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Carvedilol and vesnarinone: new antiarrhythmic approach in heart failure therapy

  
@article{APS7352,
	author = {Jian-Hua Chen and Kaichiro Kamiya and Itsuo Kodama},
	title = {Carvedilol and vesnarinone: new antiarrhythmic approach in heart failure therapy},
	journal = {Acta Pharmacologica Sinica},
	volume = {22},
	number = {3},
	year = {2016},
	keywords = {},
	abstract = {Carvedilol and vesnarinone are drugs attracting recent interest in the treatment of chronic heart failure. Electrophysiologic studies have revealed that these drugs cause a moderate prolongation of action potential duration (APD) of ventricular muscles with minimal \"reverse frequency-dependence\" through different ionic mechanisms. Carvedilol blocks L-type Ca2+ current (ICa), transient outward K+ current (Ito), and delayed rectifier K+ current (IK) preferentially for the rapidly activating component (IKr). Vesnarinone is a selective blocker of IK with a unique drug-channel interaction. From the voltage- and time-dependence of IK inhibition, vesnarinone is considered to bind the IK (mainly IKr) channel during the activated state and unbind during the closed state. These electropharmacologic profiles provide a new approach for the development of an ideal antiarrhythmic drugs in patients with structural heart diseases.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/7352}
}