Morphine receptors in immunocytes and neurons

Maynard H. Makman
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引用次数: 74

Abstract

Receptor interactions of morphine are reviewed, with particular attention given to a recently discovered opiate receptor, designated μ3, with unique selectivity for morphine and certain other opiate alkaloids. Morphine, other opiate alkaloids and related analogs are known to bind to the classical σ, R and is opioid receptor subtypes. Each of these subtypes also binds one or more of the endogenous opioid peptides with high affinity. Immunocytes have recently been found to contain a unique receptor for morphine, capable of binding morphine and certain other opiate alkaloids, but with essentially no or exceedingly low affinity for the naturally occurring endogenous opioid peptides or peptide analogs. This putative μ3 (morphine/opiate alkaloid) receptor is present in invertebrate immunocytes as well as in human peripheral blood monocytes (macrophages). More recently this same receptor has been found in certain established macrophage cell lines and in human peripheral blood granulocytes. Finally, the same or closely related opiate alkaloid-selective (μ3) receptor has been found to be present in a neuroblastoma and in a hybrid neural cell line. Studies indicate that in the immunocytes the receptor mediates inhibitory effects of morphine on cellular chemotaxis. While the functional coupling of this receptor in neurons is not known, it is postulated that the receptor may mediate effects of opiates on neuronal differentiation and cell division as well as neuronal transmission. Both for the immune system and the nervous system, the μ3 receptor may constitute a major site of action for putative endogenous morphine or morphine-like substances. This receptor system also provides an additional pharmacological site of action for exogenously administered opiate alkaloid drugs. The μ3 receptor is proposed to be an important neuro-immune link. This system is likely to play a significant role in a variety of responses involving the immune system, including the response of the organism to stress, infection and malignant transformation.

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免疫细胞和神经元中的吗啡受体
对吗啡的受体相互作用进行了综述,特别关注了最近发现的阿片受体μ3,它对吗啡和某些其他阿片生物碱具有独特的选择性。已知吗啡,其他阿片生物碱和相关类似物与经典的σ, R和is阿片受体亚型结合。这些亚型中的每一种都能以高亲和力结合一种或多种内源性阿片肽。最近发现免疫细胞含有一种独特的吗啡受体,能够结合吗啡和某些其他阿片类生物碱,但对自然产生的内源性阿片类肽或肽类似物基本上没有或极低的亲和力。这种假定的μ3(吗啡/阿片生物碱)受体存在于无脊椎动物免疫细胞和人外周血单核细胞(巨噬细胞)中。最近,在某些已建立的巨噬细胞系和人外周血粒细胞中发现了相同的受体。最后,在神经母细胞瘤和杂交神经细胞系中发现了相同或密切相关的阿片生物碱选择性(μ3)受体。研究表明,在免疫细胞中,该受体介导吗啡对细胞趋化的抑制作用。虽然该受体在神经元中的功能偶联尚不清楚,但假设该受体可能介导阿片类药物对神经元分化和细胞分裂以及神经元传递的影响。在免疫系统和神经系统中,μ3受体可能是内源性吗啡或吗啡样物质的主要作用部位。这种受体系统也为外源性给药的阿片生物碱药物提供了一个额外的药理学作用位点。μ3受体被认为是一个重要的神经免疫环节。该系统可能在涉及免疫系统的各种反应中发挥重要作用,包括生物体对应激,感染和恶性转化的反应。
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