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121.
Julia Bell-Quint Trudy Forte Paul Graham 《Biochemical and biophysical research communications》1981,99(2):700-706
Cultured rat hepatocytes were used to demonstrate that the liver can synthesize two forms of apolipoprotein B. Separation of apolipoprotein B by disc gel electrophoresis indicated that hepatocyte low density lipoprotein contains predominantly apolipoprotein B with an apparent molecular weight of 345,000 ± 5,055. In contrast, the major apolipoprotein B component of hepatocyte very low density lipoprotein is a variant form with a molecular weight of 242,000 ± 2,720. Hepatocyte high density lipoprotein, unlike plasma HDL, also contains apolipoprotein B with an apparent molecular weight of 244,000 ± 2,742. Incorporation of [3H] leucine into hepatocyte apolipoprotein B components suggested de novo synthesis. 相似文献
122.
123.
F. Perin M. Dufour J. Mispelter B. Ekert C. Künneke F. Oesch F. Zajdela 《Chemico-biological interactions》1981,35(3):267-284
The metabolism of dibenzo[c,g]carbazole (DBC), was studied in vitro using microsomal fractions of mouse and rat liver from animals, which were treated with 3-methylcholanthrene (MC). The separation of extractable metabolites by high pressure liquid chromatography (HPLC) and thinlayer chromatography (TLC) as well as identification of most of them by nuclear magnetic resonance, mass spectrometry and comparison with synthetically obtained products are described. The microsomes of both species produced the same twelve compounds of which the following have been identified: five monohydroxylated derivatives (phenols), the product of further oxidation of one of them, and a dihydrodiol. The 5-OH-DBC (60% including its spontaneously-formed dimer) and the 3-OH-DBC (14%) are the main metabolites. Three minor metabolites cochromatographed with synthetically prepared 2-OH-DBC, 4-OH-DBC and 6-OH-DBC. The dihydrodiol detectable in small quantity (4–6%) was tentatively identified as 3,4-dihydroxy-3,4-dihydro-DBC by the sensitivity of its formation to very low concentrations of the inhibitor of microsomal epoxide hydrolase, 1,1,1-trichloropropene oxide, by its molecular ion and major fragment in mass spectrometry and by its dehydration product 3-OH-DBC. No other dihydrodiols were detected. The qualitative and quantitative effects of various modulators of metabolism (enzyme inhibitors, apparently homogeneous epoxide hydrolase, glutathione, supernatant fraction) were investigated. The results are discussed with respect to possible ultimate carcinogens. 相似文献
124.
Some pharmacological properties of ellipticine (E) and its derivatives linked to their interaction with cytochrome P-450 have been investigated with human liver microsomes. 9-Hydroxyellipticine (9-OHE) interacts with human liver cytochrome P-450 exhibiting a type II spectrum (λmax: 428 nm, Ks = 1.1 μM). After incubation with human liver microsomes the E was converted to 9-OHE; 7-hydroxyellipticine was not produced. The cytotoxic effect of this biotransformation has been evaluated on leukemic L1210 cells, in vitro, and found to be equal to those elicited by liver microsomes of control or phenobarbital (PB) pretreated rats. Moreover, 9-OHE and 9-fluoroellipticine (9-FE) strongly inhibit the benzo[a]pyrene hydroxylase (AHH) activity of human liver microsomes (I50 = 2.6 μM and 1.6 μM, respectively) as well as the mutagenesis induced by the polycyclic aromatic hydrocarbon 2-acetylaminofluorene (AAF); 1 μg/plate of each of these compounds is able to inhibit by more than 50% the mutagenicity of 5 μg/plate AAF. 相似文献
125.
The chemical reaction between (±)-styrene oxide and N-acetylcysteine produces both positional isomers ( and ) as a mixture of diastereoisomers with a preference for the benzylic thioether isomer (2 : 1). Synthesis of the mercapturic acid conjugates from either (+)- or (?)-styrene oxide produces only two of the four possible stereoisomers. The single diastereoisomers of and were separated by high pressure liquid chromatography (HPLC) and identified by 1H- and 13C-nuclear magnetic resonance (NMR). The relative stereochemistry at the benzylic carbon center of the mercapturic acid conjugates was assigned on the basis of the established chemical correlation between optically pure styrene oxide and its precursor mandelic acid, and considerations on the mechanism of ring opening of epoxides by sulfur nucleophiles. The stereochemical definition of the isomers – should prove useful in investigations of the biotransformation of the glutathione (GSH) conjugates of styrene oxide. 相似文献
126.
Phytoplankton ecology of the Lake of Menteith,Scotland 总被引:1,自引:1,他引:0
The results discussed in this paper represent the first seasonal ecological study carried out on the phytoplankton of the Lake of Menteith. All measured nutrients reached maximum levels during the winter, with silicate showing particularly high concentrations (up to 85 µg at Si l–1). During the summer period phosphate, nitrate and silicate showed almost complete exhaustion in surface waters. The lake water was consistently alkaline, never falling below pH 7, while the alkalinity ranged from 20 to 24 mg CaCO3 l–1. Generally, the nutrient status of the main inflow had a rapid effect on the water quality of the lake.The region of the lake under investigation showed no thermal stratification at any period of the year, although continuous thermal gradients were recorded in the winter. The continual circulation of the water mass probably prevented oxygen saturation from falling below 77% even following a large phytoplankton bloom and subsequent decomposition.From an examination of net phytoplankton samples the Lake of Menteith could be described as blue-green or blue-green/diatom in nature. From the quantitative study, large pulses of Melosira, Asterionella and Fragilaria were recorded in the spring. The disappearance of the species appears to be related to silicate limitation. The summer growth of Asterionella may have been promoted by a nitrogen source other than nitrate and nitrite, both of which were reduced to critical levels. This alternative source of combined nitrogen may have been contributed by nitrogen-fixing algae in the lake. Three species of Anabaena were recorded, all of which produced large populations during the year.Department of Botany, The University of GlasgowPresent Address: Department of Biology, College of Science, University of Sulaimaniyah, Sulaimaniyah, Iraq 相似文献
127.
H. Stam H. Jansen W.C. Hülsmann 《Biochemical and biophysical research communications》1980,96(2):899-906
Chylomicron degradation by hearts from fed and fasted rats was studied using a perfusion technique, which allows the separate collection of coronary (Qrv) and interstitial effluent (Qi). Upon perfusion with [3H]-cholesterol-containing chylomicrons the tissue recovery of label was highest in the fasted state, while label recovered in Qi was highest in the fed state. Density gradient centrifugation of Qi indicated that the label was recovered in lipoproteins with higher densities: low density lipoproteins (1.019<d<1.050), high density lipoproteins (1.050<d<1.21) and a fraction of d>1.21. These particles probably represent chylomicron degradation products (remnants and “surface fragments”). Our results indicate that tissue cholesterol uptake during chylomicron degradation may be inhibited in the fed state. Furthermore, the role of the myocyte (or interstitial) lipoprotein lipase in chylomicron degradation is discussed. 相似文献
128.
The principal products of the photooxidation of 7,12-dimethylbenz[a]-anthracene (DMBA) in aqueous solutions by photooxidation induced by laboratory lighting have been characterized by high performance liquid chromatograms (HPLC), ultraviolet and mass spectrograms and by comparisons with authentic samples. The products identified were the 7,12-epidioxy-7,12-dihydro-7-12-dimethyl-, 7,12-dione, 7-hydroxymethyl-12-methyl-, 12-hydroxymethyl-7-methyl-, 7-formyl-12-methyl-, 12-formyl-7-methyl-, and 12-hydroxy-12-methyl-7-one derivatives of benz[a]-anthracene. The HPLC profile of products is similar to that obtained from oxidation of DMBA by 'one-electron' reagents, singlet oxygen, or liver microsomal metabolism. The first points of attack are the 7- and 12- positions. The mechanism of photooxidation appears to be generation of singlet oxygen by photodynamic effect of DMBA. None of the products is photosensitizing, however. 相似文献
129.