Leung E, Johnston C I, Woodcock E A
Biochem Biophys Res Commun. 1983 Jan 14;110(1):208-15. doi: 10.1016/0006-291x(83)91281-0.
Adenylate cyclase in homogenates of guinea pig ventricles was inhibited by the stable adenosine analogs N6-phenylisopropyladenosine (PIA) and 5(1)-N-ethylcarboxamidoadenosine (NECA). Inhibition required GTP and was enhanced by sodium ion. The maximum inhibition observed was 35.1 +/- 1.1%, the EC50 (95% confidence limits, n) for PIA and NECA were 0.20 microM (0.17-0.25 microM, 6) and 0.66 microM (0.26-1.7 microM, 4) respectively. 8-Phenyltheophylline (10 and 100 microM) and isobutylemethylxanthine (100 microM) antagonized the inhibitory effects of the adenosine analogs. These results indicate that adenosine receptors of the inhibitory type (RI or A1) are present in guinea pig myocardium and may mediate some of the cardiac responses to adenosine.
豚鼠心室匀浆中的腺苷酸环化酶受到稳定的腺苷类似物N6-苯基异丙基腺苷(PIA)和5(1)-N-乙基甲酰胺基腺苷(NECA)的抑制。抑制作用需要GTP,且钠离子可增强该作用。观察到的最大抑制率为35.1 +/- 1.1%,PIA和NECA的半数有效浓度(EC50,95%置信区间,n)分别为0.20微摩尔(0.17 - 0.25微摩尔,6)和0.66微摩尔(0.26 - 1.7微摩尔,4)。8-苯基茶碱(10和100微摩尔)以及异丁基甲基黄嘌呤(100微摩尔)可拮抗腺苷类似物的抑制作用。这些结果表明,豚鼠心肌中存在抑制型腺苷受体(RI或A1),且可能介导了心脏对腺苷的一些反应。