Gröne H J, Helmchen U
Lab Invest. 1986 Jun;54(6):645-55.
Earlier experiments have shown that in sodium depleted hypertensive rats with bilaterally constricted renal arteries the arterial pressure normalized after blockade of the renin-angiotensin system; simultaneously acute renal failure occurred. In hypertensive rats with unilateral renal artery stenosis an impaired excretory function of the clipped kidney can be expected, but may not be detectable by conventional tests of renal function. Male Wistar rats with chronic two kidney, one clip hypertension were fed a low sodium diet. After 7 days the rats were treated with vehicle, with the vasodilator dihydralazine, or with the angiotension converting enzyme inhibitor MK 421 for 2 weeks. During the 14-day treatment period a continuous blood pressure reduction was achieved in dihydralazine and MK 421 treated rats. Overall excretory kidney function (plasma creatinine concentration) was well maintained in all three groups until the end of the antihypertensive drug treatment. At the end of drug therapy mean glomerular filtration rates of the left clipped kidneys were significantly lower in both treated groups compared to hypertensive controls, and mean glomerular filtration rate of the left clipped kidneys of dihydralazine treated rats was significantly higher than in MK 421 treated rats: controls (N = 6) 1.03 +/- 0.03, dihydralazine-group (N = 10) 0.28 +/- 0.07, MK 421-group (N = 9) 0.03 +/- 0.01 ml/min. Renal blood flows were comparable in both treated groups. Only the left kidneys of rats treated with MK 421 showed a prominent tubular atrophy. Seven days after declipping of the left renal artery and right nephrectomy a considerable restitution of the tubular structure had occurred in the MK 421-group. The recovery of tubular epithelial cells was paralleled by a rise in glomerular filtration rate: MK 421 group (N = 7) 1.25 +/- 0.08 ml/min. Thus, the clipped kidney in two kidney, one clip hypertensive rats showed functional and morphological signs of impairment when systemic arterial pressure was reduced to the normal range. The alterations of the clipped kidney were most pronounced in rats with renin-angiotensin system-blockade.
早期实验表明,在双侧肾动脉狭窄的失钠型高血压大鼠中,肾素 - 血管紧张素系统被阻断后动脉血压恢复正常;同时发生了急性肾衰竭。在单侧肾动脉狭窄的高血压大鼠中,可以预期夹闭侧肾脏的排泄功能受损,但通过传统的肾功能测试可能无法检测到。给患有慢性双肾单夹高血压的雄性Wistar大鼠喂食低钠饮食。7天后,大鼠分别用赋形剂、血管扩张剂双肼屈嗪或血管紧张素转换酶抑制剂MK 421治疗2周。在14天的治疗期间,双肼屈嗪和MK 421治疗的大鼠血压持续降低。在抗高血压药物治疗结束前,所有三组的总体肾脏排泄功能(血浆肌酐浓度)均保持良好。药物治疗结束时,与高血压对照组相比,两个治疗组中左夹闭肾脏的平均肾小球滤过率均显著降低,且双肼屈嗪治疗大鼠左夹闭肾脏的平均肾小球滤过率显著高于MK 421治疗的大鼠:对照组(N = 6)1.03±0.03,双肼屈嗪组(N = 10)0.28±0.07,MK 421组(N = 9)0.03±0.01 ml/分钟。两个治疗组的肾血流量相当。仅MK 421治疗的大鼠的左肾显示出明显的肾小管萎缩。左肾动脉夹闭解除和右肾切除7天后,MK 421组的肾小管结构有相当程度的恢复。肾小管上皮细胞的恢复与肾小球滤过率的升高平行:MK 421组(N = 7)1.25±0.08 ml/分钟。因此,在双肾单夹高血压大鼠中,当全身动脉血压降至正常范围时,夹闭侧肾脏显示出功能和形态学损伤的迹象。在肾素 - 血管紧张素系统阻断的大鼠中,夹闭侧肾脏的改变最为明显。