吕 享, 周 英, 陈克明, 赵 致, 周 建, 马小妮. 8-异戊烯基柑橘素抑制骨髓细胞向破骨细胞分化及骨吸收活性J. 药学学报, 2013,48(3): 347-351.
引用本文: 吕 享, 周 英, 陈克明, 赵 致, 周 建, 马小妮. 8-异戊烯基柑橘素抑制骨髓细胞向破骨细胞分化及骨吸收活性J. 药学学报, 2013,48(3): 347-351.
Lü Xiang,ZHOU Ying,CHEN Ke-ming,ZHAO Zhi,ZHOU Jian,MA Xiao-ni. Inhibitory effect of 8-prenylnaringenin on osteoclastogensis of bone marrow cells and bone resorption activityJ. 药学学报, 2013,48(3): 347-351.
Citation: Lü Xiang,ZHOU Ying,CHEN Ke-ming,ZHAO Zhi,ZHOU Jian,MA Xiao-ni. Inhibitory effect of 8-prenylnaringenin on osteoclastogensis of bone marrow cells and bone resorption activityJ. 药学学报, 2013,48(3): 347-351.

8-异戊烯基柑橘素抑制骨髓细胞向破骨细胞分化及骨吸收活性

Inhibitory effect of 8-prenylnaringenin on osteoclastogensis of bone marrow cells and bone resorption activity

  • 摘要:

    研究8-异戊烯基柑橘素 (8-prenylnaringenin, 8-PNG) 对骨髓细胞向破骨细胞分化及骨吸收活性的影响。从出生24 h内的青紫兰兔四肢骨髓中分离培养破骨细胞, 加入8-PNG (1×10−71×10−61×10−5 mol·L−1), 1×10−7 mol·L−1 17β-雌二醇 (17β-estradiol, E2) 作为阳性对照。培养5天后进行TRAP染色和TRAP活性检测, 7天后进行甲苯胺蓝染色和骨吸收陷窝数量与面积的分析。分别于加药后24812243648 h进行Annexin V染色, 观察破骨细胞凋亡情况; 122436 h提取总RNA, real-time RT-PCR法检测TRAP (tartrate-    resistant acid phosphatase) CTSK (cathepsin K) 的基因表达水平。结果显示, 8-PNG (1×10−61×10−5 mol·L−1) 组的TRAP染色阳性细胞即破骨细胞数量明显低于空白对照组 (P < 0.01), 但只有8-PNG (1×10−5 mol·L−1) 组显著低于E2 (P < 0.05); TRAP活性的变化呈相同趋势; 骨陷窝数和面积的计量结果亦呈相似变化趋势; E2组使破骨细胞的凋亡高峰大大提前, 且凋亡数量最多, 其次为8-PNG (1×10−5 mol·L−1) , 8-PNG (1×10−7 mol·L−1) 组与空白对照组比较无差异。8-PNG (1×10−71×10−61×10−5 mol·L−1) 可显著抑制TRAPCTSK的基因表达, 且呈剂量依赖性。结果表明, 8-PNG能抑制骨髓细胞向破骨细胞分化, 并能抑制破骨细胞的骨吸收活性, 其机制与诱导破骨细胞凋亡和抑制骨吸收关键酶的基因表达与活性有关。

     

    Abstract:

    This study is to investigate the effect of 8-prenylnaringenin (8-PNG) on osteoclastogensis of bone marrow cells and bone resorption activity of osteoclasts.  Osteoclasts were separated from long bone marrow of newborn rabbits and cultured in α-MEM containing 10% FBS.  8-PNG was added into culture media at 1×10−7, 1×10−6, 1×10−5 mol·L−1, separately.  17β-Estradiol (E2, 1×10−7 mol·L−1) was used as positive control.  TRAP staining and TRAP activity measurement were performed after 5 days, and the bone resorption pits were analyzed after 7 days.  Annexin V staining for the detection of apoptotic osteoclasts was performed after 2, 4, 8, 12, 24, 36 and 48 h separately.  The mRNA expression level of TRAP and cathepsin K (CTSK) was measured by real-time RT-PCR.  8-PNG significantly reduced the number of osteoclasts which was TRAP staining positive and with more than three nucleus, the area and number of bone resorption pits decreased obviously in 8-PNG- supplemented groups.  The apoptosis rate peaked earlier in the 8-PNG-supplemented groups and the mRNA expression level of TRAP and CTSK decreased significantly.  All these inhibitory effects were in a dose dependent manner, the highest effect was obtained by 1×10−5 mol·L−1 8-PNG.  8-PNG inhibits bone resorption activity of osteoclasts by inducing osteoclast apoptosis and inhibiting the gene expression and enzyme activity including TRAP and CTSK, and restrains bone marrow cells to osteoclast differentiation.

     

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