|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Articles in PresS, published online ahead of print April 11, 2002
Am J Physiol Heart Circ Physiol, 10.1152/ajpheart.00677.2001
Submitted on August 1, 2001
Accepted on April 8, 2002
1 Department of Medicine, Christchurch School of Medicine, Christchurch, New Zealand
2 Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC, USA
* To whom correspondence should be addressed. E-mail: leigh.ellmers{at}chmeds.ac.nz.
Atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) are cardiac hormones that regulate blood pressure and volume, and exert their biological actions via the natriuretic peptide receptor-A (Npr1). Mice lacking the Npr1 have marked cardiac hypertrophy and fibrosis, disproportionate to their increased blood pressure. This study examined the relationships between ANP and BNP gene expression, immunoreactivity and fibrosis in cardiac tissue, circulating ANP levels, and ANP and BNP mRNA during embryogenesis in Npr1-/- mice. Disruption of the Npr1-/- signaling pathway resulted in augmented ANP and BNP gene and ANP protein expression in the cardiac ventricles, most pronounced for ANP mRNA in females (414±57 in Npr1-/-, 124±25 in wild-type (WT) by Taqman assay, p<0.001). This increased expression was highly correlated to the degree of cardiac hypertrophy, and was localized to the left ventricle (LV) inner free wall and to areas of ventricular fibrosis. In contrast, plasma ANP was significantly greater than WT in male but not female Npr1-/- mice. Increased ANP and BNP gene expression was observed in Npr1-/- embryos from 16 days of gestation. Our study suggests that cardiac ventricular expression of ANP and BNP is more closely associated with local hypertrophy and fibrosis than either systemic blood pressure or circulating ANP levels.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |