Lu Yun-Fei, Wang Yan, He Ying, Zhang Fu-Kang, He Ting, Wang Rui-Rui, Chen Xue-Feng, Yang Fei, Gong Ke-Rui, Chen Jun
Institute for Biomedical Sciences of Pain and Institute for Functional Brain Disorders, Tangdu Hospital, The Fourth Military Medical University, Xi'an, 710038, China.
Neurosci Bull. 2014 Feb;30(1):1-20. doi: 10.1007/s12264-013-1344-9. Epub 2013 May 18.
To explore whether experiencing inflammatory pain has an impact upon intracortical synaptic organization, the planar multi-electrode array (MEA) technique and 2-dimensional current source density (2D-CSD) imaging were used in slice preparations of the anterior cingulate cortex (ACC) from rats. Synaptic activity across different layers of the ACC was evoked by deep layer stimulation through one electrode. The layer-localization of both local field potentials (LFPs) and the spread of current sink calculated by 2D-CSD analysis was characterized pharmacologically. Moreover, the induction of long-term potentiation (LTP) and changes in LTP magnitude were also evaluated. We found that under naïve conditions, the current sink was initially generated in layer VI, then spread to layer V and finally confined to layers II-III. This spatial pattern of current sink movement typically reflected changes in depolarized sites from deep layers (V-VI) to superficial layers (II-III) where intra- and extracortical inputs terminate. In the ACC slices from rats in an inflamed state (for 2 h) caused by intraplantar bee-venom injection, the spatial profile of intra-ACC synaptic organization was significantly changed, showing an enlarged current sink distribution and a leftward shift of the stimulus-response curves relative to the naïve and saline controls. The change was more distinct in the superficial layers (II-III) than in the deep site. In terms of temporal properties, the rate of LTP induction was significantly increased in layers II-III by inflammatory pain. However, the magnitude of LTP was not significantly enhanced by this treatment. Taken together, these results show that inflammatory pain results in distinct spatial and temporal plasticity of synaptic organization in the ACC, which may lead to altered synaptic transmission and modulation.
为了探究经历炎性疼痛是否会对皮质内突触组织产生影响,研究人员在大鼠前扣带皮层(ACC)的脑片标本中使用了平面多电极阵列(MEA)技术和二维电流源密度(2D-CSD)成像。通过一个电极对深层进行刺激,诱发ACC不同层的突触活动。通过药理学方法对局部场电位(LFP)的层定位以及通过2D-CSD分析计算出的电流汇扩散情况进行了表征。此外,还评估了长时程增强(LTP)的诱导情况以及LTP幅度的变化。我们发现,在未处理条件下,电流汇最初在VI层产生,然后扩散到V层,最终局限于II-III层。这种电流汇移动的空间模式通常反映了去极化位点从深层(V-VI层)到皮质内和皮质外输入终止的浅层(II-III层)的变化。在足底注射蜂毒导致处于炎症状态(2小时)的大鼠的ACC脑片中,ACC内突触组织的空间分布显著改变,表现为电流汇分布扩大,刺激-反应曲线相对于未处理和生理盐水对照组向左偏移。这种变化在浅层(II-III层)比深层部位更为明显。在时间特性方面,炎性疼痛使II-III层的LTP诱导速率显著增加。然而,这种处理并未显著增强LTP的幅度。综上所述,这些结果表明,炎性疼痛导致ACC中突触组织出现明显的空间和时间可塑性,这可能会导致突触传递和调制的改变。