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西拉普利的降压及肾脏效应及其在肾血管性高血压大鼠中被血管紧张素逆转的情况。

Antihypertensive and renal effects of cilazapril and their reversal by angiotensin in renovascular hypertensive rats.

作者信息

Ding Y A, Chang S T, Shieh S M, Huang W C

机构信息

Department of Medicine, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

Clin Sci (Lond). 1988 Apr;74(4):365-72. doi: 10.1042/cs0740365.

Abstract
  1. The antihypertensive and renal effects of cilazapril, a new angiotensin converting enzyme inhibitor, were evaluated in both two-kidney, one-clip Goldblatt hypertensive rats (n = 11) and normotensive rats (n = 6). 2. Intravenous infusion of cilazapril (1 mg/kg followed by 25 micrograms min-1 kg-1) caused significant reductions of blood pressure from 163 +/- 3 to 122 +/- 4 mmHg and from 157 +/- 2 to 113 +/- 3 mmHg in two separate groups of hypertensive rats and from 124 +/- 1 to 105 +/- 2 mmHg in normotensive rats. The hypotensive effect in terms of absolute value of percentage change was greater in hypertensive rats than in normotensive rats (41 +/- 6 vs 20 +/- 3 mmHg or 25 +/- 4% vs 16 +/- 2%, respectively). 3. Cilazapril increased glomerular filtration rate, urine flow, and absolute and fractional excretion rates of sodium and potassium in the non-clipped kidney of hypertensive rats. In contrast, the clipped kidney exhibited a depressed renal function during cilazapril infusion. 4. In normotensive rats, the hypotensive and enhanced renal function responses to cilazapril were much less than those of the non-clipped kidney of hypertensive rats. 5. Superimposed administration of either angiotensin II or angiotensin III during cilazapril infusion completely reversed the blood pressure and bilateral renal responses of cilazapril in both hypertensive and normotensive rats. 6. These results indicate that cilazapril reduces arterial pressure and enhances renal excretion mainly via inhibition of angiotensin II and angiotensin III formation.
摘要
  1. 在双肾单夹型戈德布拉特高血压大鼠(n = 11)和正常血压大鼠(n = 6)中评估了新型血管紧张素转换酶抑制剂西拉普利的降压和肾脏效应。2. 静脉输注西拉普利(1 mg/kg,随后以25微克/分钟·千克⁻¹)使两组高血压大鼠的血压分别从163±3 mmHg显著降至122±4 mmHg以及从157±2 mmHg显著降至113±3 mmHg,使正常血压大鼠的血压从124±1 mmHg显著降至105±2 mmHg。就变化百分比的绝对值而言,高血压大鼠的降压效果大于正常血压大鼠(分别为41±6 mmHg对20±3 mmHg或25±4%对16±2%)。3. 西拉普利增加了高血压大鼠未夹闭肾脏的肾小球滤过率、尿流量以及钠和钾的绝对排泄率和排泄分数。相比之下,在输注西拉普利期间,夹闭的肾脏表现出肾功能降低。4. 在正常血压大鼠中,西拉普利引起的降压和肾功能增强反应远小于高血压大鼠未夹闭肾脏的反应。5. 在输注西拉普利期间叠加给予血管紧张素II或血管紧张素III可完全逆转西拉普利在高血压和正常血压大鼠中的血压和双侧肾脏反应。6. 这些结果表明,西拉普利主要通过抑制血管紧张素II和血管紧张素III的形成来降低动脉血压并增强肾脏排泄。

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