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作 者:刘加强[1,2] 刘洪臣[1] 王懿[1] 冯元[1] 高辉[3]
机构地区:[1].解放军总医院口腔研究所,北京100853 [2]解放军第313医院口腔科,辽宁省葫芦岛125000 [3]武警北京总队第三医院口腔科.北京100141
出 处:《上海口腔医学》2011年第3期225-229,共5页Shanghai Journal of Stomatology
基 金:国家自然科学基金(30973354);教育部博士后科学基金(20100471816)~~
摘 要:目的:检测高糖环境对体外培养的人牙周膜细胞(hPDLF)增殖、总蛋白合成、碱性磷酸酶活性(ALP)、Ⅰ型胶原(Col-Ⅰ)和骨钙素(OCN)分泌的影响以及胰岛素在此过程中的调节作用,为探讨糖尿病型牙周炎的发病机制及治疗方法提供理论依据。方法:采用含不同糖浓度(5.5、15、25、35、45mmol/L)的培养基培养hPDLF,各组均采用胰岛素作为治疗对照。孵育24h后,采用CCK-8法检测不同糖浓度对细胞增殖的影响;同时检测其对细胞蛋白质合成、ALP活性、Col-Ⅰ和OCN分泌的影响。采用SPSS 13.0软件包对数据进行统计学分析。结果:低浓度的葡萄糖对hPDLF增殖及其他生物学活性无显著影响,随浓度的增高,葡萄糖能够浓度依赖性抑制hPDLF的增殖,减少蛋白质合成及Col-Ⅰ分泌,抑制ALP活性及OCN分泌,这一效应可被胰岛素所抑制。结论:高糖可抑制hPDLF生物学活性,胰岛素能拮抗这种抑制作用。PURPOSE:The investigate the effect of high glucose on proliferation,total protein synthesis,alkaline phosphatase(ALP) activities,collagen-Ⅰ(Col-Ⅰ) and osteocalcin(OCN) secretion of human periodontal ligament fibroblast(hPDLF) in vitro and the regulative function of insulin in this process.METHODS:Glucose of different concentration(5.5,15,25,35and 45mmol/L) was used to culture hPDLF and insulin was used for each group as treatment control.24 hrs after administration,cell proliferation was detected by cell counting kit(CCK-8),total protein synthesis,ALP activities,Col-Ⅰ and OCN secretion were investigated.Data was analyzed with SPSS 13.0 soft ware package.RESULTS:Glucose of low concentration had no effect on biological function of hPDLF,but glucose of high concentration could inhibit proliferation,total protein synthesis,ALP activities,Col-Ⅰ and OCN secretion of hPDLF significantly in a concentration-dependent manner.This effect could be blocked by insulin.CONCLUSIONS:High glucose could inhibit biological function of hPDLF and such effect could be blocked by insulin.
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