Tatsuno-Atoda H, Shigenobu K
Department of Biochemistry Meiji College of Pharmacy, University of Tokyo.
J Toxicol Sci. 1988 Feb;13(1):7-16. doi: 10.2131/jts.13.7.
Cardiac effects of ketanserin were examined mainly electrophysiologically with using rat and guinea pig heart muscle preparations. 10(-6)M ketanserin slightly antagonized the positive chronotropic but not inotropic action of serotonin in spontaneously beating guinea pig atria. Ketanserin, only at the concentration as high as 10(-4)M, produced slight rightward shift of the positive chronotropic but not inotropic dose-response curves for norepinephrine in guinea pig atria. In both rat and guinea pig atria, ketanserin per se produced negative chronotropic effect and slight prolongation of action potential duration (APD) at high concentrations, 0.1 or 0.3 mg/ml. In guinea pig ventricular preparation, 1 mg/ml of ketanserin did not affect the rate of rise of the action potential (+Vmax), action potential amplitude and APD. In rat ventricular free wall preparations, 1 mg/ml of ketanserin produced slight increase in APD without affecting the other action potential parameters. In rat ventricular papillary muscle and septum preparations, 0.3 mg/ml of ketanserin tended to produce a decrease in +Vmax and an increase in APD. However, since these changes were produced only at extremely high concentrations and slight in degree, it was concluded that ketanserin does not produce electrophysiological side effects of clinical relevance.
主要通过电生理学方法,利用大鼠和豚鼠的心肌标本,研究了酮色林对心脏的影响。10(-6)M的酮色林可轻微拮抗5-羟色胺对豚鼠自发搏动心房的正性变时作用,但不拮抗其正性变力作用。只有在高达10(-4)M的浓度下,酮色林才会使豚鼠心房去甲肾上腺素的正性变时剂量-反应曲线轻微右移,但不影响正性变力曲线。在大鼠和豚鼠的心房中,高浓度(0.1或0.3mg/ml)的酮色林本身会产生负性变时作用,并轻微延长动作电位时程(APD)。在豚鼠心室标本中,1mg/ml的酮色林不影响动作电位上升速率(+Vmax)、动作电位幅度和APD。在大鼠心室游离壁标本中,1mg/ml的酮色林使APD轻微增加,但不影响其他动作电位参数。在大鼠心室乳头肌和间隔标本中,0.3mg/ml的酮色林倾向于使+Vmax降低,使APD增加。然而,由于这些变化仅在极高浓度下产生且程度轻微,因此得出结论,酮色林不会产生具有临床相关性的电生理副作用。