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血管紧张素II拮抗剂对易卒中型自发性高血压大鼠的肾脏影响。

Renal effects of an angiotensin II antagonist in stroke-prone spontaneously hypertensive rat.

作者信息

Yo Y, Moriguchi A, Higaki J, Nagano M, Nakano N, Kamide K, Yu H, Mikami H, Ogihara T

机构信息

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

出版信息

Nephron. 1997;76(4):466-71. doi: 10.1159/000190230.

DOI:10.1159/000190230
PMID:9274845
Abstract

We evaluated the renal effects of the new angiotensin II type 1 (AT ) receptor antagonist, HR 720, in the stroke-prone spontaneously hypertensive rat. Rats were treated with either vehicle, HR 720, MK-954 (a selective AT1 receptor antagonist) or enalapril for 6 weeks. Blood pressure was decreased to a similar extent by HR 720, MK-954 and enalapril (203 +/- 4, 202 +/- 5 and 190 +/- 4 vs. 247 +/- 4 mm Hg for control). Urinary protein secretion was also decreased (5.2 +/- 0.3, 5.3 +/- 0.2 and 5.5 +/- 0.6 vs. 25.2 +/- 4.6 mg/100g/24h). The glomerular hypertensive change was improved in each drug-treated group (2.0 +/- 0.2, 3.3 +/- 0.3 and 1.6 +/- 0.1 vs. 17.6 +/- 1.5%; p < 0.0001). These results show that, in addition to its antihypertensive effect, HR 720 has a beneficial effect on renal function.

摘要

我们在易患中风的自发性高血压大鼠中评估了新型1型血管紧张素II(AT)受体拮抗剂HR 720对肾脏的影响。大鼠分别接受赋形剂、HR 720、MK - 954(一种选择性AT1受体拮抗剂)或依那普利治疗6周。HR 720、MK - 954和依那普利使血压降低的程度相似(对照组为247±4 mmHg,用药组分别为203±4、202±5和190±4 mmHg)。尿蛋白分泌也减少了(分别为5.2±0.3、5.3±0.2和5.5±0.6,对照组为25.2±4.6 mg/100g/24h)。每个药物治疗组的肾小球高血压变化均得到改善(分别为2.0±0.2、3.3±0.3和1.6±0.1,对照组为17.6±1.5%;p<0.0001)。这些结果表明,HR 720除具有降压作用外,对肾功能也有有益影响。

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