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作 者:马攀[1] 谭包生[1] 刘洪臣[2] 顾斌[2] 马军利[2] 鄂玲玲[2] 吴霞[2]
机构地区:[1]首都医科大学附属北京口腔医院种植中心,北京100050 [2]解放军总医院口腔科.北京100853
出 处:《上海口腔医学》2013年第2期175-180,共6页Shanghai Journal of Stomatology
摘 要:目的:探讨格列美脲对高糖培养的大鼠下颌骨成骨细胞增殖、分化和矿化功能的影响。方法:分离培养大鼠下颌骨成骨细胞,分别给予5.5 mmol/L(生理糖浓度)、16.5 mmol/L葡萄糖浓度的培养液培养,加入或不加入10μmol/L格列美脲后,用噻唑蓝法(MTT)观察成骨细胞7 d时的增殖情况,生化法测定7 d时的碱性磷酸酶(alkaline phosphatase,ALP)活性,Western免疫印迹检测7 d和14d时Ⅰ型胶原(collagenⅠ,ColⅠ)的表达,实时定量PCR检测21 d时的骨钙素(osteocalcin,OCN)mRNA的表达,采用SPSS13.0软件包对数据进行统计学分析。结果:高糖浓度降低了成骨细胞的增殖、ALP活性和OCN的mRNA表达,提高了14 d时的ColⅠ的表达。格列美脲能够促进2种糖浓度下的成骨细胞增殖、ALP活性、ColⅠ的蛋白表达和OCN的mRNA表达。结论:高糖浓度降低了大鼠下颌骨成骨细胞的增殖、分化和矿化能力,在2种糖浓度下,格列美脲促进大鼠下颌骨成骨细胞的增殖、分化和矿化。PURPOSE: To evaluate the effects of hyperglycemia and glimepiride on proliferation, differentiation and mineralization of rat mandibular osteoblasts to verify the hypothesis of dental implant administration. METHODS: Primary osteoblasts were isolated and cultured. Then the cells were placed in an osteogenic medium, containing 2 different concentrations of glucose (5.5 mmol/L and 16.5 mmol/L), with or without glimepiride (10 p, mol/L). Cell proliferation was evaluated through MTF assay. Alkaline phosphatase (ALP) activity was determined by biochemistric method. Col I protein levels were determined by Western blot. OCN mRNA levels were tested by RT-PCR. SPSS 13.0 software package was used for statistical analysis. RESULTS: Hyperglycemic conditions interfered with the proliferation, ALP activity and OCN mRNA expression of rat osteoblasts, but improved the expression of Col I on day 14. Glimepiride stimulated rat osteoblast proliferation, ALP activity and OCN mRNA expression. The addition of glimepiride to normoglycemic (5.5 mmol/L) cultures registered a significant increase of Col I expression at 7 d and 14 d. Glimepiride significantly increased Col I expression in cells cultured with 16.5 mmol/L glucose for 7 days, but failed to increase at 14 d. CONCLUSIONS: Hyperglycemic conditions interfered with the proliferation, differentiation and mineralization of osteoblasts in rats; however, glimepiride improved the proliferation, differentiation and mineralization of osteoblasts in rats.
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