Anand-Srivastava M B
Biochem Biophys Res Commun. 1983 Dec 16;117(2):420-8. doi: 10.1016/0006-291x(83)91217-2.
Angiotensin II (AII) inhibited adenylate cyclase from rat aorta in a concentration dependent manner. The maximal inhibition (approximately 20%) was observed at 10 microM. The inhibitory effect of angiotensin II was dependent on monovalent cations such as Na+ or Li+ and was blocked by saralasin, an antagonist of angiotensin. Guanine nucleotides such as GTP or GMP-P (NH)P were also required to elicit the inhibition by angiotensin II. In addition, angiotensin II also inhibited the stimulation exerted by catecholamines. These data suggest that angiotensin receptors are present in aorta which are negatively coupled to adenylate cyclase.
血管紧张素II(AII)以浓度依赖的方式抑制大鼠主动脉的腺苷酸环化酶。在10微摩尔时观察到最大抑制作用(约20%)。血管紧张素II的抑制作用依赖于单价阳离子,如Na+或Li+,并被血管紧张素拮抗剂沙拉新所阻断。鸟嘌呤核苷酸,如GTP或GMP-P(NH)P也参与介导血管紧张素II的抑制作用。此外,血管紧张素II还抑制儿茶酚胺所产生的刺激作用。这些数据表明,主动脉中存在与腺苷酸环化酶负性偶联的血管紧张素受体。