Behr J, Gloveli T, Heinemann U
Department of Neurophysiology, Institute of Physiology, University Hospital Charité, Humboldt University Berlin, Germany.
Eur J Neurosci. 1998 Mar;10(3):1011-8. doi: 10.1046/j.1460-9568.1998.00111.x.
Intracellular recordings were performed to examine the perforant path projection from layer III of the entorhinal cortex to the subiculum in rat combined hippocampal-entorhinal cortex slices. Electrical stimulation in the medial entorhinal cortex layer III caused short latency combined excitatory and inhibitory synaptic responses in subicular cells. In the presence of the GABA(A) antagonist bicuculline and the GABA(B) antagonist CGP-55845 A inhibition was blocked and isolated AMPA- or NMDA receptor-mediated EPSPs could be elicited. After application of the non-NMDA antagonist NBQX and the NMDA antagonist APV excitatory responses were completely blocked indicating a glutamatergic input from the neurons of the medial entorhinal cortex layer III. By stimulation from a close (< 0.2 mm) position in the presence of NBQX and APV and either CGP-55845 A or bicuculline we could record monosynaptic fast GABA(A) or slow GABA(B) receptor-mediated IPSPs, respectively. We compared synaptic responses in subicular cells induced by stimulation in the medial entorhinal cortex layer III with responses elicited by stimulation of afferent fibres in the alveus. The EPSPs of subicular cells induced by stimulation of alvear fibres could be significantly augmented by simultaneous activation of perforant path fibres originating in the medial entorhinal cortex layer III, while delayed activation of alvear fibres after stimulation of the perforant path resulted in a weak inhibition of the alveus evoked EPSPs. Thus, the perforant path projection activates monosynaptic excitation of subicular neurons. Therefore the entorhinal cortex does not only function as an important input structure of the hippocampal formation but is also able to modulate the hippocampal output via the entorhinal-subicular circuit.
采用细胞内记录法,在大鼠海马-内嗅皮层联合切片中,研究内嗅皮层第III层至海马下托的穿通通路投射。在内嗅皮层第III层进行电刺激,可在海马下托细胞中引发潜伏期短的兴奋性和抑制性突触反应。在存在GABA(A)拮抗剂荷包牡丹碱和GABA(B)拮抗剂CGP-55845 A的情况下,抑制作用被阻断,可诱发分离的AMPA或NMDA受体介导的兴奋性突触后电位(EPSP)。应用非NMDA拮抗剂NBQX和NMDA拮抗剂APV后,兴奋性反应完全被阻断,表明来自内嗅皮层第III层神经元的谷氨酸能输入。在存在NBQX和APV以及CGP-55845 A或荷包牡丹碱的情况下,从近距离(<0.2 mm)位置进行刺激,我们分别记录到单突触快速GABA(A)或慢速GABA(B)受体介导的抑制性突触后电位(IPSP)。我们比较了内嗅皮层第III层刺激诱发的海马下托细胞突触反应与齿状回纤维刺激诱发的反应。同时激活起源于内嗅皮层第III层的穿通通路纤维,可显著增强齿状回纤维刺激诱发的海马下托细胞EPSP,而穿通通路刺激后延迟激活齿状回纤维,则会对齿状回诱发的EPSP产生微弱抑制。因此,穿通通路投射激活海马下托神经元的单突触兴奋。所以,内嗅皮层不仅作为海马结构的重要输入结构发挥作用,还能够通过内嗅-海马下托回路调节海马输出。