Keywords :
Adult; Angiotensin II/antagonists & inhibitors/metabolism/pharmacology; Angiotensin Receptor Antagonists; Animals; Binding, Competitive; Biphenyl Compounds/pharmacology; Cell Line; Cells, Cultured; Cloning, Molecular; Gene Expression Regulation/drug effects; Homeostasis; Humans; Imidazoles/pharmacology; Kinetics; Losartan; Oligodeoxyribonucleotides; Oligopeptides/pharmacology; RNA, Messenger/genetics/metabolism; Receptors, Angiotensin/genetics/metabolism; Tetrazoles/pharmacology; Transfection; Zona Fasciculata/metabolism; Zona Reticularis/metabolism
Abstract :
[en] The classical concept of human adrenal physiology indicates that only glomerulosa cells are the target of A-II. Herein, we demonstrated that cultured human adrenal fasciculata-reticularis cells were also responsive to this hormone. Indeed, these cells contained high affinity (Kd = 0.9-1.1 nM) and low capacity (8,000-13,000 sites/cell) A-II receptors, and more than 95% of them were of the type-1. These AT1 receptors are functional since A-II was able to increase cortisol production after 48 h of treatment. These effects were inhibited by losartan, an AT1 antagonist, but not by CGP42112A, an AT2 antagonist. The expression of the type-1 A-II receptor mRNA was detected in the whole adrenal in both adult and fetus, and in cultured human adrenal fasciculata-reticularis cells. In these cells A-II negatively regulated AT1 receptor mRNA, and this effect was also mediated through the AT1 receptor subtype.
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