Selective β-antagonists are equally and highly potent at 5-HT sites in the rat hippocampus
- 1 January 1987
- journal article
- research article
- Published by Elsevier BV in Neuropharmacology
- Vol. 26 (1), 93-96
- https://doi.org/10.1016/0028-3908(87)90050-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Blockade of the central 5-HT autoreceptor by β-adrenoceptor antagonistsEuropean Journal of Pharmacology, 1986
- Molecular pharmacology of 5-HT1 and 5-HT2 recognition sites in rat and pig brain membranes: Radioligand binding studies with [3H]5-HT, [3H]8-OH-DPAT, (−)[125I]iodocyanopindolol, [3H]mesulergine and [3H]KetanserinEuropean Journal of Pharmacology, 1985
- Characterization of the 5-HTIB recognition site in rat brain: Binding studies with (−)[125I]IodocyanopindololEuropean Journal of Pharmacology, 1985
- β-Adrenoceptor blocking agents recognize a subpopulation of serotonin receptors in brainBrain Research, 1985
- Cyanopindolol is a highly potent and selective antagonist at the presynaptic serotonin autoreceptor in the rat brain cortexNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1985
- Stereoselective blockade at [3H]5-HT binding sites and at the 5-HT autoreceptor by propranololEuropean Journal of Pharmacology, 1984
- Binding of 125I-iodohydroxybenzylpindolol to cerebral membranes: Association with 5-hydroxytryptamine recognition sites as well as beta-adrenoceptorsBiochemical Pharmacology, 1983
- (±)[125Iodo]cyanopindolol, a new ligand for β-adrenoceptors: Identification and quantitation of subclasses of β-adrenoceptors in guinea pigNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1981