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宫内用 dexamethasone 处理的大鼠胎儿所培养的肝细胞中酪氨酸转氨酶的诱导。

Tyrosine aminotransferase induction in hepatocytes cultured from rat foetuses treated with dexamethasone in utero.

作者信息

Yeoh G C, Arbuckle T, Oliver I T

出版信息

Biochem J. 1979 Jun 15;180(3):545-9. doi: 10.1042/bj1800545.

Abstract
  1. The administration of dexamethasone to foetal rats in utero does not result in the appearance of specific tyrosine aminotransferase activity even after 24 h. 2. When foetal hepatocytes are cultured in vitro from animals treated in utero with dexamethasone, significantly higher activities of specific tyrosine aminotransferase are found than in untreated controls. 3. Dexamethasone in vitro induces specific tyrosine aminotransferase in cells cultured from control animals and the effect is maximal at 10 nM in the culture medium. 4. Actinomycin D at 0.2 microgram/ml in the culture medium completely prevents the induction of activity in vitro. 5. In cultures established from animals treated with dexamethasone in utero, the increase in specific tyrosine aminotransferase activity over the control cultures is only marginally decreased in the presence of actinomycin D. 6. The results can be interpreted to mean that dexamethasone in utero stimulates the transcription of enzyme-specific mRNA, which is not rranslated until a translational block in the foetal liver is removed by the conditions of culture in vitro.
摘要
  1. 对子宫内的胎鼠注射地塞米松,即使在24小时后也不会导致特异性酪氨酸转氨酶活性的出现。2. 当从子宫内用地塞米松处理过的动物体外培养胎肝细胞时,发现特异性酪氨酸转氨酶的活性明显高于未处理的对照。3. 地塞米松在体外可诱导从对照动物培养的细胞中产生特异性酪氨酸转氨酶,且在培养基中浓度为10 nM时效果最佳。4. 培养基中浓度为0.2微克/毫升的放线菌素D可完全阻止体外活性的诱导。5. 在从子宫内用地塞米松处理过的动物建立的培养物中,在放线菌素D存在的情况下,特异性酪氨酸转氨酶活性相对于对照培养物的增加仅略有降低。6. 这些结果可以解释为,子宫内的地塞米松刺激了酶特异性mRNA的转录,而这种转录直到胎儿肝脏中的翻译阻滞被体外培养条件消除后才会被翻译。

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