期刊
CHANNELS
卷 16, 期 1, 页码 173-184出版社
TAYLOR & FRANCIS INC
DOI: 10.1080/19336950.2022.2106025
关键词
Long QT syndrome; propranolol; induced pluripotent stems
资金
- NHLBI [3R01HL123483]
- NSTEM [C028563]
Congenital long QT syndrome (LQTS) is a common cardiac channelopathy treated with beta blockers. However, the effectiveness of this treatment has been questioned for LQT3 patients. This study found that the beta blocker propranolol selectively inhibits the ion channel current expressed by specific mutations, suggesting its protective effect in LQT3 treatment is due in part to its modulation of the ion channel current.
The congenital long QT syndrome (LQTS), one of the most common cardiac channelopathies, is characterized by delayed ventricular repolarization underlying prolongation of the QT interval of the surface electrocardiogram. LQTS is caused by mutations in genes coding for cardiac ion channels or ion channel-associated proteins. The major therapeutic approach to LQTS management is beta blocker therapy which has been shown to be effective in treatment of LQTS variants caused by mutations in K+ channels. However, this approach has been questioned in the treatment of patients identified as LQTS variant 3(LQT3) patients who carry mutations in SCN5A, the gene coding for the principal cardiac Na+ channel. LQT3 mutations are gain of function mutations that disrupt spontaneous Na+ channel inactivation and promote persistent or late Na+ channel current (I-NaL) that delays repolarization and underlies QT prolongation. Clinical investigation of patients with the two most common LQT3 mutations, the Delta KPQ and the E1784K mutations, found beta blocker treatment a useful therapeutic approach for managing arrhythmias in this patient population. However, there is little experimental data that reveals the mechanisms underlying these antiarrhythmic actions. Here, we have investigated the effects of the beta blocker propranolol on I-NaL expressed by Delta KPQ and E1784K channels in induced pluripotent stem cells derived from patients carrying these mutations. Our results indicate that propranolol preferentially inhibits I-NaL expressed by these channels suggesting that the protective effects of propranolol in treating LQT3 patients is due in part to modulation of I-NaL.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据