The steroid aldosterone plays a major role in the maintenance of total body
sodium homeostasis and also contributes to cardiovascular pathophysiology
by mediating cardiac hypertrophy and fibrosis. In addition to classical adr
enal production of aldosterone, endogenous tissue production of aldosterone
has been observed in various organs; aldosterone biosynthesis in cardiac t
issues, however, remains highly controversial. The current study provides a
comprehensive evaluation of steroid hormone biosynthethic capabilities in
multiple tissues from two distinct rat strains under unstimulated and stimu
lated conditions. Panels of tissues from Wistar and Sprague-Dawley rats wer
e probed for 11 beta-hydroxylase (P45011 beta) and aldosterone synthase (P4
50aldo) by reverse transcriptase-polymerase chain reaction (RT-PCR). Under
unstimulated conditions, cardiac P45011 beta and P450aldo were detected onl
y in Wistar rats. Angiotensin 11 (100 mu g/day) stimulated myocardial expre
ssion of both enzymes in both strains. Cerebral cortex and mesenteric arter
y message levels in both strains was reduced by angiotensin II. These data
demonstrate the potential for local steroid synthesis in vascular, cardiac,
renal, and neuronal tissues, and that biosynthesis of non-adrenal aldoster
one may be differentially regulated between strains. This variability may t
hus resolve in part or whole the current controversy over the existence of
non-adrenal steroidogenic systems. (C) 2000 Elsevier Science Ireland Ltd. A
ll rights reserved.