Diamond B I, Borison R L
Neurology. 1978 Nov;28(11):1085-8. doi: 10.1212/wnl.28.11.1805.
Unilateral lesions of the substantia nigra were made with 6-hydroxydopamine in rats. In this model, drugs such as naloxone, which block endogenous enkephalin receptors, potentiated agents with postsynaptic dopaminergic actions, while antagonizing agents with presynaptic dopaminergic actions. Drugs which increase brain enkephalin content (d-phenylalanine or methionine-enkephalin) antagonized postsynaptically active agents and potentiated presynaptic agents. Naloxone also reversed reserpine-induced parkinsonism in rats. Separate pre- and postsynaptic enkephalinergic neurons thus seem to modulate nigrostriatal function.
用6-羟基多巴胺对大鼠进行黑质单侧损伤。在这个模型中,诸如纳洛酮这类阻断内源性脑啡肽受体的药物,增强了具有突触后多巴胺能作用的药物,同时拮抗了具有突触前多巴胺能作用的药物。增加脑内脑啡肽含量的药物(d-苯丙氨酸或甲硫氨酸-脑啡肽)拮抗了突触后活性药物并增强了突触前药物。纳洛酮还逆转了利血平诱导的大鼠帕金森病。因此,独立的突触前和突触后脑啡肽能神经元似乎调节黑质纹状体功能。