Delgado C, Tamargo J, Tejerina T, Valenzuela C
Br J Pharmacol. 1987 Mar;90(3):575-82. doi: 10.1111/j.1476-5381.1987.tb11208.x.
The effects of 5-hydroxy-propafenone (5-OH-P), an active metabolite of propafenone, were studied on isolated atrial muscle fibres obtained from non-treated guinea-pigs and from animals pretreated with 5-OH-P, 3 mg kg-1, for 28 days. In untreated atria 5-OH-P, 10(-8) M-10(-4) M, produced a dose-dependent decrease in amplitude and df/dtmax and reduced the amplitude of the slow contractions induced by isoprenaline and histamine in high K+ media. 5-OH-P also produced a dose-dependent decrease in atrial rate, prolonged the sinus node recovery time and reduced the maximum chronotropic responses to isoprenaline. In untreated atrial muscle fibres 5-OH-P depressed action potential amplitude and Vmax, reduced the resting membrane potential and prolonged the action potential duration (ADP) and the effective refractory period, lengthening the effective refractory period relative to APD. Pretreatment with 5-OH-P reduced atrial rate and increased contractile force, but did not modify the action potential characteristics from the values obtained in untreated atria. Further addition of 5-OH-P produced similar but more marked changes than in untreated atria. It is concluded that in guinea-pig isolated atrial muscle fibres 5-OH-P, like propafenone, exhibits class I (membrane stabilizing), class II (antisympathetic) and class IV (Ca antagonistic) antiarrhythmic actions. Therefore, this metabolite could be responsible, at least in part, for some of the antiarrhythmic effects previously attributed to propafenone.
研究了普罗帕酮的活性代谢物5-羟基普罗帕酮(5-OH-P)对从未经处理的豚鼠以及用3mg/kg 5-OH-P预处理28天的动物所分离出的心房肌纤维的作用。在未经处理的心房中,10⁻⁸M - 10⁻⁴M的5-OH-P可使振幅和最大上升速率(df/dtmax)呈剂量依赖性降低,并减弱高钾培养基中异丙肾上腺素和组胺诱导的慢收缩振幅。5-OH-P还可使心房率呈剂量依赖性降低,延长窦房结恢复时间,并降低对异丙肾上腺素的最大变时反应。在未经处理的心房肌纤维中,5-OH-P降低动作电位振幅和最大上升速度(Vmax),降低静息膜电位,延长动作电位持续时间(ADP)和有效不应期,相对于ADP延长有效不应期。用5-OH-P预处理可降低心房率并增加收缩力,但并未改变动作电位特征,其特征与未经处理的心房中的值相同。进一步添加5-OH-P所产生的变化与未经处理的心房相似,但更为明显。得出的结论是,在豚鼠分离的心房肌纤维中,5-OH-P与普罗帕酮一样,具有I类(膜稳定)、II类(抗交感神经)和IV类(钙拮抗)抗心律失常作用。因此,这种代谢物可能至少部分地是先前归因于普罗帕酮的一些抗心律失常作用的原因。