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慢性转换酶抑制对血管肾素-血管紧张素系统的影响。

Effects of chronic converting enzyme inhibition on the vascular renin-angiotensin system.

作者信息

Saito H, Nakamaru M, Rakugi H, Mikami H, Ogihara T, Inagami T

机构信息

Department of Geriatric Medicine, Osaka University Medical School, Japan.

出版信息

Clin Exp Pharmacol Physiol. 1990 Nov;17(11):745-53. doi: 10.1111/j.1440-1681.1990.tb01276.x.

Abstract
  1. The effects of chronic oral administration of inhibitors of angiotensin converting enzyme (ACE) on the vascular renin-angiotensin system were studied. 2. Male Sprague-Dawley rats were treated orally with five ACE inhibitors, captopril, enalapril, ramipril, cilazapril and CS-622 (10 mg/kg per day), for periods of 1-2 weeks. Their mesenteric arteries were then isolated and perfused in vitro with Krebs'-Ringer solution, and the angiotensin II (AII) released into the perfusate was measured under unstimulated and isoproterenol-stimulated conditions. The vascular renin activity was also determined after treatments with ACE inhibitors. 3. Treatment with captopril for 1 week suppressed the isoproterenol-stimulated increase in AII release, but had little effect on the baseline release. Oral treatment with captopril for 2 weeks or with other ACE inhibitors for 1 week markedly inhibited both the unstimulated and stimulated release of AII from the mesenteric vasculature. 4. Both the vascular renin activity and the plasma renin activity increased on captopril treatment, but their changes with time were different. 5. These results indicate that virtually complete inhibition of the vascular renin-angiotensin system can be achieved after prolonged treatment with ACE inhibitors, and suggest that the chronic antihypertensive action of ACE inhibitors is not solely due to inhibition of the plasma renin-angiotensin system.
摘要
  1. 研究了长期口服血管紧张素转换酶(ACE)抑制剂对血管肾素-血管紧张素系统的影响。2. 雄性Sprague-Dawley大鼠口服五种ACE抑制剂,卡托普利、依那普利、雷米普利、西拉普利和CS-622(每天10毫克/千克),持续1 - 2周。然后分离它们的肠系膜动脉,在体外用Krebs-Ringer溶液灌注,并在未刺激和异丙肾上腺素刺激条件下测量灌注液中释放的血管紧张素II(AII)。在用ACE抑制剂治疗后也测定了血管肾素活性。3. 用卡托普利治疗1周可抑制异丙肾上腺素刺激引起的AII释放增加,但对基线释放影响很小。用卡托普利口服治疗2周或用其他ACE抑制剂治疗1周可显著抑制肠系膜血管系统中未刺激和刺激状态下的AII释放。4. 卡托普利治疗后血管肾素活性和血浆肾素活性均升高,但它们随时间的变化不同。5. 这些结果表明,长期用ACE抑制剂治疗后可实现对血管肾素-血管紧张素系统的几乎完全抑制,并提示ACE抑制剂的慢性降压作用并非仅归因于对血浆肾素-血管紧张素系统的抑制。

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