Reinke L A, Kauffman F C, Evans R K, Belinsky S A, Thurman R G
Res Commun Chem Pathol Pharmacol. 1979 Jan;23(1):185-93.
Conjugation of p-nitrophenol in perfused livers from control and phenobarbital-treated rats was measured spectrally by determining influent minus effluent concentration differences of the free drug. Rates of conjugation (1.0 to 2.0 mu moles/g/h) were essentially the same in livers from fasted control or fasted phenobarbital-treated rats. In control fed livers, rates of conjugation did not differ from the fasted state. However, rates of conjugation in livers from carbohydrate-rich, phenobarbital-treated rats were 6- to 10-fold greater than rates in livers from fasted phenobarbital-treated animals. Differences in rates of conjugation in phenobarbital-treated rats in different nutritional states were more closely related to carbohydrate reserves as indicated by glycogen levels than to activities of p-nitrophenyl UDP-glucuronyl transferase.
通过测定游离药物的流入浓度与流出浓度之差,以光谱法测定对照大鼠和苯巴比妥处理大鼠的灌注肝脏中对硝基苯酚的结合情况。禁食对照大鼠或禁食苯巴比妥处理大鼠肝脏中的结合速率(1.0至2.0微摩尔/克/小时)基本相同。在对照喂食的肝脏中,结合速率与禁食状态无差异。然而,富含碳水化合物的苯巴比妥处理大鼠肝脏中的结合速率比禁食苯巴比妥处理动物肝脏中的结合速率高6至10倍。不同营养状态下苯巴比妥处理大鼠结合速率的差异与糖原水平所表明的碳水化合物储备更密切相关,而非与对硝基苯基UDP-葡萄糖醛酸转移酶的活性相关。