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Chloride equilibrium potential in salamander cones
BACKGROUND: GABAergic inhibition and effects of intracellular chloride ions on calcium channel activity have been proposed to regulate neurotransmission from photoreceptors. To assess the impact of these and other chloride-dependent mechanisms on release from cones, the chloride equilibrium potentia...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539262/ https://www.ncbi.nlm.nih.gov/pubmed/15579212 http://dx.doi.org/10.1186/1471-2202-5-53 |
Sumario: | BACKGROUND: GABAergic inhibition and effects of intracellular chloride ions on calcium channel activity have been proposed to regulate neurotransmission from photoreceptors. To assess the impact of these and other chloride-dependent mechanisms on release from cones, the chloride equilibrium potential (E(Cl)) was determined in red-sensitive, large single cones from the tiger salamander retinal slice. RESULTS: Whole cell recordings were done using gramicidin perforated patch techniques to maintain endogenous Cl(- )levels. Membrane potentials were corrected for liquid junction potentials. Cone resting potentials were found to average -46 mV. To measure E(Cl), we applied long depolarizing steps to activate the calcium-activated chloride current (I(Cl(Ca))) and then determined the reversal potential for the current component that was inhibited by the Cl(- )channel blocker, niflumic acid. With this method, E(Cl )was found to average -46 mV. In a complementary approach, we used a Cl-sensitive dye, MEQ, to measure the Cl(- )flux produced by depolarization with elevated concentrations of K(+). The membrane potentials produced by the various high K(+ )solutions were measured in separate current clamp experiments. Consistent with electrophysiological experiments, MEQ fluorescence measurements indicated that E(Cl )was below -36 mV. CONCLUSIONS: The results of this study indicate that E(Cl )is close to the dark resting potential. This will minimize the impact of chloride-dependent presynaptic mechanisms in cone terminals involving GABA(a )receptors, glutamate transporters and I(Cl(Ca)). |
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