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T‐type Ca 2+ channel activity increases in rat hippocampal CA1 region during kindling epileptogenesis
Author(s) -
Aksoz Erkan,
Sara Yildirim,
Onur Rustu
Publication year - 2020
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.22155
Subject(s) - kindling , epileptogenesis , long term potentiation , excitatory postsynaptic potential , neuroscience , chemistry , hippocampal formation , inhibitory postsynaptic potential , hippocampus , tetraethylammonium , kindling model , epilepsy , psychology , receptor , biochemistry , potassium , organic chemistry
Abstract Epileptogenesis is a dynamical process that involves synaptic plasticity changes such as synaptic reorganization of excitatory and inhibitory systems and axonal sprouting in the hippocampus, which is one of the most studied epileptogenic regions in the brain. However, the early events that trigger these changes are not understood well. We investigated short‐term and long‐term synaptic plasticity parameters and T‐type Ca 2+ channel activity changes in the early phase of a rat kindling model. Chronic pentylenetetrazole (PTZ) application was used in order to induce the kindling process in rats. The recordings were obtained from hippocampal slices in the CA1 region at 25th day of PTZ application. Tetraethylammonium was used in order to induce long‐term potentiation and T‐type Ca 2+ channel activity was assessed in the presence of mibefradil. We found that tetraethylammonium‐induced long‐term potentiation was not prevented by mibefradil in the kindling group in contrast to control group. We also found an increase in paired‐pulse ratios in the PTZ‐applied group. Our findings indicate an increase in the “T‐type Ca 2+ channel component of LTP” in the kindling group, which may be an early mechanism in epileptogenesis.