Coldwell M C, Howlett D R
Beecham Pharmaceutical Research Division, Medicinal Research Centre, Harlow, Essex, U.K.
Biochem Pharmacol. 1988 Nov 1;37(21):4105-10. doi: 10.1016/0006-2952(88)90102-5.
Experiments have been performed in order to investigate the calcium and exposure time dependency of cromakalim (BRL 34915)-stimulated rubidium efflux in rabbit isolated mesenteric artery. Removal of calcium from the bathing medium prolonged the effects of cromakalim on rubidium efflux. Lanthanum was without effect on cromakalim-induced efflux whilst high concentrations of nifedipine were required to produce a significant inhibitory effect. Decreasing the exposure time to cromakalim, either in the presence or absence of calcium, led to a progressive loss of the response. However, significant increases in rubidium efflux rate were observed after very short exposures (15 sec) to the drug. In normal medium, exposure to cromakalim resulted in an inhibition of a second response when the drug was reapplied. Blockade by tetraethylammonium of the initial rubidium efflux response to cromakalim did not reverse the inhibition of the second response. These results suggest that the stimulation by cromakalim of rubidium efflux in rabbit isolated mesenteric artery is independent of calcium influx and requires only a short initial exposure to the drug in order to develop a response. The development and maintenance of the response after the removal of the drug suggest that cromakalim does not directly interact with the potassium channel through which rubidium efflux enhancement is observed.
为了研究在兔离体肠系膜动脉中,克罗卡林(BRL 34915)刺激的铷外流对钙和暴露时间的依赖性,已进行了实验。从浴液中去除钙可延长克罗卡林对铷外流的作用。镧对克罗卡林诱导的外流没有影响,而需要高浓度的硝苯地平才能产生显著的抑制作用。无论有无钙存在,缩短对克罗卡林的暴露时间都会导致反应逐渐丧失。然而,在对该药物进行非常短时间的暴露(15秒)后,观察到铷外流速率显著增加。在正常培养基中,当再次应用克罗卡林时,暴露于该药物会导致第二次反应受到抑制。用四乙铵阻断最初对克罗卡林的铷外流反应并不能逆转对第二次反应的抑制。这些结果表明,在兔离体肠系膜动脉中,克罗卡林对铷外流的刺激与钙内流无关,并且仅需要对该药物进行短时间的初始暴露即可产生反应。去除药物后反应的发展和维持表明,克罗卡林并不直接与观察到铷外流增强所通过的钾通道相互作用。