Fournier T, Mejdoubi N, Monnet D, Durand G, Porquet D
General Biochemistry Laboratory, Pharmacy Faculty, University of South Paris, Châtenay-Malabry, France.
Hepatology. 1994 Dec;20(6):1584-8. doi: 10.1002/hep.1840200630.
The serum level of rat alpha 1-acid glycoprotein is significantly increased by treatment with phenobarbital, and in vivo studies have shown that phenobarbital seems to act mainly at the transcriptional level. To show the direct mediating effect of phenobarbital on alpha 1-acid glycoprotein gene expression, we investigated the ability of primary cultured rat hepatocytes to respond to in vitro phenobarbital administration. Phenobarbital increased both alpha 1 acid glycoprotein secretion and corresponding mRNA levels in primary rat hepatocytes cultured on matrigel. Used in combination with interleukin-1, interleukin-6 and dexamethasone, phenobarbital had an additive or synergistic effect on alpha 1-acid glycoprotein synthesis. These results show that (a) phenobarbital acts directly on hepatocytes by increasing alpha 1-acid glycoprotein gene expression and (b) this effect is mediated by a specific mechanism independent of pathways involved in alpha 1-acid glycoprotein induction by interleukin-1, interleukin-6 and glucocorticoids.
用苯巴比妥治疗可使大鼠α1-酸性糖蛋白的血清水平显著升高,体内研究表明苯巴比妥似乎主要在转录水平起作用。为了显示苯巴比妥对α1-酸性糖蛋白基因表达的直接介导作用,我们研究了原代培养的大鼠肝细胞对体外给予苯巴比妥的反应能力。苯巴比妥增加了在基质胶上培养的原代大鼠肝细胞中α1酸性糖蛋白的分泌及相应的mRNA水平。与白细胞介素-1、白细胞介素-6和地塞米松联合使用时,苯巴比妥对α1-酸性糖蛋白的合成有相加或协同作用。这些结果表明:(a)苯巴比妥通过增加α1-酸性糖蛋白基因表达直接作用于肝细胞;(b) 这种作用是由一种独立于白细胞介素-1、白细胞介素-6和糖皮质激素诱导α1-酸性糖蛋白的途径的特定机制介导的。