Calixto J B, Loch S
Br J Pharmacol. 1985 May;85(1):189-95. doi: 10.1111/j.1476-5381.1985.tb08846.x.
The inhibitory effect of the intravenous anaesthetic ketamine on CaCl2-induced contractions in the isolated K+-depolarized uterus of the rat in Ca2+-free medium was compared with that produced by papaverine, theophylline and the calcium entry blocker verapamil. Pre-incubation for 20 min with either ketamine (0.3 to 3 mM), papaverine (3 to 30 microM), theophylline (0.1 to 1 mM) or verapamil (3 to 30 nM) induced parallel, concentration-dependent rightward displacements of the dose-response curves to Ca2+ (0.04 to 22 mM). The antagonism was competitive, except that due to verapamil, the Schild plot for which yielded a slope which differed significantly from unity. The calculated pA2 values (+/- s.e.mean) were: ketamine 3.90 +/- 0.07; papaverine 5.55 +/- 0.05; theophylline 3.99 +/- 0.1 and verapamil 9.54 +/- 0.24. These drugs differed in their ability to relax the sustained contraction induced by Ca2+ (1 mM) in K+-depolarizing solution. Ketamine and verapamil relaxed the preparation in a concentration-dependent manner whereas theophylline and especially papaverine were less potent and induced only partial maximal relaxation. The t1/2 of the relaxant effect was significantly less for ketamine than for verapamil (5 and 22 min, respectively). Only ketamine produced a relaxation comparable to that obtained by washing the preparation with Ca2+-free solution (t1/2 = approx. 5 min). Prior exposure of the depolarized uterine strip to a low concentration of Ca2+ (0.22 mM) increased the potency of ketamine, but decreased that of papaverine and theophylline, in antagonizing Ca2+ induced contractions. In contrast, this procedure did not affect the potency of verapamil. 5 The inhibitory effects of these drugs, excluding those of verapamil, were completely reversed after washing the preparations with a high-potassium Ca2+-free solution, 3-5 times for about 30-60 min. 6 These experiments provide further evidence that the relaxant effect produced by ketamine on the rat isolated uterus is due to its ability to antagonize Ca2+ movements competitively and also show that there are marked differences between the nature of the relaxant effects of ketamine and those of papaverine, theophylline and verapamil.
将静脉麻醉药氯胺酮对无钙培养基中大鼠离体K⁺去极化子宫CaCl₂诱导收缩的抑制作用,与罂粟碱、茶碱和钙通道阻滞剂维拉帕米所产生的抑制作用进行了比较。用氯胺酮(0.3至3 mM)、罂粟碱(3至30 μM)、茶碱(0.1至1 mM)或维拉帕米(3至30 nM)预孵育20分钟,均引起对Ca²⁺(0.04至22 mM)剂量 - 反应曲线平行、浓度依赖性的右移。除维拉帕米外,拮抗作用均为竞争性,维拉帕米的Schild图斜率显著不同于1。计算得到的pA₂值(±标准误均值)分别为:氯胺酮3.90 ± 0.07;罂粟碱5.55 ± 0.05;茶碱3.99 ± 0.1;维拉帕米9.54 ± 0.24。这些药物在松弛K⁺去极化溶液中Ca²⁺(1 mM)诱导的持续收缩的能力上存在差异。氯胺酮和维拉帕米以浓度依赖性方式松弛标本,而茶碱尤其是罂粟碱效力较弱,仅诱导部分最大松弛。氯胺酮松弛作用的t1/2显著短于维拉帕米(分别为5分钟和22分钟)。只有氯胺酮产生的松弛作用与用无钙溶液冲洗标本所获得的松弛作用相当(t1/2约为5分钟)。将去极化的子宫条预先暴露于低浓度的Ca²⁺(0.22 mM),可增强氯胺酮拮抗Ca²⁺诱导收缩的效力,但降低罂粟碱和茶碱的效力。相反,该操作不影响维拉帕米的效力。用高钾无钙溶液冲洗标本3 - 5次,每次约30 - 60分钟后,除维拉帕米外,这些药物的抑制作用完全逆转。这些实验进一步证明,氯胺酮对大鼠离体子宫产生的松弛作用是由于其竞争性拮抗Ca²⁺运动的能力,并且还表明氯胺酮与罂粟碱、茶碱和维拉帕米松弛作用的性质存在显著差异。