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淫羊藿苷对人牙周膜细胞中核因子κB受体激活因子配体及骨保护素表达的影响

[Effect of icariin on the expression of receptor activator nuclear factor-κB ligand and osteoprotegerin of human periodontal ligament cells].

作者信息

Ding Qian, Zhang Feng-qiu

机构信息

Department of Periodontology, Capital Medical University School of Stomatology, Beijing, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2013 Feb;48(2):68-71.

Abstract

OBJECTIVE

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).

METHODS

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.

RESULTS

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).

CONCLUSIONS

The concentration of 0.1 mg/L icariin can inhibit hPDLC expression of RANKL in sonicated extracts of Pg and promote OPG expression.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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