Please use this identifier to cite or link to this item: https://doi.org/10.1111/j.1750-3639.2009.00243.x
Title: Morpho-physiologic characteristics of dorsal subicular network in mice after pilocarpine-induced status epilepticus
Authors: He, D.F.
Ma, D.L.
Tang, Y.C.
Engel Jr, J.
Bragin, A.
Tang, F.R. 
Keywords: Dorsal subiculum
Electrophysiology
In vivo
Mouse
Pilocarpine
Temporal lobe epilepsy
Issue Date: Jan-2010
Citation: He, D.F., Ma, D.L., Tang, Y.C., Engel Jr, J., Bragin, A., Tang, F.R. (2010-01). Morpho-physiologic characteristics of dorsal subicular network in mice after pilocarpine-induced status epilepticus. Brain Pathology 20 (1) : 80-95. ScholarBank@NUS Repository. https://doi.org/10.1111/j.1750-3639.2009.00243.x
Abstract: The goal of this study was to examine the morpho-physiologic changes in the dorsal subiculum network in the mouse model of temporal lobe epilepsy using extracellular recording, juxtacellular and immunofluorescence double labeling, and anterograde tracing methods. A significant loss of total dorsal subicular neurons, particularly calbindin, parvalbumin (PV) and immunopositive interneurons, was found at 2 months after pilocarpine-induced status epilepticus (SE). However, the sprouting of axons from lateral entorhinal cortex (LEnt) was observed to contact with surviving subicular neurons. These neurons had two predominant discharge patterns: bursting and fast irregular discharges. The bursting neurons were mainly pyramidal cells, and their dendritic spine density and bursting discharge rates were increased significantly in SE mice compared with the control group. Fast irregular discharge neurons were PV-immunopositive interneurons and had less dendritic spines in SE mice when compared with the control mice. When LEnt was stimulated, bursting and fast irregular discharge neurons had much shorter latency and stronger excitatory response in SE mice compared with the control group. Our results illustrate that morpho-physiologic changes in the dorsal subiculum could be part of a multilevel pathologic network that occurs simultaneously in many brain areas to contribute to the generation of epileptiform activity. © 2009 International Society of Neuropathology.
Source Title: Brain Pathology
URI: http://scholarbank.nus.edu.sg/handle/10635/111437
ISSN: 10156305
DOI: 10.1111/j.1750-3639.2009.00243.x
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