Mineralocorticoid selectivity: Molecular and cellular aspects

被引:52
作者
Farman, N [1 ]
Bocchi, B [1 ]
机构
[1] Univ Paris 07, INSERM, U478, F-75870 Paris 18, France
关键词
aldosterone; glucocorticoid hormones; mineralocorticoid receptor; hypertension; 11 beta HSD2;
D O I
10.1046/j.1523-1755.2000.00976.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aldosterone acts in mineralocorticoid-sensitive cells by binding to the mineralocorticoid receptor (MR). Because the MR displays similar affinity for aldosterone and glucocorticoid hormones and because these latter hormones are 100- to 1000-fold more abundant than aldosterone in the plasma, mechanisms are required to avoid permanent illicit occupancy of MR by glucocorticoid hormones. The main mechanism of mineralo-corticoid selectivity is enzymatic: the 11 beta hydroxysteroid dehydrogenase (HSD2) metabolizes glucocorticoid hormones into derivatives with a low affinity for MR. The cell biology and regulation of HSD2 are reviewed in this article. as well as its implications in human hypertension. Other factors play a role in mineralocorticoid selectivity: the MR itself. the possibility to form homodimers (MR-MR), or heterodimers (with the glucocorticoid receptor). All of these cellular events participate to successive dynamic equilibriums, which allow fine tuning of transcriptional regulation of target genes, depending on the target tissue and the hormonal status.
引用
收藏
页码:1364 / 1369
页数:6
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