Journal
BRITISH JOURNAL OF PHARMACOLOGY
Volume 176, Issue 8, Pages 1090-1105Publisher
WILEY
DOI: 10.1111/bph.14577
Keywords
-
Categories
Funding
- Research Council of the KU Leuven [GOA/14/011]
- Fund for Scientific Research Flanders [FWO: G.0765.13]
Ask authors/readers for more resources
Background and purposeThe citrus flavanone hesperetin has been proposed for the treatment of several human pathologies, but its cardiovascular actions remain largely unexplored. Here, we evaluated the effect of hesperetin on cardiac electrical and contractile activities, on aortic contraction, on the wild-type voltage-gated Na(V)1.5 channel, and on a channel mutant (R1623Q) associated with lethal ventricular arrhythmias in the long QT syndrome type 3 (LQT3). Experimental approachWe used cardiac surface ECG and contraction force recordings to evaluate the effects of hesperetin in rat isolated hearts and aortic rings. Whole-cell patch clamp was used to record Na(V)1.5 currents (I-Na) in rat ventricular cardiomyocytes and in HEK293T cells expressing hNa(V)1.5 wild-type or mutant channels. Key resultsHesperetin increased the QRS interval and heart rate and decreased the corrected QT interval and the cardiac and aortic contraction forces at concentrations equal or higher than 30molL(-1). Hesperetin blocked rat and human Na(V)1.5 channels with an effective inhibitory concentration of approximate to 100molL(-1). This inhibition was enhanced at depolarized holding potentials and higher stimulation frequency and was reduced by the disruption of the binding site for local anaesthetics. Hesperetin increased the rate of inactivation and preferentially inhibited I-Na during the slow inactivation phase, these effects being more pronounced in the R1623Q mutant. Conclusions and implicationsHesperetin preferentially inhibits the slow inactivation phase of I-Na, more markedly in the mutant R1623Q. Hesperetin could be used as a template to develop drugs against lethal cardiac arrhythmias in LQT3.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available