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长期阻断后循环和肾内肾素-血管紧张素系统的不同调节

Divergent regulation of circulating and intrarenal renin-angiotensin systems in response to long-term blockade.

作者信息

Kasper Sherry O, Basso Nidia, Kurnjek María Luisa, Paglia Nora, Ferrario Carlos M, Ferder Leon F, Diz Debra I

机构信息

Hypertension and Vascular Disease Center and Physiology/Pharmacology Department, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

Am J Nephrol. 2005 Jul-Aug;25(4):335-41. doi: 10.1159/000086571. Epub 2005 Jun 22.

Abstract

BACKGROUND/AIMS: Long-term treatment with angiotensin-converting enzyme (ACE) inhibitors or angiotensin (Ang) II type I (AT(1)) receptor blockers can improve kidney function and attenuate the progressive decline in kidney function associated with age. In this study in Wistar rats medicated for 22 months, we determined the effects of enalapril (10 mg/kg/day) and losartan (30 mg/kg/day) treatment, in comparison with vehicle (tap water), on renal AngII receptor density and circulating and urinary components of the renin-angiotensin system (RAS).

METHODS

Kidney sections were incubated with [(125)I-sarcosine(1)-threonine(8)]AngII (0.6 nM) for Ang receptor density, and Ang peptides were determined using radioimmunoassays.

RESULTS

Receptor density was approximately 50% higher in vasa recta, glomeruli, and tubulointerstitium in enalapril-treated rats and lower in vasa recta and glomeruli in losartan-treated relative to vehicle-treated rats. Losartan and enalapril treatment elevated plasma levels of AngI and Ang-(1-7) while AngII increased only in losartan-treated rats. In contrast, both treatments were associated with a reduction in urinary excretion of all three Ang peptides as compared with control rats.

CONCLUSION

The reduction in urinary Ang peptides with losartan and enalapril treatment suggests that blockade of intrarenal AngII may be an important mechanism underlying the renoprotection seen with such treatments.

摘要

背景/目的:长期使用血管紧张素转换酶(ACE)抑制剂或血管紧张素(Ang)II 1型(AT(1))受体阻滞剂治疗可改善肾功能,并减缓与年龄相关的肾功能进行性下降。在这项对Wistar大鼠进行22个月给药的研究中,我们确定了依那普利(10毫克/千克/天)和氯沙坦(30毫克/千克/天)治疗与溶剂(自来水)相比,对肾脏AngII受体密度以及肾素-血管紧张素系统(RAS)的循环和尿液成分的影响。

方法

用[(125)I-肌氨酸(1)-苏氨酸(8)]AngII(0.6纳摩尔)孵育肾脏切片以测定Ang受体密度,并用放射免疫分析法测定Ang肽。

结果

与溶剂处理的大鼠相比,依那普利处理的大鼠直小血管、肾小球和肾小管间质中的受体密度高约50%,氯沙坦处理的大鼠直小血管和肾小球中的受体密度较低。氯沙坦和依那普利治疗可提高血浆中AngI和Ang-(1-7)的水平,而AngII仅在氯沙坦处理的大鼠中升高。相比之下,与对照大鼠相比,两种治疗均与所有三种Ang肽的尿排泄减少有关。

结论

氯沙坦和依那普利治疗使尿中Ang肽减少,这表明阻断肾内AngII可能是此类治疗中肾脏保护作用的重要机制。

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