Literature DB >> 9508805

The effect of polyamines on KATP channels in guinea-pig ventricular myocytes.

X W Niu1, R W Meech.   

Abstract

1. The effect of natural polyamines on KATP channels was studied using inside-out patches from guinea-pig ventricular myocytes. 2. At a holding potential of +40 mV, spermine at the intracellular membrane surface reduced the KATP channel open probability (Popen) in a dose-dependent manner. Half-maximal inhibition occurred at 29 microM with a Hill coefficient of 1.2. 3. The effect of spermine on Popen was not greatly influenced by the membrane potential but there appeared to be a small reduction in unitary current amplitude during strong depolarizations. 4. Analysis of KATP single channel kinetics showed that spermine inhibited the channel by decreasing the mean open time and introducing transitions to a long closed state. 5. Spermidine (0.1 mM) was found to have a similar effect to spermine. Putrescine (10 mM) was found to block more effectively at positive membrane potentials. Up to 20 mM arginine had no significant effect on KATP channels. 6. Our results indicate that natural polyamines influence native KATP channel gating in cardiac myocytes.

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Year:  1998        PMID: 9508805      PMCID: PMC2230875          DOI: 10.1111/j.1469-7793.1998.401bq.x

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


  42 in total

Review 1.  Cardiac energetics.

Authors:  C L Gibbs
Journal:  Physiol Rev       Date:  1978-01       Impact factor: 37.312

2.  Membrane current through adenosine-triphosphate-regulated potassium channels in guinea-pig ventricular cells.

Authors:  A Noma; T Shibasaki
Journal:  J Physiol       Date:  1985-06       Impact factor: 5.182

3.  Ion channel block by acetylcholine, carbachol and suberyldicholine at the frog neuromuscular junction.

Authors:  D C Ogden; D Colquhoun
Journal:  Proc R Soc Lond B Biol Sci       Date:  1985-09-23

4.  Control of rectification and gating of cloned KATP channels by the Kir6.2 subunit.

Authors:  S Shyng; T Ferrigni; C G Nichols
Journal:  J Gen Physiol       Date:  1997-08       Impact factor: 4.086

5.  ATP-sensitive K+ channels in rat ventricular myocytes are blocked and inactivated by internal divalent cations.

Authors:  I Findlay
Journal:  Pflugers Arch       Date:  1987-10       Impact factor: 3.657

6.  Voltage-dependent magnesium block of adenosine-triphosphate-sensitive potassium channel in guinea-pig ventricular cells.

Authors:  M Horie; H Irisawa; A Noma
Journal:  J Physiol       Date:  1987-06       Impact factor: 5.182

7.  Data transformations for improved display and fitting of single-channel dwell time histograms.

Authors:  F J Sigworth; S M Sine
Journal:  Biophys J       Date:  1987-12       Impact factor: 4.033

8.  Studies of the unitary properties of adenosine-5'-triphosphate-regulated potassium channels of frog skeletal muscle.

Authors:  A E Spruce; N B Standen; P R Stanfield
Journal:  J Physiol       Date:  1987-01       Impact factor: 5.182

9.  Inward-rectifying channels in isolated patches of the heart cell membrane: ATP-dependence and comparison with cell-attached patches.

Authors:  G Trube; J Hescheler
Journal:  Pflugers Arch       Date:  1984-06       Impact factor: 3.657

10.  Modulation of membrane protein lateral mobility by polyphosphates and polyamines.

Authors:  M Schindler; D E Koppel; M P Sheetz
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

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  2 in total

1.  Potassium inhibition of sodium-activated potassium (K(Na)) channels in guinea-pig ventricular myocytes.

Authors:  X W Niu; R W Meech
Journal:  J Physiol       Date:  2000-07-01       Impact factor: 5.182

2.  Functional K(ATP) channels in the rat retinal microvasculature: topographical distribution, redox regulation, spermine modulation and diabetic alteration.

Authors:  Eisuke Ishizaki; Masanori Fukumoto; Donald G Puro
Journal:  J Physiol       Date:  2009-03-16       Impact factor: 5.182

  2 in total

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