Kohn Adam, Metz Carol, Tommerdahl Mark A, Whitsel Barry L
Curriculum in Neurobiology, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
J Neurophysiol. 2002 Dec;88(6):3331-47. doi: 10.1152/jn.01012.2001.
Sensory cortical neurons display substantial receptive field dynamics during and after persistent sensory drive. Because a cell's response properties are determined by the inputs it receives, receptive field dynamics are likely to involve changes in the relative efficacy of different inputs to the cell. To test this hypothesis, we have investigated if brief repetitive stimulus drive in vitro alters the efficacy of two types of corticocortical inputs to layer V pyramidal cells. Specifically, we have used whole cell recordings to measure the effect of repetitive electrical stimulation at the layer VI/white matter (WM) border on the synaptic response of layer V pyramidal cells to corticocortical input evoked by electrical stimulation of layer I or layer II/III and emulated by local application of glutamate. Repetitive stimulation (10 Hz for 3 s) at the layer VI/WM border transiently potentiated excitatory postsynaptic potentials (EPSPs) evoked by electrical stimulation of layer II/III by 97 +/- 12% (mean +/- SE). The recovery of EPSP amplitude to its preconditioning value was well-described by a single-term decaying exponential with a time constant of 7.2 s. The same layer VI/WM conditioning train that evoked layer II/III EPSP potentiation frequently caused an attenuation of layer I EPSPs. Similarly, subthreshold postsynaptic responses to local glutamate application in layers II/III and I were potentiated and attenuated, respectively, by the conditioning stimulus. Potentiation and attenuation could be evoked in the same cell by repositioning the glutamate puffer pipette in the appropriate layer. The conditioning stimulus that led to the transient modification of upper layer EPSP efficacy also evoked a slow depolarization in glial cells. The membrane potential of glial cells recovered with a time course similar to the dissipation of the potentiation effect, suggesting that stimulus-evoked changes in extracellular potassium (ECK) play a role in layer II/III EPSP potentiation. Consistent with this proposal, increasing the bath concentration of ECK caused a substantial increase of layer II/III EPSP amplitude. EPSP potentiation was sensitive to postsynaptic membrane potential and, more importantly, was significantly weaker for synaptic currents than for synaptic potentials, suggesting that it involves the recruitment of a postsynaptic voltage-dependent mechanism. Two observations suggest that layer II/III EPSP potentiation may involve the recruitment of postsynaptic sodium channels: EPSP potentiation was strongly reduced by intracellular application of N-(2,6-dimethyl-phenylcarbamoylmethyl) triethylammonium bromide (QX-314) and responses to local glutamate application were potentiated by high ECK in the presence of cadmium but not in the presence of tetrodotoxin. The results demonstrate a novel way in which brief periods of repetitive stimulus drive are accompanied by rapid, transient, and specific alterations in the functional connectivity and information processing characteristics of sensorimotor cortex.
在持续的感觉驱动期间及之后,感觉皮层神经元表现出显著的感受野动态变化。由于细胞的反应特性由其接收到的输入决定,感受野动态变化可能涉及不同输入到细胞的相对效能的改变。为了验证这一假设,我们研究了体外短暂的重复刺激驱动是否会改变两类皮质皮质输入到V层锥体细胞的效能。具体而言,我们使用全细胞记录来测量在VI层/白质(WM)边界处的重复电刺激对V层锥体细胞对由I层或II/III层电刺激诱发并通过局部应用谷氨酸模拟的皮质皮质输入的突触反应的影响。在VI层/WM边界处的重复刺激(10 Hz,持续3 s)使由II/III层电刺激诱发的兴奋性突触后电位(EPSP)瞬时增强了97±12%(平均值±标准误)。EPSP幅度恢复到其预处理值的过程可以用一个单指数衰减函数很好地描述,时间常数为7.2 s。诱发II/III层EPSP增强的相同VI层/WM条件刺激序列经常导致I层EPSP的衰减。同样,对II/III层和I层局部谷氨酸应用的阈下突触反应分别通过条件刺激而增强和衰减。通过将谷氨酸吹管移到适当的层,可以在同一细胞中诱发增强和衰减。导致上层EPSP效能短暂改变的条件刺激也在胶质细胞中诱发了缓慢的去极化。胶质细胞的膜电位恢复的时间进程与增强效应的消散相似,表明刺激诱发的细胞外钾(ECK)变化在II/III层EPSP增强中起作用。与此提议一致,增加浴液中ECK的浓度导致II/III层EPSP幅度大幅增加。EPSP增强对突触后膜电位敏感,更重要的是,对突触电流的增强比对突触电位的增强明显更弱,这表明它涉及突触后电压依赖性机制的募集。两项观察结果表明,II/III层EPSP增强可能涉及突触后钠通道的募集:通过细胞内应用N-(2,6-二甲基苯基氨基甲酰甲基)三乙基溴化铵(QX-314),EPSP增强被强烈降低,并且在镉存在但河豚毒素不存在的情况下,对局部谷氨酸应用的反应通过高ECK而增强。结果证明了一种新的方式,即短暂的重复刺激驱动伴随着感觉运动皮层功能连接性和信息处理特征的快速、短暂和特定改变。