Intracellular protons inhibit inward rectifier K+ channel of guinea-pig ventricular cell membrane.

Pflügers Archiv : European journal of physiology
H ItoE Carmeliet

Abstract

The effect of intracellular protons (Hi+) on the inward rectifier K+ channel of the guinea-pig ventricular cell membrane was examined, using the patch-clamp technique. The inward single-channel current was recorded in "inside-out" and "outside-out" patch configurations, while the pH of the solution perfusing the intra- and extracellular side, respectively, was varied. Low intracellular pH (pHi), but not low extracellular pH, inhibited the channel. Low pHi reduced the unit amplitude, which was about 20% smaller at pHi 6.0 than that at pHi 7.4 at every voltage tested. The slope conductance decreased from 41.7 pS at pHi 7.4 to 35.1 pS at pHi 6.0. Low pHi also reduced the channel activity without apparent voltage dependence. The concentration/response curve indicated the half-maximum inhibition at pHi 6.11 and a Hill coefficient of 2.52. Lowering the pHi from 7.4 to 6.0 did not affect the distributions of the open times and the closed times below 50 ms, while the time constant of the histogram constructed from closings longer than 50 ms was approximately doubled. These results indicate that the inward rectifier K+ channel in ventricular myocytes is inhibited by H+ from the intracellular side. This might contribute to the depolariza...Continue Reading

References

Mar 1, 1987·Pflügers Archiv : European journal of physiology·O Christensen, T Zeuthen
Aug 1, 1984·Pflügers Archiv : European journal of physiology·A L Blatz
Aug 1, 1981·Pflügers Archiv : European journal of physiology·O P HamillF J Sigworth
Sep 1, 1982·Pflügers Archiv : European journal of physiology·Y Kurachi

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Citations

Jan 1, 1996·Neuroscience Research·K I Takahashi, D R Copenhagen
Feb 1, 1996·Progress in Neurobiology·J W Deitmer, C R Rose
Sep 21, 2001·British Journal of Pharmacology·M LongobardoC Valenzuela
Mar 10, 1998·The Journal of Physiology·M TareT B Bolton
Sep 8, 1998·The Journal of Physiology·E A AielloH E Cingolani
Aug 26, 2009·Journal of Molecular and Cellular Cardiology·Justus M B Anumonwo, Anatoli N Lopatin
May 6, 2004·Basic & Clinical Pharmacology & Toxicology·De-Li DongBao-Feng Yang
Mar 31, 2007·Journal of the American College of Cardiology·David N KenigsbergSubramaniam C Krishnan
May 7, 2016·International Heart Journal·Ichiro Watanabe, Leonard S Gettes
Apr 5, 2003·Stroke; a Journal of Cerebral Circulation·Naohiko SantaMitsuo Iida
Sep 16, 2000·Molecular Membrane Biology·C Brechenmacher, J L Rodeau
Feb 1, 1997·The American Journal of Physiology·A RichJ L Rae
Dec 9, 1998·The American Journal of Physiology·C M McNicholasG Giebisch
Jun 14, 2002·American Journal of Physiology. Heart and Circulatory Physiology·Kimiaki KomukaiClive H Orchard
Jul 9, 2008·Progress in Biophysics and Molecular Biology·David Nickerson, Martin Buist

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