Title

Rat supraoptic magnocellular neurones show distinct large conductance, Ca2+-activated K+ channel subtypes in cell bodies versus nerve endings

UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Publication Date

8-5-1999

Document Type

Article

Subjects

Alkaloids; Animals; *Benzylisoquinolines; Calcium; Calcium Channel Blockers; Evoked Potentials; Ion Channel Gating; Large-Conductance Calcium-Activated Potassium Channels; Male; Nerve Endings; Neurons; Patch-Clamp Techniques; Potassium Channels; *Potassium Channels, Calcium-Activated; Rats; Reaction Time; Supraoptic Nucleus

Disciplines

Biochemistry | Physiology

Abstract

1. Large conductance, Ca2+-activated K+ (BK) channels were identified in freshly dissociated rat supraoptic neurones using patch clamp techniques. 2. The single channel conductance of cell body BK channels, recorded from inside-out patches in symmetric 145 mM K+, was 246.1 pS, compared with 213 pS in nerve ending BK channels (P1.53 microM for the neurohypophysial channel, indicating the higher Ca2+ sensitivity of the cell body isochannel. 5. Cell body BK channels showed fast kinetics (open time constant, 8.5 ms; fast closed time constant, 1.6 and slow closed time constant, 12.7 ms), identifying them as 'type I' isochannels, as opposed to the slow gating (type II) of neurohypophysial BK channels. 6. Cell body BK activity was reduced by 10 nM charybdotoxin (NPo, 37% of control), or 10 nM iberiotoxin (NPo, 5% of control), whereas neurohypophysial BK channels are insensitive to charybdotoxin at concentrations as high as 360 nM. 7. Whilst blockade of nerve ending BK channels markedly slowed the repolarization of evoked single spikes, blockade of cell body channels was without effect on repolarization of evoked single spikes. 8. Ethanol reversibly increased neurohypophysial BK channel activity (EC50, 22 mM; maximal effect, 100 mM). In contrast, ethanol (up to 100 mM) failed to increase cell body BK channel activity. 9. In conclusion, we have characterized BK channels in supraoptic neuronal cell bodies, and demonstrated that they display different electrophysiological and pharmacological properties from their counterparts in the nerve endings.

Rights and Permissions

Citation: J Physiol. 1999 Aug 15;519 Pt 1:101-14.

Related Resources

Link to Article in PubMed

Journal/Book/Conference Title

The Journal of physiology

PubMed ID

10432342