Albowitz B, Kuhnt U
Max Planck Institute for Biophysical Chemistry, Department of Neurobiology, Göttingen, Germany.
Exp Brain Res. 1993;93(2):213-25. doi: 10.1007/BF00228388.
Coronal slices from guinea pig visual neocortex were stained with voltage-sensitive fluorescent dyes RH414 or RH795. Activity was evoked by electrical stimulation of either white matter or layer I. Emitted-light intensity changes representing summated changes of membrane potential were recorded by a 10 x 10 photodiode array with a temporal resolution of 0.4 ms and a spatial resolution of 60 microns or 94 microns. Following either stimulation of layer I or of white matter, maximal activity was located close to the respective stimulation electrode, in upper layer III/II, and between layer IV and V. With stimulation of the white matter, additional peak activity was recorded from upper layer VI. Non-synaptic activity was separated from mixed (synaptic and non-synaptic) activity by comparing responses obtained in standard perfusion medium with those obtained in perfusion medium from which the calcium was omitted, such that synaptic transmission was blocked. With stimulation of the white matter, most of the evoked activity in lower cortical layers was of non-synaptic origin. This non-synaptic activity consisted of early and fast potentials, which were predominant in layer VI and probably represented presynaptic fibre activity, and of slower components that were presumably of antidromic origin. Significant postsynaptic activity was only found in upper layer III/II. In contrast, with stimulation of layer I, most of the evoked activity was of postsynaptic origin. Early and fast non-synaptic potentials consisting of presynaptic fibre activity were confined to layer I. Slower non-synaptic activity, that might reflect direct dendritic activation, was minimal and was confined to upper cortical layers. Thus, following either stimulation of layer I or of white matter, the major postsynaptic components were found in upper layer III/II. It is suggested that the postsynaptic response following stimulation of white matter resulted from di- or polysynaptic activation by afferent fibres. The postsynaptic response to stimulation of layer I was presumably a monosynaptic activation of apical dendrites from pyramidal cells by layer I horizontal fibres. Activity following stimulation of white matter spread faster than activity following stimulation of layer I. This might reflect the difference in active conduction along afferent and efferent fibres on the one hand and in passive conductance along the dendritic tree on the other hand.
用电压敏感染料RH414或RH795对豚鼠视觉新皮层的冠状切片进行染色。通过电刺激白质或I层来诱发活动。由10×10光电二极管阵列记录代表膜电位总和变化的发射光强度变化,其时间分辨率为0.4毫秒,空间分辨率为60微米或94微米。在刺激I层或白质后,最大活动位于靠近各自刺激电极的位置,在III/II上层以及IV层和V层之间。刺激白质时,在VI上层记录到额外的峰值活动。通过比较在标准灌注介质中获得的反应与在省略钙的灌注介质中获得的反应,将非突触活动与混合(突触和非突触)活动分开,从而阻断突触传递。刺激白质时,皮质下层的大多数诱发活动是非突触起源的。这种非突触活动由早期和快速电位组成,在VI层中占主导,可能代表突触前纤维活动,还有较慢的成分,推测是逆行起源的。显著的突触后活动仅在上层III/II中发现。相比之下,刺激I层时,大多数诱发活动是突触后起源的。由突触前纤维活动组成的早期和快速非突触电位局限于I层。较慢的非突触活动可能反映直接的树突激活,最小且局限于皮质上层。因此,在刺激I层或白质后,主要的突触后成分都在上层III/II中发现。有人认为,刺激白质后的突触后反应是由传入纤维的双突触或多突触激活引起的。对I层刺激的突触后反应可能是I层水平纤维对锥体细胞顶树突的单突触激活。刺激白质后的活动比刺激I层后的活动传播得更快。这可能一方面反映了沿传入和传出纤维的主动传导与另一方面沿树突树的被动传导之间的差异。