Detailed Pharmacological Characterization of 5-HT1A-Receptor-Mediated [35S]GTPγS Binding in Rat Hippocampal Membranes

• Published in: Journal of Pharmacological Sciences Vol. 98; no. 1; pp. 66 - 76
• Main Authors: Odagaki, Yuji, Toyoshima, Ryoichi
• Format: Journal Article
• Language: English
• Published: Japan Elsevier B.V 2005; The Japanese Pharmacological Society; Elsevier
• Subjects: 5-HT1A receptor; [35S]GTPγS binding; Animals; Dose-Response Relationship, Drug; G protein; Guanosine 5'-O-(3-Thiotriphosphate) - metabolism; hippocampus; Hippocampus - metabolism; intrinsic activity; Male; Protein Binding - physiology; Rats; Rats, Sprague-Dawley; Receptor, Serotonin, 5-HT1A - metabolism; Serotonin Antagonists - metabolism; Sulfur Radioisotopes - metabolism; [35S]GTPγS binding; intrinsic activity; hippocampus; 5-HT1A receptor; G protein
• ISSN: 1347-8613; 1347-8648
• DOI: 10.1254/jphs.fpj05010x

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 µM GDP, 5 mM MgCl2, and 100 mM NaCl: Condition I) to the alternative one (100 µM GDP, 5 mM 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 WAY100635 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.