Actions of thienyl analogs of baclofen at GABAB receptors in rat neocortical slices
| dc.contributor.author | Ong, J. | |
| dc.contributor.author | Kerr, D. | |
| dc.contributor.author | Vaccher, C. | |
| dc.contributor.author | Berthelot, P. | |
| dc.date.issued | 1997 | |
| dc.description | Short communication | |
| dc.description.abstract | In rat neocortical slices maintained in Mg2+-free Krebs medium, baclofen and its thienyl analogs, 4-amino-3-(5-chlorothien-2-yl)-butanoic acid (5h), 4-amino-3-(5-methylthien-2-yl)-butanoic acid (5d), 4-amino-3-(5-bromothien-2-yl)-butanoic acid (5f) and 4-amino-3-(thien-3-yl)-butanoic acid (5j) dose-dependently suppressed the spontaneous discharges, antagonised by the GABA(B) receptor antagonist 2-hydroxysaclofen (200 microM). Their relative potencies were baclofen > 5h > 5d > 5f > 5j. These heterocyclic analogs may prove useful as GABA(B) receptor agonists in functional studies. | |
| dc.description.statementofresponsibility | Jennifer Ong, David I.B. Kerr, Claude Vaccher, Pascal Berthelot | |
| dc.identifier.citation | European Journal of Pharmacology, 1997; 329(2-3):133-136 | |
| dc.identifier.doi | 10.1016/S0014-2999(97)00185-4 | |
| dc.identifier.issn | 0014-2999 | |
| dc.identifier.issn | 1879-0712 | |
| dc.identifier.orcid | Ong, J. [0000-0002-0958-460X] | |
| dc.identifier.uri | http://hdl.handle.net/2440/5993 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier BV | |
| dc.rights | © 1997 Elsevier Science B.V. | |
| dc.source.uri | https://doi.org/10.1016/s0014-2999(97)00185-4 | |
| dc.subject | Baclofen: GABAB receptor agonist | |
| dc.subject | Thienyl baclofen analog | |
| dc.subject | 2-Hydroxysaclofen | |
| dc.subject | Neocortical slice, rat | |
| dc.title | Actions of thienyl analogs of baclofen at GABAB receptors in rat neocortical slices | |
| dc.title.alternative | Actions of thienyl analogs of baclofen at GABA(B) receptors in rat neocortical slices | |
| dc.type | Journal article | |
| pubs.publication-status | Published |