Mottino A D, Rodríguez Garay E A
Instituto de Fisiología Experimental, CONICET - Universidad Nacional de Rosario, Argentina.
Acta Physiol Pharmacol Latinoam. 1987;37(4):479-84.
The formation of bilirubin glucuronides was studied using liver microsomes from normal and spironolactone (SP)-treated rats. Increasing amounts of uridine diphosphoglucuronic acid (UDPGA) were added to the incubation mixture to investigate the influence of this nucleotide on bilirubin glucuronidation. The results demonstrated that microsomal preparations from SP-treated rats had a greater capability for bilirubin glucuronidation than normal microsomes which was mostly produced at the expense of bilirubin diglucuronide (BDG) formation. On the other hand, the increase in UDPGA concentration in the incubation mixture also produced an increase of BDG formation which was more important than that of monoglucuronide. These results support the hypothesis of different subunits in the glucuronyl-transferase moiety with different substrate specificities. In addition, the inducer effect of SP on bilirubin glucuronidation is in agreement to the results obtained in living rats which were described previously.
使用来自正常大鼠和螺内酯(SP)处理大鼠的肝脏微粒体研究胆红素葡萄糖醛酸苷的形成。向孵育混合物中添加越来越多的尿苷二磷酸葡萄糖醛酸(UDPGA),以研究该核苷酸对胆红素葡萄糖醛酸化的影响。结果表明,SP处理大鼠的微粒体制剂比正常微粒体具有更强的胆红素葡萄糖醛酸化能力,这主要是以胆红素二葡萄糖醛酸苷(BDG)的形成为代价产生的。另一方面,孵育混合物中UDPGA浓度的增加也导致BDG形成增加,这比单葡萄糖醛酸苷的增加更显著。这些结果支持了葡萄糖醛酸转移酶部分中具有不同底物特异性的不同亚基的假设。此外,SP对胆红素葡萄糖醛酸化的诱导作用与先前描述的在活体大鼠中获得的结果一致。