Bravo E L, Khosla M C, Bumpus F M
J Clin Endocrinol Metab. 1975 Mar;40(3):530-3. doi: 10.1210/jcem-40-3-530.
The vascular and steroidogenic responses to (1-Sarcosine, 8-Isoleucine)-, and to (1-Des (Aspartic acid), 8-Isoleucine) angiotensin II were compared in bilaterally nephrectomized, ACTH-suppressed dogs receiving constant infusions of angiotensin II. Aldosterone secretion rate was significantly inhibited by pretreatment with 200 ng/Kg/min of the heptapeptide, (1-Des(Aspartic acid), 8-Isoleucine) ang II, but not by similar doses of the octapeptide, (1-Sarcosine, 8-Isoleucine) ang II. In contrast, the pressor action of ang II was unaffected by (1-Des (Aspartic acid), 8-Isoleucine) ang II though significant inhibition occurred with relatively small doses of (1-Sarcosine, 8-Isoleucine) ang II. This study suggests that: (a) angiotensin receptors in adrenal cortex and vascular smooth muscle are functionally different, and (b) (1-Des(Aspartic acid),8-Isoleucine) angiotensin II is a specific antagonist of steroidogenic effect of ang II.
在接受血管紧张素II持续输注的双侧肾切除、促肾上腺皮质激素抑制的犬中,比较了对(1-肌氨酸,8-异亮氨酸)-和对(1-去(天冬氨酸),8-异亮氨酸)血管紧张素II的血管和类固醇生成反应。用200 ng/Kg/分钟的七肽(1-去(天冬氨酸),8-异亮氨酸)血管紧张素II预处理可显著抑制醛固酮分泌率,但相似剂量的八肽(1-肌氨酸,8-异亮氨酸)血管紧张素II则无此作用。相反,血管紧张素II的升压作用不受(1-去(天冬氨酸),8-异亮氨酸)血管紧张素II影响,而相对小剂量的(1-肌氨酸,8-异亮氨酸)血管紧张素II则可产生显著抑制作用。本研究提示:(a)肾上腺皮质和血管平滑肌中的血管紧张素受体在功能上不同,且(b)(1-去(天冬氨酸),8-异亮氨酸)血管紧张素II是血管紧张素II类固醇生成作用的特异性拮抗剂。