地塞米松对小鼠颅骨成骨细胞的影响。

S Taniuchi
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引用次数: 0

摘要

在本研究中,我们测定了地塞米松对MC3T3-E1细胞(一种来源于小鼠颅骨的成骨细胞)的影响。得到了以下结果:1)地塞米松对MC3T3-E1细胞生长的抑制作用在浓度为1微克/ml及以上时呈剂量依赖性。2) 1、10、30 μ g /ml地塞米松治疗后12、24、48 h碱性磷酸酶活性均升高。当剂量为10微克/毫升时,48小时活性最高,为对照值的311%。当使用60微克/毫升或更高剂量的地塞米松时,12小时时活性增加,但在48小时时活性低于对照组。3) 1、10、30微克/毫升地塞米松治疗24小时后,胶原蛋白的合成更容易。特别是在10微克/毫升时,合成水平最高,为对照值的232%。然而,这种合成在60微克/毫升或更高的剂量下被抑制。4) 1或10微克/毫升地塞米松治疗48小时可促进胶原蛋白的合成,30微克/毫升以上地塞米松可抑制胶原蛋白的合成。5)显微镜下观察染色后的制剂,地塞米松分别在60、150、200微克/ml时引起空泡变性、核深染、固缩。
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[Effect of dexamethasone on osteoblastic cells derived from mouse calvaria].

In the present study, the effect of dexamethasone on MC3T3-E1 cells, a strain of osteoblasts derived from mouse cranial bone, was determined. The following results were obtained. 1) Dexamethasone showed dose-dependent suppression of the growth of MC3T3-E1 cells at concentration of 1 microgram/ml or more. 2) The alkaline phosphatase activity was increased 12, 24, and 48 hours after treatment with dexamethasone at 1, 10 or 30 micrograms/ml. The activity was highest at 48 hours, the level being 311% of the control value at a dose of 10 micrograms/ml. When dexamethasone at a dose of 60 micrograms/ml or more was used, the activity was increased at 12 hours, but was lower than the control at 48 hours. 3) Synthesis of collagenous protein was facilitated after 24-hour treatment with dexamethasone at 1, 10 or 30 micrograms/ml. In particular, the level of synthesis was highest, 232% of the control value, at 10 micrograms/ml. Such synthesis, however, was suppressed at a dose of 60 micrograms/ml or more. 4) Synthesis of collagenous protein was facilitated by 48-hour treatment with dexamethasone at a dose of 1 or 10 micrograms/ml and suppressed at a dose of 30 micrograms/ml or more. 5) Microscopic observation of stained preparations revealed that dexamethasone caused vacuolar degeneration, deep staining of the nucleus, and pyknosis at 60, 150, and 200 micrograms/ml, respectively.

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