The time course of dopamine transmission in the ventral tegmental area. The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] Journal article | | Title | The time course of dopamine transmission in the ventral tegmental area. | | Author(s) | Ford CP, Phillips PE, Williams JT | | Institution | Vollum Institute, Oregon Health & Science University, Portland, Oregon 97239, USA. | | Source | J Neurosci 2009 Oct 21; 29(42):13344-52. | | MeSH | Animals Biophysics Chelating Agents Dizocilpine Maleate Dopamine Dopamine Agonists Egtazic Acid Electric Stimulation Electrochemistry Excitatory Amino Acid Antagonists Female G Protein-Coupled Inwardly-Rectifying Potassium Channels GABA Antagonists Inhibitory Postsynaptic Potentials Male Mice Mice, Inbred DBA Neurons Patch-Clamp Techniques Phosphinic Acids Picrotoxin Propanolamines Quinoxalines Quinpirole Rhodamines Signal Transduction Statistics, Nonparametric Temperature Time Factors Ventral Tegmental Area
| | Abstract | Synaptic transmission mediated by G-protein coupled receptors (GPCR) is not generally thought to be point-to-point. To determine the extent over which dopamine signals in the midbrain, the present study examined the concentration and time course of dopamine that underlies a D(2)-receptor IPSC (D(2)-IPSC) in the ventral tegmental area. Extracellular dopamine was measured electrochemically while simultaneously recording D(2)-IPSCs. The presence of dopamine was brief relative to the IPSC, suggesting that G-protein dependent potassium channel activation determined the IPSC time course. The activation kinetics of D(2) receptor-dependent potassium current was studied using outside-out patch recordings with rapid application of dopamine. Dopamine applied at a minimum concentration of 10 mum for a maximum of 100 ms mimicked the IPSC. Higher concentrations applied for as little as 5 ms did not change the kinetics of the current. The results indicate that both the intrinsic kinetics of G-protein coupled receptor signaling and a rapidly rising high concentration of dopamine determine the time course of the IPSC. Thus, dopamine transmission in the midbrain is more localized then previously proposed. | | Language | eng | | Pub Type(s) | In Vitro Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't
| | PubMed ID | 19846722 |
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