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血管紧张素 II 受体拮抗剂氯沙坦对年轻自发性高血压大鼠的血压有持续影响:与血管结构无关。

Angiotensin II receptor antagonist losartan has persistent effects on blood pressure in the young spontaneously hypertensive rat: lack of relation to vascular structure.

作者信息

Morton J J, Beattie E C, MacPherson F

机构信息

MRC Blood Pressure Unit, Western Infirmary, Glasgow, UK.

出版信息

J Vasc Res. 1992 May-Jun;29(3):264-9. doi: 10.1159/000158941.

Abstract

The persistent effects on blood pressure of the angiotensin II receptor antagonist losartan and the converting enzyme inhibitor captopril were compared in the young spontaneously hypertensive rat (SHR). Losartan (DuP753/MK954, 15 mg/kg/day) and captopril (100 mg/kg/day) were given in the drinking water of 3-week-old SHRs for 4- and 10-week durations. Blood pressure was measured during treatment and after treatment was stopped until the age of 30 weeks. Both losartan and captopril given for 4 and 10 weeks prevented the development of hypertension during treatment and redevelopment of hypertension after treatment was stopped. Treatment for 10 weeks was more effective than for 4 weeks in lowering long-term pressure. Four weeks of treatment did not affect the mesenteric resistance artery media/lumen (m1/l1) ratio. In contrast, both losartan and captopril given for 10 weeks resulted in large and significant reductions in m1/l1 [5.3 +/- 0.8 and 5.63 +/- 0.8 vs 7.7 +/- 0.8 x 10(-2) (SD), p less than 0.001]. In losartan-treated rats, plasma renin and angiotensin II concentration were increased between 4- and 7-fold at the end of both treatment periods. These findings show losartan to be an effective antihypertensive agent and support data implicating angiotensin II in the early events leading to hypertension in this model. The abilities of losartan and captopril to affect blood pressure without affecting vascular structure suggest that the latter is a poor predictor of long-term hypertensive levels in the SHR.

摘要

在年轻的自发性高血压大鼠(SHR)中比较了血管紧张素II受体拮抗剂氯沙坦和转化酶抑制剂卡托普利对血压的持续影响。给3周龄的SHR饮用含氯沙坦(DuP753/MK954,15毫克/千克/天)和卡托普利(100毫克/千克/天)的水,持续4周和10周。在治疗期间和停止治疗后直至30周龄时测量血压。给予4周和10周的氯沙坦和卡托普利均能在治疗期间预防高血压的发展,并在停止治疗后预防高血压的再次出现。治疗10周在降低长期血压方面比治疗4周更有效。治疗4周对肠系膜阻力动脉中膜/管腔(m1/l1)比值没有影响。相比之下,给予10周的氯沙坦和卡托普利均导致m1/l1大幅显著降低[分别为5.3±0.8和5.63±0.8,而对照组为7.7±0.8×10(-2)(标准差),p<0.001]。在氯沙坦治疗的大鼠中,在两个治疗期结束时血浆肾素和血管紧张素II浓度增加了4至7倍。这些发现表明氯沙坦是一种有效的抗高血压药物,并支持了在该模型中血管紧张素II参与导致高血压早期事件的数据。氯沙坦和卡托普利在不影响血管结构的情况下影响血压的能力表明,血管结构对于SHR长期高血压水平的预测性较差。

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