
Professor Jules Hancox
DSc (Bristol), B.Sc.(Leeds), Ph.D.(St.And.)
Current positions
Professor of Cardiac Electrophysiology
School of Physiology, Pharmacology & Neuroscience
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Research interests
I am interested in elucidating the function of small membrane proteins (ion channels and exchangers) responsible for generating electrical activity of cells in the heart. I have a long-standing interest is the basis of the activity of a key part of the heart's electrical conducting system called the atrioventricular (AV) node, which co-ordinates the normal sequence of beating of the heart's upper and lower chambers (the atria and ventricles). We study single AV node cells using electrophysiological and imaging techniques. Recent work in collaboration with Clive Orchard , Andrew James and Prof Godfrey Smith (Glasgow) has been focused on the effects of acidosis, endothelin-1 and calcium-cycling on AV node cellular electrophysiology. Collaborative work with colleagues in Manchester (Prof Mark Boyett, Prof Henggui Zhang) and Kings College London (Dr Oleg Aslanidi) is focused on producing biophysically accurate models of the AV node and atrium.
I also have a long-standing interest in the electrophysiology and pharmacology of the hERG potassium channel, which plays an important role in drug-induced arrhythmias and in the congenital 'Short QT syndrome'. Using a combination of molecular and electrophysiological methods, we have studied mechanisms of hERG blockade by a range of drugs and identified in vitro the antiarrhythmic disopyramide as an effective inhibitor of the hERG mutant K+ channel responsible for one form of Short QT syndrome. We are also investigating different K+ channel mutations involved in other forms of this syndrome and are focused both on identifying pharmacological agents that can inhibit Short QT mutant channels and on identifying arrhythmia substrates in the syndrome (in collaboration with Prof Henggui Zhang and colleagues, Manchester).
Projects and supervisions
Research projects
Investigation of pharmacological modulators of TASK-1 K+ channels on electrophysiology of the atrioventricular node.
Principal Investigator
Managing organisational unit
School of Physiology, Pharmacology & NeuroscienceDates
01/02/2017 to 31/01/2020
INVESTIGATION OF CARDIAC LATE SODIUM CURRENT AS A THERAPEUTIC TARGET IN RETT SYNDROME
Principal Investigator
Managing organisational unit
School of Physiology, Pharmacology & NeuroscienceDates
01/10/2016 to 30/09/2019
Potassium channel linked short QT syndrome ¬タモ a mechanical as well as electrical disorder?
Principal Investigator
Managing organisational unit
School of Physiology, Pharmacology & NeuroscienceDates
23/07/2016 to 22/07/2019
New pathogenic mechanisms in the long QT syndrome: KCNE1 modulation of hERG.
Principal Investigator
Managing organisational unit
School of Physiology, Pharmacology & NeuroscienceDates
29/03/2015 to 28/09/2017
IP3 receptor modulation of the atrioventricular node
Principal Investigator
Managing organisational unit
School of Physiology, Pharmacology & NeuroscienceDates
01/10/2014 to 01/10/2016
Thesis supervisions
Structural requirements for high-affinity block of hERG K⁺ channels using electrophysiology and mutagenesis with simplified blockers
Supervisors
Characterisation of two short QT syndrome potassium channel mutations
Supervisors
Modulation of the herg potassium channel function by extracellular acidosis
Supervisors
Recapitulation of respiratory sinus arrhythmia suppresses alternans in guinea pig ventricular myocytes
Supervisors
Development of iPSC-derived human cardiac myocytes for the targeting of SK channels
Supervisors
Publications
Recent publications
07/02/2024In situ monolayer patch clamp of acutely stimulated human iPSC-derived cardiomyocytes promotes consistent electrophysiological responses to SK channel inhibition
Scientific Reports
Nitazene opioids and the heart
Journal of molecular and cellular cardiology plus
Human atrial fibrillation and genetic defects in transient outward currents: mechanistic insights from multi-scale computational models
Philosophical Transactions of the Royal Society B: Biological Sciences
Inhibition of the hERG Potassium Channel by a Methanesulphonate-Free E-4031 Analogue
Pharmaceuticals
New synthetic cannabinoids and the potential for cardiac arrhythmia risk
Journal of Molecular and Cellular Cardiology