Levinson Simon, Tran Conny H, Barry Joshua, Viker Brett, Levine Michael S, Vinters Harry V, Mathern Gary W, Cepeda Carlos
IDDRC, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Section of Neuropathology, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Front Cell Neurosci. 2020 Mar 20;14:54. doi: 10.3389/fncel.2020.00054. eCollection 2020.
In the present study, we characterized the effects of bath application of the proconvulsant drug 4-aminopyridine (4-AP) alone or in combination with GABA and/or GABA receptor antagonists, in cortical dysplasia (CD type I and CD type IIa/b), tuberous sclerosis complex (TSC), and non-CD cortical tissue samples from pediatric epilepsy surgery patients. Whole-cell patch clamp recordings in current and voltage clamp modes were obtained from cortical pyramidal neurons (CPNs), interneurons, and balloon/giant cells. In pyramidal neurons, bath application of 4-AP produced an increase in spontaneous synaptic activity as well as rhythmic membrane oscillations. In current clamp mode, these oscillations were generally depolarizing or biphasic and were accompanied by increased membrane conductance. In interneurons, membrane oscillations were consistently depolarizing and accompanied by bursts of action potentials. In a subset of balloon/giant cells from CD type IIb and TSC cases, respectively, 4-AP induced very low-amplitude, slow membrane oscillations that echoed the rhythmic oscillations from pyramidal neurons and interneurons. Bicuculline reduced the amplitude of membrane oscillations induced by 4-AP, indicating that they were mediated principally by GABA receptors. 4-AP alone or in combination with bicuculline increased cortical excitability but did not induce seizure-like discharges. Ictal activity was observed in pyramidal neurons and interneurons from CD and TSC cases only when phaclofen, a GABA receptor antagonist, was added to the 4-AP and bicuculline solution. These results emphasize the critical and permissive role of GABA receptors in the transition to an ictal state in pediatric CD tissue and highlight the importance of these receptors as a potential therapeutic target in pediatric epilepsy.
在本研究中,我们对惊厥药物4-氨基吡啶(4-AP)单独应用或与GABA和/或GABA受体拮抗剂联合应用于皮质发育异常(I型和IIa/b型CD)、结节性硬化症(TSC)以及小儿癫痫手术患者的非CD皮质组织样本中的作用进行了表征。通过全细胞膜片钳记录,在电流钳和电压钳模式下从皮质锥体细胞(CPN)、中间神经元以及气球样/巨细胞中获取数据。在锥体细胞中,浴加4-AP可使自发突触活动增加以及出现节律性膜振荡。在电流钳模式下,这些振荡通常是去极化的或双相的,并伴有膜电导增加。在中间神经元中,膜振荡持续去极化并伴有动作电位爆发。在分别来自IIb型CD和TSC病例的一部分气球样/巨细胞中,4-AP诱导出非常低幅度、缓慢的膜振荡,这些振荡与锥体细胞和中间神经元的节律性振荡相似。荷包牡丹碱降低了4-AP诱导的膜振荡幅度,表明它们主要由GABA受体介导。单独的4-AP或与荷包牡丹碱联合应用可增加皮质兴奋性,但未诱发癫痫样放电。仅当将GABA受体拮抗剂法氯芬添加到4-AP和荷包牡丹碱溶液中时,才在来自CD和TSC病例的锥体细胞和中间神经元中观察到发作期活动。这些结果强调了GABA受体在小儿CD组织向发作期状态转变中的关键和允许作用,并突出了这些受体作为小儿癫痫潜在治疗靶点的重要性。