期刊
CARDIOVASCULAR TOXICOLOGY
卷 15, 期 3, 页码 232-240出版社
HUMANA PRESS INC
DOI: 10.1007/s12012-014-9289-4
关键词
Azithromycin; Ventricular contraction; QT prolongation; I-Kr; Torsade de pointes; Atrioventricular block
资金
- Japan Science and Technology Agency [AS2116907E]
- Toho University School of Medicine [25-25]
- Toho University [H25-3, H26-2]
- Grants-in-Aid for Scientific Research [24591074, 15K09103] Funding Source: KAKEN
Azithromycin has been reported to increase the risk of death from cardiovascular causes among patients with high baseline risk. Since the information is still limited to bridge the gap between electrophysiological properties of azithromycin in vitro and cardiac death in patients, we initially assessed its electropharmacological effects in doses of 3 and 30 mg/kg, i.v., with the halothane-anesthetized dogs (n = 4). The low dose provided 5.2 times higher than the therapeutic concentration, whereas the high dose attained 17.0 times higher. The high dose delayed the ventricular repolarization in a reverse use-dependent manner, reflecting blockade of the rapid component of delayed rectifier K+ current, and the potency was relatively weak; namely, maximum change in QTc was +20 ms (+5.6 %). The high dose also induced the negative inotropic effect possibly through Ca2+ channel-independent pathway. In order to clarify proarrhythmic risk, 30 mg/kg, i.v., of azithromycin was examined with the chronic atrioventricular block dogs (n = 4). Azithromycin neither induced torsade de pointes nor affected beat-to-beat variability of repolarization. Thus, azithromycin can be considered to lack proarrhythmic potential, but caution has to be paid on its use for patients with left ventricular dysfunction.
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