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Genetic variability in response to dietary calcium
P E Huie1, D C Hatton, M S Muntzel
1Department of Medical Psychology, Oregon Health Sciences University, Portland 97201.
Life Sciences
|November 9, 1987
Summary
Dietary calcium and sodium intake affect blood pressure differently across rat strains. Fisher 344 rats showed elevated blood pressure on low calcium/sodium diets, unlike other strains, indicating genetic variability in nutrient-ion regulation.
Area of Science:
- Nutritional Physiology
- Cardiovascular Research
- Genetics
Background:
- Dietary calcium supplementation can lower blood pressure in hypertensive rats.
- Calcium-restricted diets can elevate blood pressure, especially with sodium restriction.
- These effects are linked to changes in serum ionized calcium concentrations.
Purpose of the Study:
- To investigate the influence of altered dietary calcium and sodium on blood pressure in genetically normotensive rats.
- To determine if blood pressure responses to dietary changes vary across different rat strains.
Main Methods:
- Three rat strains (Fisher 344, Wistar Furth, ACI) were fed either low (0.1% Ca, 0.25% Na) or normal (1.0% Ca, 0.45% Na) diets from 4 to 29 weeks of age.
- Systolic blood pressure was measured indirectly.
- Serum electrolytes (ionized calcium, phosphorus, magnesium) were analyzed.
Main Results:
- Only Fisher 344 rats consistently showed elevated blood pressure on low calcium/low sodium diets.
- All strains exhibited reduced ionized calcium and increased phosphorus and magnesium on restricted diets.
- In Fisher 344 rats, blood pressure correlated inversely with ionized/total calcium and positively with phosphorus/magnesium; no such correlations were found in other strains.
Conclusions:
- Significant genetic variability exists in blood pressure responses to dietary calcium and sodium alterations.
- Diet-induced changes in serum electrolytes, particularly calcium, do not always predict blood pressure changes.
- Strain-specific differences in calcium-sensitive physiological processes likely mediate blood pressure regulation.