GLYCOCHENODEOXYCHOLIC ACID INHIBITS CALCIUM-PHOSPHATE PRECIPITATION INVITRO BY PREVENTING THE TRANSFORMATION OF AMORPHOUS CALCIUM-PHOSPHATE TO CALCIUM HYDROXYAPATITE

被引:21
|
作者
QIU, SM [1 ]
WEN, G [1 ]
HIRAKAWA, N [1 ]
SOLOWAY, RD [1 ]
HONG, NK [1 ]
CROWTHER, RS [1 ]
机构
[1] UNIV TEXAS, MED BRANCH,DEPT INTERNAL MED,DIV GASTROENTEROL, 4 106 MCCULLOUGH BLDG,G-64, GALVESTON, TX 77550 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 1991年 / 88卷 / 04期
基金
美国国家卫生研究院;
关键词
BILE SALTS; BIOMINERALIZATION; CALCIFICATION; FOURIER TRANSFORM INFRARED SPECTROSCOPY; GALLSTONES;
D O I
10.1172/JCI115430
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Calcium hydroxyapatite can be a significant component of black pigment gallstones. Diverse molecules that bind calcium phosphate inhibit hydroxyapatite precipitation. Because glycine-conjugated bile acids, but not their taurine counterparts, bind calcium phosphate, we studied whether glycochenodeoxycholic acid inhibits calcium hydroxyapatite formation. Glycochenodeoxycholic acid (2 mM) totally inhibited transformation of amorphous calcium phosphate microprecipitates to macroscopic crystalline calcium hydroxyapatite. This inhibition was not mediated by decreased Ca2+ activity. Taurocholic acid (2-12 mM) did not affect hydroxyapatite formation, but antagonized glycochenodeoxycholic acid. Both amorphous and crystalline precipitates contained a surface fraction relatively rich in phosphate. The surface phosphate content was diminished by increasing glycochenodeoxycholic acid concentrations, and this relationship was interpreted as competition between bile acid and HPO42- for binding sites on the calcium phosphate surface. A phosphate-rich crystal surface was associated with rapid transition from amorphous to crystalline states. These results indicate that glycochenodeoxycholic acid prevents transformation of amorphous calcium phosphate to crystalline hydroxyapatite by competitively inhibiting the accumulation of phosphate on the crystal embryo surface.
引用
收藏
页码:1265 / 1271
页数:7
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