Banke Tue G
Danish Neuroscience Centre, Aarhus University Hospital/Aarhus University, Nørrebrogade 44, Bygning 10G, 2.sal, 8000, Aarhus C, Denmark.
Pflugers Arch. 2016 Apr;468(4):717-26. doi: 10.1007/s00424-015-1775-4. Epub 2016 Jan 4.
The transient receptor potential vanilloid 1 (TRPV1) channel is a non-selective cation channel that is mainly found in nociceptive neurons of the peripheral nervous system; however, these channels have also been located within the CNS, including the entorhinal cortex. Whole-cell patch-clamp recordings of principal entorhinal cortex (EC) layers II/III neurons revealed that evoked inhibitory postsynaptic currents were depressed by application of the TRPV1 agonist capsaicin (CAP), accompanied by a change in the pair-pulse ratio (PPR). In addition, recordings of miniature inhibitory postsynaptic currents (mIPSCs) revealed that inter-event intervals but not amplitude were decreased in wild-type (WT) after application of CAP. This suggests that TRPV1 channels are functional in the entorhinal cortex and are located on inhibitory neurons with their axonal arborization within layers II/III. In order to study TRPV1 channels and their involvement in long-term potentiation (LTP) induction in a more intact circuit, extracellular field potential recordings were performed in EC layers II/III. It was found that activated TRPV1 channels preclude induction of long-term potentiation. In sharp contrast, clear LTP was observed when antagonizing TRPV1 channels or recording from TRPV1 knock-out mice. Thus, these results suggests that signaling through activating inhibitory presynaptic TRPV1 channels represents a novel mechanism by which a shift in feed-forward inhibition of layers II/III cortical principal neurons prompt changes in synaptic strength and thereby contribute to a change of information storage within the brain.
瞬时受体电位香草酸亚型1(TRPV1)通道是一种非选择性阳离子通道,主要存在于外周神经系统的伤害性神经元中;然而,这些通道也存在于中枢神经系统内,包括内嗅皮层。对内侧内嗅皮层(EC)II/III层主要神经元进行的全细胞膜片钳记录显示,应用TRPV1激动剂辣椒素(CAP)会抑制诱发的抑制性突触后电流,并伴有配对脉冲比率(PPR)的变化。此外,微小抑制性突触后电流(mIPSCs)记录显示,应用CAP后,野生型(WT)小鼠的事件间期缩短,但幅度未变。这表明TRPV1通道在内嗅皮层中具有功能,且位于抑制性神经元上,其轴突分支位于II/III层内。为了在更完整的回路中研究TRPV1通道及其在长时程增强(LTP)诱导中的作用,对内嗅皮层II/III层进行了细胞外场电位记录。研究发现,激活的TRPV1通道会阻止长时程增强的诱导。与之形成鲜明对比的是,在拮抗TRPV1通道或从TRPV1基因敲除小鼠进行记录时,观察到了明显的LTP。因此,这些结果表明,通过激活抑制性突触前TRPV1通道进行信号传导代表了一种新机制,通过这种机制,II/III层皮质主要神经元前馈抑制的转变促使突触强度发生变化,从而有助于大脑中信息存储的改变。