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大鼠肾血管性高血压中因转化酶抑制所致肾形态学损伤的后果

Consequences of renal morphologic damage induced by inhibition of converting enzyme in rat renovascular hypertension.

作者信息

Michel J B, Nochy D, Choudat L, Dussaule J C, Philippe M, Chastang C, Corvol P, Menard J

机构信息

Unité 36, Institut National de la Santé et de la Recherche Médicale 17, Paris.

出版信息

Lab Invest. 1987 Oct;57(4):402-11.

PMID:2823006
Abstract

The consequences of morphologic changes in the kidney distal to a stenosis induced by chronic administration of a converting enzyme inhibitor were determined after induction of experimental renovascular hypertension in rats. The relationship between changes in morphology in the clipped kidney and diuresis, creatinine, and mortality was studied by converting a two-kidney, one-clip model into a one-kidney, one-clip model after 1 month of converting enzyme inhibition. The right renal artery was constricted with a clip of 0.2 mm diameter to increase blood pressure, the left kidney was left untouched. After 1 month, systolic blood pressure had increased to 173 +/- 27 mm Hg in the clipped animals (n = 47) compared with 139 +/- 8 mm Hg in sham-operated animals (n = 15; group 1). An inhibitor of angiotensin-converting enzyme, MK421 (2 mg/kg, po), or an equivalent volume of vehicle was then administered daily for 1 month. After treatment with the converting enzyme inhibitor, blood pressure (148 +/- 28 mm Hg) was virtually identical with that of a sham-operated, vehicle-treated control group (145 +/- 16 mm Hg, n = 15), and was significantly lower than that of untreated hypertensive rats (186 +/- 30 mm Hg, n = 17) (group 2). The weight of the left kidney was increased in the untreated hypertensive animals as compared with sham-operated controls (1260 +/- 168 mg for group 2 versus 1075 +/- 100 mg for group 1). After treatment with MK421, the weight of the contralateral kidney (1472 +/- 190 mg) was further increased. After 1 month of treatment with MK421 or vehicle, the unclipped left kidney was removed from all animals. The treated animals were then randomly divided into two groups: one in which treatment with MK421 was stopped (treated/untreated, n = 24; group 3) and a second in which the treatment was continued (treated/treated, n = 23; group 4). The ability of the rats to excrete a water load of 15 ml was then examined 12 hours after removal of the unclipped left kidney. In the two groups of treated rats, the urinary excretion of the water load was decreased and frequency of oliguria was increased as compared with controls and hypertensive untreated rats. Survival rates were affected by the treatment: 3 deaths occurred in the hypertensive untreated group 2, 10 in the treated/untreated group 3, and 12 in the treated/treated group 4. The majority of these deaths could be attributed to renal insufficiency.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在大鼠实验性肾血管性高血压诱导后,确定了慢性给予转化酶抑制剂所导致的狭窄远端肾脏形态学改变的后果。通过在转化酶抑制1个月后将双肾单夹模型转变为单肾单夹模型,研究了夹闭肾形态学改变与利尿、肌酐及死亡率之间的关系。用直径0.2毫米的夹子夹闭右肾动脉以升高血压,左肾未处理。1个月后,夹闭动物(n = 47)的收缩压升至173±27毫米汞柱,而假手术动物(n = 15;第1组)为139±8毫米汞柱。然后每天给予血管紧张素转化酶抑制剂MK421(2毫克/千克,口服)或等量的赋形剂,持续1个月。用转化酶抑制剂治疗后,血压(148±28毫米汞柱)与假手术、赋形剂处理的对照组(145±16毫米汞柱,n = 15)基本相同,且显著低于未治疗的高血压大鼠(186±30毫米汞柱,n = 17)(第2组)。与假手术对照组相比,未治疗的高血压动物左肾重量增加(第2组为1260±168毫克,第1组为1075±100毫克)。用MK421治疗后,对侧肾重量(1472±190毫克)进一步增加。用MK421或赋形剂治疗1个月后,从所有动物身上切除未夹闭的左肾。然后将治疗动物随机分为两组:一组停止用MK421治疗(治疗/未治疗,n = 24;第3组),另一组继续治疗(治疗/治疗,n = 23;第4组)。在切除未夹闭的左肾12小时后,检测大鼠排泄15毫升水负荷的能力。与对照组和未治疗的高血压大鼠相比,两组治疗大鼠的水负荷尿排泄减少,少尿频率增加。存活率受治疗影响:未治疗的高血压第2组有3只死亡,治疗/未治疗第3组有10只死亡,治疗/治疗第4组有12只死亡。这些死亡大多可归因于肾功能不全。(摘要截断于400字)

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