T. Sasaki et al., Oestrogen attenuates the increases in blood pressure and platelet aggregation in ovariectomized and salt-loaded Dahl salt-sensitive rats, J HYPERTENS, 18(7), 2000, pp. 911-917
Citations number
34
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective To investigate the effects of oestrogen supplementation after ova
riectomy on systolic blood pressure and platelet aggregation on different s
odium content diet in the female Dahl salt-sensitive rats.
Methods At 12 weeks of age, rats were ovariectomized or sham-operated and w
ere fed either a high NaCl (8%) or low NaCl (0.3%) diet Ovariectomized rats
were treated with either 17 beta-oestradiol or placebo for 8 weeks, wherea
s sham-operated rats received placebo alone. After 8 weeks, the systolic bl
ood pressure and platelet aggregation were measured and analysed by two-way
analysis of variance.
Results The systolic blood pressure of ovariectomized rats was significantl
y higher than that of sham-operated rats, and this increase in systolic bro
od pressure was suppressed by oestrogen supplementation. Systolic blood pre
ssure was inversely correlated with plasma 17 beta-oestradiol levels (r = -
0.77, P < 0.01) and with the uterus weight to body weight ratio (r = -0.47,
P < 0.01). Platelet aggregation was significantly enhanced by salt loading
. Salt loading and female hormonal manipulation significantly interacted on
platelet aggregation. Only in Dahl salt-sensitive rats fed a low sodium di
et, ovariectomy increased platelet aggregation, whereas hormone replacement
did not improve it. In Dahl salt-sensitive rats fed a high sodium diet, ho
rmone replacement reduced platelet aggregation.
Conclusions Oestrogen replacement suppresses the development of hypertensio
n and attenuates platelet aggregatory function in the salt-loaded ovariecto
mized Dahl salt-sensitive rats. It has a potential to inhibit the atheroscl
erotic process in postmenopausal hypertension. J Hypertens 2000, 18:911-917
(C) Lippincott Williams & Wilkins.