Biomedical subjects
D Emmerling
Publications and source records attributed to D Emmerling.
[40 years of the microcensus].
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[On voluntary responding to microcensus questions].
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[Analyses of voluntary responses in the microcensus: are survey results distorted by voluntary responses?].
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The use of high pressure liquid chromatography to study chemically induced alterations in the pattern of benzo[a]pyrene metabolism.
The metabolism of radiolabeled benzo[a]pyrene (BP) by control, 3-methyl-cholanthrene (3-MC) induced, and 1,1,1-trichloropropene-2,3-oxide (TCPO)-inhibited rat liver microsomes was measured using fluorescence, radiometric, and high-pressure liquid chromatographic (HPLC) assays. Significant differences in the total measurable metabolism of BP by the three microsomal enzyme incubations resulted from the use of the three assay procedures. Appreciable differences in the concentration of the metabolite fractions after 3-MC induction and TCPO inhibition are clearly demonstrated. NMR analysis revealed that while the 3-hydroxy-BP fraction is greater than 90% pure, the 9-hydroxy fraction contains a number of metabolites having essentially identical retention times.
Partial characterization of hepatic micorsomes from tupaia glis.
The dithionite difference spectrum of Tupaia microsomal cytochrome P-450-CO complex has an absorbance maximum at 449 nm, rather than at 450 nm as found for rat, rabbit, mouse, guinea pig, and human microsomes. N-octylamine difference spectroscopy showed the ratio of high- and low-spin forms of cytochrome P-450 to be different from that of the rat, indicating that the 449 nm absorption maximum might be due to a high concentration of the high-spin form, cytochrome P-448. The Tupaia microsomes demonstrated greater aryl hydrocarbon activity than microsomes prepared from male rats. These preliminary results suggest that Tupaia microsomes contain a modified terminal oxygenase which is responsible for the observed rapid metabolism of benzo[alpha]pyrene.
Characterization of the hepatic microsomal mixed-function oxidase enzyme system in miniature pigs.
Hepatic microsomal protein, cytochrome P-450, UDP-glucuronyltransferase, ethylmorphine demethylase, aniline hydroxylase, and aryl hydrocarbon hydroxylase levels were measured in the 2-, 4-, 5-, 6-, and 8-month-old Hanford miniature pig. The activities or concentrations of all of the liver parameters measured had apparently reached their adult plateau level by 2 months of age. The use of the miniature pig in toxicology research programs is discussed.
A comprehensive study of in vitro drug metabolism in several laboratory species.
A shortage of rhesus monkeys for use in drug toxicity studies has made it necessary to search for a potential replacement species in the event that one should be needed in the near future. To this end, 14 parameters of drug metabolism in hepatic microsomal and soluble fractions were examined in preparations from adult male and female rhesus monkeys, squirrel monkeys, Hanford miniature pigs, common tree shrews, and Sprague-Dawley rats. Model substrates were utilized and comparisons were made on a quantitative basis. All species tested demonstrated activity in all but one test assay and all showed some similarity to the rhesus. None of the species, however, was totally comparable to the rhesus in drug-metabolizing ability. The squirrel monkey showed the least similarity to the rhesus and the miniature pig was the most similar. With the exception of the expected differences in the rat, the tree shrew demonstrated the only sex difference in drug metabolism, the enzyme activities of females being higher than the male in several pathways. The data suggest that any of the four species tested could be a suitable replacement for the rhesus in studies of drug metabolism in vitro.