Zhang Zizhen, Gadotti Vinicius M, Chen Lina, Souza Ivana A, Stemkowski Patrick L, Zamponi Gerald W
Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
Cell Rep. 2015 Aug 4;12(5):752-9. doi: 10.1016/j.celrep.2015.07.001. Epub 2015 Jul 23.
Noxious stimuli are detected by peripheral nociceptors and then transmitted to higher CNS centers, where they are perceived as an unpleasant sensation. The mechanisms that govern the emotional component associated with pain are still incompletely understood. Here, we used optogenetic approaches both in vitro and in vivo to address this issue. We found that peripheral nerve injury inhibits pyramidal cell firing in the prelimbic area of the prefrontal cortex as a result of feed-forward inhibition mediated by parvalbumin-expressing GABAergic interneurons. In addition, activation of inhibitory archaerhodopsin or excitatory channelrhodopsin-2 in these neurons decreased and increased pain responses, respectively, in freely moving mice and accordingly modulated conditioned place preference scores and place escape/avoidance behavior. Our findings thus demonstrate an important role of the prelimbic area in sensory and emotional aspects of pain and identify GABAergic circuits in this region as a potential target for pain therapeutics.
伤害性刺激由外周伤害感受器检测到,然后传递到中枢神经系统的高级中枢,在那里它们被感知为一种不愉快的感觉。与疼痛相关的情感成分的调控机制仍未完全了解。在这里,我们在体外和体内使用光遗传学方法来解决这个问题。我们发现,由于表达小白蛋白的γ-氨基丁酸能中间神经元介导的前馈抑制,外周神经损伤会抑制前额叶皮质前边缘区的锥体细胞放电。此外,在这些神经元中激活抑制性古紫质或兴奋性通道视紫红质-2,分别降低和增加了自由活动小鼠的疼痛反应,并相应地调节了条件性位置偏好得分和位置逃避/回避行为。因此,我们的研究结果证明了前边缘区在疼痛的感觉和情感方面的重要作用,并确定该区域的γ-氨基丁酸能回路是疼痛治疗的潜在靶点。