Detailed pharmacological characterization of 5-HT1A-receptor- mediated [35S]GTPγS binding in rat hippocampal membranes

Abstract

5-HT-stimulated [35S]GTPγS binding to rat hippocampal membranes was pharmacologically characterized. Signal/noise ratio or percent increase over basal was optimized with 100 μM GDP, 2-10 mM MgCl2, and 150-200 mM NaCl. However, we preferred the standard condition (20 mu;M GDP, 5 mM MgCl2, and 100 mM NaCl: Condition I) to the alternative one (100 μM GDP, 5mM MgCl2, and 150 mM NaCl: Condition II) because 1) absolute values of basal and 5-HT-sensitive bindings decreased with higher concentrations of GDP and NaCl; 2) EC50 values determined under Condition II were 2-6 fold higher than those under Condition I; 3) some partial agonists had less intrinsic activities in the presence of higher concentrations of GDP; and 4) Inhibitory effects of WAY10063 5 were complete under Condition I, while incomplete under Condition II. Pharmacological profile of concentration-dependent stimulation by a series of 5-HT ligands and concentration-dependent inhibition of 5-HT-stimulated binding by several 5-HT-receptor antagonists clearly indicated that this response under Condition I was mediated solely through 5-HT1A receptors. Although caution should be paid especially to the apparent intrinsic activities susceptible to the assay conditions, this method appears useful to investigate functional coupling between 5-HT1A receptors and their coupled G proteins in native hippocampal membranes. © 2005 The Japanese Pharmacological Society.