Kocić I, Korolkiewicz K Z
Department of Pharmacology, Medical University of Gdańsk, Poland.
Pharmacol Res. 1998 Jan;37(1):67-73. doi: 10.1006/phrs.1997.0270.
The aim of this study was to examine the influence of pre-treatment with rimalkalim (formerly HOE 234), an activator of ATP-sensitive K+ channels (KATP), on the chronotropic, inotropic and electrophysiological effects of digoxin in the guinea pig heart. To study these effects we used spontaneously beating right atria and isolated papillary muscles from the guinea pig heart. The following parameters were measured: the heart rate (b.p.m.), force of contraction (Fc), rate of rise (+dF/dt) and rate of fall (-dF/dt) of force of contraction, time to peak contraction (ttp) and time to 10% of total amplitude of force (tt10), action potential (RP, APA, APD, Vmax) and effective refractory period (ERP). Apart from the positive inotropic effect, digoxin induced negative chronotropic action at the concentration of 30 microM. Digoxin also significantly decreased APD50 and APD90 duration and reduced APA and RP. Rimalkalim itself, has similar electrophysiological and chronotropic effects to digoxin, but opposite to digoxin, a negative inotropic action and hyperpolarisation of the isolated tissue. After pre-treatment with rimalkalim (1 microM), the significant potentiation of maximum positive inotropic effect (Emax) of digoxin has been observed, as well as a significant shortening of the duration of ttp, tt10 and ERP when compared with the values obtained with digoxin alone. Furthermore, a significant increase in Vmax occurred, compared to the value obtained with rimalkalim. Glibenclamide (1 microM), a selective inhibitor of ATP-sensitive K+ channels, added to rimalkalim, prevented the changes in digoxin action observed after pre-treatment with rimalkalim. The results demonstrate significant influence of pre-treatment with rimalkalim on digoxin-induced inotropic and electrophysiological effects in the guinea pig heart. An abolishing action of glibenclamide on this effect of rimalkalim suggests that an activation of ATP-sensitive K+ channels might cause these changes.
本研究的目的是考察瑞马卡林(原名HOE 234,一种ATP敏感性钾通道(KATP)激活剂)预处理对豚鼠心脏中地高辛变时、变力及电生理效应的影响。为研究这些效应,我们使用了豚鼠心脏的自发搏动右心房和分离的乳头肌。测量了以下参数:心率(次/分钟)、收缩力(Fc)、收缩力上升速率(+dF/dt)和下降速率(-dF/dt)、收缩峰值时间(ttp)和收缩力总幅度10%的时间(tt10)、动作电位(RP、APA、APD、Vmax)和有效不应期(ERP)。除正性变力作用外,地高辛在30微摩尔浓度时可诱发负性变时作用。地高辛还显著缩短了APD50和APD90的时程,并降低了APA和RP。瑞马卡林本身具有与地高辛相似的电生理和变时效应,但与地高辛相反,它对分离组织具有负性变力作用和超极化作用。用瑞马卡林(1微摩尔)预处理后,观察到地高辛最大正性变力效应(Emax)显著增强,与单独使用地高辛时相比,ttp、tt10和ERP的时程也显著缩短。此外,与瑞马卡林单独作用时相比,Vmax显著增加。加入瑞马卡林的同时添加格列本脲(1微摩尔),一种ATP敏感性钾通道的选择性抑制剂,可阻止瑞马卡林预处理后观察到的地高辛作用变化。结果表明,瑞马卡林预处理对豚鼠心脏中地高辛诱发的变力和电生理效应有显著影响。格列本脲对瑞马卡林这一效应的消除作用表明,ATP敏感性钾通道的激活可能导致了这些变化。