Literature DB >> 28062187

Dentate gyrus autonomous ictal activity in the status epilepticus rat model of epilepsy.

Florian Weissinger1, Matthias Wawra2, Pawel Fidzinski1, Mark Elsner1, Hartmut Meierkord1, Martin Holtkamp1, Katharina Buchheim1.   

Abstract

The dentate gyrus (DG) as part of the hippocampal formation is believed to serve as a gatekeeper with strong inhibitory properties against uncontrolled propagation of neuronal activity from the entorhinal cortex and neocortical structures. In temporal lobe epilepsy, the DG becomes hyperexcitable and loses its gate function, enabling propagation of ictal activity into downstream structures such as CA3 and CA1 areas. Furthermore, the DG, apart from facilitating propagation, may also be able to autonomously generate ictal activity, but this point has remained open so far. To tackle this question, we used intrinsic optical imaging in combination with electrophysiological recordings in brain slice preparations from rats in which status epilepticus had been induced electrically several weeks prior to measurements. Upon omission of Mg++ from the artificial cerebrospinal fluid, in 15 out of 33 slices (45.4%) from 9 out of 13 epileptic animals (69.2%), spontaneous and autonomous ictal activity, mostly seizure-like events (SLE), was observed in the DG. This activity manifested independently from SLE generated in adjacent cortices and never occurred in slices from control animals. SLE generated in the DG differed from those with origin in the entorhinal or temporal cortex by longer latency to the first event after Mg++ omission (p<0.001), a higher SLE frequency (p<0.05), higher amplitude (p<0.001) and a longer SLE duration (p<0.05). We conclude that in epilepsy, the DG, in addition to facilitated gating of activity from upstream structures, can serve as an independent generator of ictal activity.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Hippocampus; Intrinsic optical signal; Low Mg(++) model; Slice electrophysiology; Sustained stimulation

Mesh:

Year:  2017        PMID: 28062187     DOI: 10.1016/j.brainres.2016.12.030

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  2 in total

1.  Astaxanthin Attenuates Neuroinflammation in Status Epilepticus Rats by Regulating the ATP-P2X7R Signal.

Authors:  Ming Wang; Xiaolin Deng; Yangmei Xie; Yinghui Chen
Journal:  Drug Des Devel Ther       Date:  2020-04-30       Impact factor: 4.162

2.  Direct Medial Entorhinal Cortex Input to Hippocampal CA3 Is Crucial for eEF2K Inhibitor-Induced Neuronal Oscillations in the Mouse Hippocampus.

Authors:  Ziyang Liu; Cheng Peng; Yinghan Zhuang; Ying Chen; Thomas Behnisch
Journal:  Front Cell Neurosci       Date:  2020-03-06       Impact factor: 5.505

  2 in total

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