Kraut M A, Arezzo J C, Vaughan H G
Department of Radiology, Beth Israel Hospital, Boston, MA 02215.
Electroencephalogr Clin Neurophysiol. 1990 Nov;76(5):440-52. doi: 10.1016/0013-4694(90)90097-4.
Flash visual evoked potentials (VEP) and concurrent multiple unit activity (MUA) were recorded from closely spaced intracortical sites in unanesthetized monkeys before and after intracortical injection of the GABAA antagonist bicuculline. Laminar VEP profiles were subjected to current source density (CSD) analysis to localize the transmembrane current flows contributing to the generation of the field potentials. Before bicuculline, the first large VEP component, N40, was generated principally within the parvocellular thalamorecipient sublamina 4Cb. After bicuculline injection, the current sinks associated with N40 spread throughout lamina 4, consistent with a release of intracortical inhibition mediated by GABA. A subsequent component, P65, believed to represent recurrent inhibitory activity within 4Cb, was greatly diminished in size after bicuculline injection. The laminar pattern of current sources and sinks coincident with this component was more complicated after bicuculline, reflecting the summation of current flows associated with disinhibited lamina 4 activity. Bicuculline also altered the responses of neuronal elements in laminae 3 and 5, evidenced by large increases in MUA in these laminae that began approximately 50 msec after stimulation. Finally, bicuculline diminished the degree of intracortical ocular dominance, implicating GABAergic mechanisms in the maintenance and refinement of ocular input segregation within cortical columns.
在未麻醉的猴子皮层内注射GABAA拮抗剂荷包牡丹碱前后,从紧密间隔的皮层内位点记录闪光视觉诱发电位(VEP)和同步多单位活动(MUA)。对层状VEP剖面图进行电流源密度(CSD)分析,以定位导致场电位产生的跨膜电流流动。在注射荷包牡丹碱之前,第一个大的VEP成分N40主要在小细胞丘脑接受层4Cb内产生。注射荷包牡丹碱后,与N40相关的电流汇扩散到整个第4层,这与GABA介导的皮层内抑制的释放一致。随后的成分P65被认为代表4Cb内的反复抑制活动,在注射荷包牡丹碱后其大小大大减小。注射荷包牡丹碱后,与该成分一致的电流源和电流汇的层状模式更为复杂,反映了与第4层去抑制活动相关的电流流动的总和。荷包牡丹碱还改变了第3层和第5层神经元成分的反应,这些层中MUA的大幅增加证明了这一点,这种增加在刺激后约50毫秒开始。最后,荷包牡丹碱降低了皮层内眼优势的程度,这表明GABA能机制参与了皮层柱内眼输入分离的维持和细化。