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首页> 外文期刊>Frontiers in Cellular Neuroscience >Synaptic Conductances during Interictal Discharges in Pyramidal Neurons of Rat Entorhinal Cortex
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Synaptic Conductances during Interictal Discharges in Pyramidal Neurons of Rat Entorhinal Cortex

机译:大鼠内嗅皮层锥体神经元间放电过程中的突触传导。

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摘要

In epilepsy, the balance of excitation and inhibition underlying the basis of neural network activity shifts, resulting in neuronal network hyperexcitability and recurrent seizure-associated discharges. Mechanisms involved in ictal and interictal events are not fully understood, in particular, because of controversial data regarding the dynamics of excitatory and inhibitory synaptic conductances. In the present study, we estimated AMPAR-, NMDAR-, and GABAA R-mediated conductances during two distinct types of interictal discharge (IID) in pyramidal neurons of rat entorhinal cortex in cortico-hippocampal slices. Repetitively emerging seizure-like events and IIDs were recorded in high extracellular potassium, 4-aminopyridine, and reduced magnesium-containing solution. An original procedure for estimating synaptic conductance during IIDs was based on the differences among the current-voltage characteristics of the synaptic components. The synaptic conductance dynamics obtained revealed that the first type of IID is determined by activity of GABAA R channels with depolarized reversal potential. The second type of IID is determined by the interplay between excitation and inhibition, with early AMPAR and prolonged depolarized GABAA R and NMDAR-mediated components. The study then validated the contribution of these components to IIDs by intracellular pharmacological isolation. These data provide new insights into the mechanisms of seizures generation, development, and cessation.
机译:在癫痫病中,神经网络活动基础的兴奋和抑制平衡发生变化,导致神经网络过度兴奋和与癫痫发作相关的反复发作。尤其是由于有关兴奋性和抑制性突触电导动力学的有争议的数据,尚不完全了解涉及发作和发作间事件的机制。在本研究中,我们估计了皮质海马片大鼠内嗅皮质锥体神经元的两种不同类型的间隙放电(IID)期间AMPAR-,NMDAR-和GABAA R介导的电导。在高细胞外钾,4-氨基吡啶和还原的含镁溶液中记录到反复出现的癫痫样事件和IID。估计IID期间突触电导的原始程序是基于突触组件电流-电压特性之间的差异。获得的突触电导动力学表明,IID的第一种类型是由具有去极化反转电位的GABAA R通道的活性决定的。 IID的第二种类型取决于激发和抑制之间的相互作用,以及早期AMPAR和延长的去极化GABAAR R和NMDAR介导的成分。然后,该研究通过细胞内药理学分离验证了这些成分对IID的贡献。这些数据为癫痫发作的发生,发展和停止的机制提供了新的见解。

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