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PMID: 2952874 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Pharmacological characterization of two 5-hydroxytryptamine receptors coupled to adenylate cyclase in guinea pig hippocampal membranes.

Molecular pharmacology ·Vol. 31 ·No. 4 ·1987-04-00 ·Pages 357-67

Shenker A, Maayani S, Weinstein H, Green JP

Abstract

Two 5-hydroxytryptamine (5-HT) receptors mediate stimulation of adenylate cyclase activity in membranes of adult guinea pig hippocampus. The two receptors were characterized with agonists and antagonists and with the aid of computerized curve-fitting procedures. Each receptor mediates about 50% of the maximal response to 5-HT. 5-HT is about 10-fold more potent in eliciting response through one cyclase-linked receptor (RH) than the other (RL). The concentrations of 5-HT that elicit half-maximal response through RH and RL are 43 +/- 6 nM and 414 +/- 53 nM, respectively. 5-Methoxytryptamine (5-MeOT) and 5-HT are approximately equipotent at each receptor. The agonists tryptamine and bufotenine are less potent than 5-HT at both receptors, and each is about 50-fold selective for RH. The two receptors are best discriminated by the agonists 5-carboxamidotryptamine (5-CONH2-T) and 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT), both of which are selective for RH. 5-CONH2-T is about 7-fold more potent than 5-HT at RH. The rank order of agonist potencies at RH (5-CONH2-T greater than 8-OH-DPAT = 5-HT = 5-MeOT greater than bufotenine greater than tryptamine) differs from that at RL (5-HT = 5-MeOT greater than bufotenine greater than tryptamine = 5-CONH2-T greater than 8-OH-DPAT). Spiperone acts as a simple competitive antagonist at RH, with a dissociation constant of 20 nM, but it is at least 100-fold less potent as an antagonist at RL. The relatively low affinities of the selective 5-HT antagonists ketanserin and MDL 72222 for RH and RL indicate that neither receptor may be classified as the 5-HT2 or as the 5-HT3 (i.e., peripheral neuronal) type. The characteristics of RH suggest that it is a functional correlate of the 5-HT1A-binding site in brain. RL appears not to correspond to a known 5-HT-binding site, but it may be homologous to receptors that mediate 5-HT-stimulated adenylate cyclase activity in other systems such as infant rat colliculi. RH and RL may also mediate stimulation of adenylate cyclase activity by 5-HT in hippocampal membranes of adult rat.

MeSH Terms
5-Methoxytryptamine/metabolism 8-Hydroxy-2-(di-n-propylamino)tetralin Adenylyl Cyclases/metabolism Animals Bufotenin/metabolism Guinea Pigs Hippocampus/metabolism Kinetics Male Mathematics Membranes/metabolism Rats Rats, Inbred Strains Receptors, Serotonin/metabolism Serotonin/analogs & derivatives,metabolism Spiperone/metabolism Tetrahydronaphthalenes/metabolism Tryptamines/metabolism
Chemicals
Receptors, Serotonin Tetrahydronaphthalenes Tryptamines Bufotenin Serotonin 5-Methoxytryptamine tryptamine Spiperone 8-Hydroxy-2-(di-n-propylamino)tetralin 5-carboxamidotryptamine Adenylyl Cyclases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shenker A
Maayani S
Weinstein H
Green J P
Article Info
Journal
Molecular pharmacology
Abbr.
Mol Pharmacol
ISSN
0026-895X
Published
1987-04-00
Pages
357-67
Language
English
Region
United States
NLM ID
0035623
Subset
IM
Grants
NIDA NIH HHS · DA 01875 · United States
NIGMS NIH HHS · GM-07280 · United States
NIDA NIH HHS · K02 DA 00060 · United States
Corrections
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