Doggrell S A
Department of Pharmacology, School of Medicine, University of Auckland, New Zealand.
J Pharmacol Methods. 1988 Apr;19(2):93-107. doi: 10.1016/0160-5402(88)90030-7.
Three consecutive challenges of the rat isolated left atria with electrical stimulation and then electrical stimulation and isoprenaline were made. The responses to electrical stimulation decreased and the responses to isoprenaline increased with consecutive challenges such that the maximal combined response to electrical stimulation and isoprenaline remained constant. The sensitivity (pD2) to isoprenaline decreased with successive challenges. Thus, in studies of the effects of drugs on the responses to electrical stimulation and isoprenaline, it is necessary to perform parallel experiments with untreated atria to monitor changes in the responses unrelated to the addition of drug. Analysis of the effects of procaine, metoprolol, and propranolol on the responses to electrical stimulation and/or isoprenaline demonstrated distinct contractile manifestations of beta-adrenoceptor blocking and membrane stabilizing activity. The beta-adrenoceptor blocking activity of metroprolol at 10(-7) M and propranolol (3 X 10(-9)-10(-6) M) consisted of parallel rightward shifts of the concentration-response curves to isoprenaline alone. There were three components to the membrane-stabilizing action of drugs: first, there was a decrease in the responses to electrical stimulation alone, which was observed with procaine at greater than or equal to 10(-4) M and propranolol at greater than or equal to 3 X 10(-9) M, second, there was a small parallel rightward shift of concentration-response curve to isoprenaline alone with metoprolol at 10(-6) M and propranolol at 3 X 10(-6) M (that the inhibitory effects of metoprolol at 10(-6) M or propranolol at 3 X 10(-6) M are greater than can be explained by beta-adrenoceptor blockade only may be detected either by determining pA2 values from the formula pA2 = pAx + log(x - 1) or by Schild analysis); third, the highest concentrations of procaine (3 X 10(-4) M) and propranolol (10(-5) M) tested decreased the maximal combined response to electrical stimulation and isoprenaline.
对大鼠离体左心房进行了连续三次电刺激挑战,然后进行电刺激和异丙肾上腺素挑战。随着连续挑战,对电刺激的反应降低,对异丙肾上腺素的反应增加,使得对电刺激和异丙肾上腺素的最大联合反应保持恒定。对异丙肾上腺素的敏感性(pD2)随着连续挑战而降低。因此,在研究药物对电刺激和异丙肾上腺素反应的影响时,有必要对未处理的心房进行平行实验,以监测与添加药物无关的反应变化。对普鲁卡因、美托洛尔和普萘洛尔对电刺激和/或异丙肾上腺素反应的影响分析表明,β-肾上腺素能受体阻断和膜稳定活性有明显的收缩表现。10^(-7) M的美托洛尔和3×10^(-9) - 10^(-6) M的普萘洛尔的β-肾上腺素能受体阻断活性表现为单独对异丙肾上腺素的浓度-反应曲线平行右移。药物的膜稳定作用有三个组成部分:第一,单独对电刺激的反应降低,在大于或等于10^(-4) M的普鲁卡因和大于或等于3×10^(-9) M的普萘洛尔中观察到;第二,10^(-6) M的美托洛尔和3×10^(-6) M的普萘洛尔使单独对异丙肾上腺素的浓度-反应曲线有小的平行右移(10^(-6) M的美托洛尔或3×10^(-6) M的普萘洛尔的抑制作用大于仅由β-肾上腺素能受体阻断所解释的作用,这可以通过从公式pA2 = pAx + log(x - 1)确定pA2值或通过Schild分析来检测);第三,所测试的最高浓度的普鲁卡因(3×10^(-4) M)和普萘洛尔(10^(-5) M)降低了对电刺激和异丙肾上腺素的最大联合反应。