Actions of barium and rubidium on membrane currents in canine Purkinje fibres

The actions of Ba2+ and Rb+, two blockers of background K+ conductance, were investigated. Recent studies performed on ungulate Purkinje fibres have suggested that the pace-maker current is an inward current activated by hyperpolarization. This hypothesis is based on the assumption that Ba2+ reduces...

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Veröffentlicht in:The Journal of physiology 1983-05, Vol.338 (1), p.589-612
Hauptverfasser: Cohen, I S, Falk, R T, Mulrine, N K
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description The actions of Ba2+ and Rb+, two blockers of background K+ conductance, were investigated. Recent studies performed on ungulate Purkinje fibres have suggested that the pace-maker current is an inward current activated by hyperpolarization. This hypothesis is based on the assumption that Ba2+ reduces the inwardly rectifying background K+ conductance without affecting the pace-maker current. Addition of 5 mM-BaCl2 to the bathing Tyrode solution decreases background K+ permeability and eliminates the reversal of the pace-maker current. The reversal reappears on return to Ba2+-free Tyrode solution. 5 mM-BaCl2 also reduces the time-dependent current at pace-maker potentials positive to about -95 mV in 4 mM-K+ Tyrode solution. The pace-maker current in Ba2+ Tyrode solution usually does not have an exponential time course, and often decays non-monotonically. It can take more than two minutes to reach a steady state. The fast initial component of membrane current, which is observed on hyperpolarizing in the pace-maker potential range in Purkinje fibres and which has been called the 'depletion current', is still present in Ba2+ Tyrode solution, but is reduced or eliminated if 10 mM-CsCl is added to the Ba2+ Tyrode solution. The addition of Cs+ is accompanied by an outward shift in membrane current in Ba2+ Tyrode solution. Ba2+ reduces the background K+ permeability in a dose-dependent manner. Addition of between 0.5 and 1 mM-BaCl2 achieves a maximum effect. Raising the amount of BaCl2 above this level reduces the time-dependent current even when no further effect on background permeability is observed. Rb+ substitution for K+ reduces the magnitude of the pace-maker current at potentials positive to -100 mV, eliminates the reversal of the pace-maker current, shifts the activation range to more negative potentials, and decreases the voltage dependence of pace-maker current kinetics. Rb+ addition to Tyrode solution has little effect on pace-maker current magnitude or time course positive to -90 mV, but does shift the reversal to more negative potentials. The available evidence suggests that the pace-maker current in Ba2+ Tyrode solution is an inward current activated by hyperpolarization. However, Ba2+ blocks an unknown fraction of the pace-maker current in a dose-dependent, and possibly voltage-dependent manner. Also, the presence of a slow component of pace-maker decay suggests that the standard Hodgkin-Huxley formalism for the analysis of pace-maker currents is ina
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Recent studies performed on ungulate Purkinje fibres have suggested that the pace-maker current is an inward current activated by hyperpolarization. This hypothesis is based on the assumption that Ba2+ reduces the inwardly rectifying background K+ conductance without affecting the pace-maker current. Addition of 5 mM-BaCl2 to the bathing Tyrode solution decreases background K+ permeability and eliminates the reversal of the pace-maker current. The reversal reappears on return to Ba2+-free Tyrode solution. 5 mM-BaCl2 also reduces the time-dependent current at pace-maker potentials positive to about -95 mV in 4 mM-K+ Tyrode solution. The pace-maker current in Ba2+ Tyrode solution usually does not have an exponential time course, and often decays non-monotonically. It can take more than two minutes to reach a steady state. The fast initial component of membrane current, which is observed on hyperpolarizing in the pace-maker potential range in Purkinje fibres and which has been called the 'depletion current', is still present in Ba2+ Tyrode solution, but is reduced or eliminated if 10 mM-CsCl is added to the Ba2+ Tyrode solution. The addition of Cs+ is accompanied by an outward shift in membrane current in Ba2+ Tyrode solution. Ba2+ reduces the background K+ permeability in a dose-dependent manner. Addition of between 0.5 and 1 mM-BaCl2 achieves a maximum effect. Raising the amount of BaCl2 above this level reduces the time-dependent current even when no further effect on background permeability is observed. Rb+ substitution for K+ reduces the magnitude of the pace-maker current at potentials positive to -100 mV, eliminates the reversal of the pace-maker current, shifts the activation range to more negative potentials, and decreases the voltage dependence of pace-maker current kinetics. Rb+ addition to Tyrode solution has little effect on pace-maker current magnitude or time course positive to -90 mV, but does shift the reversal to more negative potentials. The available evidence suggests that the pace-maker current in Ba2+ Tyrode solution is an inward current activated by hyperpolarization. However, Ba2+ blocks an unknown fraction of the pace-maker current in a dose-dependent, and possibly voltage-dependent manner. 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Recent studies performed on ungulate Purkinje fibres have suggested that the pace-maker current is an inward current activated by hyperpolarization. This hypothesis is based on the assumption that Ba2+ reduces the inwardly rectifying background K+ conductance without affecting the pace-maker current. Addition of 5 mM-BaCl2 to the bathing Tyrode solution decreases background K+ permeability and eliminates the reversal of the pace-maker current. The reversal reappears on return to Ba2+-free Tyrode solution. 5 mM-BaCl2 also reduces the time-dependent current at pace-maker potentials positive to about -95 mV in 4 mM-K+ Tyrode solution. The pace-maker current in Ba2+ Tyrode solution usually does not have an exponential time course, and often decays non-monotonically. It can take more than two minutes to reach a steady state. The fast initial component of membrane current, which is observed on hyperpolarizing in the pace-maker potential range in Purkinje fibres and which has been called the 'depletion current', is still present in Ba2+ Tyrode solution, but is reduced or eliminated if 10 mM-CsCl is added to the Ba2+ Tyrode solution. The addition of Cs+ is accompanied by an outward shift in membrane current in Ba2+ Tyrode solution. Ba2+ reduces the background K+ permeability in a dose-dependent manner. Addition of between 0.5 and 1 mM-BaCl2 achieves a maximum effect. Raising the amount of BaCl2 above this level reduces the time-dependent current even when no further effect on background permeability is observed. Rb+ substitution for K+ reduces the magnitude of the pace-maker current at potentials positive to -100 mV, eliminates the reversal of the pace-maker current, shifts the activation range to more negative potentials, and decreases the voltage dependence of pace-maker current kinetics. Rb+ addition to Tyrode solution has little effect on pace-maker current magnitude or time course positive to -90 mV, but does shift the reversal to more negative potentials. The available evidence suggests that the pace-maker current in Ba2+ Tyrode solution is an inward current activated by hyperpolarization. However, Ba2+ blocks an unknown fraction of the pace-maker current in a dose-dependent, and possibly voltage-dependent manner. Also, the presence of a slow component of pace-maker decay suggests that the standard Hodgkin-Huxley formalism for the analysis of pace-maker currents is inappropriate.</description><subject>Action Potentials</subject><subject>Animals</subject><subject>Barium - pharmacology</subject><subject>Cell Membrane Permeability - drug effects</subject><subject>Cesium - pharmacology</subject><subject>Dogs</subject><subject>Dose-Response Relationship, Drug</subject><subject>Heart Conduction System - drug effects</subject><subject>In Vitro Techniques</subject><subject>Kinetics</subject><subject>Membrane Potentials - drug effects</subject><subject>Potassium - metabolism</subject><subject>Purkinje Fibers - drug effects</subject><subject>Purkinje Fibers - metabolism</subject><subject>Purkinje Fibers - physiology</subject><subject>Rubidium - pharmacology</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUU1v1DAUtBCoXQo_gSon6GUXPzuJ7QvSUpUvFdFDOVuO_dL1ksSLvaHaf4-jbCu4IE5P78280YyGkHOgKwDgb7e7zSH50K1ASb5KOwplreAJWUxzKYTiT8mCUsaWXFRwSp6ntKUUOFXqhJzUUlRKsAX5urZ7H4ZUhLZoTPRjX5jBFXFsvJuWMBQ99k00AxZ2jBGHfSr8UFgz-Hy6GeMPP2yxaH0TMb0gz1rTJXx5nGfk-4er28tPy-tvHz9frq-XtuI8u0NolamVkCgVs5RLWTqUkiqHTIkaUPLsFUqnGtcoUyrrOFrgTVtzYRw_I-9m3d3Y9OhsdhVNp3fR9yYedDBe_40MfqPvwi8NkFMDywKvjwIx_Bwx7XXvk8WuyznDmLSklWRMlZl48U8iCKpAMMF5ptYz1caQUsT20Q9QPXWmHzrTU2f6obP8-OrPNI9vx5Iy_n7G732Hh_9U1bdfbqYD5xIqqbLIm1lk4-829z6int9SsB73B515GvTE_A2jbbmS</recordid><startdate>19830501</startdate><enddate>19830501</enddate><creator>Cohen, I S</creator><creator>Falk, R T</creator><creator>Mulrine, N K</creator><general>The Physiological Society</general><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>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19830501</creationdate><title>Actions of barium and rubidium on membrane currents in canine Purkinje fibres</title><author>Cohen, I S ; Falk, R T ; Mulrine, N K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5339-7e1f9a6978e892c03884de8809de29761e8300114d9bdb9a49cd3ec13bf637ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Action Potentials</topic><topic>Animals</topic><topic>Barium - pharmacology</topic><topic>Cell Membrane Permeability - drug effects</topic><topic>Cesium - pharmacology</topic><topic>Dogs</topic><topic>Dose-Response Relationship, Drug</topic><topic>Heart Conduction System - drug effects</topic><topic>In Vitro Techniques</topic><topic>Kinetics</topic><topic>Membrane Potentials - drug effects</topic><topic>Potassium - metabolism</topic><topic>Purkinje Fibers - drug effects</topic><topic>Purkinje Fibers - metabolism</topic><topic>Purkinje Fibers - physiology</topic><topic>Rubidium - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cohen, I S</creatorcontrib><creatorcontrib>Falk, R T</creatorcontrib><creatorcontrib>Mulrine, N K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, I S</au><au>Falk, R T</au><au>Mulrine, N K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Actions of barium and rubidium on membrane currents in canine Purkinje fibres</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>1983-05-01</date><risdate>1983</risdate><volume>338</volume><issue>1</issue><spage>589</spage><epage>612</epage><pages>589-612</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>The actions of Ba2+ and Rb+, two blockers of background K+ conductance, were investigated. Recent studies performed on ungulate Purkinje fibres have suggested that the pace-maker current is an inward current activated by hyperpolarization. This hypothesis is based on the assumption that Ba2+ reduces the inwardly rectifying background K+ conductance without affecting the pace-maker current. Addition of 5 mM-BaCl2 to the bathing Tyrode solution decreases background K+ permeability and eliminates the reversal of the pace-maker current. The reversal reappears on return to Ba2+-free Tyrode solution. 5 mM-BaCl2 also reduces the time-dependent current at pace-maker potentials positive to about -95 mV in 4 mM-K+ Tyrode solution. The pace-maker current in Ba2+ Tyrode solution usually does not have an exponential time course, and often decays non-monotonically. It can take more than two minutes to reach a steady state. The fast initial component of membrane current, which is observed on hyperpolarizing in the pace-maker potential range in Purkinje fibres and which has been called the 'depletion current', is still present in Ba2+ Tyrode solution, but is reduced or eliminated if 10 mM-CsCl is added to the Ba2+ Tyrode solution. The addition of Cs+ is accompanied by an outward shift in membrane current in Ba2+ Tyrode solution. Ba2+ reduces the background K+ permeability in a dose-dependent manner. Addition of between 0.5 and 1 mM-BaCl2 achieves a maximum effect. Raising the amount of BaCl2 above this level reduces the time-dependent current even when no further effect on background permeability is observed. Rb+ substitution for K+ reduces the magnitude of the pace-maker current at potentials positive to -100 mV, eliminates the reversal of the pace-maker current, shifts the activation range to more negative potentials, and decreases the voltage dependence of pace-maker current kinetics. Rb+ addition to Tyrode solution has little effect on pace-maker current magnitude or time course positive to -90 mV, but does shift the reversal to more negative potentials. The available evidence suggests that the pace-maker current in Ba2+ Tyrode solution is an inward current activated by hyperpolarization. However, Ba2+ blocks an unknown fraction of the pace-maker current in a dose-dependent, and possibly voltage-dependent manner. Also, the presence of a slow component of pace-maker decay suggests that the standard Hodgkin-Huxley formalism for the analysis of pace-maker currents is inappropriate.</abstract><cop>England</cop><pub>The Physiological Society</pub><pmid>6875972</pmid><doi>10.1113/jphysiol.1983.sp014691</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection
subjects Action Potentials
Animals
Barium - pharmacology
Cell Membrane Permeability - drug effects
Cesium - pharmacology
Dogs
Dose-Response Relationship, Drug
Heart Conduction System - drug effects
In Vitro Techniques
Kinetics
Membrane Potentials - drug effects
Potassium - metabolism
Purkinje Fibers - drug effects
Purkinje Fibers - metabolism
Purkinje Fibers - physiology
Rubidium - pharmacology
title Actions of barium and rubidium on membrane currents in canine Purkinje fibres
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