División de Investigación y Estudios de Posgrado, Facultad de Psicología, Universidad Nacional Autónoma de México, 04510, México City, D.F., México.
Eur J Neurosci. 2013 Apr;37(8):1248-59. doi: 10.1111/ejn.12141. Epub 2013 Feb 7.
Changes in synaptic efficacy and morphology are considered as the downstream mechanisms of consolidation of memories and other adaptive behaviors. In the last decade, neurotrophin-3 (NT-3) has emerged as one potent mediator of synaptic plasticity. In the adult brain, expression of NT-3 is largely confined to the hippocampal dentate gyrus (DG). Our previous studies show that application of high-frequency stimulation (HFS) sufficient to elicit long-term potentiation (LTP) at the DG-CA3 pathway as well as acute intrahippocampal microinfusion of brain-derived neurotrophin factor produce mossy fiber (MF) structural reorganization. Here, we show that intrahippocampal microinfusion of NT-3 induces a long-lasting potentiation of synaptic efficacy in the DG-CA3 projection accompanied by an MF structural reorganization of adult rats in vivo. It is considered that the capacity of synapses to express plastic changes is itself subject to variation depending on previous experience; taking into consideration the effects of NT-3 on MF synaptic plasticity, we thus used intrahippocampal microinfusion of NT-3 to analyse its effects on functional and structural plasticity induced by subsequent MF-HFS sufficient to induce LTP in adult rats, in vivo. Our results show that NT-3 modifies the ability of the MF pathway to present subsequent LTP by HFS, and modifies the structural reorganization pattern. The modifications in synaptic efficacy and morphology elicited by NT-3 at the MF-CA3 pathway were blocked by the presence of a Trk receptor inhibitor (K252a). These findings support the idea that NT-3 actions modify subsequent synaptic plasticity, a homeostatic mechanism thought to be essential for maintaining synapses in the adult mammalian brain.
突触效能和形态的变化被认为是记忆巩固和其他适应行为的下游机制。在过去的十年中,神经生长因子-3(NT-3)已成为突触可塑性的一个有力介质。在成年大脑中,NT-3 的表达主要局限于海马齿状回(DG)。我们之前的研究表明,应用足以在 DG-CA3 通路中引发长时程增强(LTP)的高频刺激(HFS)以及急性海马内微灌注脑源性神经营养因子会导致苔藓纤维(MF)结构重组。在这里,我们显示海马内微灌注 NT-3 可诱导 DG-CA3 投射中突触效能的持久增强,同时伴有成年大鼠体内 MF 结构的重组。认为突触表达可塑性变化的能力本身取决于先前的经验;考虑到 NT-3 对 MF 突触可塑性的影响,我们因此使用海马内微灌注 NT-3 来分析其对随后 MF-HFS 诱导的功能和结构可塑性的影响,在成年大鼠体内足以诱导 LTP。我们的结果表明,NT-3 通过 HFS 改变了 MF 通路呈现随后的 LTP 的能力,并改变了结构重组模式。在 MF-CA3 通路中,NT-3 引起的突触效能和形态变化被 Trk 受体抑制剂(K252a)阻断。这些发现支持 NT-3 作用修饰随后的突触可塑性的观点,这是一种被认为对于维持成年哺乳动物大脑中的突触至关重要的平衡机制。