Department of Neurology, University of Virginia, Health Sciences Center, Charlottesville, VA 22908-0394, USA.
Neurobiol Dis. 2010 Nov;40(2):490-501. doi: 10.1016/j.nbd.2010.07.016. Epub 2010 Aug 1.
Neurosteroid sensitivity of GABA(A) receptor mediated inhibition of the hippocampal dentate granule cells (DGCs) is reduced in animal models of temporal lobe epilepsy. However, the properties and subunit composition of GABA(A) receptors mediating tonic inhibition in DGCs of epileptic animals have not been described. In the DGCs of epileptic animals, allopregnanolone and L-655708 sensitivity of holding current was diminished and δ subunit was retained in the endoplasmic reticulum and its surface expression was decreased the in the hippocampus. Ro15-4513 and lanthanum had distinct effects on holding current recorded from DGCs of control and epileptic animals suggesting that the pharmacological properties of GABA(A) receptors maintaining tonic inhibition in DGCs of epileptic animals were similar to those containing the α4βxγ2 subunits. Furthermore, surface expression of the α4 subunit increased and a larger fraction of the subunit co-immunoprecipitated with theγ2 subunit in hippocampi of epileptic animals. Together, these studies revealed that functional α4βxδ and α5βxγ2 receptors were reduced in the hippocampi of epileptic animals and that novel α4bxγ2 receptors contributed to the maintenance of tonic inhibition. The presence of α4βxγ2 receptors resulted in low GABA affinity and neurosteroid sensitivity of tonic currents in the DGCs of epileptic animals that could potentially increase seizure vulnerability. These receptors may represent a novel therapeutic target for anticonvulsant drugs without sedative actions.
神经甾体对颞叶癫痫动物模型中海马齿状回颗粒细胞(DGC)中 GABA(A) 受体介导的抑制作用的敏感性降低。然而,癫痫动物 DGC 中介导紧张性抑制的 GABA(A) 受体的特性和亚基组成尚未描述。在癫痫动物的 DGC 中,别孕烯醇酮和 L-655708 对保持电流的敏感性降低,δ亚基保留在内质网中,其表面表达在海马体中减少。Ro15-4513 和镧对来自对照和癫痫动物的 DGC 记录的保持电流有明显的影响,表明维持癫痫动物 DGC 中紧张性抑制的 GABA(A) 受体的药理学特性与那些含有 α4βxγ2 亚基的受体相似。此外,α4 亚基的表面表达增加,并且亚基与γ2 亚基的更大比例共同免疫沉淀在癫痫动物的海马体中。总之,这些研究表明,功能性 α4βxδ 和 α5βxγ2 受体在癫痫动物的海马体中减少,并且新型的 α4βxγ2 受体有助于维持紧张性抑制。α4βxγ2 受体的存在导致癫痫动物 DGC 中紧张性电流的 GABA 亲和力和神经甾体敏感性降低,这可能增加癫痫发作的易感性。这些受体可能代表具有抗惊厥作用而无镇静作用的新型治疗靶点。