Xy. Wu et al., HYPERTENSION DEVELOPMENT IN DAHL-S AND DAHL-R RATS ON HIGH-SALT LOW POTASSIUM DIET - CALCIUM, MAGNESIUM AND SYMPATHETIC NERVOUS-SYSTEM, Clinical and experimental hypertension, 20(7), 1998, pp. 795-815
Dietary combination of high salt with low potassium (HSLK) exacerbates
hypertension development in Dahl salt-sensitive (S) rats, and produce
s a mild degree of hypertension in otherwise salt-resistant (R) rats.
Increased blood pressure in both strains is associated with increased
urinary excretion of calcium and magnesium. The objective of this stud
y was to determine the effect of blood pressure on body balance of the
se ions in Dahl rats on HSLK diet. Two groups of S and two groups of R
weanlings were all placed on HSLK diet (NaCl=8%, K=0.2%) for eight we
eks. One group of each strain was subjected to chemical sympathectomy
with 6-hydroxydopamine (6-OHDA) to counteract hypertension development
. Urinary norepinephrine was used to determine efficacy of 6-OHDA trea
tment. Systolic blood pressures of conscious animals were measured dai
ly throughout the study. The last three days on the diet were used to
determine total dietary intake and urinary as well as fecal excretion
of sodium, calcium and magnesium. At the end of the study, extracellul
ar fluid volume, serum aldosterone and parathyroid hormone were analyz
ed. Final systolic blood pressures in the 4 groups were as follows: S
= 235+/-9 mmHg (n=9); R = 155+/-3 mmHg (n=8); 6-OHDA S = 151+/-6 mm Hg
(n=8); 6-OHDA R = 117+/-6 mm Hg. Chemical sympathectomy decreased blo
od pressure in both S and R rats. There was no indication of sodium ac
cumulation in S rats. Associated with reduced parathyroid hormone leve
ls the S strain had significantly less positive balance for calcium th
an the R strain, primarily due to increased urinary excretion. A less
positive balance for magnesium was also observed, due mainly to relati
vely reduced intestinal absorption of the ion. We conclude that the HS
LK diet is associated with inappropriate activation of the sympathetic
nervous system and increased arterial pressure in both strains. In ad
dition, since divalent cations may influence blood pressure, we sugges
t that the observed abnormalities in calcium and magnesium metabolism
might independently promote hypertension development in the S strain.