Campbell W B, Brooks S N, Pettinger W A
Science. 1974 May 31;184(4140):994-6. doi: 10.1126/science.184.4140.994.
The potential role of angiotensin II and its heptapeptide metabolite, des-aspartyl-angiotensin II, was studied in the conscious unanesthetized rat. Aldosterone release was induced by both peptides at physiologic doses (0.72 nanogram per minute). [I-Sarcosyl-8-alanyl]-angiotensin II (P-113 inhibited angiotensin II more effectively than des-aspartyl-angiotensin II (101 percent as compared to 82 percent). These results indicate that angiotensin controls aldosterone release in the rat and that des-aspartyl-angiotensin II (that is, angiotensin III) may be important in this sequence.
在清醒未麻醉的大鼠中研究了血管紧张素II及其七肽代谢产物去天冬氨酰血管紧张素II的潜在作用。两种肽在生理剂量(每分钟0.72纳克)时均可诱导醛固酮释放。[I-肌氨酰-8-丙氨酰] -血管紧张素II(P-113)抑制血管紧张素II的作用比去天冬氨酰血管紧张素II更有效(分别为101%和82%)。这些结果表明,血管紧张素控制大鼠体内醛固酮的释放,而去天冬氨酰血管紧张素II(即血管紧张素III)在这一过程中可能起重要作用。