Correlation between low/high affinity ratios for 5-HT(1A) receptors and intrinsic activity

Marie Bernadette Assié, Cristina Cosi, Wouter Koek

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

G protein-coupled receptors exist in G protein-coupled and -uncoupled forms that exhibit high and low affinity for agonists, respectively. Consequently, affinity differences of a compound for the high vs. the low affinity state of a receptor have been used to estimate its intrinsic activity at that receptor. We examined the affinity of a series of compounds for 5-hydroxytryptamine(1A) (5-HT(1A)) receptor sites labeled with 0.2 nM [3H](±)-8-hydroxy-2-(di-n-propylamino)tetralin ([3H]8-OH-DPAT) (high affinity), or with 0.25 nM [3H]4-(2'-methoxy-)-phenyl-1-[2'-(N-2''-pyridyl)- p-fluorobenzamido]ethyl-piperazine ([3H]p-MPPF) in the presence of 100 μM guanylylimidodiphosphate (Gpp(NH)p) (low affinity) in rat hippocampal membranes. For a variety of 5-HT(1A) receptor ligands, the low/high affinity ratio (ranging from 110 for 5-HT to 0.12 for spiperone) was in good agreement with their reported intrinsic activity. Positive rank correlations were found between low/high affinity ratios and intrinsic activities (E(max) values) reported in the literature. The high efficacy 5-HT(1A) receptor agonists, 1[2-(4-fluorobenzoylamino)ethyl]-4-(7-methoxynaphtyl)piperazine (S-14506) and dihydroergotamine, however, had similar, high affinity for both G protein- coupled and -uncoupled forms of the receptor. The Hill coefficients for both compounds were markedly higher than 1.0, suggesting that positive cooperativity could be responsible for the unexpected results. The 5-HT(1A) receptor agonist activity of dihydroergotamine and S-14506, assessed by measuring the inhibition of forskolin-stimulated cAMP accumulation, was blocked completely by pertussis toxin, reinforcing the suggested involvement of an inhibitory G protein in their effects. Taken together, the results suggest that, although the low/high affinity ratio of a ligand for 5-HT(1A) receptors generally covaries with its intrinsic activity, dihydroergotamine and S-14506 may interact with 5-HT(1A) receptors in a manner different from that of other 5-HT(1A) receptor agonists. Their effects, however, appear to be G(i) protein-dependent.

Original languageEnglish (US)
Pages (from-to)97-103
Number of pages7
JournalEuropean Journal of Pharmacology
Volume386
Issue number1
DOIs
StatePublished - Dec 10 1999
Externally publishedYes

Fingerprint

Receptor, Serotonin, 5-HT1A
1-((4-fluorobenzoylamino)ethyl)-4-(7-methoxy-1-naphthyl)piperazine hydrochloride
Dihydroergotamine
GTP-Binding Proteins
8-Hydroxy-2-(di-n-propylamino)tetralin
Guanylyl Imidodiphosphate
Ligands
Spiperone
Pertussis Toxin
Colforsin
G-Protein-Coupled Receptors
Serotonin
Membranes

Keywords

  • 5-HT(1A) receptor ligand
  • Affinity
  • Dihydroergotamine
  • Efficacy
  • Gpp(NH)p shift
  • Intrinsic activity
  • S-14506

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Pharmacology

Cite this

Correlation between low/high affinity ratios for 5-HT(1A) receptors and intrinsic activity. / Assié, Marie Bernadette; Cosi, Cristina; Koek, Wouter.

In: European Journal of Pharmacology, Vol. 386, No. 1, 10.12.1999, p. 97-103.

Research output: Contribution to journalArticle

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