抑制前列腺素合成可降低环AMP水平并抑制培养鸡肢体间质软骨形成。

D M Biddulph, M M Dozier, A A Capehart
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引用次数: 13

摘要

本研究研究了抑制前列腺素合成对培养鸡肢间质环AMP浓度和软骨形成的影响。吲哚美辛在50- 200微米的浓度范围内对PGE(2)合成和软骨形成产生浓度依赖性的抑制作用。50微米浓度的药物对PGE(2)的抑制达到了最大抑制的一半,在培养第6天的阿利新绿染色中,细胞培养中软骨基质的数量也明显减少。吲哚美辛对软骨形成的抑制作用在加入1mm二丁基cAMP后被很大程度上逆转,表明细胞仍能对循环AMP刺激产生反应。内源性环AMP水平在对照细胞培养的6天内增加了6倍,而在经吲哚美辛处理的培养物中,在培养皿时(第0天),游离细胞的环AMP水平没有显著增加。结果表明,抑制肢体间充质中PGE(2)浓度的成软骨前升高可以防止在同一时期发生的环状AMP水平的升高,从而抑制软骨形成。这些数据进一步支持了PGE(2)通过其对腺苷酸环化酶- camp系统的影响,在软骨分化中发挥重要作用的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of prostaglandin synthesis reduces cyclic AMP levels and inhibits chondrogenesis in cultured chick limb mesenchyme.

The present study investigated effects of inhibiting the synthesis of prostaglandins (PGs) on cyclic AMP concentrations and chondrogenesis in cultured chick limb mesenchyme. Indomethacin produced concentration-dependent inhibition of both PGE(2) synthesis and chondrogenesis over a concentration range of 50--200 microM. Half maximal inhibition of PGE(2) was achieved with 50 microM concentrations of the drug which also produced visibly reduced amounts of cartilage matrix in cell cultures as evaluated by Alcian green staining on day 6 of culture. The inhibitory effects of indomethacin on chondrogenesis were largely reversed by addition of 1 mM dibutyryl cAMP, indicating that cells could still respond to cyclic AMP stimulation. Endogenous levels of cyclic AMP, which increased by 6 fold during the six days of culture in control cells, did not increase significantly from dissociated cells at the time of plating (day 0) in indomethacin- treated cultures. The results indicate that inhibition of the prechondrogenic rise in PGE(2) concentrations in limb mesenchyme prevents the increase in cyclic AMP levels which occur during this same period resulting in inhibition of chondrogenesis. The data provide further support for the hypothesis that PGE(2), through its effects on the adenylate cyclase-cAMP system, plays an important role in the differentiation of cartilage.

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