Tanabe A, Naruse M, Arai K, Naruse K, Yoshimoto T, Seki T, Imaki T, Miyazaki H, Zeng Z P, Demura R, Demura H
Department of Medicine, Institute of Clinical Endocrinology, Tokyo Women's Medical College, Japan.
Horm Metab Res. 1998 Aug;30(8):490-5. doi: 10.1055/s-2007-978918.
Although stimulation of aldosterone secretion is one of the functions of angiotensin II, the gene expression and biological significance of the angiotensin II receptor subtypes, AT1 and AT2, in the human adrenal have not been characterized. We therefore investigated the transcription levels of the receptor subtype genes and their roles in regulation of steroid secretion by human adrenals. The expression of AT1 and AT2 receptor mRNA was assessed by reverse transcription-polymerase chain reaction followed by Southern blot analysis in normal adrenocortical tissues (n = 6) and a series of adrenal tumour tissues: aldosterone-producing adrenocortical adenoma (n=6), Cushing's syndrome (n = 6) and pheochromocytoma (n = 6). The role of the two receptor subtypes in steroid secretion in vitro was examined by incubating the tissue with angiotensin II(1 microM) with or without the selective AT1 antagonist CV-11974 (1 microM). Both AT1 and AT2 receptor mRNA transcripts were demonstrated in all of the human adrenal tissues tested. Angiotensin II-induced aldosterone secretion was suppressed 50% upon the addition of CV-11974. The selective AT2 agonist CGP-42112 increased aldosterone secretion by 55% over the control, which was not suppressed by CV-11974. Angiotensin II and CGP-42112 did not affect cortisol secretion. These results suggest that both AT2 and AT1 receptors may be involved in the regulation of aldosterone secretion and tumorigenesis of the human adrenals.
虽然刺激醛固酮分泌是血管紧张素II的功能之一,但血管紧张素II受体亚型AT1和AT2在人肾上腺中的基因表达及生物学意义尚未明确。因此,我们研究了受体亚型基因的转录水平及其在人肾上腺类固醇分泌调节中的作用。通过逆转录-聚合酶链反应,随后在正常肾上腺皮质组织(n = 6)和一系列肾上腺肿瘤组织中进行Southern印迹分析,评估AT1和AT2受体mRNA的表达:醛固酮分泌性肾上腺皮质腺瘤(n = 6)、库欣综合征(n = 6)和嗜铬细胞瘤(n = 6)。通过将组织与血管紧张素II(1 microM)一起孵育,添加或不添加选择性AT1拮抗剂CV-11974(1 microM),来检测两种受体亚型在体外类固醇分泌中的作用。在所有测试的人肾上腺组织中均证实了AT1和AT2受体mRNA转录本。添加CV-11974后,血管紧张素II诱导的醛固酮分泌被抑制了50%。选择性AT2激动剂CGP-42112使醛固酮分泌比对照增加了55%,且未被CV-11974抑制。血管紧张素II和CGP-42112不影响皮质醇分泌。这些结果表明,AT2和AT1受体可能都参与了人肾上腺醛固酮分泌的调节和肿瘤发生。