Tseng L L, Suh H H
Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee.
Eur J Pharmacol. 1989 Dec 7;173(2-3):171-6. doi: 10.1016/0014-2999(89)90515-3.
Intrathecal (i.t.) injection of antibody directed to [Met5]enkephalin antagonized intracerebroventricularly (i.c.v.) administered beta-endorphin-induced inhibition of the tail-flick response but not the hot-plate response. [Met5]enkephalin antibody injected i.t., however, did not affect inhibition of either the tail-flick and hot-plate response induced by morphine given i.c.v. The antibodies to [Leu5]enkephalin, dynorphin A-(1-13) and beta-endorphin even at a high dose injected i.t. did not affect the inhibition induced by i.c.v. administered beta-endorphin or morphine either in the tail-flick and hot-plate test. Our results with antibodies support the results of previous studies that beta-endorphin but not morphine produces its analgesic action by selectively releasing [Met5]enkephalin.
鞘内注射针对[Met5]脑啡肽的抗体可拮抗脑室内注射β-内啡肽所诱导的甩尾反应抑制,但不影响热板反应。然而,鞘内注射[Met5]脑啡肽抗体并不影响脑室内注射吗啡所诱导的甩尾反应和热板反应的抑制。即使高剂量鞘内注射针对[Leu5]脑啡肽、强啡肽A-(1-13)和β-内啡肽的抗体,在甩尾试验和热板试验中也不影响脑室内注射β-内啡肽或吗啡所诱导的抑制。我们使用抗体的研究结果支持了先前的研究结果,即β-内啡肽而非吗啡通过选择性释放[Met5]脑啡肽产生镇痛作用。