1. The oxidation of aromatic hydrocarbons to arene oxides and the reduction of these oxides to the parent hydrocarbons are both catalysed by enzymes in the microsomal fraction of rat liver. A suggested name for the enzyme concerned in the reduction of these epoxides is 'epoxide reductase'. 2. 'Epoxide reductase' is NADPH-dependent and is inhibited by oxygen. 3. Preliminary investigations suggest that the enzyme is specific for both 'K-region' and 'non-K-region' arene oxides.
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http://dx.doi.org/10.3109/00498257509052066 | DOI Listing |
Toxicol Mech Methods
January 2025
Drug Safety Research and Evaluation, Research, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
The rat S9 microsome fraction is commonly used to assess compound metabolite formation during genotoxicity assessments. However, methods using S9 have not been standardized for genotoxicity studies, and different experimental methods are used at various facilities. Therefore, this study investigated whether the differences between the two experimental conditions (1) S9 inducers, phenobarbital + beta-naphthoflavones vs.
View Article and Find Full Text PDFSci Rep
December 2024
Intercollegiate Faculty of Biotechnology, University of Gdansk and Medical University of Gdansk, Gdansk, 80-307, Poland.
This study presents characterisation of diatom's PtLPCAT1 (acyl-CoA: lysophosphatidylcholine acyltransferase) activity in phospholipid remodelling. In this research microsomal fractions of yeast Δale1 mutant overexpressing PtLPCAT1 were used as a source of the tested enzyme. In the assays evaluating remodelling of different phospholipids by PtLPCAT1 not modified microsomal fractions of the tested yeast were used.
View Article and Find Full Text PDFEur J Drug Metab Pharmacokinet
December 2024
Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Objective: The objective of this study was to determine the apparent intrinsic clearance (Cl) and fraction unbound in human liver microsomes (f) of 86 marketed central nervous system (CNS) drugs and to predict the in vivo hepatic blood clearance (CL).
Methods: Cl in human liver microsomes (HLM) was determined by substrate depletion, and f was determined by equilibrium dialysis. The relationship between lipophilicity (logP) and unbound intrinsic clearance (Cl) was explored using the Biopharmaceutical Drug Disposition Classification System (BDDCS) and Extended Clearance Classification System (ECCS).
J Agric Food Chem
December 2024
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China.
A better understanding of the metabolic differences between chiral pesticide enantiomers in organisms is crucial for accurately assessing their risk. The enantioselective metabolism of mefentrifluconazole was investigated by the human liver microsome reaction system. The metabolic rate of -mefentrifluconazole was found to be 4 times that of -mefentrifluconazole.
View Article and Find Full Text PDFEnviron Pollut
January 2025
Programa de Pós-graduação Em Ecologia, Universidade Federal Do Rio Grande Do Sul (UFRGS), Av. Bento Gonçalves, 9500, 91501-970, Cx Postal 15007, Porto Alegre, RS, Brazil; Divisão de Laboratórios, Fundação Estadual de Proteção Ambiental Henrique Luís Roessler (FEPAM), Rua Aurélio Porto, 37, 90620-090, Porto Alegre, RS, Brazil. Electronic address:
This study investigated the presence of mutagenic compounds in raw and treated waters at four water treatment plants (WTP01 to WTP04), in southern Brazil. Samples were concentrated using Amberlite XAD4 resin and the acidic and neutral pH fractions tested by mutagenesis in Salmonella/microsome assay, using TA98, TA100 and YG7108 strains in presence and absence of metabolic activation (in vitro human S9). Mutagenesis in raw water was found only by strain TA98 at WTP03, with and without S9.
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