Jackson B, Franze L, Sumithran E, Johnston C I
Department of Medicine, University of Melbourne, Austin Hospital, Victoria, Australia.
J Lab Clin Med. 1990 Jan;115(1):21-7.
Angiotensin converting enzyme (ACE) inhibitor treatment in renovascular hypertension is associated with acute compromise of renal function in patients with bilateral renal artery stenosis or with arterial stenosis to a single functioning kidney. Recent evidence has suggested that renal function is also compromised in the stenosed kidney of patients with unilateral renal artery stenosis. The long-term consequence of this reduction in renal function is not known. We have studied the effect of chronic ACE inhibition with enalapril on renal structure and function in rats with the two-kidney one-clip model of renovascular hypertension. Four weeks after placement of a clip on the left renal artery, hypertensive rats were randomized to treatment with enalapril, minoxidil, or to a no treatment group. Twelve months later split kidney function was determined by chromium 51-labeled ethylenediamine-tetraacetic acid clearance in surviving rats. Clearance of the clipped kidney was 0.0 ml/min (enalapril group), 0.26 +/- 0.23 ml/min (minoxidil group), and 0.74 +/- 0.13 ml/min (untreated group). The clipped kidney from the enalapril treated rats weighed much less than the minoxidil group or the untreated group (0.46 +/- 0.1 gm, 1.2 +/- 0.07 gm, and 1.14 +/- 0.10 gm, respectively). Enalapril treatment was stopped for 2 weeks in five rats. The clipped kidney remained small and nonfunctional. Histologic examination revealed marked interstitial fibrosis and tubular atrophy of the clipped kidneys from the enalapril treated group in contrast to minor changes in the minoxidil treated and untreated groups. After 12 months of treatment, survival in the enalapril group was 84%, 48% in the minoxidil group, and 15% in the untreated group.(ABSTRACT TRUNCATED AT 250 WORDS)
血管紧张素转换酶(ACE)抑制剂用于治疗肾血管性高血压时,对于双侧肾动脉狭窄患者或单肾动脉狭窄至仅存一个功能肾的患者,会导致肾功能急性受损。近期证据表明,单侧肾动脉狭窄患者的狭窄肾肾功能也会受损。这种肾功能降低的长期后果尚不清楚。我们采用双肾单夹肾血管性高血压大鼠模型,研究了依那普利长期抑制ACE对肾脏结构和功能的影响。在左肾动脉夹闭四周后,将高血压大鼠随机分为依那普利治疗组、米诺地尔治疗组或不治疗组。十二个月后,通过对存活大鼠进行铬51标记乙二胺四乙酸清除率测定来确定分肾功能。夹闭肾的清除率在依那普利组为0.0 ml/分钟,米诺地尔组为0.26±0.23 ml/分钟,未治疗组为0.74±0.13 ml/分钟。依那普利治疗组大鼠的夹闭肾重量远低于米诺地尔组或未治疗组(分别为0.46±0.1克、1.2±0.07克和1.14±0.10克)。五只大鼠停用依那普利治疗两周。夹闭肾仍保持较小且无功能。组织学检查显示,依那普利治疗组夹闭肾有明显的间质纤维化和肾小管萎缩,而米诺地尔治疗组和未治疗组变化较小。治疗十二个月后,依那普利组的存活率为84%,米诺地尔组为48%,未治疗组为15%。(摘要截选至250词)