Brock T A, Lewis L J, Smith J B
Proc Natl Acad Sci U S A. 1982 Mar;79(5):1438-42. doi: 10.1073/pnas.79.5.1438.
Angiotensin markedly altered the Na+ permeability of smooth muscle cells cultured from explants of rat aorta. The rate of net Na+ uptake was followed in the presence of ouabain in order to block Na+ efflux via the Na+/K+ pump. Angiotensin II (AII) or angiotensin III (AIII) increased net Na+ uptake by about 3-fold. Maximal stimulation of Na+ uptake was produced by about 10 nM AII. Bradykinin and the angiotensin antagonist [Sar1, Ileu5, Ala8]AII had no significant effect on net Na+ uptake. Angiotensin also enhanced the activity of the Na+/K+ pump, which was assayed by following the rate of ouabain-sensitive 86Rb+ uptake by the cells. AII and AIII nearly doubled ouabain-sensitive 86Rb+ uptake, but bradykinin, norepinephrine, and [Sar1, Ileu5, Ala8]AII had no effect. In the presence of ouabain, 86Rb+ uptake was not significantly affected by AII or AIII, indicating that angiotensin did not alter passive permeability to Rb+. Loading the cells with Na+, either by incubation in K+-free medium or exposure to the Na+-selective ionophore monensin, markedly increased ouabain-sensitive 86RB+ uptake. This result indicates that the activity of the Na+/K+ pump is limited by the low level of Na+ that is normally in the cells. AII had no effect on the activity of the Na+/K+ pump in Na+-loaded cells. These results suggest that AII or AIII stimulates the Na+/K+ pump in cultured aortic muscle cells by increasing its Na+ supply.
血管紧张素显著改变了从大鼠主动脉外植体培养的平滑肌细胞的钠通透性。在哇巴因存在的情况下追踪净钠摄取速率,以阻断通过钠钾泵的钠外流。血管紧张素II(AII)或血管紧张素III(AIII)使净钠摄取增加约3倍。约10 nM的AII产生了钠摄取的最大刺激作用。缓激肽和血管紧张素拮抗剂[Sar1,Ileu5,Ala8]AII对净钠摄取没有显著影响。血管紧张素还增强了钠钾泵的活性,这是通过追踪细胞对哇巴因敏感的86Rb +摄取速率来测定的。AII和AIII使对哇巴因敏感的86Rb +摄取几乎增加了一倍,但缓激肽、去甲肾上腺素和[Sar1,Ileu5,Ala8]AII没有作用。在哇巴因存在的情况下,AII或AIII对86Rb +摄取没有显著影响,表明血管紧张素没有改变对Rb +的被动通透性。通过在无钾培养基中孵育或暴露于钠选择性离子载体莫能菌素使细胞加载钠,显著增加了对哇巴因敏感的86RB +摄取。这一结果表明钠钾泵的活性受到细胞中正常低水平钠的限制。AII对钠加载细胞中的钠钾泵活性没有影响。这些结果表明,AII或AIII通过增加钠供应来刺激培养的主动脉肌细胞中的钠钾泵。