Second‐generation antipsychotic quetiapine blocks voltage‐dependent potassium channels in coronary arterial smooth muscle cells

Author:

Zhuang Wenwen1,Mun Seo‐Yeong1,Park Minju1,Jeong Junsu1,Kim Hye Ryung1,Park Hongzoo2,Han Eun‐Taek3,Han Jin‐Hee3,Chun Wanjoo4,Li Hongliang5,Park Won Sun1ORCID

Affiliation:

1. Institute of Medical Sciences, Department of Physiology Kangwon National University School of Medicine Chuncheon South Korea

2. Institute of Medical Sciences, Department of Urology, Kangwon National University Hospital Kangwon National University School of Medicine Chuncheon South Korea

3. Department of Medical Environmental Biology and Tropical Medicine Kangwon National University School of Medicine Chuncheon South Korea

4. Department of Pharmacology Kangwon National University School of Medicine Chuncheon South Korea

5. Institute of Translational Medicine, Medical College, Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment for Senile Diseases Yangzhou University Yangzhou Jiangsu China

Abstract

AbstractVoltage‐dependent K+ (Kv) channels play an important role in restoring the membrane potential to its resting state, thereby maintaining vascular tone. In this study, native smooth muscle cells from rabbit coronary arteries were used to investigate the inhibitory effect of quetiapine, an atypical antipsychotic agent, on Kv channels. Quetiapine showed a concentration‐dependent inhibition of Kv channels, with an IC50 of 47.98 ± 9.46 μM. Although quetiapine (50 μM) did not alter the steady‐state activation curve, it caused a negative shift in the steady‐state inactivation curve. The application of 1 and 2 Hz train steps in the presence of quetiapine significantly increased the inhibition of Kv current. Moreover, the recovery time constants from inactivation were prolonged in the presence of quetiapine, suggesting that its inhibitory action on Kv channels is use (state)‐dependent. The inhibitory effects of quetiapine were not significantly affected by pretreatment with Kv1.5, Kv2.1, and Kv7 subtype inhibitors. Based on these findings, we conclude that quetiapine inhibits Kv channels in both a concentration‐ and use (state)‐dependent manner. Given the physiological significance of Kv channels, caution is advised in the use of quetiapine as an antipsychotic due to its potential side effects on cardiovascular Kv channels.

Funder

National Research Foundation of Korea

China Scholarship Council

Publisher

Wiley

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