Takeda R
2nd Department of Internal Medicine, School of Medicine Kanazawa University.
Nihon Naibunpi Gakkai Zasshi. 1993 Dec 20;69(11):1101-22. doi: 10.1507/endocrine1927.69.11_1101.
With the recent advance in immunohistochemical and molecular-genetic techniques, all of the components of the renin-angiotensin system (RAS) have been shown to exist in the vascular tissue of various animal species as well as in humans. The author's group previously reported that angiotensin II (AII) was generated in the mesenteric arteries of several experimental rat models. Vascular AII generation appears to be regulated independently of circulating renin levels, as suggested by the expression of tissue-specific angiotensinogen mRNA. In the light of recent reports that aldosterone may be synthesized in the cultured endothelial cells from bovine aorta, and that 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD) plays a key role in determining the specificity in mineralocorticoid activity in various mineralocorticoid-responsive tissues, the author wishes to review the studies carried out by colleagues on the production of aldosterone with its precursor steroids and enzyme expression for aldosterone synthesis in the blood vessels as the components of the vascular auto-/paracrine system. The first part of the present paper is summarized as follows: 1) With Northern blotting and RT-PCR of the RNA which was prepared from rat arterial tissue or cultured human arterial smooth muscle cells (SMC), the expression of mineralo- and glucocorticoid receptors was confirmed. 2) The vascular production of aldosterone and corticosterone from the rat mesenteric artery was demonstrated in analyzing the arterial perfusates using a HPLC and GC/MS. Moreover, in this ex vivo experiment, the production of aldosterone in the vasculature was found to be partially controlled by angiotensin II generated locally. 3) It was clearly demonstrated using an RT-PCR method for the first time that aldosterone synthase, cytochrome P450aldo (c 18 or c mo); CYP 11B2 messenger RNA is expressed in the cultured endothelial cells (EC) from human pulmonary artery. From these data, the author would like to propose the concept of a vascular renin-angiotensin-aldosterone system under which paracrinaly produced mineralocorticoid in the vascular EC may easily reach the vascular SMC and in turn act to increase the vascular tone through binding to the receptor there. The second part can be summarized as follows: 1) The expression of 11 beta-HSD in the vasculature was confirmed by bioassay using ex vivo experiment of the isolated rat mesenteric artery perfusion system, immunocytochemical staining methods, in situ hybridization and also by Northern blot analysis.(ABSTRACT TRUNCATED AT 400 WORDS)
随着免疫组织化学和分子遗传学技术的最新进展,肾素-血管紧张素系统(RAS)的所有组分已被证明存在于各种动物物种以及人类的血管组织中。作者团队此前报道,在几种实验大鼠模型的肠系膜动脉中可生成血管紧张素II(AII)。组织特异性血管紧张素原mRNA的表达表明,血管AII的生成似乎独立于循环肾素水平而受到调节。鉴于最近有报道称醛固酮可能在牛主动脉的培养内皮细胞中合成,并且11β-羟基类固醇脱氢酶(11β-HSD)在决定各种盐皮质激素反应性组织中盐皮质激素活性的特异性方面起关键作用,作者希望回顾同事们关于醛固酮及其前体类固醇的产生以及作为血管自身/旁分泌系统组分的血管中醛固酮合成的酶表达的研究。本文第一部分总结如下:1)通过对从大鼠动脉组织或培养的人动脉平滑肌细胞(SMC)制备的RNA进行Northern印迹和RT-PCR,证实了盐皮质激素和糖皮质激素受体的表达。2)使用HPLC和GC/MS分析动脉灌注液,证实了大鼠肠系膜动脉可产生醛固酮和皮质酮。此外,在这个离体实验中,发现血管中醛固酮的产生部分受局部生成的血管紧张素II控制。3)首次使用RT-PCR方法清楚地证明,醛固酮合成酶,细胞色素P450aldo(c 18或c mo);CYP 11B2信使RNA在人肺动脉的培养内皮细胞(EC)中表达。根据这些数据,作者想提出血管肾素-血管紧张素-醛固酮系统的概念,在该系统中,血管内皮细胞旁分泌产生的盐皮质激素可能很容易到达血管平滑肌细胞,进而通过与那里的受体结合来增加血管张力。第二部分总结如下:1)通过使用离体大鼠肠系膜动脉灌注系统的实验、免疫细胞化学染色方法、原位杂交以及Northern印迹分析的生物测定,证实了11β-HSD在血管中的表达。(摘要截断于400字)