA1 field of the hippocampus. On the other hand, an increased post-tetanic potentiation was shown by mdx, but not mdx3cv mice, which might be linked to calcium-regulatory defects. Otherwise, immunoblot analyses suggested an increased expression of a 400,000 mol. wt protein in brain extracts from both mdx and mdx3cv mice, but not in those from control mice. This protein might correspond to the dystrophin-homologue utrophin. The present results suggest that altered expression of dystrophin or C-terminal dystrophin proteins in brain did not markedly affect hippocampus-dependent spatial learning and CA1 hippocampal long-term potentiation in mdx and mdx3cv mice. The role of these membrane cytoskeleton-associated proteins in normal brain function and pathology remains to be elucidated. Furthermore, the possibility that redundant mechanisms could partially compensate for dystrophins' deficiency in the mdx and mdx3cv models should be further considered.
机译:杜兴氏肌营养不良症通常与非进展性认知功能障碍有关,归因于缺乏427,000 mol。重度肌营养不良蛋白,或该蛋白Dp71和/或Dp140的其他C末端产物的表达改变。为了进一步探索这些膜细胞骨架相关蛋白在脑功能中的作用,我们研究了缺少427,000 mol的mdx小鼠的空间学习和离体突触可塑性。 wt肌营养不良蛋白,以及mdx3cv突变体中,显示出迄今已知的所有肌营养不良蛋白基因产物的表达大大降低。我们显示参考和工作记忆在径向突变的迷宫中执行空间区分任务的两个突变小鼠在很大程度上不受损害。但是,与对照小鼠相比,mdx3cv小鼠表现出增强的情绪反应性,并且在学习任务方面发展出不同的策略。我们还显示,这两个突变体在海马CA1场中均显示出明显的正常水平的长期增强作用和成对脉冲促进作用。另一方面,mdx显示了强直性强直后增强作用,但mdx3cv小鼠却没有,这可能与钙调节缺陷有关。否则,免疫印迹分析表明表达增加了400,000 mol。 mdx和mdx3cv小鼠的脑部提取物中的wt蛋白,但对照小鼠的脑部提取物中的wt蛋白。该蛋白可能对应于肌营养不良蛋白-同源性的卵磷脂。目前的结果表明,神经营养不良蛋白或C端营养不良蛋白表达的改变不会明显影响mdx和mdx3cv小鼠的海马依赖性空间学习和CA1海马长期增强。这些膜细胞骨架相关蛋白在正常脑功能和病理中的作用仍有待阐明。此外,应进一步考虑冗余机制可以部分弥补mdx和mdx3cv模型中营养不良蛋白缺乏症的可能性。

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