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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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 |
format | Article |
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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.</description><identifier>ISSN: 0363-6143</identifier><identifier>ISSN: 0002-9513</identifier><identifier>EISSN: 1522-1563</identifier><identifier>DOI: 10.1152/ajpcell.1991.261.2.c310</identifier><identifier>PMID: 1872373</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cadmium - pharmacology ; cations ; Cations, Divalent - pharmacology ; currents ; Electrophysiology ; Heart - physiology ; Kinetics ; modulation ; Myocardium - cytology ; myocytes ; Rats ; ventricle ; Zinc - pharmacology</subject><ispartof>American Journal of Physiology: Cell Physiology, 1991-08, Vol.261 (2), p.C310-C318</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-445e56f98e934c434d08bf0fcca0b36a1e875167e1d0705a38c3fa0434e00ab43</citedby><cites>FETCH-LOGICAL-c443t-445e56f98e934c434d08bf0fcca0b36a1e875167e1d0705a38c3fa0434e00ab43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1872373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Agus, Z. 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. 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.</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. S</creator><creator>Dukes, I. D</creator><creator>Morad, M</creator><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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19910801</creationdate><title>Divalent cations modulate the transient outward current in rat ventricular myocytes</title><author>Agus, Z. S ; Dukes, I. 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 & 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. D</au><au>Morad, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divalent cations modulate the transient outward current in rat ventricular myocytes</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol</addtitle><date>1991-08-01</date><risdate>1991</risdate><volume>261</volume><issue>2</issue><spage>C310</spage><epage>C318</epage><pages>C310-C318</pages><issn>0363-6143</issn><issn>0002-9513</issn><eissn>1522-1563</eissn><abstract>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.</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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