Study of a myo-inositol hexaphosphate-based cream to prevent dystrophic calcinosis cutis

被引:19
作者
Grases, F [1 ]
Perelló, J [1 ]
Isern, B [1 ]
Prieto, RM [1 ]
机构
[1] Univ Balearic Isl, Univ Inst Hlth Sci Res, IUNICS, Lab Renal Lithiasis Res & Biomineralizat, Palma de Mallorca 07122, Spain
关键词
calcinosis cutis; crystallization inhibitor; myo-inositol hexaphosphate; phytate;
D O I
10.1111/J.1365-2133.2005.06382.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Calcinosis cutis is a disorder caused by abnormal deposits of calcium phosphate in the skin and is observed in diverse disorders. Myo-inositol hexaphosphate (InsP(6)) is a diet-dependent molecule found in all mammalian fluids and tissues, which exhibits an extraordinary capacity as a crystallization inhibitor of calcium salts. To establish the effects of topically administered InsP(6) cream on artificially provoked dystrophic calcifications in soft tissues. Fourteen male Wistar rats were randomly assigned into two groups: control and treated groups. Rats were fed with an InsP(6)-free or phytate diet. Plaque formation was induced by subcutaneous injection of 0.1% KMnO4 solution. From 4 days before plaque induction to the end of the experiment, control rats were treated topically with a standard cream, whereas treated rats were treated with the same cream with 2% InsP(6) or phytate (as sodium salt). Calcification of plaques was allowed to proceed for 10 days. InsP(6) in urine was determined. The plaques were excised and weighed. It was found that when InsP(6) was administered topically through a moisturizing cream (2% InsP(6)-rich), the plaque size and weight were notably and significantly reduced compared with the control group (1.6 +/- 1.1 mg InsP(6)-treated, 26.7 +/- 3.0 mg control). The InsP(6) urinary levels for animals treated with the InsP(6)-enriched cream were considerably and significantly higher than those found in animals treated topically with the cream without InsP(6) (16.96 +/- 4.32 mg L-1 InsP(6)-treated, 0.06 +/- 0.03 mg L-1 control). This demonstrates the important capacity of InsP(6) as a crystallization inhibitor and also demonstrates that it is possible to propose topical use as a new InsP(6) administration route.
引用
收藏
页码:1022 / 1025
页数:4
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