Makó E, Rónai A Z
Department of Pharmacology and Pharmacotherapy, Semmelweis University, H-1445, Budapest, P.O.B. 370, Hungary.
Med Sci Monit. 2001 May-Jun;7(3):350-6.
The kappa and delta opioid receptors were characterized in longitudinal muscle strip of guinea-pig ileum (GPI, mu, kappa), mouse (MVD, delta, mu, kappa) and rabbit (LVD, kappa) vas deferens and rabbit ear artery (ART, delta, kappa) with particular attention to the presence of receptor subtypes.
For this purpose, type/subtype selective agonist and antagonist were used such as [D-Ala2, D-Leu5]-enkephalin (delta agonist) [D-Pen2,5]-enkephalin (delta 1 agonist), deltorphin II (delta 2 agonist) naltriben (NTB, delta 2 antagonist), BOC-YPGFLT(OtBu) (delta antagonist) on the one hand and ethylketocyclazocine (EKC, kappa/(agonist), PD-117 302 (kappa 1 agonist), [Met5]-enkephalin-Arg6, Phe7 (ME-RF, delta/kappa 2/(agonist) and its amide ME-RF-NH2, kappa 2/(agonist), naltrexone (NTX, mu > delta = kappa antagonist) and norbinaltorphimine (nBNI, kappa antagonist) on the other hand.
In MVD the Ke of NTB against different (agonists revealed no receptor type heterogeneity. In LVD the Ke of nBNI but not of NTX against EKC versus the ones against ME-RF and ME-RF-NH2 indicated inhomogenous (receptor population. The (receptor antagonist BOC-YPGFLT(OtBu) antagonized the action of ME-RF-NH2 in ART but not in MVD or LVD indicating a special receptor subtype in ART (kappa, possibly delta).
在豚鼠回肠纵行肌条(GPI,μ、κ)、小鼠输精管(MVD,δ、μ、κ)和兔输精管(LVD,κ)以及兔耳动脉(ART,δ、κ)中对κ和δ阿片受体进行了表征,特别关注受体亚型的存在情况。
为此,使用了类型/亚型选择性激动剂和拮抗剂,一方面有[D - Ala2,D - Leu5] - 脑啡肽(δ激动剂)、[D - Pen2,5] - 脑啡肽(δ1激动剂)、强啡肽II(δ2激动剂)、纳曲苄(NTB,δ2拮抗剂)、BOC - YPGFLT(OtBu)(δ拮抗剂),另一方面有乙基酮环唑辛(EKC,κ/激动剂)、PD - 117 302(κ1激动剂)、[Met5] - 脑啡肽 - Arg6,Phe7(ME - RF,δ/κ2/激动剂)及其酰胺ME - RF - NH2,κ2/激动剂、纳曲酮(NTX,μ>δ = κ拮抗剂)和去甲二氢吗啡酮(nBNI,κ拮抗剂)。
在MVD中,NTB对不同激动剂的解离常数未显示受体类型异质性。在LVD中,nBNI而非NTX对EKC的解离常数与对ME - RF和ME - RF - NH2的解离常数相比表明受体群体不均匀。受体拮抗剂BOC - YPGFLT(OtBu)拮抗ME - RF - NH2在ART中的作用,但在MVD或LVD中无此作用,表明ART中存在一种特殊的受体亚型(κ,可能是δ)。