Abstract

BackgroundGABAergic 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 (ECl) was determined in red-sensitive, large single cones from the tiger salamander retinal slice.ResultsWhole 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 ECl, we applied long depolarizing steps to activate the calcium-activated chloride current (ICl(Ca)) and then determined the reversal potential for the current component that was inhibited by the Cl- channel blocker, niflumic acid. With this method, ECl 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 ECl was below -36 mV.ConclusionsThe results of this study indicate that ECl is close to the dark resting potential. This will minimize the impact of chloride-dependent presynaptic mechanisms in cone terminals involving GABAa receptors, glutamate transporters and ICl(Ca).

Highlights

  • GABAergic inhibition and effects of intracellular chloride ions on calcium channel activity have been proposed to regulate neurotransmission from photoreceptors

  • Regulation of intracellular chloride levels results in a chloride equilibrium potential (ECl) that is hyperpolarized with respect to the resting potential in many nerve cells, but depolarized in others [1,2,3,4,5]

  • The light-evoked hyperpolarization of horizontal cells causes a cessation of GABA release and this disinhibition leads to a "feedback depolarization" in cones

Read more

Summary

Introduction

GABAergic inhibition and effects of intracellular chloride ions on calcium channel activity have been proposed to regulate neurotransmission from photoreceptors. The value of ECl in cones is an important parameter for determining the strength and polarity of these effects It has been suggested GABAa receptors in the terminals of cones may mediate inhibitory synaptic feedback from horizontal cells to cones [8]. Under this hypothesis, the light-evoked hyperpolarization of horizontal cells causes a cessation of GABA release and this disinhibition leads to a "feedback depolarization" in cones. The light-evoked hyperpolarization of horizontal cells causes a cessation of GABA release and this disinhibition leads to a "feedback depolarization" in cones There is evidence both for [e.g., [8]] and against [e.g., [12,13]; see review in (page number not for citation purposes)

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call