Tortella F C, Cowan A, Adler M W
Peptides. 1980 Fall;1(3):237-41. doi: 10.1016/0196-9781(80)90060-1.
Changes in pupil size after peripheral administration of met-enkephalin, leu-enkephalin, or morphine were studied in the rat. With a simple pupillographic technique, the pupil diameter of male, S.D. rats (250--300 g) was measured by a series of photographs taken every 60 sec for at least 45 min after the last drug injection. Morphine (8 mg/kg, SC) caused mydriasis characterized by rapid and marked fluctuations of pupil size. Mydriasis also occurred after leu-enkephalin (5 and 10 mg/kg, IP) and met-enkephalin (20 mg/kg, IP) Both peptides induced morphine-like fluctuations. When given 15 min after morphine, leu-enkephalin (5 and 10 mg/kg) increased the mydriatic effect of morphine from 172 percent of control to 224 and 272 percent, respectively. Met-enkephalin (20 mg/kg, but not 10 mg/kg) also enhanced the mydriatic response of morphine, to 244 percent of control. These interactions appear to represent simple addition rather than potentiation. The effects of both peptides were reversed by naloxone (1 mg/kg, SC), suggesting an opiate receptor interaction for the pupillary effect of the enkephalins. The rat pupil thus provides one of the few in vivo models permitting quantification of enkephalin action after parenteral administration.
研究了在大鼠外周给予甲硫氨酸脑啡肽、亮氨酸脑啡肽或吗啡后瞳孔大小的变化。采用一种简单的瞳孔描记技术,在最后一次注射药物后,每隔60秒拍摄一系列照片,测量雄性SD大鼠(250 - 300克)的瞳孔直径,至少持续45分钟。吗啡(8毫克/千克,皮下注射)引起瞳孔散大,其特征是瞳孔大小迅速且明显波动。亮氨酸脑啡肽(5和10毫克/千克,腹腔注射)和甲硫氨酸脑啡肽(20毫克/千克,腹腔注射)后也出现瞳孔散大。两种肽均诱导出类似吗啡的波动。在吗啡给药15分钟后给予亮氨酸脑啡肽(5和10毫克/千克),分别将吗啡的散瞳作用从对照的172%增加到224%和272%。甲硫氨酸脑啡肽(20毫克/千克,但10毫克/千克无效)也增强了吗啡的散瞳反应,达到对照的244%。这些相互作用似乎代表简单相加而非增强作用。两种肽的作用均被纳洛酮(1毫克/千克,皮下注射)逆转,提示脑啡肽的瞳孔效应存在阿片受体相互作用。因此,大鼠瞳孔提供了少数几个允许对肠外给药后脑啡肽作用进行定量的体内模型之一。