Steinfels G F, Tam S W, Cook L
E. I. du Pont de Nemours & Co., Inc., Medical Products Department, Wilmington, DE 19898.
Eur J Pharmacol. 1987 Sep 2;141(1):163-6. doi: 10.1016/0014-2999(87)90426-2.
The role of the dopaminergic, noradrenergic and serotonergic systems in the production of the discriminative stimulus (DS) properties of the sigma receptor agonist (+)-N-allylnormetazocine [(+)-NANM/(+)-SKF 10,047] was measured in rats. The partial generalization of the noradrenergic agonist clonidine with (+)-NANM and partial antagonism of (+)-NANM by yohimbine suggest that the noradrenergic system may play a role in (+)-NANM DS. Activation of the dopaminergic system by apomorphine did not produce (+)-NANM DS however, haloperidol, which binds to the sigma receptor with high affinity, antagonized (+)-NANM DS. These data suggest that the haloperidol antagonism of (+)-NANM DS is a function of antagonism at the sigma receptor rather than antagonism at the dopamine receptor. Since yohimbine does not bind to the sigma receptor, yohimbine antagonizes (+)-NANM by a mechanism different from that of haloperidol. There was no evidence to suggest serotonergic mediation of (+)-NANM DS.
在大鼠中测定了多巴胺能、去甲肾上腺素能和血清素能系统在西格玛受体激动剂(+)-N-烯丙基去甲左啡诺[(+)-NANM/(+)-SKF 10,047]辨别刺激(DS)特性产生中的作用。去甲肾上腺素能激动剂可乐定与(+)-NANM的部分泛化以及育亨宾对(+)-NANM的部分拮抗表明,去甲肾上腺素能系统可能在(+)-NANM DS中起作用。阿扑吗啡对多巴胺能系统的激活并未产生(+)-NANM DS,然而,与西格玛受体具有高亲和力结合的氟哌啶醇拮抗了(+)-NANM DS。这些数据表明,氟哌啶醇对(+)-NANM DS的拮抗作用是西格玛受体拮抗作用的结果,而非多巴胺受体拮抗作用的结果。由于育亨宾不与西格玛受体结合,育亨宾通过与氟哌啶醇不同的机制拮抗(+)-NANM。没有证据表明血清素能介导(+)-NANM DS。