Interactions of Midazolam and Propofol on alpha(1)beta(2)gamma L-2 and alpha(1)beta(2)gamma S-2 Gamma Aminobutyric Acid Type A Receptors Expressed in Human Embryonic Kidney Cells

초록

BACKGROUND: The gamma aminobutyric acid type A (GABA(A)) receptor is a prime target of many anesthetics, including midazolam and propofol. Although these anesthetics have sedative and hypnotic properties by enhancing GABA(A) receptor activity, their interactions at the GABA(A) receptors have not been explored. We investigated the interaction of midazolam and propofol with alpha(1)beta(2)gamma L-2 and alpha(1)beta(2)gamma S-2 GABA(A) receptors. METHODS: Using the whole-cell patch clamp technique, we tested the effects of midazolam and propofol on GABA-induced currents in human embryonic kidney 293 T cells transfected with alpha beta(2)gamma L-2 and alpha(1)beta(2)gamma S-2 GABA(A) receptors. RESULTS: Midazolam and propofol on their own enhanced the amplitude of GABA(A) receptor responses in a dose-dependent manner, and they had additive effects on alpha(1)beta(2)gamma S-2 GABA(A) receptors, but not on alpha(1)beta(2)gamma L-2 GABA(A) receptors. However, additive interactions of midazolam and propofol on the alpha(1)beta(2)gamma L-2 GABA(A) receptors were observed when protein kinase C was inhibited. CONCLUSIONS: The interaction between midazolam and propofol is affected by receptor subtype, and protein kinase phosphorylation influences their interaction on the alpha(1)beta(2)gamma L-2 receptor. (Anesth Analg 2011;112:1096-102)

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