Action potential clamp characterization of the S631A hERG mutation associated with short QT syndrome

Content Provider	Semantic Scholar
Author	Butler, Andrew Zhang, Yihong Stuart, Alan Graham Dempsey, Christopher E. Hancox, Jules C.
Copyright Year	2018
Abstract	The hERG potassium channel is critical to normal repolarization of cardiac action potentials (APs) and loss- and gain-of-function hERG mutations are associated, respectively, with long and short QT syndromes, pathological conditions that can lead to arrhythmias and sudden death. hERG current (IhERG ) exhibits uniquely fast inactivation involving conformational changes to the channel pore. The S631A hERG pore mutation was originally engineered to interrogate hERG channel inactivation, but has very recently been found in a family with short QT syndrome (SQTS). Accordingly, this study characterized the effects of the S631A mutation on IhERG profile during ventricular, atrial, and Purkinje fiber (PF) AP waveforms, using patch clamp recording from hERG expressing HEK 293 cells at 37°C. Under conventional voltage clamp, the current-voltage (I-V) relation for IhERG exhibited a marked right-ward shift in the region of negative slope at positive membrane potentials. Under ventricular AP clamp, the S631A mutation resulted in augmented IhERG , which also peaked much earlier during the AP plateau than did wild-type (WT) IhERG . Instantaneous I-V relations showed a marked positive shift in peak repolarizing current during the ventricular AP in the S631A setting, while the instantaneous conductance-voltage relation showed an earlier and more sustained rise in S631A compared to WT IhERG conductance during ventricular repolarization. Experiments with atrial and PF APs in each case also showed augmented and positively shifted IhERG in the S631A setting, indicating that the S631A mutation is likely to accelerate repolarization in all three cardiac regions. Ventricular AP clamp experiments showed retained effectiveness of the class Ia antiarrhythmic drug quinidine (1 μmol/L) against S631A IhERG . Quinidine is thus likely to be effective in reducing excessively fast repolarization in SQTS resulting from the S631A hERG mutation.
File Format	PDF HTM / HTML
DOI	10.14814/phy2.13845
PubMed reference number	30175559
Journal	Medline
Volume Number	6
Alternate Webpage(s)	https://research-information.bristol.ac.uk/files/167840624/Butler_et_al_2018_Physiological_Reports.pdf
Alternate Webpage(s)	https://research-information.bris.ac.uk/files/167840624/Butler_et_al_2018_Physiological_Reports.pdf
Alternate Webpage(s)	https://doi.org/10.14814/phy2.13845
Journal	Physiological reports
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article