Chapman D B, Hu J, Way E L
Eur J Pharmacol. 1980 Aug 8;65(4):369-77. doi: 10.1016/0014-2999(80)90341-6.
Intracerebroventricular (i.c.v.) administration of subanalgesic doses of beta- and leucine-endorphin in mice 15 min before subcutaneous morphine injection, significantly enhanced the analgesic effects of the morphine as measured by the tail-flick assay. A similar effect was seen with levorphanol analgesia but not enhancement of leucine- or methionine-enkephalin analgesia by beta-endorphin was observed. The same doses of the endorphins did not affect the development of single-dose morphine tolerance and dependence. Leucine-enkephalin failed to affect morphine analgesia, tolerance or dependence development, while low doses of methionine-enkephalin administered i.c.v. were observed to have an antagonistic effect on morphine analgesia without affecting tolerance or dependence development. Neither endephalin had any effect on beta-endorphin analgesia.
在小鼠皮下注射吗啡前15分钟,脑室内(i.c.v.)给予亚镇痛剂量的β-内啡肽和亮氨酸-内啡肽,通过甩尾试验测量发现,显著增强了吗啡的镇痛效果。左啡诺镇痛也观察到类似效果,但未观察到β-内啡肽增强亮氨酸-脑啡肽或甲硫氨酸-脑啡肽的镇痛作用。相同剂量的内啡肽不影响单剂量吗啡耐受性和依赖性的形成。亮氨酸-脑啡肽不影响吗啡镇痛、耐受性或依赖性的形成,而脑室内给予低剂量的甲硫氨酸-脑啡肽对吗啡镇痛有拮抗作用,且不影响耐受性或依赖性的形成。两种内啡肽对β-内啡肽镇痛均无影响。