Herz A
J Neural Transm Suppl. 1983;18:227-33.
There is ample evidence from studies of peripheral isolated organs, binding of opiate receptor ligands to brain membranes and behavioural experiments that opiate receptors are not homogeneous but consist of different types such as the mu- (= morphine), delta- (= enkephalin), kappa- (= ketocyclazocine) and the epsilon- (= beta-endorphin) receptors. In addition, there are indications for subtypes within the particular classes of receptors, at least in the case of mu- and kappa-receptors. In one organ or particular brain structure, several types of receptors can be present-though big differences in the relative concentrations between various brain areas exist. The precise nature of the relationship between the multiplicity of opiate receptors and the multiplicity of endogenous opioids is not clear. The enkephalins and dynorphin appear to be, however, related to, respectively, delta- and kappa-receptors. According to our present knowledge, there is no strict relationship between certain physiological functions (or pharmacological actions) and the activation of a particular receptor type; for example, mu-, delta- and kappa-receptors are involved in pain modulation.
对外周孤立器官的研究、阿片受体配体与脑膜的结合以及行为实验都提供了充分证据,表明阿片受体并非同质,而是由不同类型组成,如μ-(=吗啡)、δ-(=脑啡肽)、κ-(=酮环唑辛)和ε-(=β-内啡肽)受体。此外,至少在μ-和κ-受体的情况下,特定受体类别中存在亚型的迹象。在一个器官或特定脑结构中,可能存在多种类型的受体——尽管不同脑区之间的相对浓度存在很大差异。阿片受体多样性与内源性阿片类物质多样性之间关系的确切性质尚不清楚。然而,脑啡肽和强啡肽似乎分别与δ-和κ-受体相关。根据我们目前的知识,特定生理功能(或药理作用)与特定受体类型的激活之间没有严格的关系;例如,μ-、δ-和κ-受体都参与疼痛调节。