Bührle C P, Rosivall L, Taugner R
Am J Physiol. 1987 Apr;252(4 Pt 2):F635-44. doi: 10.1152/ajprenal.1987.252.4.F635.
Angiotensin II (ANG II) reversibly depolarizes renin-containing juxtaglomerular epithelioid cells (JGECs) of the hydronephrotic mouse kidney afferent arteriole. This depolarizing response was utilized to assess changes in ANG II concentration in the vicinity of JGECs in order to test whether ANG II is generated from ANG I and artificial renin substrate (ARS) in this preparation. Depolarizations were also produced by the application of ANG I and ARS in the superfusing medium. These responses to ANG I and ARS were completely blocked by saralasin. Hence, our findings are indicative for an intrarenal, local generation of ANG II. As opposed to saralasin, several converting enzyme and renin inhibitors only diminished but generally did not abolish the actions of ANG I and ARS, respectively. These results suggest an alternative, nonrenin and non-converting enzyme-dependent pathway of ANG II generation in renal tissue.
血管紧张素II(ANG II)可使肾积水小鼠肾脏传入小动脉中含肾素的球旁上皮样细胞(JGECs)发生可逆性去极化。这种去极化反应被用于评估JGECs附近ANG II浓度的变化,以测试在此制剂中ANG II是否由血管紧张素I(ANG I)和人工肾素底物(ARS)产生。在灌注培养基中应用ANG I和ARS也会产生去极化。对ANG I和ARS的这些反应被沙拉新完全阻断。因此,我们的研究结果表明肾脏内局部产生ANG II。与沙拉新不同,几种转化酶和肾素抑制剂仅分别减弱但通常并未消除ANG I和ARS的作用。这些结果提示在肾组织中存在一种替代的、非肾素和非转化酶依赖性的ANG II生成途径。