Mathiasen J R, Vaught J L
Eur J Pharmacol. 1987 Apr 29;136(3):405-7. doi: 10.1016/0014-2999(87)90314-1.
Jimpy (B6CBA-A W-J/A-Ta jp) mice, which are known to be deficient in neuronal cerebroside sulfate (a putative component of the mu opioid receptor), were non-responsive in the tail flick test (compared to littermate controls and a standard Swiss strain of mouse) to analgesic doses of two mu opioid receptor agonists, morphine sulfate and [D-Ala2,MePhe4,Gly-ol5]enkephalin (DAGO). However, the jimpy mice responded normally (compared to controls) to the analgesic effects of the selective delta opioid receptor agonist [D-Pen2,L-Pen5]enkephalin (DPLPE). These results suggest (1) that delta opioid receptors can mediate analgesia and (2) that cerebroside sulfate is not necessary for delta opioid receptor activation.
已知Jimpy(B6CBA - A W - J/A - Ta jp)小鼠缺乏神经节苷脂硫酸酯(一种推测的μ阿片受体成分),在甩尾试验中(与同窝对照和标准瑞士小鼠品系相比),对两种μ阿片受体激动剂硫酸吗啡和[D - Ala2,MePhe4,Gly - ol5]脑啡肽(DAGO)的镇痛剂量无反应。然而,Jimpy小鼠(与对照相比)对选择性δ阿片受体激动剂[D - Pen2,L - Pen5]脑啡肽(DPLPE)的镇痛作用反应正常。这些结果表明:(1)δ阿片受体可介导镇痛作用;(2)硫酸脑苷脂对于δ阿片受体的激活并非必需。