Literature DB >> 9807763

The influence of dietary phosphorus and magnesium concentrations on the calcium content of heart and kidneys of DBA/2 and NMRI mice.

F A van den Broek1, A C Beynen.   

Abstract

Dystrophic cardiac calcification (DCC) is often found in DBA/2 mice, reportedly in association with low plasma magnesium levels in this mouse strain. It was hypothesized that high-phosphorus diets and low-magnesium diets that are known to lower plasma magnesium concentrations would promote the development of DCC. DBA/2 mice were fed diets with either low-magnesium (0.02%, w/w) or high-phosphorus (0.8%) concentrations or a combination of the two variables. NMRI mice were given either a low- (0.2%) or high- (0.6%) phosphorus diet. Female, but not male, NMRI mice accumulated calcium in the heart when fed the high-phosphorus diet; neither gender developed kidney calcification. DBA/2 mice with either a low-magnesium or a high-phosphorus intake developed marked cardiac calcifications. The combination of low-magnesium and high-phosphorus intake caused severe calcification of the heart, kidney and tongue. Increasing the dietary magnesium content (0.08%) and reducing phosphorus (0.2%) did not fully prevent cardiac calcification, but reduced heart calcium concentrations in male DBA/2 mice. It is concluded that diets for DCC-susceptible mice should contain adequate amounts of magnesium and low, but sufficient amounts of phosphorus in order not to additionally stimulate cardiac calcification.

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Year:  1998        PMID: 9807763     DOI: 10.1258/002367798780599758

Source DB:  PubMed          Journal:  Lab Anim        ISSN: 0023-6772            Impact factor:   2.471


  15 in total

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2.  Calcification of myocardial necrosis is common in mice.

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4.  Gas6 protein: its role in cardiovascular calcification.

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7.  The serum protein alpha 2-Heremans-Schmid glycoprotein/fetuin-A is a systemically acting inhibitor of ectopic calcification.

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8.  Identification of Abcc6 as the major causal gene for dystrophic cardiac calcification in mice through integrative genomics.

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9.  Effect of genetic background on the dystrophic phenotype in mdx mice.

Authors:  William D Coley; Laurent Bogdanik; Maria Candida Vila; Qing Yu; Jack H Van Der Meulen; Sree Rayavarapu; James S Novak; Marie Nearing; James L Quinn; Allison Saunders; Connor Dolan; Whitney Andrews; Catherine Lammert; Andrew Austin; Terence A Partridge; Gregory A Cox; Cathleen Lutz; Kanneboyina Nagaraju
Journal:  Hum Mol Genet       Date:  2015-11-12       Impact factor: 6.150

10.  Evaluation of calcium acetate/magnesium carbonate as a phosphate binder compared with sevelamer hydrochloride in haemodialysis patients: a controlled randomized study (CALMAG study) assessing efficacy and tolerability.

Authors:  Angel L M de Francisco; Michael Leidig; Adrian C Covic; Markus Ketteler; Ewa Benedyk-Lorens; Gabriel M Mircescu; Caecilia Scholz; Pedro Ponce; Jutta Passlick-Deetjen
Journal:  Nephrol Dial Transplant       Date:  2010-06-07       Impact factor: 5.992

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