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Effects of imipramine on the transient outward current in rabbit atrial single cells
Author(s) -
Delpón Eva,
Tamargo Juan,
SánchezChapula José
Publication year - 1992
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1992.tb14357.x
Subject(s) - imipramine , repolarization , depolarization , chemistry , medicine , biophysics , electrophysiology , endocrinology , membrane potential , resting potential , biology , biochemistry , alternative medicine , pathology
1 . The effects of imipramine on action potential characteristics and transient outward potassium current ( I t ) of rabbit isolated atrial myocytes were studied using the whole‐cell configuration of the patch‐clamp technique. 2 Imipramine, 3 μ m , decreased action potential amplitude and lengthened the action potential duration measured at 50% of repolarization, whereas it did not modify the final phase of repolarization or the resting membrane potential. These results are similar to those reported in multicellular rabbit atrial preparations. 3 Imipramine, 0.1–100 μ m , induced a concentration‐dependent inhibition of the peak amplitude of I t , a shortening of the time to peak current and an increase in the inactivation rate. The acceleration of the current inactivation is to a major extent responsible for the decrease in the integral of the outward current measured at 50 ms after the start of the pulse. 4 The drug‐induced block of I t was not associated with changes in the voltage‐dependence of the steady‐state inactivation curve or in the process of recovery from inactivation of the current. Extrapolation to zero block shows that imipramine did not block I t before its activation at the onset of the depolarization. These results suggested that imipramine does not affect the inactivated or the resting state of I t channels. 5 It is concluded that in rabbit isolated atrial cells, imipramine inhibits I t and that this effect is responsible for the lengthening of the action potential duration produced by this drug.