Jp. Tolvanen et al., EFFECTS OF CALCIUM AND POTASSIUM SUPPLEMENTS ON ARTERIAL TONE IN-VITRO IN SPONTANEOUSLY HYPERTENSIVE RATS, British Journal of Pharmacology, 124(1), 1998, pp. 119-128
1 Calcium and potassium intakes inversely correlate with blood pressur
e in experimental hypertension. Therefore, we examined the effects of
calcium and potassium supplements alone and in combination on arterial
tone in spontaneously hypertensive rats (SHR). Wistar-Kyoto (WKY) rat
s served as normotensive controls. Calcium and potassium contents in t
he control diet were both 1%, while those in supplemented chows were 3
% and 3.5%, respectively. The sodium content of all diets was moderate
ly elevated to 1.1%. 2 After 12 weeks of the study systolic blood pres
sures in SHR on high calcium and on high potassium diets were markedly
lower (about 53 and 58 mmHg, respectively) than in hypertensive contr
ols, while combined supplementation of these cations reduced blood pre
ssure even further (about 69 mmHg). 3 Responses of mesenteric arterial
rings in vitro were examined at the end of the study. Both high calci
um and high potassium diets improved the impaired relaxation to acetyl
choline (ACh) in SHR, while the combination of these supplements compl
etely normalized this response. Cyclo-oxygenase inhibition by diclofen
ac augmented the relaxation to ACh in hypertensive controls but not in
the other groups. Nevertheless, enhanced endothelium-mediated dilatat
ion was still observed in the presence of diclofenac and the nitric ox
ide synthase inhibitor N-G-nitro-L-arginine methyl ester (L-NAME) in a
ll supplemented groups. Interestingly, additional blockade of Ca2+-act
ivated K+ channels by tetraethylammonium abolished the improved relaxa
tion to ACh in SHR on high calcium and on high potassium, but distinct
responses were still observed in WKY rats and SHR on the combined sup
plement. 4 When hyperpolarization of smooth muscle was prevented by pr
econtraction of the preparations with 50 mM KCl, only marginal differe
nces were observed in the diclofenac and L-NAME-resistant relaxations
to ACh between the study groups. Finally, endothelium-independent vaso
relaxations of noradrenaline-precontracted rings to nitroprusside, iso
prenaline and cromakalim were comparably augmented by all supplements.
5 In conclusion, the vascular mechanisms underlying the antihypertens
ive effect of high calcium and high potassium diets during moderately
elevated sodium intake in SHR may involve enhanced arterial hyperpolar
ization, increased smooth muscle sensitivity to nitric oxide and decre
ased production of vasoconstrictor prostanoids. The administration of
these cations in combination was more effective than either of them al
one in reducing blood pressure and restoring arterial tone.