Dills R L, Howell S R, Klaassen C D
Drug Metab Dispos. 1987 May-Jun;15(3):281-8.
Hepatic synthesis rates of UDP-glucose and UDP-glucuronic acid were determined in rats. Two high pressure liquid chromatographic methods were developed to quantitate and isolate UTP, UDP-glucose, and UDP-glucuronic acid from perchloric acid extracts of rat liver. The specific activities of UTP, UDP-glucose, and UDP-glucuronic acid were determined in liver samples obtained from rats killed by cervical dislocation at various times after [6-14C]orotic acid administration. Synthesis rates were calculated from the rate of change in specific activities of the compound of interest and its immediate precursor and the concentration of the compound of interest. Synthesis rates of UDP-glucose and UDP-glucuronic acid were 102 +/- 9 and 99 +/- 1 nmol X min-1 X g of liver-1, respectively. UDP-glucuronic acid synthesis apparently accounts for most of the UDP-glucose produced during a period (8 a.m.-10 a.m.) when glycogen synthesis is low. The effect of an ethionine-induced reduction of energy state on these basal synthesis rates was examined. UDP-Glucose and UDP-glucuronic acid synthesis rates were decreased by approximately 80%. In summary, the hepatic synthesis rates of UDP-glucose and UDP-glucuronic acid are approximately 100 nmol X min-1 X g of liver-1, and a reduced energy state can decrease these synthesis rates in vivo.
在大鼠中测定了UDP-葡萄糖和UDP-葡萄糖醛酸的肝脏合成速率。开发了两种高压液相色谱方法,用于从大鼠肝脏的高氯酸提取物中定量和分离UTP、UDP-葡萄糖和UDP-葡萄糖醛酸。在给予[6-¹⁴C]乳清酸后不同时间通过颈椎脱臼处死大鼠所获得的肝脏样本中,测定了UTP、UDP-葡萄糖和UDP-葡萄糖醛酸的比活性。根据目标化合物及其直接前体的比活性变化率以及目标化合物的浓度计算合成速率。UDP-葡萄糖和UDP-葡萄糖醛酸的合成速率分别为102±9和99±1 nmol·min⁻¹·g肝脏⁻¹。在糖原合成较低的时间段(上午8点至10点),UDP-葡萄糖醛酸的合成显然占所产生的UDP-葡萄糖的大部分。研究了乙硫氨酸诱导的能量状态降低对这些基础合成速率的影响。UDP-葡萄糖和UDP-葡萄糖醛酸的合成速率降低了约80%。总之,UDP-葡萄糖和UDP-葡萄糖醛酸的肝脏合成速率约为100 nmol·min⁻¹·g肝脏⁻¹,能量状态降低可在体内降低这些合成速率。