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Anti-arrhythmic action of cycloprotobuxine-A

  
@article{APS5581,
	author = {Yong-xiao Wang and Jin-wen Liu and Yue-hua Tan and Bao-heng Sheng},
	title = {Anti-arrhythmic action of cycloprotobuxine-A},
	journal = {Acta Pharmacologica Sinica},
	volume = {10},
	number = {5},
	year = {2016},
	keywords = {},
	abstract = {Cycloprotobuxine-A (CPB-A) 1-4 mg/kg (1/100-1/25 LD50) produced therapeutic and prophylactic effects which were found to be dose-dependent on experimental arrhythmias induced by BaCl2, aconitine and chloroform. Given at equitoxic doses, the anti-arrhythmic action of CPB-A was as potent as cyclovirobuxine-D (CVB-D) and amiodarone (Amio). However, its therapeutic index (LD50/ED50) was 1.8 times that of CVB-D and 1.2 times that of Amio. The most pronounced effects of CPB-A (0.3-30 mumol/L) on the electrophysiology of ventricular muscle of guinea pig were the lengthening of APD50, APD90 and ERP. This may contribute to its anti-arrhythmic action and suggests that CPB-A most likely belongs to class III anti-arrhythmic drugs (prolongation of APD). Perfused with the same concentration (3 mumol/L), CPB-A brought about more significant increases in APD50, APD90 and ERP than CVB-D and Amio did.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/5581}
}