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用喹那普利(CI-906)和卡托普利对肾素-血管紧张素系统受抑制的自发性高血压大鼠进行血管紧张素转换酶抑制作用研究。

Angiotensin-converting enzyme inhibition with quinapril (CI-906) and captopril in spontaneously hypertensive rats with suppressed renin-angiotensin system.

作者信息

Säynävälammi P, Pörsti I

机构信息

Department of Biomedical Sciences, University of Tampere, Finland.

出版信息

Methods Find Exp Clin Pharmacol. 1987 Jun;9(6):325-31.

PMID:3309510
Abstract

Renin- and nonrenin-mediated antihypertensive actions of angiotensin-converting enzyme (ACE) inhibitors were investigated in young spontaneously hypertensive rats (SHR). Renin was suppressed either by removal of 2/3 of the renal mass, deoxycorticosterone (DOC) treatment, or 1% of NaCl in drinking water. Blood pressure responses to the nonsulfhydryl ACE inhibitor quinapril (CI-906) and the sulfhydryl inhibitor captopril, given orally for 2 days each, were examined by the tail cuff method. The marked depressor responses observed in control SHR were attenuated by the different manipulations in a manner clearly related to suppression of plasma renin activity (PRA). The decrease in blood pressure falls and in PRA was smallest in partially nephrectomized SHR. The mineralocorticoid (DOC) administration or 1% NaCl reduced PRA and the responses to ACE inhibitors markedly, though not completely. In a further experiment, severe salt retention induced by DOC and NaCl in uninephrectomized SHR suppressed PRA to an unmeasurable level and prevented the depressor action of a large dose of captopril. The results suggest that in SHR the acute blood pressure-lowering effect of ACE inhibitors is completely dependent on the renin-angiotensin system. The experiments also show that this system clearly participates in the support of rapidly increasing blood pressure in young SHR.

摘要

在年轻的自发性高血压大鼠(SHR)中研究了血管紧张素转换酶(ACE)抑制剂的肾素介导和非肾素介导的降压作用。通过切除2/3的肾组织、给予脱氧皮质酮(DOC)或在饮用水中添加1%的氯化钠来抑制肾素。采用尾套法检测了连续2天口服非巯基ACE抑制剂喹那普利(CI-906)和巯基抑制剂卡托普利后的血压反应。在对照SHR中观察到的明显降压反应因不同处理而减弱,其减弱方式与血浆肾素活性(PRA)的抑制明显相关。部分肾切除的SHR中血压下降和PRA的降低最小。给予盐皮质激素(DOC)或1%氯化钠可显著降低PRA以及对ACE抑制剂的反应,尽管不是完全消除。在进一步的实验中,DOC和氯化钠在单侧肾切除的SHR中诱导的严重盐潴留将PRA抑制到无法测量的水平,并阻止了大剂量卡托普利的降压作用。结果表明,在SHR中,ACE抑制剂的急性降压作用完全依赖于肾素-血管紧张素系统。实验还表明,该系统明显参与了年轻SHR中快速升高血压的维持。

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