Aktories K, Schultz G, Jakobs K H
Eur J Pharmacol. 1981 Apr 24;71(1):157-60. doi: 10.1016/0014-2999(81)90401-5.
Membrane preparations of hamster adipocytes were used to study the inhibition of adenylate cyclase by the adenosine analogue, N6-phenylisopropyladenosine (PIA). Inhibition by PIA was half-maximal and maximal (about 40%) at about 0.03 and 1 micro M, respectively, and was antagonized by 3-isobutyl-1-methylxanthine in a competitive manner. Like other hormone receptor-mediated inhibitions of the adipocyte adenylate cyclase, the adenosine receptor-mediated action on the enzyme was absolutely dependent on GTP and was amplified by sodium ions.
利用仓鼠脂肪细胞的膜制剂研究腺苷类似物N6-苯异丙基腺苷(PIA)对腺苷酸环化酶的抑制作用。PIA的抑制作用在约0.03微摩尔和1微摩尔时分别达到半数最大抑制和最大抑制(约40%),且被3-异丁基-1-甲基黄嘌呤以竞争性方式拮抗。与其他激素受体介导的脂肪细胞腺苷酸环化酶抑制作用一样,腺苷受体对该酶的作用绝对依赖于GTP,并被钠离子放大。