Disturbances of vitamin D metabolism and action during clinical and experimental magnesium deficiency. 1988

T O Carpenter
Yale University School of Medicine, Department of Pediatrics (Endocrinology), New Haven, Connecticut.

It has been known since the 1920s that magnesium is influential in calcium homeostasis. In the 1970s it was documented that parathyroid secretion and activity may be impaired in magnesium deficiency. In the past two decades a variety of studies have indicated alterations in circulating vitamin D metabolites in humans, although these observations are not entirely consistent. Animal studies have not consistently demonstrated impaired vitamin D metabolism during relatively brief periods of magnesium deprivation, despite in vitro magnesium dependence of 1 alpha-hydroxylase activity. Studies of the administration of active vitamin D metabolites to humans and animals suggest that skeletal resistance to these compounds in magnesium deficiency may, in part, explain their reduced calcaemic effect during magnesium deficiency.

UI MeSH Term Description Entries
D008275 Magnesium Deficiency A nutritional condition produced by a deficiency of magnesium in the diet, characterized by anorexia, nausea, vomiting, lethargy, and weakness. Symptoms are paresthesias, muscle cramps, irritability, decreased attention span, and mental confusion, possibly requiring months to appear. Deficiency of body magnesium can exist even when serum values are normal. In addition, magnesium deficiency may be organ-selective, since certain tissues become deficient before others. (Harrison's Principles of Internal Medicine, 12th ed, p1936) Deficiency, Magnesium,Deficiencies, Magnesium,Magnesium Deficiencies
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013250 Steroid Hydroxylases Cytochrome P-450 monooxygenases (MIXED FUNCTION OXYGENASES) that are important in steroid biosynthesis and metabolism. Steroid Hydroxylase,Steroid Monooxygenases,Hydroxylase, Steroid,Hydroxylases, Steroid,Monooxygenases, Steroid
D014807 Vitamin D A vitamin that includes both CHOLECALCIFEROLS and ERGOCALCIFEROLS, which have the common effect of preventing or curing RICKETS in animals. It can also be viewed as a hormone since it can be formed in SKIN by action of ULTRAVIOLET RAYS upon the precursors, 7-dehydrocholesterol and ERGOSTEROL, and acts on VITAMIN D RECEPTORS to regulate CALCIUM in opposition to PARATHYROID HORMONE.
D053493 Cholestanetriol 26-Monooxygenase An NAPH-dependent cytochrome P450 enzyme that catalyzes the oxidation of the side chain of sterol intermediates such as the 27-hydroxylation of 5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol. 5-beta-Cholestane-3-alpha,7-alpha,12-alpha-triol 27-Hydroxylase,C27-Steroid 26-Hydroxylase,Cytochrome P-450 Steroid 27-Hydroxylase,Cytochrome P-450 Sterol 26-Hydroxylase,Steroid 25-Hydroxylase,Steroid 27-Hydroxylase,Sterol 26-Hydroxylase,Sterol 27-Hydroxylase,Vitamin D3 25-Hydroxylase,C27 Steroid 26 Hydroxylase,Cholestanetriol 26 Monooxygenase,Cytochrome P 450 Steroid 27 Hydroxylase,Cytochrome P 450 Sterol 26 Hydroxylase,Steroid 25 Hydroxylase,Steroid 27 Hydroxylase,Sterol 26 Hydroxylase,Sterol 27 Hydroxylase,Vitamin D3 25 Hydroxylase

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