Cp. Aloamaka et al., THE EFFECT OF INDOMETHACIN AND ENDOTHELIUM DENUDATION ON THE REACTIVITY OF VASCULAR SMOOTH-MUSCLE FROM PREGNANT RATS WITH SALT-INDUCED HYPERTENSION, Hypertension in pregnancy, 14(2), 1995, pp. 213-226
Objective: The study examined the effects of salt-induced hypertension
on vascular contractile responses during pregnancy and the mechanisms
of the effects.Methods: Aortic rings from pregnant Wistar rats, fed f
or 6 weeks on diets containing 0.3% (control) and 8.0% (test) sodium c
hloride were contracted by phenylephrine, 5-hydroxytryptamine, and pot
assium chloride, in the presence and absence of either endothelium or
10(-6) M indomethacin. Contractile responses to calcium chloride were
also assessed. Results: High salt intake increased the systolic blood
pressure of the rats. Rings from the high-salt-fed rats showed enhance
d reactivity to phenylephrine, but not to potassium chloride and 5-hyd
roxytryptamine. Indomethacin treatment decreased the contractions of r
ings from the test rats to phenylephrine, but did not significantly af
fect the responses of rings from the control rats. Removal of endothel
ium resulted in similar increase in the contractile responses of rings
from both groups of rats to phenylephrine but had no effect on respon
ses to 5-hydroxytryptamine and potassium chloride. Rings from hyperten
sive rats showed significantly increased maximal contractions to calci
um chloride when pretreated with phenylephrine but not potassium chlor
ide. Contractile responses to phenylephrine in calcium-free medium wer
e similar in both groups of rats.Conclusions: The results suggest that
the enhanced contractions of aortic rings from pregnant rats with sal
t-induced hypertension are related to alterations in adrenergic mechan
isms, and are mediated by vasoconstrictor prostaglandin and enhanced c
alcium influx through a phenylephrine-activated receptor operated calc
ium entry pathway. The capacity to produce endothelium-dependent relax
ation appears unaltered in this form of hypertension in pregnancy.