Open AccessCarbamazepine modulates the spatiotemporal activity in the dentate gyrus of rats and pharmacoresistant humans in vitro
Author(s) -
Cappaert Natalie L. M.,
Werkman Taco R.,
Benito Nuria,
Witter Menno P.,
Baayen Johannes C.,
Wadman Wytse J.
Publication year - 2016
Publication title -
brain and behavior
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.915
H-Index - 41
ISSN - 2162-3279
DOI - 10.1002/brb3.463
Subject(s) - dentate gyrus , hippocampal formation , carbamazepine , hippocampus , epilepsy , neuroscience , granular layer , human brain , anticonvulsant , medicine , pharmacology , chemistry , biology , cerebellum
Abstract Introduction Human hippocampal tissue resected from pharmacoresistant epilepsy patients was investigated to study the effect of the antiepileptic drug CBZ (carbamazepine) and was compared to similar experiments in the hippocampus of control rats. Methods The molecular layer of the DG (dentate gyrus) of human epileptic tissue and rat nonepileptic tissue was electrically stimulated and the evoked responses were recorded with voltage‐sensitive dye imaging to characterize the spatiotemporal properties. Results Bath applied CBZ (100 μ mol/L) reduced the amplitude of the evoked responses in the human DG, albeit that no clear use‐dependent effects were found at frequencies of 8 or 16 Hz. In nonepileptic control DG from rats, CBZ also reduced the amplitude of the evoked response in the molecular layer of the DG as well as the spatial extent of the response. Conclusions This study demonstrates that CBZ still reduced the activity in the DG, although the patients were clinically diagnosed as pharmacoresistant for CBZ. This suggests that in the human epileptic brain, the targets of CBZ, the voltage‐gated Na + channels, are still sensitive to CBZ, although we used a relative high concentration and it is not possibility to assess the actual CBZ concentration that reached the target in the patient. We also concluded that the effect of CBZ was found in the activated region of the DG, quite comparable to the observations in the nonepileptic rat.