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2 Institute of Hypertension, First Affiliated Hospital, Fujian Medical University, Fuzhou 350005, People's Republic of China; and 1 Metabolic Research Unit and Department of Medicine, University of California at San Francisco, San Francisco, California 94143
Treatment of spontaneously hypertensive
rats (SHR) with captopril (100 mg · kg
1 · day
1)
throughout development and during the first 16 wk of life leads to a
reduction in blood pressure and left ventricular hypertrophy. Blood
pressures and hypertrophy are reduced in these animals (vs. untreated
SHR) for up to 24 wk after discontinuation of the drug. We used
conventional blot hybridization and Western analysis to examine
hypertrophy-dependent gene expression during this period. Ventricular
expression of the atrial natriuretic peptide gene was reduced by
>90% at 16 wk of age in the captopril-treated SHR. Expression
increased in the 24 wk after discontinuation of treatment, but remained
well below that of the untreated SHR. A similar reduction in
ventricular c-myc gene expression was
seen with captopril treatment. Neither renal expression of the atrial
natriuretic peptide gene nor ventricular expression of the
c-fos gene was affected by captopril. This study demonstrates that captopril treatment during a critical period of development in the SHR leads to a sustained reduction in
hypertrophy-dependent myocardial gene expression, which does not revert
to levels seen in the untreated SHR after discontinuation of the drug.
atrial natriuretic peptide; cardiac hypertrophy; spontaneously hypertensive rat
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