Bhargava H N, Matwyshyn G A, Gudehithlu K P
Department of Pharmaceutics and Pharmacodynamics (M/C 865), University of Illinois at Chicago 60612, USA.
Pharmacology. 1995 Nov;51(5):323-30. doi: 10.1159/000139342.
In male Sprague-Dawley rats, acute and chronic effects of dizocilpine (MK-801), a noncompetitive antagonist of the N-methyl-D-aspartate (NMDA) receptor, were determined on the analgesic and hypothermic actions of U-50,488H, a kappa-opioid receptor agonist. In addition, the in vitro effects of MK-801 on the binding of [3H]ethylketocyclazocine ([3H]EKC) to kappa-opioid receptors in brain and spinal cord of the rat were determined. A single injection of MK-801 given 10 min prior to U-50,488H or given twice a day for 4 days dose-dependently enhanced the analgesic action of U-50,488H. The enhancement of the analgesic response was much greater in rats injected chronically with MK-801 as compared with those injected acutely. Both single and multiple injections of MK-801 failed to affect the hypothermic action of U-50,488H. In vitro, MK-801 inhibited the binding of [3H]EKC to brain and spinal cord membranes with IC50 values of 9.80 +/- 1.7 and 1.37 +/- 0.58 microM, respectively. Chronic administration of MK-801 twice a day for 4 days increased the Bmax value of [3H]EKC binding in the brain, but had no effect on Kd. On the other hand, chronic treatment with MK-801 decreased the Kd of [3H]EKC binding in spinal cord without affecting Bmax. It is concluded that blockade of NMDA receptor enhances the analgesic response to a kappa-opioid receptor agonist and upregulates brain and spinal cord kappa-opioid receptors. Finally, the results suggest that the NMDA receptor may have a role in the regulation of kappa-opioid systems.
在雄性斯普拉格-道利大鼠中,研究了N-甲基-D-天冬氨酸(NMDA)受体的非竞争性拮抗剂地佐环平(MK-801)对κ-阿片受体激动剂U-50,488H的镇痛和降温作用的急性和慢性影响。此外,还测定了MK-801在体外对大鼠脑和脊髓中[3H]乙基酮环唑辛([3H]EKC)与κ-阿片受体结合的影响。在U-50,488H给药前10分钟单次注射MK-801或每天注射两次,连续注射4天,均剂量依赖性地增强了U-50,488H的镇痛作用。与急性注射MK-801的大鼠相比,慢性注射MK-801的大鼠镇痛反应增强更为明显。单次和多次注射MK-801均未影响U-50,488H的降温作用。在体外,MK-801抑制[3H]EKC与脑和脊髓膜的结合,IC50值分别为9.80±1.7和1.37±0.58微摩尔/升。每天两次,连续4天慢性给予MK-801可增加脑中[3H]EKC结合的Bmax值,但对Kd无影响。另一方面,MK-801慢性治疗可降低脊髓中[3H]EKC结合的Kd,而不影响Bmax。得出的结论是,NMDA受体的阻断增强了对κ-阿片受体激动剂的镇痛反应,并上调了脑和脊髓中的κ-阿片受体。最后,结果表明NMDA受体可能在κ-阿片系统的调节中发挥作用。