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

โœ Scribed by Hiroyuki Ito; Johan Vereecke; Edward Carmeliet


Publisher
Springer
Year
1992
Tongue
English
Weight
774 KB
Volume
422
Category
Article
ISSN
0031-6768

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โœฆ Synopsis


The effect of intracellular protons (Hi +) on the inward rectifier K + channel of the guinea-pig ventricular ceil 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 intraand extracellular side, respectively, was varied. Low intracellular pH (pHi) , but not low extracellular pH, inhibited the channel. Low pH i reduced the unit amplitude, which was about 20~ smaller at pH i 6.0 than that at pH i 7.4 at every voltage tested. The slope conductance decreased from 41.7 pS at pH i 7.4 to 35.1 pS at pH i 6.0. Low pH i also reduced the channel activity without apparent voltage dependence. The concentration/response curve indicated the half-maximum inhibition at pH i 6.11 and a Hill coefficient of 2.52. Lowering the pH i 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 depolarization of the resting membrane potential induced by intracellular acidosis during myocardial ischaemia.


๐Ÿ“œ SIMILAR VOLUMES


Pinacidil activates the ATP-sensitive K+
โœ Zheng Fan; Keiko Nakayama; Masayasu Hiraoka ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer ๐ŸŒ English โš– 966 KB

Patch-clamp techniques were used to study the effects of pinacidil on the adenosine-5'-triphosphate (ATP)sensitive K + channel current in guinea-pig ventricular myocytes. In inside-out patches, the ATP-sensitive K + channel current could be recorded at an internal ATP concentration of 0.5 mM or tess