Qu W, Kauffman F C, Thurman R G
Department of Pharmacology, University of North Carolina at Chapel Hill 27599-7365, USA.
Arch Biochem Biophys. 1995 Jun 1;319(2):451-6. doi: 10.1006/abbi.1995.1316.
Rates of conjugation of p-nitrophenol were studied in livers from normal and food-restricted rats perfused with either p-nitroanisole or p-nitrophenol. Female Sprague-Dawley rats had ad libitum access to a Purina 5001 nonpurified diet (control) or were given 65% of the intake of controls for 3 weeks. Livers were perfused with oxygenated Krebs-Henseleit buffer using a nonrecirculating system. Maximal rates of conjugation of p-nitrophenol, generated either from the O-demethylation of p-nitroanisole (200 microM) or from the infusion of p-nitrophenol (70 microM), were elevated significantly nearly twofold by food restriction. Thus, food restriction stimulates conjugation in the intact liver cell. Specifically, rates of conjugation were increased from 2.1 +/- 0.2 to 3.7 +/- 0.4 and from 3.3 +/- 0.6 to 5.8 +/- 0.5 mumol/g/h when 200 microM p-nitroanisole or 70 microM p-nitrophenol were infused, respectively. On the other hand, rates of conjugation were not affected by food restriction when low concentrations of p-nitroanisole (50 microM) or p-nitrophenol (20 microM) were infused. Further, food restriction did not alter rates of conjugation in isolated microsomes supplemented with excess UDPGA. Interestingly, both UDP-glucose and UDP-glucuronic acid were increased significantly in liver extracts from food-restricted rats when livers were perfused with high but not low concentrations of p-nitrophenol. Under these conditions, the increase in UDP-glucuronic acid was threefold. Moreover, food restriction increased carbohydrate release from the liver about twofold. Glycogen content was also increased significantly in liver extracts from 8.4 +/- 1.9 to 60.4 +/- 13.8 mmol/kg wet weight by food restriction. Taken together, these data support the hypothesis that food restriction stimulates conjugation of p-nitrophenol concentrations by increasing the supply of the pivotal cofactor UDP-glucuronic acid from carbohydrate reserves (e.g., glycogen).
在分别用对硝基苯甲醚或对硝基苯酚灌注的正常大鼠和限食大鼠的肝脏中,研究了对硝基苯酚的结合率。雌性斯普拉格 - 道利大鼠可随意摄取普瑞纳5001非纯化饮食(对照),或在3周内给予对照组摄入量65%的食物。使用非循环系统用含氧的克雷布斯 - 亨泽莱特缓冲液灌注肝脏。对硝基苯甲醚(200微摩尔)O - 去甲基化产生的对硝基苯酚或灌注对硝基苯酚(70微摩尔)产生的对硝基苯酚的最大结合率,通过限食显著提高了近两倍。因此,限食刺激完整肝细胞中的结合作用。具体而言,当分别灌注200微摩尔对硝基苯甲醚或70微摩尔对硝基苯酚时,结合率分别从2.1±0.2增加到3.7±0.4以及从3.3±0.6增加到5.8±0.5微摩尔/克/小时。另一方面,当灌注低浓度的对硝基苯甲醚(50微摩尔)或对硝基苯酚(20微摩尔)时,结合率不受限食影响。此外,限食并未改变补充了过量尿苷二磷酸葡萄糖醛酸(UDPGA)的分离微粒体中的结合率。有趣的是,当用高浓度而非低浓度的对硝基苯酚灌注肝脏时,限食大鼠肝脏提取物中的尿苷二磷酸葡萄糖(UDP - 葡萄糖)和尿苷二磷酸葡萄糖醛酸均显著增加。在这些条件下,尿苷二磷酸葡萄糖醛酸增加了三倍。此外,限食使肝脏碳水化合物释放增加约两倍。限食还使肝脏提取物中的糖原含量从8.4±1.9显著增加到60.4±13.8毫摩尔/千克湿重。综上所述,这些数据支持以下假设:限食通过增加碳水化合物储备(如糖原)中关键辅助因子尿苷二磷酸葡萄糖醛酸的供应来刺激对硝基苯酚浓度的结合。