Illes P, Schulz R
Br J Pharmacol. 1980;71(1):195-200. doi: 10.1111/j.1476-5381.1980.tb10926.x.
1 The amplitude of excitatory junction potentials (e.j.ps) recorded intracellularly from smooth muscle cells of the mouse vas deferens varied with the strength of stimulation. Normorphine (0.4, 2 and 10 microM) shifted the stimulus-response curve to the right, without any change in slope. This shift of the curve was proportional to the concentration of the opiate in the bath. Naloxone (0.4 and 2 microM) antagonized this effect of normorphine. 2 The action of normorphine (2 and 10 microM) was studied in vasa deferentia prepared from control mice and mice that had been implanted with morphine pellets. Both groups of tissues were continuously exposed to a low concentration of normorphine (0.4 microM), to simulate the plasma concentration in the morphine-treated mice. Addition of 10 microM normorphine produced a parallel displacement of the curve in vasa deferentia from control animals, and a non-parallel displacement in tissues from morphine pellet-implanted mice. In the preparations from morphine-treated mice a pronounced degree of tolerance to normorphine was observed at a low stimulus strength. 3 Naloxone (0.4 and 2 microM) had a greater effect on vasa deferentia prepared from morphine-treated animals than on tissues from control mice, when both organs were continuously exposed to 0.4 microM normorphine. The difference in the effect of the antagonist in the two groups of preparations was absent when the incubating solution contained 2 microM normorphine. 4 It is concluded that a low intensity of stimulation the e.j.ps are more readily depressed by normorphine and also the degree of tolerance displayed is larger than at a high intensity of stimulation.
从小鼠输精管平滑肌细胞内记录到的兴奋性突触后电位(e.j.ps)的幅度随刺激强度而变化。去甲吗啡(0.4、2和10微摩尔)使刺激 - 反应曲线向右移动,斜率无任何变化。曲线的这种移动与浴槽中阿片类药物的浓度成正比。纳洛酮(0.4和2微摩尔)拮抗去甲吗啡的这种作用。
在由对照小鼠和已植入吗啡丸剂的小鼠制备的输精管中研究了去甲吗啡(2和10微摩尔)的作用。两组组织都持续暴露于低浓度的去甲吗啡(0.4微摩尔),以模拟吗啡处理小鼠的血浆浓度。添加10微摩尔去甲吗啡会使对照动物输精管中的曲线发生平行位移,而在植入吗啡丸剂小鼠的组织中则发生非平行位移。在来自吗啡处理小鼠的制剂中,在低刺激强度下观察到对去甲吗啡有明显程度的耐受性。
当两个器官都持续暴露于0.4微摩尔去甲吗啡时,纳洛酮(0.4和2微摩尔)对由吗啡处理动物制备的输精管的作用比对对照小鼠组织的作用更大。当孵育溶液含有2微摩尔去甲吗啡时,两组制剂中拮抗剂作用的差异不存在。
得出的结论是,在低强度刺激下,兴奋性突触后电位更容易被去甲吗啡抑制,并且所表现出的耐受程度也比高强度刺激时更大。