Duman R S, Enna S J
Brain Res. 1986 Oct 8;384(2):391-4. doi: 10.1016/0006-8993(86)91179-0.
The alpha 2-adrenergic receptor regulation of cyclic adenosine monophosphate (cAMP) accumulation in rat brain slices was examined. using a prelabeling technique for measuring second messenger production. The mixed alpha-adrenergic agonist 6-fluoronorepinephrine, as well as the more selective alpha 2-agonists clonidine and UK-14,304, caused a concentration-dependent inhibition of forskolin-stimulated cAMP accumulation in cerebral cortical slices, whereas phenylephrine, a selective alpha 1-adrenergic agonist, had no inhibitory effect in this system. Moreover, alpha 2-adrenergic receptor antagonists were more potent than alpha 1-adrenergic antagonists in blocking the inhibitory response to UK-14,304. Neither alpha 1- nor alpha 2-adrenergic agonists displayed any inhibitory effect when cAMP accumulation was stimulated by isoproterenol, vasoactive intestinal peptide or 2-chloroadenosine. The results provide further evidence that some alpha 2-adrenergic receptors are negatively coupled to adenylate cyclase in brain, and yield a procedure for studying this phenomenon in intact central nervous system tissue.
运用预标记技术测量第二信使生成,对大鼠脑片中环磷酸腺苷(cAMP)积累的α2 - 肾上腺素能受体调节进行了研究。混合α - 肾上腺素能激动剂6 - 氟去甲肾上腺素,以及更具选择性的α2 - 激动剂可乐定和UK - 14,304,均导致大脑皮层切片中福斯高林刺激的cAMP积累呈浓度依赖性抑制,而选择性α1 - 肾上腺素能激动剂去氧肾上腺素在该系统中无抑制作用。此外,在阻断对UK - 14,304的抑制反应方面,α2 - 肾上腺素能受体拮抗剂比α1 - 肾上腺素能拮抗剂更有效。当异丙肾上腺素、血管活性肠肽或2 - 氯腺苷刺激cAMP积累时,α1 - 和α2 - 肾上腺素能激动剂均未显示出任何抑制作用。这些结果进一步证明,大脑中的一些α2 - 肾上腺素能受体与腺苷酸环化酶呈负偶联,并提供了一种在完整中枢神经系统组织中研究该现象的方法。