Volume 35 Issue 6
Nov.  2019
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WANG Hua-jun, QIAO Chen, ZHAO Rong, YIN Jiang-ning. Study on the Mechanism of Circular-Icaritin Against Glucocorticoid-Induced Osteoporosis[J]. Journal of Nanjing University of traditional Chinese Medicine, 2019, 35(6): 708-713.
Citation: WANG Hua-jun, QIAO Chen, ZHAO Rong, YIN Jiang-ning. Study on the Mechanism of Circular-Icaritin Against Glucocorticoid-Induced Osteoporosis[J]. Journal of Nanjing University of traditional Chinese Medicine, 2019, 35(6): 708-713.

Study on the Mechanism of Circular-Icaritin Against Glucocorticoid-Induced Osteoporosis

  • Publish Date: 2019-11-10
  • OBJECTIVE To elucidate the reversal effect of cyclic-icaritin(CICT) on prednisolone -induced osteoporosis, and to explore its mechanism of action with BMPs signaling pathway. METHODS Prednisolone-induced osteoporosis model of zebrafish was used. The stained area, cumulative optical density, calcium and phosphorus contents of the skull of zebrafish were observed by fluorescence inverted microscope (×100). qPCR was used to quantitatively detect the expression of Runx 2 and AKP genes. RESULTS Compared with the control group, the cumulative optical density and mineralized area of zebrafish skull significantly decreased (P<0.01),the Ca and P levels significantly decreased (P<0.01), the expression of Runx 2 and AKP genes decreased significantly (P<0.01) after incubation with prednisolone (25 μmol/L).After the intervention with different doses of CICT (0.1, 1.0, 10.0 μmol/L),the cumulative optical density and bone mineralization area of zebrafish skull significantly increased (P<0.01), and the levels of Ca and P significantly increased (P<0.01). Molecular docking techniques showed that CICT could stably dock with target protein BMPs (BMP-2/BMP-4), and the docking scores were - 5.49325609 and - 5.99361658, respectively. The expressions of Runx-2 and AKP genes significantly increased (P<0.01). CONCLUSION CICT can reverse glucocorticoid-induced osteoporosis, which plays an anti-osteoporosis role by binding CICT to BMPs protein target and regulating BMPs signaling pathway to promote osteogenic differentiation.

     

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