Jiang Q, Takemori A E, Sultana M, Portoghese P S, Bowen W D, Mosberg H I, Porreca F
Department of Pharmacology, University of Arizona Health Sciences Center, Tucson.
J Pharmacol Exp Ther. 1991 Jun;257(3):1069-75.
The present study has investigated the direct opioid delta receptor-mediated antinociception produced by i.c.v. administration of the highly selective delta agonists, [D-Pen2,D-Pen5]enkephalin (DPDPE) and [D-Ala2]deltorphin II, as well as that of the less delta-selective [D-Ser2,Leu5,Thr6]enkephalin (DSLET), by using two novel nonequilibrium opioid antagonists, [D-Ala2,Leu5,Cys6] enkephalin (DALCE) and naltrindole 5'-isothiocyanate (5'-NTII). At times ranging from 8 to 48 hr after a single i.c.v. pretreatment of mice with 5'-NTII, the antinociceptive effects of [D-Ala2] deltorphin II were significantly antagonized. In contrast, 5'-NTII pretreatment at times between 10 min and 24 hr failed to antagonize the antinociceptive effects of DPDPE. Previous studies have shown that pretreatment with i.c.v. DALCE produces a dose- and time-related antagonism of DPDPE, but not morphine, antinociception. However, pretreatment with i.c.v. DALCE failed to antagonize the antinociceptive effects of [D-Ala2]deltorphin II. Similarly, i.c.v. administration of DSLET produced time- and dose-related antinociception which was partially antagonized by either beta-funaltrexamine (beta-FNA) or by ICI 174,864 (N,N-dialyl-Tyr-Aib-Aib-Phe-Leu-OH), suggesting mixed activity at mu and delta receptors. ICI 174,864 produced essentially complete antagonism of DSLET antinociception in beta-FNA-pretreated mice. Pretreatment with 5'-NTII (at -8 to -48 hr), blocked the antinociception produced by DSLET in control or in beta-FNA-pretreated mice. In contrast, pretreatment with DALCE failed to antagonize the antinociception produced by i.c.v. DSLET in either control or in beta-FNA-pretreated mice.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究通过使用两种新型非平衡阿片类拮抗剂,即[D-Ala2,Leu5,Cys6]脑啡肽(DALCE)和纳曲吲哚5'-异硫氰酸盐(5'-NTII),研究了脑室内注射高选择性δ激动剂[D-Pen2,D-Pen5]脑啡肽(DPDPE)和[D-Ala2]强啡肽II,以及δ选择性较低的[D-Ser2,Leu5,Thr6]脑啡肽(DSLET)所产生的直接阿片δ受体介导的抗伤害感受作用。在单次脑室内用5'-NTII预处理小鼠后的8至48小时内,[D-Ala2]强啡肽II的抗伤害感受作用被显著拮抗。相比之下,在10分钟至24小时之间用5'-NTII预处理未能拮抗DPDPE的抗伤害感受作用。先前的研究表明,脑室内注射DALCE预处理会产生与剂量和时间相关的对DPDPE而非吗啡抗伤害感受作用的拮抗。然而,脑室内注射DALCE预处理未能拮抗[D-Ala2]强啡肽II的抗伤害感受作用。同样,脑室内注射DSLET产生了与时间和剂量相关的抗伤害感受作用,该作用被β-氟奈曲胺(β-FNA)或ICI 174,864(N,N-二烯丙基-Tyr-Aib-Aib-Phe-Leu-OH)部分拮抗,表明其对μ和δ受体具有混合活性。ICI 174,864在β-FNA预处理的小鼠中基本上完全拮抗了DSLET的抗伤害感受作用。在-8至-48小时用5'-NTII预处理可阻断DSLET在对照或β-FNA预处理小鼠中产生的抗伤害感受作用。相比之下,在对照或β-FNA预处理小鼠中,用DALCE预处理未能拮抗脑室内注射DSLET所产生的抗伤害感受作用。(摘要截选至250字)