Mulder A H, Wardeh G, Hogenboom F, Frankhuyzen A L
Nature. 1984;308(5956):278-80. doi: 10.1038/308278a0.
At least three different families of endogenous opioid peptides, the enkephalins, endorphins and dynorphins, are present in the mammalian central nervous system (CNS). Immunocytochemical studies have demonstrated their localization in neurones, which supports the view that these peptides may have a role as neurotransmitter or neuromodulators. However, the target cells and cellular processes acted upon by the opioid peptides are still largely unknown. One possible function of neuropeptides, including the opioid peptides, may be presynaptic modulation of neurotransmission in certain neuronal pathways, for example, by inhibition or promotion of neurotransmitter release from the nerve terminals. Here we report that dynorphin and some benzomorphans potently and selectively inhibit the release of (radiolabelled) dopamine from slices of rat corpus striatum, by activating kappa-opioid receptors. In contrast, [Leu5]enkephalin and [D-Ala2, D-Leu5]enkephalin selectively inhibit acetylcholine release by activating delta-opioid receptors.
至少有三种不同家族的内源性阿片肽,即脑啡肽、内啡肽和强啡肽,存在于哺乳动物的中枢神经系统(CNS)中。免疫细胞化学研究已证实它们在神经元中的定位,这支持了这些肽可能作为神经递质或神经调质发挥作用的观点。然而,阿片肽作用的靶细胞和细胞过程在很大程度上仍然未知。包括阿片肽在内的神经肽的一种可能功能可能是在某些神经元通路中对神经传递进行突触前调节,例如,通过抑制或促进神经末梢释放神经递质。在此我们报告,强啡肽和一些苯并吗啡烷通过激活κ-阿片受体,有力且选择性地抑制大鼠纹状体切片中(放射性标记的)多巴胺的释放。相比之下,亮氨酸脑啡肽和[D-丙氨酸2,D-亮氨酸5]脑啡肽通过激活δ-阿片受体选择性地抑制乙酰胆碱的释放。