TY - JOUR
T1 - Zonisamide at clinically relevant concentrations inhibits field EPSP but not presynaptic fiber volley in rat frontal cortex
AU - Huang, Chin Wei
AU - Ueno, Shinya
AU - Okada, Motohiro
AU - Kaneko, Sunao
N1 - Funding Information:
The first author was sponsored by the Fujusawa Medical Research Foundation and a grant from National Cheng Kung University Hospital. Part of this study published in the abstract form in the Japanese Pharmacological Society, Yokohama, 2005.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2005/10
Y1 - 2005/10
N2 - We investigated the effect of Zonisamide (ZNS), a newer anti-epileptic drug, on field potentials and neuropropagation in rat frontal cortex, with the aid of the 64-channel multi-electrode dish (MED64) system. The amplitude and propagation of field potentials were expressed dimensionally in the MED64 system. ZNS (3-100 μM) inhibited the amplitude and propagation of field excitatory postsynaptic potentials (fEPSP) in a concentration dependent manner. In contrast, ZNS could not suppress the amplitude and propagation of the presynaptic fiber volley (PrV) at clinically relevant concentrations (10-30 μM). Stimulating dependency with reduction fEPSP was seen in the presence of ZNS at clinically relevant concentrations, but not with PrV. The reduction of fEPSP amplitude was not accompanied by a change in paired-pulse facilitation. These data suggest that at clinically relevant concentrations of ZNS, the suppression of neuronal propagation is at least partially due to the postsynaptic mechanism, probably through α-amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid (AMPA) receptors.
AB - We investigated the effect of Zonisamide (ZNS), a newer anti-epileptic drug, on field potentials and neuropropagation in rat frontal cortex, with the aid of the 64-channel multi-electrode dish (MED64) system. The amplitude and propagation of field potentials were expressed dimensionally in the MED64 system. ZNS (3-100 μM) inhibited the amplitude and propagation of field excitatory postsynaptic potentials (fEPSP) in a concentration dependent manner. In contrast, ZNS could not suppress the amplitude and propagation of the presynaptic fiber volley (PrV) at clinically relevant concentrations (10-30 μM). Stimulating dependency with reduction fEPSP was seen in the presence of ZNS at clinically relevant concentrations, but not with PrV. The reduction of fEPSP amplitude was not accompanied by a change in paired-pulse facilitation. These data suggest that at clinically relevant concentrations of ZNS, the suppression of neuronal propagation is at least partially due to the postsynaptic mechanism, probably through α-amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid (AMPA) receptors.
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U2 - 10.1016/j.eplepsyres.2005.08.006
DO - 10.1016/j.eplepsyres.2005.08.006
M3 - Article
C2 - 16188429
AN - SCOPUS:27644526414
VL - 67
SP - 51
EP - 60
JO - Journal of Epilepsy
JF - Journal of Epilepsy
SN - 0920-1211
IS - 1-2
ER -