期刊
LIVER INTERNATIONAL
卷 33, 期 7, 页码 1029-1038出版社
WILEY
DOI: 10.1111/liv.12153
关键词
bile acids; bone mass; cholestasis; osteoporosis; primary biliary cirrhosis
资金
- Centro de Investigacion Biomedica en Red de Enfermedades Hepaticas y Digestivas (CIBEREHD)
- Instituto de Salud Carlos III, Ministerio de Economia y Competitividad, Spain [PI080105, PI1100281]
Background Osteoporosis resulting from decreased bone formation is a common complication in patients with chronic cholestasis. Lithocholic acid (LCA) and bilirubin may play a role in osteoporosis given that both substances have detrimental effects on survival of human osteoblasts, the cells involved in bone formation. Aims As ursodeoxycholic acid (UDCA) improves cholestasis, we have assessed if this bile acid may neutralize the harmful effects of LCA, bilirubin and sera from jaundiced patients on osteoblastic cells. Methods The experiments were performed in primary human osteoblasts and human osteosarcoma cell line (Saos-2) at different times and concentrations of UDCA, LCA, cholic acid (CA), bilirubin and sera from jaundiced patients to assess cell viability, differentiation and mineralization. Results UDCA significantly decreased cell survival at concentrations 10 times higher (1mM) than that observed with LCA, whereas CA did not decrease osteoblast survival. UDCA (100M) neutralized the damaging effects of bilirubin (50M) and sera from jaundiced patients on survival. Moreover, UDCA (1M and 10M) increased osteoblast differentiation in cells treated with harmful concentrations of LCA or bilirubin. UDCA (100M) increased cell differentiation in osteoblasts cultured with a mix of serum from cholestatic patients by 23%. Furthermore, UDCA increased osteoblast mineralization by 35% and neutralized the negative consequences of 50M bilirubin. Conclusions UDCA increases osteoblast differentiation and mineralization, and neutralizes the detrimental effects of lithocholic acid, bilirubin and sera from jaundiced patients on osteoblastic cells. Therefore, UDCA may exert a favourable effect on bone in patients which chronic cholestasis.
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