Wojcik W J, Neff N H
Neurosci Lett. 1983 Oct 31;41(1-2):55-60. doi: 10.1016/0304-3940(83)90222-7.
Stimulation of either adenosine A1 or A2 receptors results in a decrease or an increase in the adenylate cyclase activity, respectively. With various concentrations of the adenosine agonist N6-phenylisopropyladenosine, both responses on cyclase are observed in a crude membrane preparation from rat striatum. The A2 receptors appeared to be associated primarily with intrinsic striatal neurons, as a kainic acid injection into the striatum resulted in about a 70% loss of receptor responsiveness to cyclase. The A1 receptors were more diffuse, being associated with intrinsic neurons and with cortical-striatal nerve terminals. From studies with 6-hydroxydopamine, we were unable to associate either receptor with dopaminergic nerve terminals within the striatum.
腺苷A1或A2受体的刺激分别导致腺苷酸环化酶活性降低或升高。使用不同浓度的腺苷激动剂N6-苯基异丙基腺苷,在大鼠纹状体的粗制膜制剂中观察到对环化酶的两种反应。A2受体似乎主要与纹状体内在神经元相关,因为向纹状体注射 kainic 酸导致受体对环化酶的反应性丧失约70%。A1受体分布更广泛,与内在神经元和皮质-纹状体神经末梢相关。通过6-羟基多巴胺的研究,我们无法将任何一种受体与纹状体内的多巴胺能神经末梢联系起来。