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唑来膦酸对人牙周膜成纤维细胞增殖和凋亡的影响

[Effect of zoledronic acid on cell proliferation and apoptosis of human periodontal fibroblasts].

作者信息

Fu Qingbiao, Cui Caiwen, Xuan Bin, Guo Yuxuan, Liu Chunlin, Zhang Jian

机构信息

Department of Oral and Maxillofacial Surgery, Stomatological Hospital of Tianjin Medical University, Tianjin 300070, China.

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出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2015 Nov;50(11):667-70.

Abstract

OBJECTIVE

To observe the effect of different concentrations of zoledronic acid on human gingival fibroblast (HGF) cells proliferation and apoptosis, and to investigate the mechanism of bisphosphonate-related osteonecrosis of the jaw (BRONJ) caused by zoledronic acid.

METHODS

Different concentrations (0, 0.5, l.0, 5.0, 10.0 µmol/L) of zoledronic acid acted on the HGF. After 24 hours, flow cytometry was used to detect the rate of apoptosis and methyl thiazolyl terazolium (MTT) assay used to observe the proliferation of HGF. The effect of different concentrations of zoledronic acid on cell proliferation was examined by proliferation test on day 2, 4 and 7.

RESULTS

Flow cytometry showed that when the concentration of zoledronic acid was 0, 0.5, 1.0, 5.0, 10.0 µmol/L, the apoptosis rate was (0.67 ± 0.50)%, (2.13 ± 0.21)%, (3.27 ± 0.23)%, (4.17 ± 0.35)%, (9.87 ± 1.79)% respectively. The difference in HGF cells between control group and zoledronic acid groups was significant (P < 0.05) at three concentrations of zoledronic acid (1.0, 5.0, 10.0 µmol/L). The cell proliferation test showed an concentration-time dependent effect. With increase of concentration and time, the cell proliferation was significantly inhibited. There was significant difference in absorbance value among the different concentration groups (P < 0.05).

CONCLUSIONS

Zoledronic acid can inhibit HGF proliferation and promote its apoptosis.

摘要

目的

观察不同浓度唑来膦酸对人牙龈成纤维细胞(HGF)增殖和凋亡的影响,探讨唑来膦酸所致双膦酸盐相关性颌骨坏死(BRONJ)的机制。

方法

不同浓度(0、0.5、1.0、5.0、10.0 μmol/L)的唑来膦酸作用于HGF。24小时后,采用流式细胞术检测凋亡率,噻唑蓝(MTT)法观察HGF的增殖情况。在第2、4和7天通过增殖试验检测不同浓度唑来膦酸对细胞增殖的影响。

结果

流式细胞术显示,当唑来膦酸浓度为0、0.5、1.0、5.0、10.0 μmol/L时,凋亡率分别为(0.67±0.50)%、(2.13±0.21)%、(3.27±0.23)%、(4.17±0.35)%、(9.87±1.79)%。在唑来膦酸三个浓度(1.0、5.0、10.0 μmol/L)时,对照组与唑来膦酸组的HGF细胞差异有统计学意义(P<0.05)。细胞增殖试验显示出浓度 - 时间依赖性效应。随着浓度和时间的增加,细胞增殖受到显著抑制。不同浓度组间吸光度值差异有统计学意义(P<0.05)。

结论

唑来膦酸可抑制HGF增殖并促进其凋亡。

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