L. Virag et al., The slow component of the delayed rectifier potassium current in undiseased human ventricular myocytes, CARDIO RES, 49(4), 2001, pp. 790-797
Citations number
25
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective: The purpose of this study was to investigate the properties of t
he slow component of the delayed rectifier potassium current (I-Ks) in myoc
ytes isolated from undiseased human left ventricles. Methods: The whole-cel
l configuration of the patch-clamp technique was applied in 58 left ventric
ular myocytes from 15 hearts at 37 degreesC. Nisoldipine (1 muM) was used t
o block inward calcium current (I-Ca) and E-4031 (1-5 muM) was applied to i
nhibit the rapid component of the delayed rectifier potassium current (I-Ks
). Results: In 31 myocytes an E-4031 insensitive, but L-735,821 and chroman
ol 293B sensitive, tail current was identified which was attributed to the
slow component of I-K (I-Ks). Activation of I-Ks was slow (tau = 903 +/- 10
1 ms at 50 mV, n = 24), but deactivation of the current was relatively rapi
d ( tau =122.4 +/- 11.7 ms at -40 mV, n = 19). The activation of I-Ks was v
oltage independent but its deactivation showed clear voltage dependence. Th
e deactivation was faster at negative voltages (about 100 ms at -50 mV) and
slower at depolarized potentials (about 300 ms at 0 mV). In six cells, the
reversal potential was -81.6 +/- 2.8 mV on an average which is close to th
e K+ equilibrium potential suggesting K+ as the main charge carrier. Conclu
sion: In undiseased human ventricular myocytes, I-Ks exhibits slow activati
on and fast deactivation kinetics. Therefore, in humans I-Ks differs from t
hat reported in guinea pig, and it best resembles I-Ks described in dog and
rabbit ventricular myocytes. (C) 2001 Elsevier Science B.V. All rights res
erved.