Divalent cations modulate the transient outward current in rat ventricular myocytes

Z. S. Agus, I. D. Dukes and M. Morad Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085. The modulation of the transient outward K+ current (Ito) by divalent cations was studied in enzymatically isolated rat ventricular myocytes with the whole cell patch...

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Veröffentlicht in:American Journal of Physiology: Cell Physiology 1991-08, Vol.261 (2), p.C310-C318
Hauptverfasser: Agus, Z. S, Dukes, I. D, Morad, M
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container_issue 2
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container_title American Journal of Physiology: Cell Physiology
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creator Agus, Z. S
Dukes, I. D
Morad, M
description Z. S. Agus, I. D. Dukes and M. Morad Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085. The modulation of the transient outward K+ current (Ito) by divalent cations was studied in enzymatically isolated rat ventricular myocytes with the whole cell patch-clamp technique. At holding potentials negative to -70 mV, 1 mM Cd2+ suppressed Ito, whereas, at potentials positive to -50 mV, the current was augmented. These effects were caused by shifts in the voltage dependence of both activation and inactivation of Ito toward more positive potentials. Cd2+ also slowed the activation kinetics of Ito by shifting the voltage dependence of its rate of activation, but the rate of inactivation was unaffected. Other divalent cations produced similar shifts but at markedly different concentrations. Thus, in the millimolar range, a rightward shift of approximately 20 mV was produced by 3 Co2+, 5 Ni2+, and 10 Ca2+, whereas 10 microM concentrations of Cu2+ and Zn2+ produced equivalent shifts. Similar effects were seen in hippocampal neurons with micromolar concentrations of Zn2+. Thus divalent cations have marked and specific effects on the kinetics and voltage dependence of Ito and may serve as a regulatory mechanism in its activation, particularly in cells with resting potentials positive to -60 mV.
doi_str_mv 10.1152/ajpcell.1991.261.2.c310
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S</creatorcontrib><creatorcontrib>Dukes, I. D</creatorcontrib><creatorcontrib>Morad, M</creatorcontrib><title>Divalent cations modulate the transient outward current in rat ventricular myocytes</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol</addtitle><description>Z. S. Agus, I. D. Dukes and M. Morad Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085. The modulation of the transient outward K+ current (Ito) by divalent cations was studied in enzymatically isolated rat ventricular myocytes with the whole cell patch-clamp technique. At holding potentials negative to -70 mV, 1 mM Cd2+ suppressed Ito, whereas, at potentials positive to -50 mV, the current was augmented. These effects were caused by shifts in the voltage dependence of both activation and inactivation of Ito toward more positive potentials. 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Thus divalent cations have marked and specific effects on the kinetics and voltage dependence of Ito and may serve as a regulatory mechanism in its activation, particularly in cells with resting potentials positive to -60 mV.</description><subject>Animals</subject><subject>Cadmium - pharmacology</subject><subject>cations</subject><subject>Cations, Divalent - pharmacology</subject><subject>currents</subject><subject>Electrophysiology</subject><subject>Heart - physiology</subject><subject>Kinetics</subject><subject>modulation</subject><subject>Myocardium - cytology</subject><subject>myocytes</subject><subject>Rats</subject><subject>ventricle</subject><subject>Zinc - pharmacology</subject><issn>0363-6143</issn><issn>0002-9513</issn><issn>1522-1563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LwzAYx4Moc04_gtiTt84nTZq2R5mvMPCgnkOWpltG28wk3ei3N6VDvXl4eJ7wfwn8ELrBMMc4Te7EdidVXc9xUeB5wsLMJcFwgqZBTWKcMnKKpkAYiRmm5BxdOLcFAJqwYoImOM8SkpEpen_Qe1Gr1kdSeG1aFzWm7GrhVeQ3YaxonR5k0_mDsGUkO2uHt24jK3y0D7fVMiRs1PRG9l65S3RWidqpq-Oeoc-nx4_FS7x8e35d3C9jSSnxMaWpSllV5KogVFJCS8hXFVRSClgRJrDKsxSzTOESMkgFySWpBASjAhArSmboduzdWfPVKed5o91ARbTKdI5nCZA8o8m_RszSnKQ5BGM2GqU1zllV8Z3VjbA9x8AH7vzInQ_ceeDOE74I3EPy-vhFt2pU-ZsbQQc9HvWNXm8O2iq-2_ROm9qs-5_SP33f0neR5w</recordid><startdate>19910801</startdate><enddate>19910801</enddate><creator>Agus, Z. 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D ; Morad, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-445e56f98e934c434d08bf0fcca0b36a1e875167e1d0705a38c3fa0434e00ab43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Cadmium - pharmacology</topic><topic>cations</topic><topic>Cations, Divalent - pharmacology</topic><topic>currents</topic><topic>Electrophysiology</topic><topic>Heart - physiology</topic><topic>Kinetics</topic><topic>modulation</topic><topic>Myocardium - cytology</topic><topic>myocytes</topic><topic>Rats</topic><topic>ventricle</topic><topic>Zinc - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Agus, Z. S</creatorcontrib><creatorcontrib>Dukes, I. D</creatorcontrib><creatorcontrib>Morad, M</creatorcontrib><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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American Journal of Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agus, Z. S</au><au>Dukes, I. 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These effects were caused by shifts in the voltage dependence of both activation and inactivation of Ito toward more positive potentials. Cd2+ also slowed the activation kinetics of Ito by shifting the voltage dependence of its rate of activation, but the rate of inactivation was unaffected. Other divalent cations produced similar shifts but at markedly different concentrations. Thus, in the millimolar range, a rightward shift of approximately 20 mV was produced by 3 Co2+, 5 Ni2+, and 10 Ca2+, whereas 10 microM concentrations of Cu2+ and Zn2+ produced equivalent shifts. Similar effects were seen in hippocampal neurons with micromolar concentrations of Zn2+. Thus divalent cations have marked and specific effects on the kinetics and voltage dependence of Ito and may serve as a regulatory mechanism in its activation, particularly in cells with resting potentials positive to -60 mV.</abstract><cop>United States</cop><pmid>1872373</pmid><doi>10.1152/ajpcell.1991.261.2.c310</doi></addata></record>
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source MEDLINE; Alma/SFX Local Collection
subjects Animals
Cadmium - pharmacology
cations
Cations, Divalent - pharmacology
currents
Electrophysiology
Heart - physiology
Kinetics
modulation
Myocardium - cytology
myocytes
Rats
ventricle
Zinc - pharmacology
title Divalent cations modulate the transient outward current in rat ventricular myocytes
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