Influence of the consumption pattern of magnesium from magnesium-rich mineral water on magnesium bioavailability.

It is generally considered that the absorption of Mg is inversely related to the ingested dose. The objective of the present study was to determine if the mode of administration (bolus v. consumption throughout the day) could influence Mg bioavailability from Mg-rich natural mineral water comparing the same nutritional Mg amount (126 mg). Using a 2 d cross-over design, twelve healthy men were asked to drink 1·5 litres Mg-rich mineral water either as 2 × 750 ml or 7 × 212 ml throughout the day. Two stable isotopes ((25)Mg and (26)Mg) were used to label the water in order to distinguish both regimens. Fractional apparent Mg absorption was determined by faecal monitoring and Mg retention was determined by measuring urinary excretion of Mg isotopes. Higher Mg absorption (50·7 (SD 12·7) v. 32·4 (SD 8·1) %; P = 0·0007) and retention (47·5 (SD 12·9) v. 29·0 (SD 7·5) %; P = 0·0008) from Mg-rich mineral water were observed when it was consumed in seven servings compared with larger servings. Thus, regular water consumption throughout the day is an effective way to increase Mg bioavailability from Mg-rich mineral water.

Vascular function of MGH and MGL mice, two strains which differ by a genetic variation of magnesium metabolism.

Mg deficiency is considered as a risk factor of cardiovascular disorders like hypertension and atherosclerosis. MGH and MGL mice, selected for high and low Mg status, are animal models which present variations of Mg metabolism of genetic origin. The cardiovascular functions of these mice have never been studied. In this study, the arterial blood pressure of MGH and MGL strains was measured by plethysmography. Morphology and reactivity to vasoconstrictor agents were also investigated by a pressurized and perfused system in mesenteric resistance artery. It is shown that: (1) MGH mice presented a higher plasma Mg concentration than MGL; (2) arterial blood pressure and heart rates were similar between the two groups; (3) media thickness, media cross-sectional area, and internal and external diameters were smaller in pressurized mesenteric resistance arteries from MGH mice than in those from MGL mice; (4) the vasoconstriction induced by vasopressin (but not norepinephrine) was higher in the mesenteric arteries from MGH mice than in those from MGL ones. In summary, MGH mice as compared to MGL mice present differences in arterial geometry and higher reactivity to vasopressin without repercussions on arterial blood pressure. The real repercussion of these observations on the cardiovascular system of the MGH and MGL models is at present unknown. More experiments are needed to clarify the influence of differences in Mg metabolism of genetic origin on cardiovascular function.