Racine R J, Moore K A, Wicks S
Department of Psychology, McMaster University, Hamilton, Ont., Canada.
Brain Res. 1991 Aug 16;556(2):226-39. doi: 10.1016/0006-8993(91)90310-r.
Stimulation trains, but not stimulation pulses, are capable of inducing long-term potentiation (LTP). In this paper we report experiments designed to examine, in chronic preparations, the characteristics of a component unique to the train-evoked response. Stimulation trains applied to the perforant path evoked population EPSP's and population spikes in the dentate gyrus that were nearly identical to those evoked by single pulses of comparable intensity. The trains also triggered a prolonged potential, negative at the dendritic pole of our electrodes, which far outlasted the pulse-evoked response. We substracted pulse-evoked responses from these train-evoked responses which left us with a waveform that peaked at about 15 ms and lasted for about 50-70 ms. The GABA agonists, diazepam and sodium pentobarbital, had no significant effect on this component, but the NMDA antagonists, ketamine and MK-801, both depressed it by over 30%. The late component had a very low threshold, which might account for the frequent observation of LTP induction at very low thresholds. Also, the late component is reliably seen in all animals showing LTP, even in the occasional animals that show no population spikes. The late component did not appear to be affected by the induction of LTP, and was either not affected or was depressed following the completion of kindling. When the 'NMDA-component' of the train-evoked response was monitored, along with LTP, in an ascending intensity train series, it was found that both the NMDA-component and the LTP increased smoothly. There was no sudden appearance of the NMDA-component at the LTP threshold. The presence of an NMDA component in the field potential of the chronic preparation allows the monitoring of the levels of NMDA activation over prolonged periods.
刺激串而非刺激脉冲能够诱导长时程增强(LTP)。在本文中,我们报告了旨在研究慢性制备物中刺激串诱发反应所特有的一个成分特征的实验。施加于穿通路径的刺激串在齿状回诱发的群体兴奋性突触后电位(EPSP)和群体锋电位与强度相当的单个脉冲诱发的几乎相同。刺激串还引发了一个持续时间较长的电位,在我们电极的树突极呈负性,其持续时间远远超过脉冲诱发反应。我们从这些刺激串诱发反应中减去脉冲诱发反应,得到一个在约15毫秒达到峰值且持续约50 - 70毫秒的波形。GABA激动剂地西泮和戊巴比妥钠对该成分无显著影响,但NMDA拮抗剂氯胺酮和MK - 801均使其降低超过30%。晚期成分阈值非常低,这可能解释了在非常低的阈值下频繁观察到LTP诱导的现象。此外,在所有表现出LTP的动物中都能可靠地观察到晚期成分,即使在偶尔未出现群体锋电位的动物中也是如此。晚期成分似乎不受LTP诱导的影响,在点燃完成后要么不受影响要么降低。当在强度递增的刺激串系列中监测刺激串诱发反应的“NMDA成分”以及LTP时,发现NMDA成分和LTP均平稳增加。在LTP阈值处未突然出现NMDA成分。慢性制备物场电位中NMDA成分的存在使得能够长时间监测NMDA激活水平。