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机构地区:[1]上海市口腔医学研究所.上海市口腔医学重点实验室,上海200011
出 处:《口腔医学研究》2012年第11期1138-1140,共3页Journal of Oral Science Research
基 金:上海市科学技术委员会基金资助(编号:10JC1408800)
摘 要:目的:探讨EDTA凝胶(EDTA gel)和氯亚明(chloramine-T)对人牙周膜细胞(periodontal ligament cell,PDLC)增殖和碱性磷酸酶(alkaline phosphatase,ALP)活性的影响。方法:将5种不同浓度的EDTA凝胶和氯亚明溶液分别作用于体外培养的PDLC。MTT法观察PDLC的增殖情况,酶动力学方法检测PDLC的碱性磷酸酶活性。结果:浓度为0.005%、0.0025%和0.00125%的EDTA凝胶溶液及浓度为0.0025%和0.00125%的氯亚明对PDLC的增殖和ALP活性无抑制作用。浓度为0.02%和0.01%的EDTA凝胶溶液及浓度为0.02%、0.01%和0.005%的氯亚明对PDLC的增殖和ALP活性有抑制作用(P<0.05),抑制作用随药物浓度和作用时间的增加而增加。结论:EDTA凝胶和氯亚明对PDLC的增殖和碱性磷酸酶活性具有一定的抑制作用。Objective: To examine the effect of chloramine--T and EDTA gel on the proliferation and the alkaline phosphatase (ALP) activity of the periodontal ligament cell (PDLC). Methods: We have added five different con- centrations of chloramine--T and EDTA gel on the PDLC in vitro. Then we observed the proliferation of PDLC by MTT and detected ALP activity of PDLC by enzyme dynamics. Results: When the concentrati6ns of EDTA gel solu- tion were 0. 005~, 0. 0025~/6o and 0. 00125~ and the concentrations of chloramine-- T were 0. 0025~//00 and 0. 00125 ~, the proliferation and ALP activity of PDLC was not inhibited. When the concentrations of EDTA gel solu- tion were 0.02~ and 0.01~ and the concentrations of chloramine--T were 0.02%, 0.01%and 0. 005%, the pro- liferation and ALP activity of PDLC was inhibited (P〈0.05). The effects of inhibition increase as the action time and concentration of drugs. Conclusion: EDTA gel and chloramine--T can inhihit the proliferation and ALP activity of PDLC to a certain extent.
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