Masmoudi T, Planells R, Mounié J, Artur Y, Magdalou J, Goudonnet H
Formation de Biochimie Pharmacologique, UFR de Pharmacie, Dijon, France.
FEBS Lett. 1996 Jan 29;379(2):181-5. doi: 10.1016/0014-5793(95)01507-8.
The effects of 3,3',5 triiodo-L-thyronine (L-T3) on the constitutive levels of hepatic mRNA encoding two UDP-glucuronosyltransferase (UGT) isoforms implicated in the glucuronidation of planar phenolic substrates (UGT106) and bilirubin (UGT10) were investigated in rat liver. The amount of UGT mRNA was quantitated by reverse transcription and amplification methods (RT-PCR). Treatment with L-T3 significantly increased UGT106 and decreased UGT10 mRNA levels by 41% and 54%, respectively. The opposite situation was observed in thyroidectomised animals. A good relationship observed between UGT activity toward 4-nitrophenol and bilirubin and mRNA levels emphasizes the key role played by the thyroid hormone L-T3 on UGT expression.
研究了3,3',5-三碘-L-甲状腺原氨酸(L-T3)对大鼠肝脏中两种尿苷二磷酸葡萄糖醛酸基转移酶(UGT)同工型编码的肝mRNA组成水平的影响,这两种同工型分别参与平面酚类底物(UGT106)和胆红素(UGT10)的葡萄糖醛酸化。通过逆转录和扩增方法(RT-PCR)对UGT mRNA的量进行定量。用L-T3处理可使UGT106显著增加,UGT10 mRNA水平分别降低41%和54%。在甲状腺切除的动物中观察到相反的情况。观察到UGT对4-硝基苯酚和胆红素的活性与mRNA水平之间存在良好的关系,这强调了甲状腺激素L-T3对UGT表达所起的关键作用。