Correlation of the apparent affinities and efficacies of γ-aminobutyric acid(C) receptor agonists

Yong Chang, Douglas F. Covey, David S Weiss

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

γ-Aminobutyric acid (GABA), trans-4-aminocrotonic acid (TACA), muscimol, imidazole-4-acetic acid (14AA), cis-4-aminocrotonic acid (CACA), and isoguvacine are all GABA(C) receptor agonists. These compounds have different apparent sensitivities (EC50) and efficacies (/(max)) on exogenously expressed human ρ1 homomeric GABA(c) receptors. It is not clear if these differences are due to distinct binding affinities and/or distinct gating kinetics. In this study, using a recently developed single oocyte binding technique, we determined the apparent dissociation constants (K(i) values) of these compounds from their IC50 values for [3H]GABA displacement. The apparent K(i) values fell into two distinct groups. The high affinity group was comprised of agonists with longer distances between the nitrogen atom of the amino or imidazole group and the carbon atom of the carboxyl or isoxazole group. The single oocyte binding technique, in conjunction with two-electrode voltage clamp, has allowed a direct correlation of the apparent affinity, efficacy, and potency of agonists on intact functional GABA(c) receptors. The correlation and coupling of these parameters are discussed in terms of a simple proposed activation mechanism.

Original languageEnglish (US)
Pages (from-to)1375-1380
Number of pages6
JournalMolecular Pharmacology
Volume58
Issue number6
StatePublished - 2000
Externally publishedYes

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Aminobutyrates
GABA Receptors
gamma-Aminobutyric Acid
Oocytes
GABA Agonists
Isoxazoles
Muscimol
Inhibitory Concentration 50
Electrodes
Nitrogen
Carbon
4-aminocrotonic acid
isoguvacine
imidazole
imidazoleacetic acid
GABA-C receptor

ASJC Scopus subject areas

  • Pharmacology

Cite this

Correlation of the apparent affinities and efficacies of γ-aminobutyric acid(C) receptor agonists. / Chang, Yong; Covey, Douglas F.; Weiss, David S.

In: Molecular Pharmacology, Vol. 58, No. 6, 2000, p. 1375-1380.

Research output: Contribution to journalArticle

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