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乙醇对大鼠肝脏胆红素UDP-葡萄糖醛酸基转移酶的转录诱导作用

Transcriptional induction of bilirubin UDP-glucuronosyltransrase by ethanol in rat liver.

作者信息

Kardon T, Coffey M J, Bánhegyi G, Conley A A, Burchell B, Mandl J, Braun L

机构信息

Department of Medical Chemistry, Semmelweis University of Medicine, P.O. Box 260, H-1444, Budapest, Hungary.

出版信息

Alcohol. 2000 Jul;21(3):251-7. doi: 10.1016/s0741-8329(00)00095-1.

Abstract

Several drug-metabolizing enzymes including bilirubin UDP-glucuronosyltransferase (UGT1A1) are influenced by long-term ethanol consumption. In the present study, the activity and expression of UGT1A1 were investigated in livers of ethanol-treated rats. Animals were treated daily for 15 days with ethanol or isocaloric amount of glucose solution by gastric intubation. Microsomes and total RNA were prepared from the liver of rats and analyzed by Western blot and Northern hybridization using UGT1A1 specific antibody and cDNA probe. Microsomal bilirubin UGT activity was also measured. The elevation of UGT1A1 mRNA was observed in the liver of ethanol consumer animals with the simultaneous increase in microsomal UGT1A1 protein leading to stimulated bilirubin glucuronidation both in vivo and in microsomal vesicles. These results arise the possibility of the transcriptional induction and/or the mRNA stabilization by ethanol consumption, which can be caused by ethanol itself or the metabolic changes due to the treatment.

摘要

包括胆红素UDP-葡萄糖醛酸基转移酶(UGT1A1)在内的几种药物代谢酶会受到长期乙醇摄入的影响。在本研究中,对乙醇处理大鼠肝脏中UGT1A1的活性和表达进行了研究。通过胃插管,每天用乙醇或等热量的葡萄糖溶液对动物进行15天的处理。从大鼠肝脏中制备微粒体和总RNA,并使用UGT1A1特异性抗体和cDNA探针通过蛋白质免疫印迹法和Northern杂交进行分析。还测定了微粒体胆红素UGT活性。在摄入乙醇的动物肝脏中观察到UGT1A1 mRNA升高,同时微粒体UGT1A1蛋白增加,导致体内和微粒体囊泡中胆红素葡萄糖醛酸化增强。这些结果提示了乙醇摄入可能导致转录诱导和/或mRNA稳定,这可能是由乙醇本身或处理引起的代谢变化所致。

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