Literature DB >> 6090649

High selectivity of calcium channels in single dialysed heart cells of the guinea-pig.

K S Lee, R W Tsien.   

Abstract

Membrane currents and action potentials were recorded in single ventricular cells obtained from guinea-pig hearts by enzymatic dissociation. Ca2+ channel currents carried by Ba2+ or Ca2+ were recorded with a suction pipette (5-10 microns diameter) for voltage clamp and internal dialysis. Currents through Na+, K+ and non-selective monovalent cation channels were suppressed by suitable holding potentials and external and internal solutions. The dialysis method allowed exchange within minutes of alkali metal cations (e.g. Cs+) and small molecules (e.g. quaternary derivatives of lidocaine and verapamil). Nevertheless, Ca2+ channels remained functional for considerable periods, typically 20 min and sometimes more than 1 h. With Ba2+ outside and Cs+ inside, current flow through Ca2+ channels changed from inward to outward at strongly positive levels beyond a clear-cut reversal potential Erev. Several methods for defining Erev were in close agreement: (1) zero-crossing of leak-subtracted peak current, (2) inversion of time-dependent current changes during channel activation or inactivation, (3) inversion of drug-sensitive current as defined by channel blockers such as Cd2+ or D-600. Erev varied with external Ba2+ or internal Cs+. Erev increased by 29 mV per 10-fold increase in Ba2+. Interpreted with constant-field theory, Erev values correspond to PBa/PCs of approximately 1360. With 5 mM-Ca2+ outside and 151 mM-Cs+ inside, Ca2+ channel current reversed near + 75 mV, corresponding to PCa/PCs approximately 6000. Earlier measurements of Erev (Lee & Tsien, 1982) suggest that PCa/PK greater than 1000. At strongly positive membrane potentials where channel activation is maximal, the Ca2+ channel current-voltage relationship is strongly non-linear, with conductance increasing on either side of an inflexion point near Erev. Activation of inward or outward currents through Ca2+ channels follows a sigmoid time course, as expected if activation were a multi-step process.

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Year:  1984        PMID: 6090649      PMCID: PMC1193410          DOI: 10.1113/jphysiol.1984.sp015374

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  37 in total

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Journal:  Annu Rev Physiol       Date:  1982       Impact factor: 19.318

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Journal:  Nature       Date:  1982-06-10       Impact factor: 49.962

4.  Single channel Ca2+ currents in Helix pomatia neurons.

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5.  Reversal of current through calcium channels in dialysed single heart cells.

Authors:  K S Lee; R W Tsien
Journal:  Nature       Date:  1982-06-10       Impact factor: 49.962

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Journal:  J Physiol       Date:  1982-10       Impact factor: 5.182

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Journal:  J Physiol       Date:  1982-08       Impact factor: 5.182

9.  Does the organic calcium channel blocker D600 act from inside or outside on the cardiac cell membrane?

Authors:  J Hescheler; D Pelzer; G Trube; W Trautwein
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10.  Block of outward current in cardiac Purkinje fibers by injection of quaternary ammonium ions.

Authors:  R S Kass; T Scheuer; K J Malloy
Journal:  J Gen Physiol       Date:  1982-06       Impact factor: 4.086

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  92 in total

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Authors:  K Ono; H A Fozzard
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9.  Energy variational analysis of ions in water and channels: Field theory for primitive models of complex ionic fluids.

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10.  Permeation and gating in CaV3.1 (alpha1G) T-type calcium channels effects of Ca2+, Ba2+, Mg2+, and Na+.

Authors:  Nilofar Khan; I Patrick Gray; Carlos A Obejero-Paz; Stephen W Jones
Journal:  J Gen Physiol       Date:  2008-08       Impact factor: 4.086

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