Jf. Norman et al., THORACIC AORTA PROSTACYCLIN PRODUCTION IS NOT ALTERED DURING EARLY ATHEROSCLEROSIS DEVELOPMENT IN YOUNG SWINE, Journal of nutritional biochemistry, 6(3), 1995, pp. 163-169
Decreased prostacyclin synthesis by atherosclerotic vascular tissue ha
s been demonstrated in both adult animal models and man. The purpose o
f this study was to determine whether the decrease in prostacyclin syn
thesis by the vessel wall was evident during the initial stages of ath
erosclerosis development and thus a potential contributor to atherogen
esis. Thirty-two Yucatan miniature swine entered the study at 3 months
of age and were placed on either an atherogenic or regular diet for 1
0, 30, 90, or 180 days. At that time, the thoracic and abdominal aorta
were harvested. Pairs of discs were punched out of the distal thoraci
c aorta and placed in Krebs Henseleit HEPES buffer, The buffer was the
n exchanged for either fresh buffer or stimulated with calcium ionopho
re A23187 (10(-4) M). Aliquots were collected at 10 min for analysis o
f prostacyclin production by radioimmunoassay of its stable metabolite
6-keto-prostaglandin F-1 alpha. Thoracic aorta sections were prepared
for atherosclerosis assessment by light microscopy, and the abdominal
aorta was stained with Sudan N. No significant differences were noted
between the diet groups at 10 and 30 days. After 90 days, a significa
nt difference was noted (P < 0.05) between the diet groups with regard
to (ii the early development of atherosclerosis in the thoracic aorta
and (2) the percent of abdominal aorta surface area sudanophilically
stained. However, no differences (P > 0.05) were noted between the die
t groups with regard to the basal and stimulated rates of prostacyclin
production. Our findings showed that prostacyclin synthesis was not a
ltered during the initial development or early progression of aortic a
therosclerosis induced by hypercholesteralemia.