Sim M K, Yuan H T
Department of Pharmacology, Faculty of Medicine, National University of Singapore.
Eur J Pharmacol. 1995 May 15;278(2):175-8. doi: 10.1016/0014-2999(95)00163-f.
Nanomolar concentrations of des-Asp-angiotensin I potentiated the contractile action of angiotensin II on the rabbit aortic ring but attenuated the contractile action of angiotensin III in the same tissue. Indomethacin had no effect on the potentiation of angiotensin II but inhibited the attenuation of angiotensin III. The action of angiotensin II, angiotensin III and des-Asp-angiotensin I was not inhibited by (S)-1-}[4-(dimethylamino)-3-methylphenyl]methyl}-5-(diphenylacetyl )-4,5,6, 7-tetrahydro-1H-imidazo-[4,5-c]pyridine-6-carboxylic acid, ditrifluoroacetate, dihydrate (PD123319), an angiotensin AT2 receptor antagonist. The data show that angiotensin II and angiotensin III act on different subclasses of angiotensin receptors and that their actions are differentially modulated by des-Asp-angiotensin I. The data also indicate the possibility that des-Asp-angiotensin I is a functional peptide that modulates the contractile action of the two angiotensins at sub-nanomolar concentrations.
纳摩尔浓度的去天冬氨酸血管紧张素I增强了血管紧张素II对兔主动脉环的收缩作用,但减弱了血管紧张素III在同一组织中的收缩作用。吲哚美辛对血管紧张素II的增强作用无影响,但抑制了血管紧张素III的减弱作用。血管紧张素II、血管紧张素III和去天冬氨酸血管紧张素I的作用不受血管紧张素AT2受体拮抗剂(S)-1-}[4-(二甲基氨基)-3-甲基苯基]甲基}-5-(二苯基乙酰基)-4,5,6,7-四氢-1H-咪唑并-[4,5-c]吡啶-6-羧酸,二水合二氟乙酸盐(PD123319)的抑制。数据表明,血管紧张素II和血管紧张素III作用于不同亚类的血管紧张素受体,且它们的作用受到去天冬氨酸血管紧张素I的不同调节。数据还表明,去天冬氨酸血管紧张素I可能是一种功能性肽,在亚纳摩尔浓度下调节这两种血管紧张素的收缩作用。