首页> 美国卫生研究院文献>The Journal of Neuroscience >β/γ Oscillatory Activity in the CA3 Hippocampal Area is Depressed by Aberrant GABAergic Transmission from the Dentate Gyrus after Seizures
【2h】

β/γ Oscillatory Activity in the CA3 Hippocampal Area is Depressed by Aberrant GABAergic Transmission from the Dentate Gyrus after Seizures

机译:癫痫发作后来自齿状回的GABA异常传递抑制了CA3海马区的β/γ振荡活性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Oscillatory activity in the CA3 region is thought to be involved in the encoding and retrieval of information. These oscillations originate from the recurrent excitation between pyramidal cells that are entrained by the synchronous rhythmic inhibition of local interneurons. We show here that, after seizures, the dentate gyrus (DG) tonically inhibits β/γ (20–24 Hz) field oscillations in the CA3 area through GABA-mediated signaling. These oscillations originate in the interneuron network because they are maintained in the presence of ionotropic glutamate receptor antagonists, and they can be blocked by GABAA receptor antagonists or by perfusion of a calcium-free extracellular medium. Inhibition of this oscillatory activity requires intact DG-to-CA3 connections, and it is suppressed by the activation of metabotropic glutamate receptors (mGluR). The influence of mGluR activation was reflected in the spontaneous subthreshold membrane oscillations of CA3 interneurons after one seizure but could also be observed in pyramidal cells after several seizures. Coincident stimulation of the DG at θ and β/γ frequencies produced a frequency-dependent excitation of interneurons and the inhibition of pyramidal cells. Indeed, these effects were maximal at the frequency that matched the mGluR-sensitive spontaneous field oscillations, suggesting a resonance phenomenon. Our results shed light on the mechanisms that may underlie the deficits in memory and cognition observed after epileptic seizures.
机译:人们认为,CA3区的振荡活动与信息的编码和检索有关。这些振荡源自锥体细胞之间的反复激发,而锥体细胞之间的周期性节律抑制则通过局部中间神经元的同步节律抑制而产生。我们在这里显示,癫痫发作后,齿状回(DG)通过GABA介导的信号传导抑制CA3区的β/γ(20-24 Hz)场振荡。这些振荡源自中间神经元网络,因为它们在存在离子型谷氨酸受体拮抗剂的情况下得以维持,并且可以被GABAA受体拮抗剂或无钙细胞外介质的灌注所阻断。抑制这种振荡活性需要完整的DG至CA3连接,并且可以通过代谢型谷氨酸受体(mGluR)的激活来抑制它。 mGluR激活的影响反映在一次癫痫发作后CA3神经元的自发性亚阈膜振动中,但也可能在几次发作后在锥体细胞中观察到。在θ和β/γ频率上对DG的同时刺激会产生中间神经元的频率依赖性激发并抑制锥体细胞。实际上,这些效应在与mGluR敏感的自发场振荡相匹配的频率处最大,表明存在共振现象。我们的研究结果揭示了可能是癫痫发作后观察到的记忆和认知缺陷的潜在机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号