Ding Qian, Zhang Feng-qiu
Department of Periodontology, Capital Medical University School of Stomatology, Beijing, China.
Zhonghua Kou Qiang Yi Xue Za Zhi. 2013 Feb;48(2):68-71.
To investigate the effect of icariin on the expression of receptor activator nuclear factor-κB ligand (RANKL) and osteoprotegerin (OPG) of human periodontal ligament cells (hPDLC) inhibited by sonicated extracts of Porphyromonas gingivalis (Pg).
hPDLC were extracted from 14 premolars extracted from 11 to 18-year-old patients for orthodontic purpose and cultured. The 7th passages of hPDLC were divided into six groups, each group was stimulated with 0, 0.001, 0.01, 0.1, 1 mg/L icariin and 50 mg/L sonicated extracts for 48 h. Reverse transcription polymerase chain reaction (RT-PCR) and Western blotting were used to detect the expression of RANKL and OPG.
Pg extracts group expressed more RANKL than the control group (3.60 ± 0.11 vs 1.08 ± 0.19), OPG expression decreased (0.32 ± 0.08 vs 1.01 ± 0.08), and RANKL/OPG ratio significantly increased (11.20 ± 0.13 vs 1.00 ± 0.10). Compared with control group, RANKL and OPG expression changed in groups stimulated with 0.001, 0.01, 0.1, 1 mg/L icariin. OPG expression was higher in 0.1 mg/L group than in the control (36.84 ± 0.05 vs 1.01 ± 0.08), RANKL/OPG ratio was significantly lower than the control group (0.04 ± 0.03 vs 1.00 ± 0.10) (P < 0.01).
The concentration of 0.1 mg/L icariin can inhibit hPDLC expression of RANKL in sonicated extracts of Pg and promote OPG expression.
探讨淫羊藿苷对牙龈卟啉单胞菌(Pg)超声裂解物抑制人牙周膜细胞(hPDLC)中核因子κB受体活化因子配体(RANKL)和骨保护素(OPG)表达的影响。
从11至18岁患者因正畸拔除的14颗前磨牙中提取hPDLC并进行培养。将第7代hPDLC分为6组,每组分别用0、0.001、0.01、0.1、1 mg/L淫羊藿苷和50 mg/L Pg超声裂解物刺激48小时。采用逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法检测RANKL和OPG的表达。
Pg提取物组RANKL表达高于对照组(3.60±0.11 vs 1.08±0.19),OPG表达降低(0.32±0.08 vs 1.01±0.08),RANKL/OPG比值显著升高(11.20±0.13 vs 1.00±0.10)。与对照组相比,用0.001、0.01、0.1、1 mg/L淫羊藿苷刺激的组中RANKL和OPG表达发生变化。0.1 mg/L组OPG表达高于对照组(36.84±0.05 vs 1.01±0.08),RANKL/OPG比值显著低于对照组(0.04±0.03 vs 1.00±0.10)(P<0.01)。
0.1 mg/L淫羊藿苷可抑制Pg超声裂解物中hPDLC的RANKL表达并促进OPG表达。