Voltage-clamp analysis of halothane effects on GABAA fast and GABAA slow inhibitory currents |
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Authors: | Heath S Lukatch M.Bruce MacIver |
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Affiliation: | Stanford Neuroscience Program and Neuropharmacology Laboratory, Department of Anesthesia, Stanford University School of Medicine, Stanford, CA 94305-5117, USA |
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Abstract: | Voltage-clamped GABAA fast and GABAA slow inhibitory postsynaptic currents (IPSCs) were selectively elicited in hippocampal area CA1 pyramidal neurons. Clinically relevant concentrations of halothane (1.2 vol.%) prolonged both GABAA fast and GABAA slow IPSC decay times approximately 2.5 fold, while having little to no effect on current amplitudes or rise times. Current–voltage analysis revealed that IPSC reversal potentials (−70 to −75 mV) remained constant in the presence of halothane. Under control conditions, GABAA slow IPSC decay times increased linearly with membrane depolarization, and this IPSC decay time voltage dependence was not significantly altered by halothane. These results confirm the existence of separable GABAA fast and GABAA slow IPSCs in hippocampus, and further elucidate the effects of halothane on these currents. |
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Keywords: | Anesthetic Decay kinetics γ -Aminobutyric acid (GABA) Halothane Half-width Hippocampus Inhibitory postsynaptic current (IPSC) Prolongation |
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