Effect of five dental pulp capping agents on cell proliferation, viability, apoptosis and mineralization of human dental pulp cells

被引:18
|
作者
Dou, Lei [1 ,2 ,3 ]
Yan, Qifang [4 ]
Yang, Deqin [1 ,2 ,3 ]
机构
[1] Chongqing Med Univ, Stomatol Hosp, Dept Conservat Dent & Endodont, 426 Song Shi Bei Lu, Chongqing 401147, Peoples R China
[2] Chongqing Key Lab Oral Dis & Biomed Sci, Chongqing 401147, Peoples R China
[3] Chongqing Municipal Key Lab Oral Biomed Engn High, Chongqing 401147, Peoples R China
[4] Southwest Med Univ, Affiliated Stomatol Hosp, Dept Endodont, Luzhou 646000, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; concentrated growth factors; dental pulp cells; platelet-rich fibrin; proliferation; CONCENTRATED GROWTH-FACTOR; PLATELET-RICH FIBRIN; TRIOXIDE AGGREGATE; CALCIUM HYDROXIDE; IN-VITRO; IROOT BP; PULPOTOMY;
D O I
10.3892/etm.2020.8444
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
The aim of the present study was to investigate the effect of calcium hydroxide [Ca(OH)(2)], mineral trioxide aggregate (MTA), iRoot BP, platelet-rich fibrin (PRF) and concentrated growth factors (CGF) on the proliferation, viability, apoptosis and mineralization of human dental pulp cells (HDPCs). HDPCs were treated with Ca(OH)(2), MTA, iRoot BP, PRF and CGF exudates. Cell viability, apoptosis, proliferation, cell cycle and alkaline phosphatase (ALP) activity were evaluated in vitro. PRF significantly increased the cell proliferation as compared with that in the MTA and iRoot BP groups on day 3. The CGF group displayed higher proliferation rates as compared with that in the MTA group on days 3 and 7. The MTA group displayed the highest ALP activity on days 1 and 3, and the CGF group on day 7. Ca(OH)(2) inhibited cell proliferation and the percentages of dead and apoptotic cells were relatively higher in the Ca(OH)(2) group on days 1, 3 and 7 compared with those in the other groups. In conclusion, PRF and CGF may be potential pulp-capping materials for vital pulp therapy. Future in vivo studies are required to confirm this.
引用
收藏
页码:2377 / 2383
页数:7
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