Van Ree J M, Innemee H, Louwerens J W, Kahn R S, De Wied D
Neuropharmacology. 1982 Nov;21(11):1095-101. doi: 10.1016/0028-3908(82)90166-6.
In rats, the beta-endorphin fragment, 6-17 (des-enkephalin-gamma-endorphin, DE gamma E), dose-dependently antagonized the reduction of the rate of locomotion and rearing induced by small doses of apomorphine. Structure-activity studies revealed that the active moiety of gamma-endorphin fragments with respect to counteracting apomorphine-induced behavioural changes resides in the fragment 6-17. The influence of DE gamma E appeared to be specific for dopamine systems mediating apomorphine-induced hypomotility, since DE gamma E hardly affected apomorphine-induced stereotypy and amphetamine-induced behavioural changes. These data suggest that DE gamma E acts as a dopamine antagonist selectively, on those dopamine receptor systems which are stimulated by small doses of apomorphine and which may be located presynaptically. In contrast to acute treatment, administration of DE gamma E for 4 days resulted in an enhancement of apomorphine-induced hypomotility. Thus, the receptor systems involved in these effects of apomorphine may become supersensitive upon (sub)chronic treatment with DE gamma E. The significance of the present findings are discussed in relation to the neuroleptic-like and antipsychotic action of gamma-type endorphins.
在大鼠中,β-内啡肽片段6-17(去甲脑啡肽-γ-内啡肽,DEγE)剂量依赖性地拮抗小剂量阿扑吗啡诱导的运动和竖毛速率降低。构效关系研究表明,γ-内啡肽片段中对抗阿扑吗啡诱导行为变化的活性部分位于片段6-17。DEγE的影响似乎对介导阿扑吗啡诱导运动减少的多巴胺系统具有特异性,因为DEγE几乎不影响阿扑吗啡诱导的刻板行为和苯丙胺诱导的行为变化。这些数据表明,DEγE作为一种多巴胺拮抗剂,选择性地作用于那些被小剂量阿扑吗啡刺激且可能位于突触前的多巴胺受体系统。与急性给药不同,连续4天给予DEγE会导致阿扑吗啡诱导的运动减少增强。因此,在用DEγE进行(亚)慢性治疗后,参与阿扑吗啡这些效应的受体系统可能会变得超敏。本文的研究结果结合γ型内啡肽的抗精神病样和抗精神病作用进行了讨论。