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Strategies for Preventing Wrong Site, Wrong Procedure, Wrong Patient Surgery

机译:预防错误部位,错误程序,错误患者手术的策略

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In this article, Fournierand colleagues ask whether epilepsy-induced newborn cells could also be involved in cognitive impairments, a common comorbidity of TLE. This question is all the more relevant since the dentate gyrus plays a critical role in certain forms of memory (7) and newborn cells in epilepsy migrate, differentiate, and integrate abnormally in the dentate gyrus. In addition, a large number of studies—although there are some discrepancies—report alterations of memory performance after blockade of adult neurogenesis in non-epileptic rodents (3). Taken together, one would therefore expect that epilepsy-induced newborn cells would negatively impact dentate and memory function. While previous attempts have been made to test this hypothesis by blocking adult neurogenesis after SE (8), it is possible that the behavioral improvements observed could be caused directly by the treatment (here, valproate) and not the decreased neurogenesis. In this study, Fournier and colleagues used a different approach: Instead of blocking adult neurogenesis in their epilepsy model, they let newborn neurons develop freely and asked whether these neurons show signs of involvement in a memory task.
机译:在这篇文章中,Fournierand的同事们询问癫痫诱发的新生细胞是否也可能与认知障碍(TLE的常见合并症)有关。由于齿状回在某些形式的记忆中起着至关重要的作用(7),并且癫痫中的新生细胞异常地迁移,分化和整合在齿状回中,因此这个问题变得更加重要。此外,尽管有一些差异,但大量研究报告了在非癫痫性啮齿动物中,成年神经发生受阻后记忆功能的改变(3)。两者合计,因此可以预期癫痫诱发的新生细胞会对齿状和记忆功能产生负面影响。尽管先前尝试通过阻断SE后的成人神经发生来检验该假设(8),但观察到的行为改善可能直接由治疗(此处为丙戊酸盐)而非减少的神经发生引起。在这项研究中,Fournier及其同事使用了另一种方法:他们不是在癫痫模型中阻止成人神经发生,而是让新生神经元自由发育,并询问这些神经元是否显示出参与记忆任务的迹象。

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