Angiotensin II and the adrenal.

G Giacchetti, G Opocher, R Sarzani, A Rappelli, F Mantero
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Abstract

1. Angiotensin II (AngII) evokes a variety of physiological responses in the adrenal gland. It is the major regulator of aldosterone secretion, in the medulla it enhances catecholamine release and it exerts trophic effects in the adrenal and stimulates growth factor secretion. 2. Angiotensin II acts via binding to specific receptors, located on the plasma membrane. Two pharmacologically distinct AngII receptor subtypes, type 1 (AT1) and type 2 (AT2) receptors, have been identified using the non-peptide antagonists Dup753 and PD 123177, respectively, and cDNA encoding each type have been identified. 3. In the adrenal, the AT1 receptor modulates all the known biological effects of AngII. The expression of the AT1 receptor is modulated at the mRNA and protein levels by many factors: conditions that increase levels of AngII (low sodium diet, renovascular hypertension, AngII infusion) up-regulate AT1 receptor mRNA levels and binding and increase aldosterone secretion. 4. A tissue renin-angiotensin system has been found in the adrenal, suggesting an important paracrine role for AngII in aldosterone regulation. 5. The possible involvement of AT1 receptors in human disease has been investigated by examining the role of AngII receptors in adrenal tumours. Binding and gene expression studies have shown that AngII receptors are abundantly expressed in aldosterone-producing adenoma (APA). 6. Densitometric analysis of AT1 expression in APA showed no significant differences compared with normal and non-tumorous adrenal. In addition, no mutations in the coding sequence of the AT1 receptor have been found to date in adrenal tumours.

血管紧张素II和肾上腺。
1. 血管紧张素II (AngII)在肾上腺中引起多种生理反应。它是醛固酮分泌的主要调节剂,在髓质中促进儿茶酚胺的释放,在肾上腺中发挥营养作用,刺激生长因子的分泌。2. 血管紧张素II通过与位于质膜上的特定受体结合而起作用。用非肽拮抗剂Dup753和PD 123177分别鉴定了两种药理学上不同的AngII受体亚型,1型(AT1)和2型(AT2)受体,并鉴定了每种受体的cDNA编码。3.在肾上腺中,AT1受体调节所有已知的AngII生物学效应。AT1受体的表达在mRNA和蛋白水平上受到多种因素的调节:AngII水平升高的条件(低钠饮食、肾血管性高血压、AngII输注)上调AT1受体mRNA水平和结合,增加醛固酮分泌。4. 在肾上腺中发现了组织肾素-血管紧张素系统,提示AngII在醛固酮调节中具有重要的旁分泌作用。5. 通过检查AngII受体在肾上腺肿瘤中的作用,研究了AT1受体在人类疾病中的可能参与。结合和基因表达研究表明,AngII受体在醛固酮生成腺瘤(APA)中大量表达。6. APA中AT1表达的密度分析显示,与正常和非肿瘤肾上腺相比,AT1表达无显著差异。此外,在肾上腺肿瘤中尚未发现AT1受体编码序列的突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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