Renin was secreted by rat renal cortical slices incubated at 37 degrees C in a physiological saline solution. 2. Secretion was nearly abolished by incubation in a medium containing 60 mM-K. Secretion could be restored to the control level by the addition of 5 X 10(-7) M-D-600 (methoxy verapamil) to 60 mM-K medium. 3. Angiotensin II inhibited renin secretion in a concentration-dependent manner. Concentrations of D-600 ranging from 1 to 3 X 10(-6) M (two to sixfold higher than required to block the inhibitory effect of high K) failed to antagonize the inhibitory effect of angiotensin II. 4. Ca is required for the inhibitory effect of angiotensin II, however, as Ca-depletion (incubation of slices in a medium with Na2EGTA and no added CaCl2)( progressively decreased and finally abolished any inhibitory effect. 5. These results confirm and extend previous observations suggesting that Ca plays an inhibitory coupling role in the control of renin secretion from the juxtaglomerular apparatus. Moreover, they suggest that although voltage-sensitive channels exist on juxtaglomerular cells, angiotensin II activates an independent pathway for Ca mobilization.
摘要
肾素由在37摄氏度的生理盐溶液中孵育的大鼠肾皮质切片分泌。2. 在含60 mM - K的培养基中孵育时,分泌几乎被消除。通过向60 mM - K培养基中添加5×10(-7) M - D - 600(甲氧基维拉帕米),分泌可恢复到对照水平。3. 血管紧张素II以浓度依赖的方式抑制肾素分泌。浓度范围为1至3×10(-6) M的D - 600(比阻断高钾抑制作用所需浓度高两至六倍)未能拮抗血管紧张素II的抑制作用。4. 血管紧张素II的抑制作用需要钙,然而,随着钙耗竭(将切片在含Na2EGTA且未添加CaCl2的培养基中孵育),抑制作用逐渐降低并最终消除。5. 这些结果证实并扩展了先前的观察结果,表明钙在肾小球旁器肾素分泌的控制中起抑制性偶联作用。此外,它们表明尽管肾小球旁细胞上存在电压敏感通道,但血管紧张素II激活了一条独立的钙动员途径。