Neusy A J, Pessah M, Steele J M, Lowenstein J
Kidney Int. 1980 Jan;17(1):66-73. doi: 10.1038/ki.1980.8.
We examined the effects of an angiotensin III (AIII) analog, isoleucine-7 AIII (Ile7-AIII), on the steroidogenic and pressor responses to angiotensin II (AII) and AIII. AII or AIII (25 ng/kg/min) were infused alone or superimposed on an infusion of Ile7-AIII (100 ng/kg/min) in conscious male New Zealand rabbits. AII and AIII induced comparable increases in plasma aldosterone concentration, but AII exhibited significantly greater pressor effect. Ile7-AIII infusion resulted in significant inhibition of AII- but not AIII-induced steroidogenesis. Despite inhibition of aldosterone production, Ile7-AIII failed to block the pressor or renin-suppressing effect of AII. Inhibition of the steroidogenic effect of AII, but not of AII, by Ile7-AIII may be taken as evidence that adrenal stimulation by AII is direct and is not mediated by in vivo conversion to the heptapeptide. The ability of the heptapeptide analog to block aldosterone stimulation by the octapeptide AII suggests that adrenal receptors may, however, have a greater affinity for the heptapeptide.
我们研究了血管紧张素III(AIII)类似物异亮氨酸-7 AIII(Ile7-AIII)对血管紧张素II(AII)和AIII的类固醇生成及升压反应的影响。在清醒的雄性新西兰兔中,单独输注AII或AIII(25 ng/kg/分钟),或在输注Ile7-AIII(100 ng/kg/分钟)的基础上叠加输注AII或AIII。AII和AIII引起血浆醛固酮浓度的相似升高,但AII表现出明显更强的升压作用。输注Ile7-AIII导致对AII诱导的类固醇生成有显著抑制作用,但对AIII诱导的类固醇生成无抑制作用。尽管醛固酮生成受到抑制,但Ile7-AIII未能阻断AII的升压或肾素抑制作用。Ile7-AIII对AII而非AIII的类固醇生成作用的抑制,可能被视为AII对肾上腺的刺激是直接的,且不是由体内转化为七肽介导的证据。然而,七肽类似物阻断八肽AII对醛固酮刺激的能力表明,肾上腺受体可能对七肽具有更高的亲和力。