Calcium currents in rat cerebellar purkinje cells maintained in culture

Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these...

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Veröffentlicht in:Neuroscience 1989, Vol.30 (3), p.605-617
Hauptverfasser: Bossu, J.-L., Dupont, J.-L., Feltz, A.
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Dupont, J.-L.
Feltz, A.
description Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these were shown to be generated by Na and Ca components, the Na one being tetrodotoxin-sensitive. At the dendritic level, Ca currents were better resolved than at the soma. In dendrites, Ca entry was shown to occur through at least two distinct currents. The first was a low-threshold transient current (elicited above −60 mV from a holding potential of −80 mV) which was reduced by almost 30% by 50μ M cadmium. The second was a high-threshold current (above −20 mV) which gave rise to (1) a transient component exhibiting a steady-state inactivation and so requiring holding potentials at −80 mV, and (2) a sustained component. Both components were suppressed by 50 μm cadmium. We measured a total Ca current at the dendritic level reaching values of up to 1 nA. In another culture medium (Leibovitz medium) known to allow expression of three types of calcium currents in nodose cells we observed the development of the dendritic tree of Purkinje cells but with no simultaneous expression of the high-threshold Ca current.
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When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these were shown to be generated by Na and Ca components, the Na one being tetrodotoxin-sensitive. At the dendritic level, Ca currents were better resolved than at the soma. In dendrites, Ca entry was shown to occur through at least two distinct currents. The first was a low-threshold transient current (elicited above −60 mV from a holding potential of −80 mV) which was reduced by almost 30% by 50μ M cadmium. The second was a high-threshold current (above −20 mV) which gave rise to (1) a transient component exhibiting a steady-state inactivation and so requiring holding potentials at −80 mV, and (2) a sustained component. Both components were suppressed by 50 μm cadmium. We measured a total Ca current at the dendritic level reaching values of up to 1 nA. 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Psychology</subject><subject>Purkinje Cells - cytology</subject><subject>Purkinje Cells - drug effects</subject><subject>Purkinje Cells - physiology</subject><subject>Rats</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMo67r6DxR6ENFDNZ9tchFk0VVY8LL3kKZTiKbtmrSC_97UXfZoIARmnhnePAhdEnxPMCkeMMNFzgWlt1LdKUyEyNkRmhNZsrwUnB-j-QE5RWcxfuB0BGczNKNlSTDHc7RaGm_d2GZ2DAG6IWauy4IZMgsBKvDehGw7hk_XfUCqeR-z1rhuSBfqibWjH8YA5-ikMT7Cxf5doM3L82b5mq_fV2_Lp3VuBaFDLrBSDVCguDalkLJOAYtC8KaAilmqZIXBGkytwrJsCsJNo0T6Ea4JV4awBbrZrd2G_muEOOjWxSmW6aAfoyaCEUK5SiDfgTb0MQZo9Da41oQfTbCe9OnJjZ7caKn0nz7N0tjVfv9YtVAfhva-Uv963zfRGt8E01kXD1ghado0xXzcYZBUfDsIOloHnYXaBbCDrnv3f45fO66KZQ</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>Bossu, J.-L.</creator><creator>Dupont, J.-L.</creator><creator>Feltz, A.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope></search><sort><creationdate>1989</creationdate><title>Calcium currents in rat cerebellar purkinje cells maintained in culture</title><author>Bossu, J.-L. ; Dupont, J.-L. ; Feltz, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-5099fe2e20da7588d3066654f6eb3c298b0eca02c9087f614af951870d149a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Action Potentials - drug effects</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Cadmium - pharmacology</topic><topic>Calcium - physiology</topic><topic>Cells, Cultured</topic><topic>Central nervous system</topic><topic>Dendrites - physiology</topic><topic>Electrophysiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Purkinje Cells - cytology</topic><topic>Purkinje Cells - drug effects</topic><topic>Purkinje Cells - physiology</topic><topic>Rats</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bossu, J.-L.</creatorcontrib><creatorcontrib>Dupont, J.-L.</creatorcontrib><creatorcontrib>Feltz, A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bossu, J.-L.</au><au>Dupont, J.-L.</au><au>Feltz, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Calcium currents in rat cerebellar purkinje cells maintained in culture</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>1989</date><risdate>1989</risdate><volume>30</volume><issue>3</issue><spage>605</spage><epage>617</epage><pages>605-617</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. 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source MEDLINE; Elsevier ScienceDirect Journals
subjects Action Potentials - drug effects
Animals
Animals, Newborn
Biological and medical sciences
Cadmium - pharmacology
Calcium - physiology
Cells, Cultured
Central nervous system
Dendrites - physiology
Electrophysiology
Fundamental and applied biological sciences. Psychology
Purkinje Cells - cytology
Purkinje Cells - drug effects
Purkinje Cells - physiology
Rats
Tetrodotoxin - pharmacology
Vertebrates: nervous system and sense organs
title Calcium currents in rat cerebellar purkinje cells maintained in culture
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