Osborne N N
Nuffield Laboratory of Ophthalmology, Oxford University, U.K.
Brain Res. 1991 Jul 5;553(1):84-8. doi: 10.1016/0006-8993(91)90233-l.
Adenylate cyclase activity in rabbit retinal homogenates can be stimulated directly by forskolin or through a receptor-mediated mechanism by vasoactive intestinal peptide (VIP). In contrast the alpha 2-adrenoceptor agonists clonidine and UK-14,304 reduce the basal cAMP level slightly. This was more evident following application of forskolin and VIP where the decrease of cAMP caused by clonidine and UK-14,304 is dose-dependent. The alpha 2-adrenoceptor agonist response is blocked by pertussis toxin and is insensitive to the phosphodiesterase inhibitor, isobutylmethylxanthine, suggesting the involvement of a Gi-protein. Clonidine and UK-14,304 attenuation of elevated cAMP levels can be inhibited by the alpha 2-receptor antagonist yohimbine and phentolamine but not by the specific alpha 1-receptor antagonist, prazosin. Serotonergic, cholinergic and beta-adrenergic receptor antagonists were without effect. The results demonstrate that alpha 2-adrenergic receptors in the retina exert inhibitory effects on adenylate cyclase activity mediated by an inhibitory guanine nucleotide regulating protein.
福司可林可直接刺激兔视网膜匀浆中的腺苷酸环化酶活性,血管活性肠肽(VIP)则可通过受体介导机制刺激该活性。相比之下,α2 -肾上腺素能受体激动剂可乐定和UK - 14,304可轻微降低基础cAMP水平。在应用福司可林和VIP后,这种情况更为明显,此时可乐定和UK - 14,304引起的cAMP降低呈剂量依赖性。α2 -肾上腺素能受体激动剂反应被百日咳毒素阻断,且对磷酸二酯酶抑制剂异丁基甲基黄嘌呤不敏感,提示有Gi蛋白参与。可乐定和UK - 14,304对升高的cAMP水平的减弱作用可被α2 -受体拮抗剂育亨宾和酚妥拉明抑制,但不能被特异性α1 -受体拮抗剂哌唑嗪抑制。5-羟色胺能、胆碱能和β-肾上腺素能受体拮抗剂均无作用。结果表明,视网膜中的α2 -肾上腺素能受体对由抑制性鸟嘌呤核苷酸调节蛋白介导的腺苷酸环化酶活性发挥抑制作用。