Background: The modulation of N-methyl-D-aspartate receptors is associated with a molar water solubility cut-off effect of approximately 1.1 mmol/l and hence are unaffected by significantly less soluble compounds. However, compounds with this molar water solubility are still able to modulate #x03B3;-aminobutyric acid type A (GABA
A) receptors. We hypothesized that GABA
A receptor modulation by phenolic compounds would exhibit cut-off at a molar water solubility value less than 1.1 mmol/l.
Methods: GABA
A receptors consisting of human α
1 and rat β
2 and #x03B3;
2s subunits were expressed in
Xenopus laevis oocytes, and drug responses were measured using standard 2-electrode voltage clamp techniques. Twenty substituted phenols and benzenes of similar size and molecular volume were studied at saturated aqueous concentrations. Reversible and statistically significant change in GABA
A receptor current that was 10% or greater in magnitude from the baseline response defined a positive drug effect.
Results: All phenyl ring compounds with a molar water solubility value equal to or greater than 0.46 mmol/l positively modulated GABA
A receptor currents. No compounds with a molar water solubility value equal to or less than 0.10 mmol/l had any effect on GABA
A receptor currents. Saturated solutions of phenols with 2,6-dimethyl and 2,6-diisopropyl substituents also caused channel opening in the absence of GABA.
Conclusions: The molar water solubility cut-off for GABA
A receptor modulation by phenyl ring compounds lies between 0.10 and 0.46 mmol/l. Data suggest that hydrocarbons, perhaps including inhaled anesthetics, might modulate GABA
A receptors by displacing water from one or more low-affinity amphipathic binding sites to induce conformational changes that increase ion conductance.
Pharmacology 2016;98:13-19
from #AlexandrosSfakianakis via Alexandros G.Sfakianakis on Inoreader http://ift.tt/1RQlmYi
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