Literature DB >> 6692500

Intra- and extracellular potassium activities, acetylcholine and resting potential in guinea pig atria.

C M Baumgarten, D H Singer, H A Fozzard.   

Abstract

Intracellular potassium activity in guinea pig left atria was measured using potassium ion-selective microelectrodes and conventional microelectrodes. The effects of extracellular potassium concentration and acetylcholine on both intracellular potassium activity and the relationship between the resting membrane potential and the potassium equilibrium potential were investigated. Intracellular potassium activity was 102.1 mM in bathing media with a potassium concentration of 5 mM. Neither increasing extracellular potassium concentration to 10 mM nor exposure to acetylcholine (2 x 10(-6) to 10(-3) M) significantly altered intracellular potassium activity. In contrast, intracellular potassium activity decreased to 92.9 mM in 2.5 mM potassium concentration solutions. Resting membrane potential was 18.6, 9.6, and 7.3 mV positive to the potassium equilibrium potential in 2.5, 5, and 10 mM potassium, respectively. Acetylcholine caused a significant hyperpolarization at each extracellular potassium activity, confirming that resting membrane potential was positive to the potassium equilibrium potential. Even after exposure to 10(-3) M acetylcholine, the resting membrane potential apparently remained positive to the potassium equilibrium potential. If potassium accumulates in extracellular clefts during acetylcholine exposure, the calculated potassium equilibrium potentials are too negative, and the resting membrane potential might closely approximate the potassium equilibrium potential under these conditions. Fading of the acetylcholine-induced hyperpolarization and overshoot of the resting membrane potential on washout of acetylcholine were observed and are consistent with an accumulation of potassium during exposure to acetylcholine. In 5.0 mM potassium bathing solution, preparation-to-preparation variability of resting membrane potential can largely be explained by variability of intracellular potassium activity.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1984        PMID: 6692500     DOI: 10.1161/01.res.54.1.65

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  6 in total

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Authors:  Antony J Workman; Andrew C Rankin
Journal:  Heart Rhythm       Date:  2010-04-08       Impact factor: 6.343

2.  Late Na channels in cardiac cells: the physiological role of background Na channels.

Authors:  C F Starmer; J Starobin; A O Grant
Journal:  Biophys J       Date:  1994-07       Impact factor: 4.033

3.  Intracellular sodium activity and its regulation in guinea-pig atrial myocardium.

Authors:  G X Wang; R Schmied; F Ebner; M Korth
Journal:  J Physiol       Date:  1993-06       Impact factor: 5.182

4.  The effects of various anions and cations on the regulation of pyruvate dehydrogenase complex activity from pig kidney cortex.

Authors:  T Pawelczyk; R A Easom; M S Olson
Journal:  Biochem J       Date:  1988-08-01       Impact factor: 3.857

5.  The fade of the response to acetylcholine at the rabbit isolated sino-atrial node.

Authors:  M R Boyett; A Roberts
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

6.  Pronounced cholinergic but only moderate purinergic effects in isolated atrial and ventricular heart muscle from cats.

Authors:  M Kemmer; H Jakob; H Nawrath
Journal:  Br J Pharmacol       Date:  1989-08       Impact factor: 8.739

  6 in total

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