Tang L C, Cotzias G C
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1546-8. doi: 10.1073/pnas.75.3.1546.
The effect of several concentrations of morphine on the activity of adenylate cyclase [ATP pyrophosphate-lyase (cyclizing): EC 4.6.1.1.] was measured in homogenates of caudate nuclei of mice. Morphine stimulated the enzyme at 500 micron and inhibited slightly at 5 micron. Morphine stimulation was blocked by naloxone. Depending on its dose, morphine also increased or decreased the stimulating effect of dopamine on the dopamine-sensitive adenylate cyclase activity of caudate homogenate. Like dopamine, morphine'e effect on the adenylate cyclase activity was increased or decreased, respectively, by pretreating the animals with poly(I).poly(C) or with chloramphenicol. Thus, both dopamine and morphine appear to act on the same receptor. This "new" receptor differs from the one described by Snyder et al. and others, who demonstrated only binding affinity and no enzymatic activity. These data indicate that certain functions of the opiates might be mediated through the dopamine-sensitive adenylate cyclase of the caudate nuclei, which are the dopamine receptors in the brain.
在小鼠尾状核匀浆中测定了几种浓度的吗啡对腺苷酸环化酶[ATP焦磷酸裂解酶(环化):EC 4.6.1.1]活性的影响。吗啡在500微摩尔时刺激该酶,在5微摩尔时略有抑制。纳洛酮可阻断吗啡的刺激作用。根据剂量不同,吗啡还会增强或减弱多巴胺对尾状核匀浆中多巴胺敏感性腺苷酸环化酶活性的刺激作用。与多巴胺一样,预先用聚(I)·聚(C)或氯霉素处理动物后,吗啡对腺苷酸环化酶活性的作用分别增强或减弱。因此,多巴胺和吗啡似乎作用于同一受体。这种“新”受体不同于斯奈德等人及其他研究者所描述的受体,他们仅证明了结合亲和力,而未证明酶活性。这些数据表明,阿片类药物的某些功能可能通过尾状核的多巴胺敏感性腺苷酸环化酶介导,而尾状核中的这些酶是大脑中的多巴胺受体。