(Hypertension. 1995;25:809-813.)
© 1995 American Heart Association, Inc.
Articles |
From the Boston (Mass) University School of Medicine.
Correspondence to Peter Brecher, PhD, Boston University School of Medicine, 80 E Concord St, Boston, MA 02118.
Abstract In this study we infused phenylephrine into adult
Wistar rats and used losartan to test for a possible role of
angiotensin II in the phenylephrine-induced fibrosis.
Phenylephrine, given by Alzet minipumps at a rate of 25
mg · kg-1 · d-1, produced a
rapid and striking fibrotic response that was obvious after 1 day and
progressed throughout a 3-day infusion period. Northern and Western
blot analyses showed large increases in cardiac fibronectin
expression and atrial natriuretic peptide mRNA, corresponding to
fibroblast proliferation and myocyte hypertrophy, respectively. Cardiac
fibrosis, fibronectin mRNA, and atrial natriuretic peptide mRNA were
blocked by prazosin (7
mg · kg-1 · d-1). Administration of
losartan (10 mg · kg-1 · d-1)
resulted in a threefold decrease in interstitial and perivascular
fibroblast proliferation, as measured by proliferating cell nuclear
antigen immunoreactivity (P<.05), a marked reduction of
fibronectin mRNA in the heart, and a moderate reduction of cardiac
atrial natriuretic peptide mRNA. The data suggest that effects mediated
by
1-adrenergic and angiotensin type 1 receptors may
promote cardiac fibrosis.
Key Words: fibrosis angiotensin II hypertension, experimental extracellular matrix receptors, adrenergic losartan
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