Tierney Patrick L, Dégenètais Eric, Thierry Anne-Marie, Glowinski Jacques, Gioanni Yves
Chaire de Neuropharmacologie, INSERM U114, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, France.
Eur J Neurosci. 2004 Jul;20(2):514-24. doi: 10.1111/j.1460-9568.2004.03501.x.
The hippocampus and prefrontal cortex (PFC), two structures implicated in learning and memory processes, are linked by a direct hippocampo-prefrontal pathway. It has been shown that PFC pyramidal cells receive monosynaptic excitatory inputs from the hippocampus and, in this study, we sought to determine the influence of the hippocampus on PFC interneurons in anesthetized rats. Extracellular recordings were coupled to juxtacellular injections of neurobiotin or biotinylated dextran amine to morphologically differentiate interneurons from pyramidal cells. In all cases, the action potentials of labeled interneurons were of shorter duration (< 0.70 ms) than those of identified pyramidal cells (> 0.70 ms). Single pulse stimulation of the hippocampal CA1/subiculum region induced an excitatory response in 70% of recorded interneurons in the prelimbic and medial-orbital areas of the PFC. In contrast to the one to two action potentials generated by pyramidal cells, an important group of interneurons fired a burst of action potentials in response to hippocampal stimulation. A large proportion of these excitatory responses was probably monosynaptic as their latency is consistent with the conduction time of the hippocampo-prefrontal pathway. In addition, when both a pyramidal cell and an interneuron were simultaneously recorded and both responded to stimulation, the interneuron consistently fired before the pyramidal cell. In conclusion, the hippocampus exerts a direct excitatory influence on PFC interneurons and is thus capable of feedforward inhibition of pyramidal cells. Hippocampal output is spatially and temporally focalized via this inhibitory process and consequently could facilitate the synchronization of a specific subset of PFC neurons with hippocampal activity.
海马体和前额叶皮质(PFC)这两个与学习和记忆过程相关的结构,通过一条直接的海马体 - 前额叶通路相连。已有研究表明,PFC锥体细胞接受来自海马体的单突触兴奋性输入,在本研究中,我们试图确定海马体对麻醉大鼠PFC中间神经元的影响。细胞外记录与神经生物素或生物素化葡聚糖胺的近细胞注射相结合,以便从形态上区分中间神经元和锥体细胞。在所有情况下,标记的中间神经元的动作电位持续时间(<0.70毫秒)比已识别的锥体细胞(>0.70毫秒)短。对海马体CA1/下托区域的单脉冲刺激在PFC的前边缘区和内侧眶区70%的记录中间神经元中诱发了兴奋性反应。与锥体细胞产生的一到两个动作电位不同,一组重要的中间神经元在受到海马体刺激时会引发一阵动作电位。这些兴奋性反应中的很大一部分可能是单突触的,因为它们的潜伏期与海马体 - 前额叶通路的传导时间一致。此外,当同时记录一个锥体细胞和一个中间神经元,且两者都对刺激有反应时,中间神经元总是比锥体细胞先放电。总之,海马体对PFC中间神经元施加直接的兴奋性影响,因此能够对锥体细胞进行前馈抑制。通过这种抑制过程,海马体输出在空间和时间上聚焦,从而可能促进PFC神经元的特定子集与海马体活动的同步。