Kintz P, Himber J, de Burlet G, Andermann G
Alcon France, Research and Development, Kaysersberg.
Curr Eye Res. 1988 Mar;7(3):287-92. doi: 10.3109/02713688809047034.
Inhibition of ciliary process adenylate cyclase was studied on rabbit membrane preparations. When considered individually, epinephrine, GTP and NaCl did not inhibit adenylate cyclase activity. On the other hand, when present together, epinephrine, GTP (10(-5) M) and NaCl (200 mM) acted synergistically to cause a 27% inhibition of basal activity. A similar inhibition was observed with 1-norepinephrine. Clonidine and BHT 920, two alpha 2-agents were found to be partial agonists causing 63% and 82% as much inhibition as epinephrine. Phenylephrine, an alpha 1-agonist did not inhibit adenylate cyclase activity at concentrations up to 10(-4) M. Yohimbine and phentolamine prevented the inhibition of adenylate cyclase by epinephrine, while prazosin was ineffective. Alpha 2-receptor selectivity in rabbit ciliary processes and their negative coupling to an adenylate cyclase via a NaCl-dependent GTP binding protein, Ni, is thus well established.
在兔膜制剂上研究了睫状突腺苷酸环化酶的抑制作用。单独考虑时,肾上腺素、GTP和NaCl均不抑制腺苷酸环化酶活性。另一方面,当它们同时存在时,肾上腺素、GTP(10⁻⁵M)和NaCl(200mM)协同作用,使基础活性受到27%的抑制。用1-去甲肾上腺素也观察到类似的抑制作用。发现可乐定和BHT 920这两种α₂-剂是部分激动剂,其抑制作用分别为肾上腺素的63%和82%。苯肾上腺素是一种α₁-激动剂,在浓度高达10⁻⁴M时不抑制腺苷酸环化酶活性。育亨宾和酚妥拉明可阻止肾上腺素对腺苷酸环化酶的抑制作用,而哌唑嗪则无效。因此,兔睫状突中的α₂-受体选择性及其通过依赖NaCl的GTP结合蛋白Ni与腺苷酸环化酶的负偶联已得到充分证实。