Yue Q Y, Odar-Cederlöf I, Svensson J O, Säwe J
Department of Clinical Pharmacology, Huddinge University Hospital, Sweden.
Pharmacol Toxicol. 1988 Nov;63(5):337-41. doi: 10.1111/j.1600-0773.1988.tb00965.x.
The UDP-glucuronyltransferase (GT) activity with morphine as substrate was measured in microsomes prepared from seven human adult kidneys including one whose cortex and medulla had been separated. The formation of morphine-3- and 6-glucuronides (M3G and M6G) was determined by HPLC methods. All kidney specimen formed M3G and M6G when incubated with morphine and UDP-glucuronic acid (UDPGA). The estimated Vmax and Km of morphine to form M3G and M6G were 2.2 and 0.18 nmol per mg protein and min. and 8.2 and 4.6 mM, respectively. The corresponding values for UDPGA were 1.3 and 0.13 nmol per mg protein and min. and 5.4 and 4.1 mM, respectively. The GT activity in cortex was 2.8-fold higher than in the medulla. The human kidney thus contains glucuronyltransferase activities towards morphine, which is in contrast to previous findings in the rat.
在从七个成年人类肾脏制备的微粒体中测定了以吗啡为底物的UDP - 葡糖醛酸基转移酶(GT)活性,其中一个肾脏的皮质和髓质已分离。通过高效液相色谱法测定吗啡 - 3 - 和6 - 葡糖醛酸苷(M3G和M6G)的形成。所有肾脏标本与吗啡和UDP - 葡糖醛酸(UDPGA)一起孵育时均形成M3G和M6G。形成M3G和M6G的吗啡的估计Vmax和Km分别为每毫克蛋白质每分钟2.2和0.18 nmol以及8.2和4.6 mM。UDPGA的相应值分别为每毫克蛋白质每分钟1.3和0.13 nmol以及5.4和4.1 mM。皮质中的GT活性比髓质高2.8倍。因此,人类肾脏含有针对吗啡的葡糖醛酸基转移酶活性,这与先前在大鼠中的发现相反。