Blockade of Kv1.5 channels by the antidepressant drug sertraline.
10.4196/kjpp.2016.20.2.193
- Author:
Hyang Mi LEE
1
;
Sang June HAHN
;
Bok Hee CHOI
Author Information
1. Department of Pharmacology, Institute for Medical Sciences, Chonbuk National University Medical School, Jeonju 54097, Korea. bhchoi@jbnu.ac.kr
- Publication Type:Original Article
- Keywords:
Kv1.5;
Open channel block;
Selective serotonin reuptake inhibitor;
Sertraline;
Shaker-type K+ channel
- MeSH:
Animals;
Arrhythmias, Cardiac;
Cardiovascular System;
Clone Cells;
Cricetinae;
Cricetulus;
Death, Sudden, Cardiac;
Female;
Inhibitory Concentration 50;
Ion Channels;
Kinetics;
Neurons;
Ovary;
Patch-Clamp Techniques;
Rats;
Serotonin;
Sertraline*;
Tail
- From:The Korean Journal of Physiology and Pharmacology
2016;20(2):193-200
- CountryRepublic of Korea
- Language:English
-
Abstract:
Sertraline, a selective serotonin reuptake inhibitor (SSRI), has been reported to lead to cardiac toxicity even at therapeutic doses including sudden cardiac death and ventricular arrhythmia. And in a SSRI-independent manner, sertraline has been known to inhibit various voltage-dependent channels, which play an important role in regulation of cardiovascular system. In the present study, we investigated the action of sertraline on Kv1.5, which is one of cardiac ion channels. The eff ect of sertraline on the cloned neuronal rat Kv1.5 channels stably expressed in Chinese hamster ovary cells was investigated using the whole-cell patch-clamp technique. Sertraline reduced Kv1.5 whole-cell currents in a reversible concentration-dependent manner, with an IC50 value and a Hill coefficient of 0.71 microM and 1.29, respectively. Sertraline accelerated the decay rate of inactivation of Kv1.5 currents without modifying the kinetics of current activation. The inhibition increased steeply between -20 and 0 mV, which corresponded with the voltage range for channel opening. In the voltage range positive to +10 mV, inhibition displayed a weak voltage dependence, consistent with an electrical distance delta of 0.16. Sertraline slowed the deactivation time course, resulting in a tail crossover phenomenon when the tail currents, recorded in the presence and absence of sertraline, were superimposed. Inhibition of Kv1.5 by sertraline was use-dependent. The present results suggest that sertraline acts on Kv1.5 currents as an open-channel blocker.
