Lang J, Timour Q, Lançon J P, Aupetit J F, Faucon G
Laboratoire de Pharmacologie Médicale, Lyon, France.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Aug;338(2):196-201. doi: 10.1007/BF00174870.
The effects of a calcium channel blocker, verapamil, on the atrioventricular (AV) node, are antagonized by calcium, intravenously infused, so long as plasma calcium concentration does not reach 5.0 or 5.5 mmol.l-1, as previously shown. Beyond this, the antagonistic effects decrease progressively, so that there is a bell-shaped relationship between dose (or concentration) and response. The purpose of the present experiments has been to investigate a possible similar dose-response curve with a calcium channel activator, Bay k 8644. The study was carried out in anaesthetized, atropinized dogs, with cardiac pacing. The His bundle potentials were recorded by endocavitary electrodes and the AV nodal effective refractory period was measured by the extrastimulus method. Verapamil impaired AV nodal conduction and additional infusion of Bay k 8644 at a rate of 1 microgram.kg-1.min-1 partly antagonized this effect. Increasing the infusion rate of Bay k 8644 to 5 micrograms.kg-1.min-1 did not further increase but reduced the antagonism. In other experiments where infusion of calcium had partly antagonized the effect of verapamil, Bay k 8644 infused after cessation of calcium infusion did not further antagonize the effect of verapamil which even became again increasingly marked. Consequently, in the AV node depressed by a calcium channel blocker, Bay k 8644 gives rise to a bell-shaped dose-response relationship of its verapamil-antagonistic action and the reversal of this action by high doses of Bay k 8644 can be observed after both administration of either calcium or Bay k 8644 in moderate doses.
如先前所示,只要血浆钙浓度未达到5.0或5.5 mmol·l-1,静脉输注钙就能拮抗钙通道阻滞剂维拉帕米对房室(AV)结的作用。超过此浓度,拮抗作用逐渐减弱,因此剂量(或浓度)与反应之间呈钟形关系。本实验的目的是研究钙通道激活剂Bay k 8644是否可能有类似的剂量反应曲线。该研究在麻醉、阿托品化且进行心脏起搏的犬身上进行。通过心腔内电极记录希氏束电位,并采用额外刺激法测量房室结有效不应期。维拉帕米损害房室结传导,以1微克·千克-1·分钟-1的速率额外输注Bay k 8644可部分拮抗这种作用。将Bay k 8644的输注速率增加至5微克·千克-1·分钟-1并未进一步增强反而减弱了这种拮抗作用。在其他实验中,钙输注部分拮抗了维拉帕米的作用,停止钙输注后输注Bay k 8644并未进一步拮抗维拉帕米的作用,甚至其作用再次变得越来越明显。因此,在被钙通道阻滞剂抑制的房室结中,Bay k 8644对其维拉帕米拮抗作用产生钟形剂量反应关系,并且在中等剂量的钙或Bay k 8644给药后,高剂量的Bay k 8644均可观察到这种作用的逆转。