Differences in the Biophysical Properties of the Benzodiazepine/γ‐Aminobutyric Acid Receptor Chloride Channel Complex in the Long‐Sleep and Short‐Sleep Mouse Lines

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Abstract
Significant differences in the thermal stability of benzodiazepine receptors were found in cerebral cortical membranes prepared from the long-sleep (LS) and short-sleep (SS) selected mouse lines. Thus, benzodiazepine receptors from LS mice were heat inactivated (55°C) at a significantly faster rate than those from SS mice. Although γ-aminobutyric acid (GABA) reduced the rate of heat inactivation in both lines, the more rapid rate of inactivation in the LS line was maintained. Furthermore, the potency of GABA to enhance [3H]flunitrazepam binding decreased threefold in membranes from LS mice as the incubation temperature was increased from 0° to 37°C, but was unaltered in membranes from SS mice. These differences in the biophysical properties of the benzodiazepine/GABA receptor chloride channel complex (“supramolecular complex”), together with a higher KD for t-[35S]butylbicyclophosphoro-thionate in membranes from LS compared to SS mice, suggest that the supramolecular complex may modulate the differential sensitivity to some depressants and convulsants in these lines.

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