Russell V A, Lamm M C, Taljaard J J
Department of Chemical Pathology, University of Stellenbosch, Tygerberg Hospital, R.S.A.
Neurochem Res. 1993 Mar;18(3):285-9. doi: 10.1007/BF00969084.
The alpha 2-adrenoceptor agonist, UK14304, dose-dependently inhibited the electrically stimulated release of dopamine (DA) from rat nucleus accumbens slices. This effect was antagonized by idazoxan, confirming that it was an alpha 2-adrenoceptor mediated effect. There was no evidence of endogenous activation of noradrenergic receptors suggesting that the alpha 2-adrenoceptor agonist was not acting presynaptically to inhibit noradrenaline release. An in vitro superfusion technique was used to investigate whether there was any interaction between alpha 2-adrenoceptors and DA D2-receptors in mediating their inhibitory effects on [3H]DA release from rat nucleus accumbens slices. alpha 2-Adrenoceptors and DA D2-receptors interact with similar second messenger systems and it was considered that they may compete for a common pool of G-proteins. The inhibitory effects of the alpha 2-adrenoceptor agonist, UK14304, and the DA receptor agonists, quinpirole, apomorphine and pergolide were not independent. However, there was no evidence of any interaction between UK14304 and the DA D2-receptor antagonists, sulpiride or haloperidol, suggesting that the two receptors do not compete for a common pool of G-proteins in mediating their inhibitory effects on DA release.
α2 - 肾上腺素能受体激动剂UK14304能剂量依赖性地抑制大鼠伏隔核切片中电刺激诱导的多巴胺(DA)释放。咪唑克生可拮抗此效应,证实这是一种由α2 - 肾上腺素能受体介导的效应。没有证据表明去甲肾上腺素能受体存在内源性激活,这表明α2 - 肾上腺素能受体激动剂并非通过作用于突触前膜来抑制去甲肾上腺素释放。采用体外灌流技术研究在介导对大鼠伏隔核切片[3H]DA释放的抑制作用时,α2 - 肾上腺素能受体与DA D2 - 受体之间是否存在相互作用。α2 - 肾上腺素能受体和DA D2 - 受体与相似的第二信使系统相互作用,人们认为它们可能竞争共同的G蛋白池。α2 - 肾上腺素能受体激动剂UK14304以及DA受体激动剂喹吡罗、阿扑吗啡和培高利特的抑制作用并非相互独立。然而,没有证据表明UK14304与DA D2 - 受体拮抗剂舒必利或氟哌啶醇之间存在任何相互作用
,这表明在介导对DA释放的抑制作用时,这两种受体并不竞争共同的G蛋白池。