| Title | Presynaptic actions of propofol enhance inhibitory synaptic transmission in isolated solitary tract nucleus neurons. | | Author(s) | Jin YH, Zhang Z, Mendelowitz D, Andresen MC | | Institution | Department of Physiology and Pharmacology, Oregon Health and Science University, Portland, OR 97239; Department of Physiology, Kyung Hee University, Seoul 130-701, Korea. | | Source | Brain Res 2009 Jun 24. | | Abstract | General anesthetics variably enhance inhibitory synaptic transmission that relies on (-aminobutyric acid (GABA) and GABA(A) receptor function with distinct differences across brain regions. Activation of "extra-synaptic" GABA(A) receptors produces a tonic current considered the most sensitive targets for general anesthetics, particularly in forebrain neurons. To evaluate the contribution of poor drug access to neurons in slices, we tested the intravenous anesthetic propofol in mechanically isolated neurons from the solitary tract nucleus (NTS). Setting chloride concentrations to E(Cl)=-29 mV made GABA currents inward at holding potentials of -60 mV. Propofol triggered pronounced but slowly developing tonic currents that reversed with 5 min washing. Effective concentrations in isolated cells were lower than in slices and propofol enhanced phasic IPSCs more potently than tonic currents (1 muM increased phasic decay time constant vs. >3 muM tonic currents). Propofol increased IPSC frequency (>3 muM), a presynaptic action. Bicuculline blocked all propofol actions. Gabazine blocked only phasic IPSCs. IPSCs persisted in TTX and/or cadmium but these agents prevented propofol-induced increases in IPSC frequency. Furosemide (>1 mM) reversibly blocked propofol-evoked IPSC frequency changes without altering waveforms. We conclude that presynaptic actions of propofol depend on a depolarizing chloride gradient across presynaptic inhibitory terminals. Our results in isolated neurons indicate that propofol pharmacokinetics intrinsically trigger the tonic currents slowly and the time course is not related to slow permeation or delivery. Unlike forebrain, phasic NTS GABA(A) receptors are more sensitive to propofol than tonic receptors but that presynaptic GABA(A) receptor mechanisms regulate GABA release. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 19559683 |
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