Neuropharmacological Characterization of Voltage-Sensitive Calcium Channels: Possible Existence of Neomycin-Sensitive, ω-Conotoxin GVIA- and Dihydropyridines-Resistant Calcium Channels in the Rat Brain

Abstract

We attemped to characterize the functional roles of subtypes of voltage-sensitive calcium channels in the brain. The maximal number of [¹²⁵I]ω-conotoxin GVIA (ω-CTX) binding sites in rat brain associated with N-type calcium channels (N-channels) was approximately 10 times more than that of [³H]-PN200-110 associated with L-type calcium channels (L-channels). [¹²⁵I]ω-CTX binding was inhibited by aminoglycoside antibiotics, neomycin and dynorphin A(1-13), but not by various classes of L-channel antagonists. A 6-hydroxydopamine-induced lesion of the striatum resulted in a marked reduction of both [¹²⁵I]-ω-CTX and [³H]PN200-110 binding. Kainic acid-induced lesion of the striatum reduced [³H]PN200-110 binding by 57%, but did not reduce [¹²⁵I]ω-CTX binding. ω-CTX produced a small (18%) but significant reduction of potassium-stimulated Ca²⁺ influx into rat brain synaptosomes, although it produced a concentration-dependent inhibition in chick brain synaptosomes. Neomycin inhibited Ca²⁺ influx in both preparations in a concentration-dependent manner. Both ω-CTX and neomycin inhibited potassium-stimulated [³H]dopamine (DA) release from rat striatal slices. The L-channel antagonists had no effect on either Ca²⁺ influx or [³H]DA release. These results suggest that DA release in the striatum is regulated by Ca²⁺ influx through N-channels located in presynaptic nerve terminals, and that the most of the Ca²⁺ influx in rat brain appears to be governed by neomycin-sensitive, ω-CTX and DHP-resistant calcium channels.