Biophysical and Pharmacological Characterization of Voltage-Dependent Ca2+ Channels in Neurons Isolated From Rat Nucleus Accumbens

Author:

Churchill Dennis1,Macvicar Brian A.1

Affiliation:

1. Neuroscience Research Group, Department of Physiology and Biophysics, Faculty of Medicine, University of Calgary, Alberta T2N 4N1, Canada

Abstract

Churchill, Dennis and Brian A. MacVicar. Biophysical and pharmacological characterization of voltage-dependent Ca2+ channels in neurons isolated from rat nucleus accumbens. J. Neurophysiol. 79: 635–647, 1998. The nucleus accumbens (NA) has an integrative role in behavior and may mediate addictive and psychotherapeutic drug action. Whole cell recording techniques were used to characterize electrophysiologically and pharmacologically high- and low-threshold voltage-dependent Ca2+ currents in isolated NA neurons. High-threshold Ca2+ currents, which were found in all neurons studied and include both sustained and inactivating components, activated at potentials greater than −50 mV and reached maximal activation at ∼0 mV. In contrast, low-threshold Ca2+ currents activated at voltages greater than −64 mV with maximal activation occurring at −30 mV. These were observed in 42% of acutely isolated neurons. Further pharmacological characterization of high-threshold Ca2+ currents was attempted using nimodipine (Nim), ω-conotoxin-GVIA (ω-CgTx) and ω-agatoxin-IVA (ωAga), which are thought to identify the L, N, and P/Q subtypes of Ca2+ currents, respectively. Nim (5–10 μM) blocked 18%, ωCgTx (1–2 μM) blocked 25%, and ωAga (200 nM) blocked 17% of total Ca2+ current. Nim primarily blocked a sustained high-threshold Ca2+ current in a partially reversible manner. In contrast, ωCgTx irreversibly blocked both sustained and inactivating components. ωAga irreversibly blocked only a sustained component. In all three of these Ca2+ channel blockers, plus 5 μM ω-conotoxin-MVIIC to eliminate a small unblocked Q-type Ca2+ current (7%), a toxin-resistant high-threshold Ca2+ current remained that was 32% of total Ca2+ current. This current inactivated much more rapidly than the other high-threshold Ca2+ currents, was depressed in 50 μM Ni2+ and reached maximal activation 5–10 mV negative to the toxin-sensitive high-threshold Ca2+ currents. Thus NA neurons have multiple types of high-threshold Ca2+ currents with a large component being the toxin-resistant “R” component.

Publisher

American Physiological Society

Subject

Physiology,General Neuroscience

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