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雌激素可降低醛固酮水平,上调肾上腺血管紧张素II AT2受体,并使去卵巢大鼠的肾上腺髓质Fra-2恢复正常。

Estrogen reduces aldosterone, upregulates adrenal angiotensin II AT2 receptors and normalizes adrenomedullary Fra-2 in ovariectomized rats.

作者信息

Macova Miroslava, Armando Ines, Zhou Jin, Baiardi Gustavo, Tyurmin Dmitri, Larrayoz-Roldan Ignacio M, Saavedra Juan M

机构信息

Section on Pharmacology, Division of Intramural Research Programs, National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, Bethesda, Md, USA.

出版信息

Neuroendocrinology. 2008;88(4):276-86. doi: 10.1159/000150977. Epub 2008 Aug 4.

Abstract

We studied the effect of ovariectomy and estrogen replacement on expression of adrenal angiotensin II AT1 and AT2 receptors, aldosterone content, catecholamine synthesis, and the transcription factor Fos-related antigen 2 (Fra-2). Ovariectomy increased AT1 receptor expression in the adrenal zona glomerulosa and medulla, and decreased adrenomedullary catecholamine content and Fra-2 expression when compared to intact female rats. In the zona glomerulosa, estrogen replacement normalized AT1 receptor expression, decreased AT1B receptor mRNA, and increased AT2 receptor expression and mRNA. Estrogen treatment decreased adrenal aldosterone content. In the adrenal medulla, the effects of estrogen replacement were: normalized AT1 receptor expression, increased AT2 receptor expression, AT2 receptor mRNA, and tyrosine hydroxylase mRNA, and normalized Fra-2 expression and catecholamine content. We demonstrate that the constitutive adrenal expression of AT1 receptors, catecholamine synthesis and Fra-2 expression are partially under the control of reproductive hormones. Our results suggest that estrogen treatment decreases aldosterone production through AT1 receptor downregulation and AT2 receptor upregulation. AT2 receptor upregulation and modulation of Fra-2 expression may participate in the estrogen-dependent normalization of adrenomedullary catecholamine synthesis in ovariectomized rats. The AT2 receptor upregulation and the decrease in AT1 receptor function and in the production of the fluid-retentive, pro-inflammatory hormone aldosterone partially explain the protective effects of estrogen therapy.

摘要

我们研究了卵巢切除和雌激素替代对肾上腺血管紧张素II AT1和AT2受体表达、醛固酮含量、儿茶酚胺合成以及转录因子Fos相关抗原2(Fra-2)的影响。与完整雌性大鼠相比,卵巢切除增加了肾上腺球状带和髓质中AT1受体的表达,并降低了肾上腺髓质儿茶酚胺含量和Fra-2表达。在球状带,雌激素替代使AT1受体表达正常化,降低了AT1B受体mRNA水平,并增加了AT2受体表达和mRNA水平。雌激素治疗降低了肾上腺醛固酮含量。在肾上腺髓质中,雌激素替代的作用包括:使AT1受体表达正常化,增加AT2受体表达、AT2受体mRNA和酪氨酸羟化酶mRNA水平,并使Fra-2表达和儿茶酚胺含量正常化。我们证明,AT1受体的肾上腺组成性表达、儿茶酚胺合成和Fra-2表达部分受生殖激素控制。我们的结果表明,雌激素治疗通过下调AT1受体和上调AT2受体来降低醛固酮生成。AT2受体上调和Fra-2表达的调节可能参与了去卵巢大鼠肾上腺髓质儿茶酚胺合成的雌激素依赖性正常化过程。AT2受体上调以及AT1受体功能和保钠、促炎激素醛固酮生成的减少部分解释了雌激素治疗的保护作用。

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