Fujimoto J M, Holmes B
Research Service, Veterans Administration Medical Center, Milwaukee, Wisconsin.
J Pharmacol Exp Ther. 1990 Jul;254(1):1-7.
The antianalgesic effect of dynorphin A (1-17) (dyn A) was demonstrated by i.c.v. administration of agonists (morphine, Tyr-D-Ala2-Gly-N-MePhe4-Gly-ol5, D-Pen2-D-Pen5-enkephalin, beta-endorphin, U50,488H and physostigmine) at 10 min and intrathecal administration of dyn A at 5 min before the tail-flick test in mice. This antianalgesic effect of dyn A was eliminated by 3 or 5.5 hr pretreatment s.c. with 10 or 100 mg/kg of morphine, respectively. This desensitization lasted for about 18 hr. Three-hour pretreatment intrathecally with dyn A also desensitized the mice to dyn A. Previously we had shown that i.c.v. administration of morphine simultaneously activates analgesic and antianalgesic systems and the latter is mediated spinally by dyn A, an endogenous antianalgesic opioid. Present results are consistent with that concept and systemic pretreatment with morphine may release dyn A in the spinal cord to produce the desensitization to the subsequently elicited antianalgesic action of dyn A.
在小鼠甩尾试验前10分钟通过脑室内注射激动剂(吗啡、酪氨酰-D-丙氨酸²-甘氨酰-N-甲基苯丙氨酸⁴-甘氨醇⁵、D-青霉胺²-D-青霉胺⁵-脑啡肽、β-内啡肽、U50,488H和毒扁豆碱)以及在5分钟前鞘内注射强啡肽A(1-17)(强啡肽A),证实了强啡肽A的抗镇痛作用。分别用10或100毫克/千克吗啡皮下预处理3或5.5小时可消除强啡肽A的这种抗镇痛作用。这种脱敏持续约18小时。鞘内用强啡肽A预处理3小时也使小鼠对强啡肽A脱敏。此前我们已经表明,脑室内注射吗啡同时激活镇痛和抗镇痛系统,后者由内源性抗镇痛阿片样物质强啡肽A在脊髓中介导。目前的结果与该概念一致,吗啡的全身预处理可能会使脊髓中释放强啡肽A,从而对随后引发的强啡肽A的抗镇痛作用产生脱敏。