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大鼠海马的渐近性长期增强并不排除在后期阶段出现额外的增强。

Asymptotic hippocampal long-term potentiation in rats does not preclude additional potentiation at later phases.

作者信息

Frey U, Schollmeier K, Reymann K G, Seidenbecher T

机构信息

Federal Institute for Neurobiology, Department of Gene Regulation and Plasticity, Magdeburg, Germany.

出版信息

Neuroscience. 1995 Aug;67(4):799-807. doi: 10.1016/0306-4522(95)00117-2.

Abstract

Hippocampal long-term potentiation may serve as an elementary process underlying certain forms of learning and memory in vertebrates. As is the case with behavioural memory, hippocampal long-term potentiation in the CA1 region and in the dentate gyrus exhibits distinct phases. These comprise a short-term early potentiation which lasts one to three hours and is independent of protein synthesis and is characterized in general by the activation of N-methyl-D-aspartate receptors and protein kinases; and a later, longer lasting phase, which can be separated by inhibitors of protein synthesis. Here, we report that the prior induction of long-term potentiation, both in the dentate gyrus in vivo and in the CA1-region in vitro, precludes further long-term but not short-term potentiation by means of a newly delivered conditioning stimulus to a subset of the same activated synapse population during the early stage (approximately 1-3 hours post tetanus). In contrast, a subsequent, long-lasting potentiation can be induced after the establishment of the late phase of potentiation (> 4 h). Thus, the system preserves the capacity for short-term potentiation immediately after potentiation, but the capacity for the induction of longer lasting plastic changes is recovered only after about four hours. Our results demonstrate that, once long-term potentiation has been established, hippocampal neurons do not lose their capacity for functional plasticity during certain phases of the maintenance of long-term potentiation.

摘要

海马体长期增强作用可能是脊椎动物某些形式学习和记忆的基本过程。与行为记忆的情况一样,CA1区域和齿状回中的海马体长期增强作用表现出不同阶段。这些阶段包括持续一到三个小时且独立于蛋白质合成的短期早期增强作用,其一般特征是N-甲基-D-天冬氨酸受体和蛋白激酶的激活;以及后期持续时间更长的阶段,该阶段可被蛋白质合成抑制剂分开。在此,我们报告,在体内齿状回和体外CA1区域中预先诱导长期增强作用后,在早期阶段(破伤风后约1-3小时),通过向同一激活突触群体的一个子集施加新的条件刺激,可阻止进一步的长期增强作用,但不阻止短期增强作用。相比之下,在增强作用后期(>4小时)建立后,可以诱导随后的长期增强作用。因此,该系统在增强作用后立即保留短期增强作用的能力,但只有在大约四个小时后才恢复诱导更持久可塑性变化的能力。我们的结果表明,一旦建立了长期增强作用,海马体神经元在长期增强作用维持的某些阶段不会丧失其功能可塑性的能力。

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