Troglitazone attenuates hypoxia-induced injury in cultured term human trophoblasts |
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Authors: | Elchalal Uriel Humphrey Rachel G Smith Steven D Hu Chaobin Sadovsky Yoel Nelson D Michael |
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Affiliation: | Departments of Obstetrics and Gynecology and Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO, USA. |
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Abstract: | OBJECTIVE: The purpose of this study was to test the hypothesis that the thiazolidinedione troglitazone, a peroxisome proliferator activated receptor-gamma ligand, attenuates hypoxia-induced trophoblast injury. STUDY DESIGN: Cytotrophoblasts from 4 term human placentas were cultured in the presence or absence of 10 mumol/L troglitazone in either 20% oxygen (standard conditions) or 1% oxygen (hypoxic conditions) for variable periods before cell harvest. Medium beta-human chorionic gonadotropin and human placental lactogen were analyzed by enzyme-linked immunosorbent assay. Apoptosis was quantified by cytokeratin-18 cleavage products staining; p53 expression was examined by Western blot analysis. RESULTS: beta-human chorionic gonadotropin and human placental lactogen levels were >/=2-fold higher in troglitazone-exposed cells at 16 hours of hypoxia, compared with vehicle control cells ( P <.05). The apoptotic index was reduced by >/=30% ( P <.001), and the expression of p53 was 2-fold lower ( P <.02) in troglitazone-exposed cells under hypoxia for =16 hours but not different after >24 hours of low oxygen. CONCLUSION: Troglitazone attenuates the influence of acute hypoxia on cultured term human trophoblasts. |
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Keywords: | Placenta Hypoxia Troglitazone Peroxisome proliferator activated eceptor– γ Apoptosis |
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