Hanioka N, Hoshikawa Y, Mitsui T, Oguri K, Yoshimura H
Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
J Pharmacobiodyn. 1990 Nov;13(11):712-7. doi: 10.1248/bpb1978.13.712.
Species difference in codeine uridine diphosphate-glucuronyltransferase (UDPGT) activity was studied in liver microsomes of mice, rats, guinea pigs and rabbits. Codeine UDPGT activity was the highest in guinea pigs, followed by that in rabbits, and the lowest in mice and rats among these four animal species. The specific activities of codeine UDPGT in liver microsomes were not correlated well with those toward morphine, 4-nitrophenol, and 4-hydroxybiphenyl in liver microsomes of each of the species. Inducibility of liver microsomal codeine UDPGT activity in rats was examined by pretreatment with phenobarbital and 3-methylcholanthrene and compared with those of other UDPGT activities. The activity was inducible by phenobarbital pretreatment as the activity toward morphine and 4-hydroxybiphenyl. The inducibility of codeine UDPGT activity by phenobarbital pretreatment was not as high as that of morphine UDPGT activity.
在小鼠、大鼠、豚鼠和兔子的肝微粒体中研究了可待因尿苷二磷酸葡萄糖醛酸基转移酶(UDPGT)活性的种属差异。在这四种动物中,可待因UDPGT活性在豚鼠中最高,其次是兔子,在小鼠和大鼠中最低。各物种肝微粒体中可待因UDPGT的比活性与对吗啡、4-硝基苯酚和4-羟基联苯的比活性相关性不佳。通过苯巴比妥和3-甲基胆蒽预处理来检测大鼠肝微粒体中可待因UDPGT活性的诱导性,并与其他UDPGT活性的诱导性进行比较。该活性可被苯巴比妥预处理诱导,如同对吗啡和4-羟基联苯的活性一样。苯巴比妥预处理对可待因UDPGT活性的诱导性不如对吗啡UDPGT活性的诱导性高。