REGULATION OF ALDOSTERONE SECRETION AND A DRENAL RENIN IN TGR(MREN2)27

Citation
J. Peters et al., REGULATION OF ALDOSTERONE SECRETION AND A DRENAL RENIN IN TGR(MREN2)27, Nieren- und Hochdruckkrankheiten, 22(7), 1993, pp. 364-368
Citations number
NO
Categorie Soggetti
Urology & Nephrology
ISSN journal
03005224
Volume
22
Issue
7
Year of publication
1993
Pages
364 - 368
Database
ISI
SICI code
0300-5224(1993)22:7<364:ROASAA>2.0.ZU;2-6
Abstract
The transgenic hypertensive rat strain, TGR(mREN2)27, serves as a new model to extend the analysis of the intraadrenal renin-angiotensin sys tem (RAS). They exhibit a strong expression of an additional renin gen e (Ren-2d) in the adrenal gland. Here we demonstrate, that, in adrenal cells of TGR(mREN2)27, renin is synthetized de-novo and released in a regulated manner. Renin secretion in the adrenal gland of TGR(mREN2)2 7 is stimulated by cAMP, angiotensin II (ANGII), and calcium. This is contrary to the known regulation of renin in the kidney. The adrenal R AS of TGR(mREN2)27 may play a role in adrenal steroid metabolism. Thus , the secretion of aldosterone is elevated, and this can be partially prevented by captopril in vitro. Moreover, further stimulation of aldo sterone release in vitro by ANGII is diminished. These results indicat e elevated adrenal ANGII in TGR(mREN2)27, possibly due to local genera tion.