Journal of Pharmacobio-Dynamics · 1991 · 132 citations · 29 references
MedicineBiochemistryPharmacologyBiochemical PharmacologyDrug MetabolismHepatic PharmacokineticsDrug DispositionDrug ExcretionOpioid AnalgesicsOpioid PharmacologySpecies Differences In Drug MetabolismUrinary ExcretionComparative Drug ExcretionGlucuronidation PathwaysHigh-performance Liquid ChromatographyInter-species PharmacokineticsMouse Liver MicrosomesOpioid MetabolismRat Liver MicrosomesUrinary Metabolite Profiling
Species difference in glucuronidation of morphine was studied using mice, rats, guinea pigs and rabbits in vivo and in vitro. Morphine-3-glucuronide (M-3-G) and morphine-6-glucuronide (M-6-G) were determined by high-performance liquid chromatography. M-3-G was the major urinary metabolite of morphine in all these animal species. However, a remarkable species difference was observed in the urinary excretion of the M-6-G. Excretion ratios of the M-3-G to M-6-G were approximately 4:1 and 50:1 in guinea pigs and rabbits, respectively. The urinary excretion of M-6-G in mice and rats was too small to be determined. On the other hand, the ratios of uridine diphosphate-glucuronyltransferase (UDPGT) activities toward 3- and 6-hydroxyl groups of morphine in liver microsomes of mice, rats, guinea pigs and rabbits were approximately 300:1, 90:1, 4:1 and 40:1, respectively. Ratios of two morphine UDPGT activities in the liver microsomes of guinea pigs and rabbits, thus, reflected those of urinary excretion of morphine glucuronides.
29
Jan‐Olof Svensson, Anders Rane, Juliette Säwe et al. · Journal of Chromatography B Biomedical Sciences and Applications · 1982 · 278 citations
Purification of Rat‐Liver Microsomal UDP‐glucuronyltransferase
Karl Walter Bock, D. Josting, Werner Lilienblum et al. · European Journal of Biochemistry · 1979 · 217 citations · Full text