Details

Autor(en) / Beteiligte

• HAUGAN, KETIL
• OLSEN, KRISTINE BOISEN
• HARTVIG, LINE
• PETERSEN, JØRGEN SØBERG
• HOLSTEIN-RATHLOU, NIELS-HENRIK
• HENNAN, JAMES K.
• NIELSEN, MORTEN SCHAK

Titel

The Antiarrhythmic Peptide Analog ZP123 Prevents Atrial Conduction Slowing During Metabolic Stress

Ist Teil von

• Journal of cardiovascular electrophysiology, 2005-05, Vol.16 (5), p.537-545

Ort / Verlag

350 Main Street , Malden , MA 02148-5018 , USA , and 9600 Garsington Road , Oxford OX4 2DQ , UK: Blackwell Science Inc

Erscheinungsjahr

2005

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Objective: As atrial conduction slowing is important in the pathogenesis of atrial reentry arrhythmias, a drug that increases atrial conduction or prevents atrial conduction slowing could serve to prevent atrial reentry arrhythmias. In this study, we investigated whether the novel stable antiarrhythmic peptide analog, ZP123, was able to prevent atrial conduction slowing. Methods: We examined the effect of ZP123 on metabolic stress‐induced changes in conduction velocity (CV) and on dynamic CV restitution in isolated left atria from male Sprague‐Dawley rats. We performed binding of ZP123 to a broad panel of 80 different cardiac and noncardiac ion channels and receptors and examined the effect of ZP123 on HERG channel conductance. Results: ZP123 dose‐dependently prevented metabolic stress‐induced atrial CV slowing at doses ranging from 1 nM to 10 μM. ZP123 did not affect CV during physiological conditions nor did it affect dynamic CV restitution. ZP123 had no effect on atrial contractility. ZP123 showed no or low affinity binding to all ion channels and receptors examined. ZP123 had no effects on HERG channel activity in concentrations that affected atrial conduction. The concentration of ZP123 giving maximal effect on atrial conduction (100 nM) inhibited the outward K+‐current by 2.7 ± 0.1%. Conclusion: ZP123 has no effects on atrial conduction during physiological conditions, but it selectively prevents atrial conduction slowing during metabolic stress.