학술논문

Triggered activity in atrial myocytes is influenced by Na+/Ca2+ exchanger activity in genetically altered mice
Document Type
article
Source
Subject
Medical Physiology
Biomedical and Clinical Sciences
Heart Disease
Cardiovascular
Action Potentials
Animals
Calcium
Calcium Signaling
Female
Gene Expression
Heart Atria
Male
Membrane Potentials
Mice
Mice
Transgenic
Myocardial Contraction
Myocardium
Myocytes
Cardiac
Sarcoplasmic Reticulum
Sodium-Calcium Exchanger
Na+/Ca2+ exchanger
Afterdepolarizations
Atrial fibrillation
Atrial myocytes
Na(+)/Ca(2+) exchanger
Cardiorespiratory Medicine and Haematology
Cardiovascular System & Hematology
Biochemistry and cell biology
Cardiovascular medicine and haematology
Medical physiology
Language
Abstract
AimsIn atrial fibrillation, increased function of the Na+/Ca2+-exchanger (NCX) is one among several electrical remodeling mechanisms.Methods/resultsUsing the patch-clamp- and Ca2+ imaging-methods, we investigated atrial myocytes from NCX-homozygous-overexpressor (OE)- and heterozygous-knockout (KO)-mice and their corresponding wildtypes (WTOE; WTKO). NCX mediated Ca2+ extrusion capacity was reduced in KO and increased in OE. There was no evidence for structural or molecular remodeling. During a proarrhythmic pacing-protocol, the number of low amplitude delayed afterdepolarizations (DADs) was unaltered in OE vs. WTOE and KO vs. WTKO. However, DADs triggered full spontaneous action potentials (sAP) significantly more often in OE vs. WTOE (ratio sAP/DAD: OE:0.18±0.05; WTOE:0.02±0.02; p