Dzau V J, Ingelfinger J R
Division of Vascular Medicine, Brigham and Women's Hospital, Boston, MA 02115.
J Hypertens Suppl. 1989 Sep;7(7):S3-8. doi: 10.1097/00004872-198909007-00002.
There has been considerable interest in the existence of an intrarenal renin-angiotensin system and its physiological implications. Recent demonstrations of renin, angiotensinogen and angiotensin converting enzyme messenger (m)RNAs in the kidney have provided strong evidence for the presence of an independent local system. This has been further supported by the demonstration of tissue-specific regulation of renin and angiotensinogen mRNA expression which may lead to differential systemic and intrarenal angiotensin activities. Using in situ hybridization, we have localized the intrarenal sites of gene expression and possible angiotensin production. One major site appears to be the proximal tubule, where local angiotensin can regulate sodium reabsorption and urine pH. Renin and angiotensinogen mRNA expressions are regulated by several common factors. In particular, sodium depletion stimulates the expression of both genes in the kidney, increasing the production of intrarenal angiotensin that is important in maintaining sodium homeostasis. Renal renin and angiotensinogen mRNA levels are altered in experimental heart failure and the spontaneously hypertensive rat (SHR). These changes in intrarenal renin and angiotensinogen mRNA expression may be important in the renal pathophysiology of these diseases.
肾内肾素 - 血管紧张素系统的存在及其生理意义一直备受关注。最近在肾脏中发现肾素、血管紧张素原和血管紧张素转换酶信使核糖核酸(mRNA),为独立局部系统的存在提供了有力证据。肾素和血管紧张素原mRNA表达的组织特异性调节的证明进一步支持了这一点,这可能导致全身和肾内血管紧张素活性的差异。利用原位杂交技术,我们已经定位了基因表达的肾内位点以及可能产生血管紧张素的部位。一个主要部位似乎是近端小管,局部血管紧张素可在该处调节钠重吸收和尿液pH值。肾素和血管紧张素原mRNA的表达受几种共同因素调节。特别是,钠缺乏会刺激肾脏中这两种基因的表达,增加肾内血管紧张素的产生,这对维持钠稳态很重要。在实验性心力衰竭和自发性高血压大鼠(SHR)中,肾脏肾素和血管紧张素原mRNA水平会发生改变。肾内肾素和血管紧张素原mRNA表达的这些变化可能在这些疾病的肾脏病理生理学中起重要作用。