Home LiteratureArticle Details
PMID: 2563909 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Multiple voltage-sensitive K+ channels regulate dendritic excitability in cerebellar Purkinje neurons.

Neuroscience letters ·Vol. 97 ·No. 1-2 ·1989-02-13 ·Pages 97-102

Gruol DL, Dionne VE, Yool AJ

Abstract

Ionic conductances present in the dendritic region of the cerebellar Purkinje neuron were studied using the single-channel and whole-cell recording methods. Several types of voltage-sensitive K+ channels including a Ca2+ activated K+ channel were found to be a prominent components of the dendritic membrane. All patches studied contained K+ channel types and most patches contained more than one K+ channel type. In cell attached recordings, K+ channel activity was associated with the late phase of spontaneous action potentials suggesting a functional relationship. These data demonstrate that voltage-sensitive ion channels contribute to dendritic excitability and suggest that the transduction and integration of synaptic signals may involve both active and passive ionic conductances.

MeSH Terms
Adrenergic alpha-Antagonists/pharmacology Adrenergic beta-Antagonists/pharmacology Animals Cells, Cultured Dendrites/drug effects,metabolism,physiology Electric Stimulation Membrane Potentials/drug effects Norepinephrine/pharmacology Potassium Channels/drug effects,physiology Purkinje Cells/metabolism,physiology Rats
Chemicals
Adrenergic alpha-Antagonists Adrenergic beta-Antagonists Potassium Channels Norepinephrine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gruol D L
Division of Preclinical Neuroscience and Endocrinology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
Dionne V E
Yool A J
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1989-02-13
Pages
97-102
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
Grants
NIAAA NIH HHS · AA07456 · United States
NINDS NIH HHS · NS21777 · United States
Corrections
ErratumIn
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