Choline-Modulated Arsenic Trioxide-Induced Prolongation of Cardiac Repolarization in Guinea Pig
| Autor: | De-Li Dong, Hong-li Sun, Yun-Long Bai, Wenfeng Chu, Yan Liu, Xiao-Hui Wang, Jin Zhou, Baofeng Yang |
|---|---|
| Rok vydání: | 2006 |
| Předmět: |
Male
Patch-Clamp Techniques Guinea Pigs chemistry.chemical_element In Vitro Techniques Calcium Pharmacology Toxicology QT interval Arsenicals Calcium in biology Choline Guinea pig Electrocardiography chemistry.chemical_compound Arsenic Trioxide Animals Repolarization Myocyte Medicine Myocytes Cardiac Patch clamp business.industry Heart Oxides General Medicine Long QT Syndrome chemistry Female business |
| Zdroj: | Basic Toxicology. 98:381-388 |
| ISSN: | 1742-7843 1742-7835 |
| DOI: | 10.1111/j.1742-7843.2006.pto_319.x |
| Popis: | Arsenic trioxide (As(2)O(3)) has been found to be effective for relapsed or refractory acute promyelocytic leukaemia, but its clinical use is burdened by QT prolongation, Torsade de pointes tachycardias, and sudden cardiac death. The aim of the present study was to elucidate the ionic mechanisms of As(2)O(3)-induced abnormalities of cardiac electrophysiology and the therapeutic action of choline on As(2)O(3)-caused QT prolongation in guinea pig. Intravenous administration of As(2)O(3) prolonged the QT interval in a dose- and time-dependent manner in guinea pig hearts, and the QT prolongation could be modulated by choline. By using whole-cell patch clamp technique and confocal laser scanning microscopy, we found that As(2)O(3) significantly lengthened action potential duration measured at 50 and 90% of repolarization, enhanced L-type calcium currents (I(Ca-L)), inhibited delayed rectifier potassium currents (I(K)), and increased intracellular calcium concentration ([Ca(2+)](i)) in guinea pig ventricular myocytes. Choline corrected As(2)O(3)-mediated alterations of action potential duration, I(Ca-L) and [Ca(2+)](i), but had no effect on the I(K) inhibition. As(2)O(3) markedly disturbed the normal equilibrium of transmembrane currents (increasing I(Ca-L) and suppressing I(K)) in guinea pig cardiomyocyte, and induced prolongation of action potential duration, further degenerated into QT prolongation. Choline normalized QT interval abnormality and corrected lengthened action potential duration by inhibiting the elevated I(Ca-L) and [Ca(2+)](i) in ventricular myocytes during As(2)O(3) application. |
| Databáze: | OpenAIRE |
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