dc.contributor.author | Caesar, M. | |
dc.contributor.author | Evans, M.L. | |
dc.contributor.author | Benham, C.D. | |
dc.date.accessioned | 2009-06-08T08:44:38Z | |
dc.date.available | 2009-06-08T08:44:38Z | |
dc.date.issued | 1999 | |
dc.identifier.citation | Caesar , M , Evans , M L & Benham , C D 1999 , ' Lack of effect of the novel anticonvulsant SB 204269 on voltage dependent currents in neurones cultured from rat hippocampus ' , Neuroscience Letters , vol. 271 , pp. 57-60 . https://doi.org/10.1016/S0304-3940(99)00514-5 | |
dc.identifier.issn | 0304-3940 | |
dc.identifier.other | dspace: 2299/3503 | |
dc.identifier.uri | http://hdl.handle.net/2299/3503 | |
dc.description | Original article can be found at: http://www.sciencedirect.com/science/journal/03043940 Copyright Elsevier Ireland Ltd. DOI: 10.1016/S0304-3940(99)00514-5 [Full text of this article is not available in the UHRA] | |
dc.description.abstract | The novel anticonvulsant SB-204269 inhibits epileptiform afterdischarges induced by high K+ in rat hippocampal slices. Its effects on voltage-gated Na+ currents, measured from cultured hippocampal neurones using whole cell patch clamp, were compared to the effects of existing anticonvulsants. SB-204269 produced no significant tonic block of Na+ currents nor any voltage-dependent and frequency-dependent block at doses 50 to 500 fold higher than its anticonvulsant EC50 of 0.2 μM. In contrast, lamotrigine, phenytoin and carbamazepine at 50 μM, blocked Na+ currents in a voltage-dependent manner. SB-204269 also had no effect on action potential discharges evoked by elevating external K+. These data suggest that direct blockade of voltage-gated channels does not contribute to the anticonvulsant properties of SB-204269 and further support the hypothesis that this compound has a novel mechanism of action. | en |
dc.language.iso | eng | |
dc.relation.ispartof | Neuroscience Letters | |
dc.title | Lack of effect of the novel anticonvulsant SB 204269 on voltage dependent currents in neurones cultured from rat hippocampus | en |
dc.contributor.institution | Department of Human and Environmental Sciences | |
dc.contributor.institution | TRP Ion channels | |
dc.contributor.institution | Department of Clinical, Pharmaceutical and Biological Science | |
dc.contributor.institution | Basic and Clinical Science Unit | |
dc.contributor.institution | Centre for Health Services and Clinical Research | |
dc.contributor.institution | School of Life and Medical Sciences | |
dc.contributor.institution | Centre for Research in Mechanisms of Disease and Drug Discovery | |
dc.description.status | Peer reviewed | |
rioxxterms.versionofrecord | 10.1016/S0304-3940(99)00514-5 | |
rioxxterms.type | Journal Article/Review | |
herts.preservation.rarelyaccessed | true | |