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在饮食盐负荷期间,循环和肾内血管紧张素 II 水平升高不当会加重 Cyp1a1-Ren-2 转基因大鼠的高血压。

Inappropriately high circulating and intrarenal angiotensin II levels during dietary salt loading exacerbate hypertension in Cyp1a1-Ren-2 transgenic rats.

机构信息

Department for Experimental Medicine, Institute for Clinical and Experimental Medicine, 1958/9 Vídenská, Prague, Czech Republic.

出版信息

J Hypertens. 2010 Mar;28(3):495-509. doi: 10.1097/HJH.0b013e3283345d69.

DOI:10.1097/HJH.0b013e3283345d69
PMID:19927008
Abstract

OBJECTIVE

We evaluated the effects of salt restriction and of increasing dietary salt loading on blood pressure and the renin-angiotensin system in transgenic rats with inducible hypertension.

METHODS

Hypertension was induced in Cyp1a1-Ren-2 rats through dietary administration of the natural xenobiotic indole-3-carbinol (0.3%), which activates the renin gene. Rats were fed either a normal-salt diet (0.6% NaCl), three different high-salt diets (2, 4 and 8% NaCl) or a low-salt diet (<0.04% NaCl). Blood pressure was monitored by radiotelemetry. Angiotensin II (ANG II) levels were determined by radioimmunoassay.

RESULTS

Induction of the renin gene by administration of indole-3-carbinol resulted in normal-salt diet fed animals in the development of severe hypertension that was accompanied by marked increases in plasma and kidney ANG II levels. Feeding the low-salt diet substantially attenuated the development of hypertension. Treatment with the 2 and 4% high-salt diet did not worsen the course of hypertension and did not alter ANG II levels when compared with rats on the normal salt diet. Feeding the 8% high-salt diet exacerbated the course of hypertension and was associated with further strong increases in plasma and kidney ANG II levels.

CONCLUSION

Our results demonstrate that after induction of the renin gene in Cyp1a1-Ren-2 transgenic rats inappropriate increases in plasma and kidney ANG II levels in response to very high dietary salt intake are responsible for the development of severe hypertension in this model of inducible renin transgenic rats.

摘要

目的

我们评估了盐限制和增加膳食盐负荷对诱导高血压的 Cyp1a1-Ren-2 转基因大鼠血压和肾素-血管紧张素系统的影响。

方法

通过饮食给予天然外源性物质吲哚-3-甲醇(0.3%)诱导 Cyp1a1-Ren-2 大鼠高血压,该物质可激活肾素基因。大鼠分别喂食正常盐饮食(0.6%NaCl)、三种不同的高盐饮食(2%、4%和 8%NaCl)或低盐饮食(<0.04%NaCl)。通过无线电遥测监测血压。通过放射免疫测定法测定血管紧张素 II(ANG II)水平。

结果

吲哚-3-甲醇诱导肾素基因表达导致正常盐饮食喂养的动物发生严重高血压,同时血浆和肾脏 ANG II 水平显著升高。低盐饮食可显著减轻高血压的发生。与正常盐饮食组相比,2%和 4%高盐饮食治疗并未使高血压恶化,也未改变 ANG II 水平。而 8%高盐饮食加重了高血压的发生,并与血浆和肾脏 ANG II 水平的进一步显著升高有关。

结论

我们的研究结果表明,在 Cyp1a1-Ren-2 转基因大鼠中诱导肾素基因后,对高盐饮食的不适当增加导致的血浆和肾脏 ANG II 水平升高是该诱导型肾素转基因大鼠模型中严重高血压发生的原因。

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