Ferré S, Fredholm B B, Morelli M, Popoli P, Fuxe K
Dept of Neuroscience, Karolinska Institute, Stockholm, Sweden.
Trends Neurosci. 1997 Oct;20(10):482-7. doi: 10.1016/s0166-2236(97)01096-5.
Increasing evidence suggests that antagonistic interactions between specific subtypes of adenosine and dopamine receptors in the basal ganglia are involved in the motor depressant effects of adenosine receptor agonists and the motor stimulant effects of adenosine receptor antagonists, such as caffeine. The GABAergic striatopallidal neurons are regulated by interacting adenosine A2A and dopamine D2 receptors. On the other hand, the GABAergic striatonigral and striatoentopeduncular neurons seem to be regulated by interacting adenosine A1 and dopamine D1 receptors. Furthermore, behavioural studies have revealed interactions between adenosine A2A and dopamine D1 receptors that occur at the network level. These adenosine-dopamine receptor-receptor interactions might offer new therapeutic leads for basal ganglia disorders.
越来越多的证据表明,基底神经节中特定亚型的腺苷受体和多巴胺受体之间的拮抗相互作用,与腺苷受体激动剂的运动抑制作用以及腺苷受体拮抗剂(如咖啡因)的运动兴奋作用有关。γ-氨基丁酸能的纹状体苍白球神经元受相互作用的腺苷A2A受体和多巴胺D2受体调节。另一方面,γ-氨基丁酸能的纹状体黑质和纹状体脚内核神经元似乎受相互作用的腺苷A1受体和多巴胺D1受体调节。此外,行为学研究揭示了腺苷A2A受体和多巴胺D1受体之间在网络水平上的相互作用。这些腺苷-多巴胺受体-受体相互作用可能为基底神经节疾病提供新的治疗线索。