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大鼠海马体中同突触长时程抑制和去增强的预激发促进作用

Primed facilitation of homosynaptic long-term depression and depotentiation in rat hippocampus.

作者信息

Holland L L, Wagner J J

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, North Dakota State University, Fargo, North Dakota 58105, USA.

出版信息

J Neurosci. 1998 Feb 1;18(3):887-94. doi: 10.1523/JNEUROSCI.18-03-00887.1998.

Abstract

Previous studies have demonstrated that prior synaptic activity can influence the subsequent induction of synaptic plasticity in the brain. Such temporal modulation of synaptic plasticity has been called "metaplasticity." In this report, we describe the facilitatory effects of high-frequency stimulation on the induction of homosynaptic long-term depression (LTD) in the CA1 region of the rat hippocampus. The LTD induced by low-frequency stimulation (1 Hz) protocols was found to be homosynaptic and NMDA receptor-dependent. The facilitatory effects of the high-frequency stimulation-induced priming event itself were found to be NMDA receptor-independent and to have a duration of at least 90 min. The effects of priming also were heterosynaptic, because the induction of synaptic plasticity by low-frequency stimulation was enhanced at an unprimed synaptic pathway after the priming of an independent pathway. In addition to enhancing LTD, priming also enhanced the reversal of long-term potentiation elicited by a 5 Hz depotentiation protocol. Our results provide examples of how metaplasticity may play a key role in the ongoing modulation of the induction and stabilization of alterations in synaptic strength.

摘要

先前的研究表明,突触前的活动能够影响随后大脑中突触可塑性的诱导。这种对突触可塑性的时间调制被称为“元可塑性”。在本报告中,我们描述了高频刺激对大鼠海马体CA1区同突触长时程抑制(LTD)诱导的促进作用。发现低频刺激(1Hz)方案诱导的LTD是同突触的且依赖于NMDA受体。高频刺激诱导的引发事件本身的促进作用被发现不依赖于NMDA受体,且持续时间至少为90分钟。引发的作用也是异突触的,因为在独立通路引发后,未引发的突触通路中低频刺激诱导的突触可塑性增强。除了增强LTD外,引发还增强了由5Hz去极化方案引发的长时程增强的逆转。我们的结果提供了元可塑性如何在突触强度变化的诱导和稳定的持续调制中发挥关键作用的实例。

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