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Brazilian Journal

High dietary of Medical


calcium and Biological
and arterial Research (1998) 31: 1099-1101
blood pressure 1099
ISSN 0100-879X Short Communication

High dietary calcium decreases blood


pressure in normotensive rats
N. Buassi Departamento de Cincias Fisiolgicas, Centro de Cincias Biolgicas,
Universidade Estadual de Londrina, Londrina, PR, Brasil

Abstract

Correspondence This study evaluates the influence of different concentrations of Key words
N. Buassi calcium on blood pressure of normotensive rats. Four groups of Wistar Calcium carbonate
Departamento de Cincias rats (A, B, C and D) had free access to modified isocaloric and Arterial blood pressure
Fisiolgicas
isoproteic diets containing 0.2, 0.5, 2 and 4 g% calcium as calcium Dietary calcium
Universidade Estadual de Londrina
86051-990 Londrina, PR
carbonate for a period of 30 days. Systolic and diastolic arterial blood
Brasil pressures were monitored in awake rats by the indirect tail cuff method
using a Physiograph equipped with transducers and preamplifiers.
Research supported by CNPq and Body weight and length and food intake were monitored. Under the
CPG-UEL. conditions of the present experiment, the systolic and diastolic arterial
blood pressures of group D rats fed a diet containing 4 g% calcium
were significantly (P<0.05) lower compared to rats of the other
Received February 24, 1997
groups.
Accepted May 21, 1998

Debate on the potential role of dietary cium intake was the most consistent factor in
calcium in the prevention and/or treatment hypertensive individuals (2) and calcium in-
of hypertension has a long history and has take was inversely correlated with systolic
been fueled by recent studies reporting rela- blood pressure, but other studies detected no
tionships among several cations, including association between calcium intake and blood
calcium, in the physiology of blood pressure pressure (7,8).
regulation (1). An inverse relationship be- The results of animal studies are more
tween calcium intake and arterial blood pres- consistent in demonstrating a link between
sure has been shown (2,3), indicating that dietary calcium and hypertension than ob-
calcium is important for blood pressure regu- servations in human subjects. The effect of
lation. Animal (4) and human (5) experi- calcium supplementation was modest in nor-
ments suggest that a low calcium intake con- motensive animals but had an overall blood
tributes to the development of hypertension pressure-lowering action in several experi-
and calcium may prevent elevations in arte- mental models of hypertension (9,10). The
rial pressure. Differential effects of calcium complexity of this subject has made it diffi-
supplementation on blood pressure have been cult to draw any definitive conclusions about
observed in normotensive and hypertensive the role of dietary calcium in the prevention
subjects (5,6). Studies of major epidemio- of hypertension (1).
logic databases carried out to evaluate the Limited work has been done to determine
link between diet and hypertension have led the long-term effects of dietary calcium sup-
to contradictory conclusions. Reduced cal- plementation on normotensive animals. The

Braz J Med Biol Res 31(8) 1998


1100 N. Buassi

objective of the current study was to investi- thermally controlled, ventilated, restraining
gate the effects of diets containing different cage to facilitate recording for small con-
concentrations of calcium, as calcium car- fined, unanesthetized laboratory animals over
bonate, on the arterial blood pressure of long periods of time.
normotensive rats. Results are reported as means SEM and
Male Wistar rats, Rattus rattus, aged 49 the statistical significance of differences be-
days were used in these experiments. Ani- tween group means was assessed by the
mals were housed in individual wire mesh Tukey test. The values were considered to be
cages under conditions of constant tempera- significantly different at P<0.05. Data were
ture of 22 2oC and a normal 12-h light/dark analyzed using the statistical analysis system
cycle. Thirty-two animals weighing 165 11 (SAS) (13).
g were randomly divided into four groups In the present study we monitored cal-
(A, B, C and D). During the 30-day experi- cium intake and changes in blood pressure in
mental period, rats had free access to modi- normotensive Wistar rats fed different levels
fied diets containing 0.2, 0.5, 2 and 4 g% of calcium in their diets, with other compo-
calcium, as calcium carbonate. The compo- nents kept constant. The calcium levels added
sition of isocaloric and isoproteic diets are to the diet were low (0.2 g%), normal (0.5
given in Ref. 11. Calcium was provided as g%), moderately high (2 g%) and high (4
carbonate because this form is widely used g%) (14), with a twenty-fold difference be-
in calcium supplements (12). Distilled water tween the highest and lowest concentrations.
and diets were offered ad libitum and moni- This difference was planned to maximize the
tored weekly. Diets were offered and meas- effect of dietary calcium on changes of arte-
ured in stainless steel cups with inner rings rial blood pressure. Diets containing 0.4 to
to minimize spillage and animal body weights 0.5 g% calcium are required to support maxi-
and lengths were measured weekly. mum calcification during growth, but the 0.2
Systolic and diastolic arterial blood pres- g% calcium diet contained the lowest cal-
sures were determined weekly in awake rats cium concentration needed to support maxi-
by the indirect tail cuff method using a Phy- mum weight gain in rats (15). The 4 g%
siograph (Narco Biosystem, Houston, TX) calcium diet was the highest concentration
equipped with transducers and preamplifi- shown by other investigators to reduce arte-
ers. All measurements were made inside a rial blood pressure in the spontaneously hy-

Table 1 - High dietary calcium decreases arterial blood pressure of normotensive rats fed isoproteic and
isocaloric diets containing 0.2, 0.5, 2.0 and 4.0 g% calcium as calcium carbonate for 30 days ad libitum.

Data are reported as means SEM for 8 rats in each group. *P<0.05 compared to the arterial systolic and
diastolic blood pressures of the other groups (Tukey test).

Parameters Dietary calcium (g%)

0.2 0.5 2.0 4.0

Systolic pressure (cmHg) 11.17 0.73 11.74 0.98 11.46 0.49 9.69 1.07*
Diastolic pressure (cmHg) 6.17 0.69 7.93 0.59 7.77 0.79 5.96 0.92*
Cumulative food intake (g) 617.0 11.2 626.0 36.5 625.0 31.8 635.0 47.7
Initial body weight (g) 166.0 14.9 167.0 11.2 165.0 9.5 165.0 9.7
Final body weight (g) 200.0 10.9 204.0 10.1 206.0 13.3 203.0 17.9
Initial body length (cm) 34.3 1.5 34.4 0.8 34.7 0.9 33.8 0.7
Final body length (cm) 37.6 0.8 38.7 0.6 38.3 0.9 37.9 0.9

Braz J Med Biol Res 31(8) 1998


High dietary calcium and arterial blood pressure 1101

pertensive rat (16). blood pressure regulation. The relationship


Body weight and length and cumulative between calcium and hypertension may then
food intake (Table 1) were the same involve the energy-dependent gradient be-
(ANOVA, P>0.05) for all the experimental tween intracellular and extracellular calcium
groups. The rats of group D fed a high- (20).
calcium diet for 30 days had significantly Both systolic and diastolic arterial blood
(P<0.05) lower systolic and diastolic blood pressures were significantly influenced by
pressures than the other groups. These re- dietary calcium under the conditions of this
sults are consistent with studies showing experiment. Diet is only one of several envi-
supplemental calcium to be associated with ronmental factors that affect arterial blood
a reduction of arterial blood pressure in both pressure and in this case a high dietary cal-
normotensive and hypertensive animals (17- cium concentration led to significantly lower
19). Despite accumulating evidence, the arterial blood pressure. The present data sup-
mechanisms by which calcium lowers blood port the view that increases in dietary cal-
pressure are still unknown. A plausible hy- cium can have a hypotensive effect on nor-
pothesis is an impact on free intracellular motensive rats.
calcium ion, a significant determinant of

References

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Braz J Med Biol Res 31(8) 1998


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Braz J Med Biol Res 31(8) 1998

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