4.7 Article

Azelnidipine inhibits aldosterone synthesis and secretion in human adrenocortical cell line NCI-H295R

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 605, Issue 1-3, Pages 49-52

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2008.12.041

Keywords

Aldosterone; Azelnidipine; H295R adrenocortical cell; Efonidipine; Nifedipine

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Blockade of a mineralocorticoid receptor is a clinically useful approach to the prevention of cardiovascular disease. The present study was designed to evaluate the effect of azelnidipine, a unique dihydropyridine Ca2+ channel blocker, on aldosterone production in the human adrenocortical cell line NCI-H295R. Azelnidipine inhibited angiotensin II- and KCl-induced expression of steroid 11 beta-hydroxylase, steroid 18-hydroxylase, and the alpha 1H subunit of the T-type Ca2+ channel, and suppressed steroid biosynthesis in H295R cells by the same amount as efonidipine. On the basis of these findings, azelnidipine appears to suppress steroid biosynthesis in H295R cells beyond the blockade of L-type calcium channels. (C) 2009 Elsevier B.V. All rights reserved.

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