Neural Circuit Physiology Lab, Systems Neuroscience Group, Department of Physiology and Biophysics, University of Buenos Aires School of Medicine, Buenos Aires, Argentina.
PLoS One. 2011;6(12):e28473. doi: 10.1371/journal.pone.0028473. Epub 2011 Dec 6.
Evoked striatal field potentials are seldom used to study corticostriatal communication in vivo because little is known about their origin and significance. Here we show that striatal field responses evoked by stimulating the prelimbic cortex in mice are reduced by more than 90% after infusing the AMPA receptor antagonist CNQX close to the recording electrode. Moreover, the amplitude of local field responses and dPSPs recorded in striatal medium spiny neurons increase in parallel with increasing stimulating current intensity. Finally, the evoked striatal fields show several of the basic known properties of corticostriatal transmission, including paired pulse facilitation and topographical organization. As a case study, we characterized the effect of local GABA(A) receptor blockade on striatal field and multiunitary action potential responses to prelimbic cortex stimulation. Striatal activity was recorded through a 24 channel silicon probe at about 600 µm from a microdialysis probe. Intrastriatal administration of the GABA(A) receptor antagonist bicuculline increased by 65±7% the duration of the evoked field responses. Moreover, the associated action potential responses were markedly enhanced during bicuculline infusion. Bicuculline enhancement took place at all the striatal sites that showed a response to cortical stimulation before drug infusion, but sites showing no field response before bicuculline remained unresponsive during GABA(A) receptor blockade. Thus, the data demonstrate that fast inhibitory connections exert a marked temporal regulation of input-output transformations within spatially delimited striatal networks responding to a cortical input. Overall, we propose that evoked striatal fields may be a useful tool to study corticostriatal synaptic connectivity in relation to behavior.
激发纹状场电位很少用于研究体内皮质纹状体通讯,因为人们对其起源和意义知之甚少。在这里,我们展示了在小鼠中刺激前额皮质时诱发的纹状场反应,在将 AMPA 受体拮抗剂 CNQX 注入靠近记录电极的部位后,其幅度减少了 90%以上。此外,记录的纹状体内中型多棘神经元的局部场反应和 dPSP 的幅度与刺激电流强度的增加呈平行关系。最后,诱发的纹状场显示出皮质纹状体传递的几个基本已知特性,包括成对脉冲易化和拓扑组织。作为一个案例研究,我们描述了局部 GABA(A)受体阻断对前额皮质刺激诱发的纹状场和多单位动作电位反应的影响。纹状活性通过 24 通道硅探针在距离微透析探针约 600 µm 的位置进行记录。纹状体内给予 GABA(A)受体拮抗剂荷包牡丹碱可使诱发的场反应持续时间延长 65±7%。此外,荷包牡丹碱输注期间,相关的动作电位反应明显增强。荷包牡丹碱增强发生在所有在药物输注前对皮质刺激有反应的纹状区,但在输注荷包牡丹碱之前没有场反应的部位在 GABA(A)受体阻断期间仍无反应。因此,这些数据表明,快速抑制性连接对皮质输入反应的空间限定纹状网络中的输入-输出转换施加了明显的时间调节。总的来说,我们提出诱发的纹状场可能是研究与行为相关的皮质纹状体突触连接的有用工具。