Apoptosis is involved in neonatal remodeling of organs of the cardiova
scular system. Since are previously reported hyperplasia of these orga
ns al birth in several forms of genetic hypertension, the aim of this
study was to determine whether alterations of the apoptotic process co
uld explain our findings. The heart, aorta, and kidneys of newborn Wis
tar-Kyoto and spontaneously hypertensive rats were harvested 24 hours
after an injection of [H-3]thymidine. DNA was extracted to measure its
specific activity (index of DNA synthesis) and DNA fragmentation as a
n estimation of apoptosis. All organs studied showed an increased weig
ht to body weight ratio in spontaneously hypertensive rats. Twenty-fou
r hours after birth, DNA synthesis in all organs of spontaneously hype
rtensive rats was comparable to that in normotensive rats. However, ap
optosis was markedly decreased In the heart and kidneys of newborn spo
ntaneously hypertensive rats compared with their normotensive controls
. In the aorta, apoptosis was reduced, but not significantly. Calculat
ion of a proliferation index (DNA synthesis/fragmentation) revealed a
significant increase of heart proliferation, with a similar trend in t
he aorta and Kidneys. In addition, we found a negative correlation bet
ween heart weight and DNA fragmentation. Although other factors may in
fluence hyperplasia of the aorta, we propose that a reduction of apopt
otic activity is responsible, at least in part, for heart and kidney h
yperplasia in newborn spontaneously hypertensive rats.