Multiple types of high-threshold calcium channels in rabbit sensory neurons: High-affinity block of neuronal L-type by nimodipine

51Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.

Abstract

Whole-cell and cell-attached patch recording have been used to characterize multiple types of voltage-dependent calcium channels in neurons freshly dispersed from rabbit dorsal root ganglia. In whole-cell patch recordings, high-threshold current, strongly resistant to inactivation by depolarized holding potentials (L-type; V1/2 = -27.2 mV), was potently inhibited by nimodipine. Assuming 1:1 binding, the dissociation constant for nimodipine binding to the inactivated state of the L-type calcium channel (Kl) was 5.3 nM (n = 8). In contrast, a second type of high-threshold current less resistant to inactivation by depolarized holding potentials (N-type; V1/2 = -56.9 mV) was not blocked by nimodipine. Nimodipine-resistant N-type calcium current was inhibited by ω-conotoxin (5 μM). Cell-attached patch recordings of single calcium channel currents demonstrated the existence of three different unitary conductances; 7.4 pS, 13.1 pS, and 24.1 pS. The 24.1 pS high-threshold channel was enhanced by (-) BAY K 8644 and inhibited by nimodipine in a concentration-and voltage-dependent manner. Hyperpolarization reversed this block. These results demonstrate that, as in cardiac and smooth muscle, there is a component of neuronal high-threshold current corresponding to the L-type calcium channel that can be blocked with high affinity by nimodipine. Copyright © 1992 Society for Neuroscience.

Cite

CITATION STYLE

APA

McCarthy, R. T., & TanPiengco, P. E. (1992). Multiple types of high-threshold calcium channels in rabbit sensory neurons: High-affinity block of neuronal L-type by nimodipine. Journal of Neuroscience, 12(6), 2225–2234. https://doi.org/10.1523/jneurosci.12-06-02225.1992

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free