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Activation of GABA A receptors containing the α4 subunit by GABA and pentobarbital
Author(s) -
Akk Gustav,
Bracamontes John,
Steinbach Joe Henry
Publication year - 2004
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2003.058230
Subject(s) - pentobarbital , gabaa receptor , receptor , chemistry , biophysics , activator (genetics) , hek 293 cells , patch clamp , biochemistry , pharmacology , biology
The activation properties of GABA A receptors containing α4β2γ2 and α4β2δ subunits were examined in the presence of GABA or pentobarbital. The receptors were expressed transiently in HEK 293 cells, and the electrophysiological experiments were carried out using cell‐attached single‐channel patch clamp or whole‐cell macroscopic recordings. The data show that GABA is a stronger activator of α4β2γ2 receptors than α4β2δ receptors. Single‐channel clusters were recorded from α4β2γ2 receptors in the presence of 10–5000 μ m GABA. The maximal intracluster open probability was 0.35, with a half‐maximal response elicited by 32 μ m GABA. Simultaneous kinetic analysis of single‐channel currents obtained at various GABA concentrations yields a channel opening rate constant of 250 s −1 , and a K D of 20 μ m . In contrast, only isolated openings were observed in the presence of GABA for the α4β2δ receptor. Pentobarbital was a strong activator of both α4β2γ2 and α4β2δ receptors. The maximal cluster open probability, recorded in the presence of 100 μ m pentobarbital, was 0.7. At higher pentobarbital concentrations, the cluster open probability was reduced, probably due to channel block. The results from single‐channel experiments were confirmed by macroscopic recordings from HEK cells in the presence of GABA or pentobarbital.