ABSTRACT
Aflatoxin B1 (AFB1) photolysis in presence of pyridine N-oxide was studied. It was established that AFB1 ethanol solution irradiated with UV-light lambda = 362 nm demonstrated an increase of the fluorescence as a result of appearance of AFB1 product which was formed by pyridine N-oxide oxygen binding to AFB1 molecules in position 2,3.
Subject(s)
Aflatoxins/radiation effects , Carcinogens/radiation effects , Photolysis , Pyridines/radiation effects , Aflatoxin B1 , Aflatoxins/analysis , Carcinogens/analysis , Chromatography, High Pressure Liquid , Drug Interactions , In Vitro Techniques , Kinetics , Photochemistry , Pyridines/analysis , Solutions , Spectrometry, Fluorescence , Ultraviolet RaysSubject(s)
Carcinogens/analysis , Mud Therapy , Mutagens/analysis , Soil/analysis , Animals , Female , Humic Substances , Male , RatsABSTRACT
The UV irradiation (lambda = 362 nm) of aflatoxin B1 (AfB1) dissolved in water resulted in the formation of an oxidized product. The process was not inhibited by ionol, a routine inhibitor of the radical processes. The oxidized product was not found in the system where AfB1 was metabolized by the 3-methylcholanthrene-activated rat liver microsomes. It is suggested that the product is identical with 2,3-dihydrodiol of AfB1.
Subject(s)
Aflatoxins/metabolism , Carcinogens/metabolism , Microsomes, Liver/enzymology , Aflatoxin B1 , Aflatoxins/analysis , Aflatoxins/radiation effects , Animals , Carcinogens/analysis , Carcinogens/radiation effects , Chromatography, High Pressure Liquid , In Vitro Techniques , Kinetics , Methylcholanthrene/pharmacology , Microsomes, Liver/drug effects , Oxidation-Reduction/drug effects , Oxidation-Reduction/radiation effects , Photolysis , Rats , Ultraviolet RaysABSTRACT
Three new morphologically different strains of stabilized transplantable hepatomas in C3HA mice were obtained using continuous transplantation of nitrosodiethylamine induced primary liver tumour by the method of parallel sublines. Morphology and development of biological properties of substrains of hepatomas are described. All differences between substrains arose gradually throughout a number of generations, with malignization of hepatomas occurring. If the development of hepatomas was accompanied with differentiation, as was the case in some substrains in our experiments, the rate of a successful transplantation diminished, and it was impossible to obtain stabilized strains of transplantable hepatomas.
Subject(s)
Liver Neoplasms, Experimental/pathology , Mice, Inbred C3H , Animals , Cell Transformation, Neoplastic/pathology , Diethylnitrosamine , Liver Neoplasms, Experimental/chemically induced , Male , Mice , Neoplasm Transplantation , Time FactorsABSTRACT
Seven new morphologically different strains of stabilized transplantable hepatomas were obtained, using a continuous subcutaneous transplantation of a highly differentiated orthoaminoazotoluol-induced primary hepatoma by the method of parallel sublines. Morphology and biological properties of all substrains are described. Differences between substrains of the highly differentiated primary hepatoma, according to their biological properties and morphology, were greater than those between substrains obtained by transplantation of a lowly differentiated primary hepatoma as a parent tumour. Some aspects of differentiation of hepatomas during their progression and stabilization are discussed.
Subject(s)
Liver Neoplasms, Experimental/pathology , Mice, Inbred C3H , Animals , Cell Transformation, Neoplastic/pathology , Liver Neoplasms, Experimental/chemically induced , Male , Mice , Neoplasm Transplantation , Time Factors , o-AminoazotolueneABSTRACT
After the administration of colchicine (5 mcg/ml) into nutritive medium of primary tissue culture there is a remarkable decrease in the volume and number of fibroblast-membrane organoids during the first 3 hours. The removing of colchicine-damaged fibroblasts into the medium without colchicine leads to the renewal of the most of intracellular membranes during the following 24 hours. Probable reasons and mechanisms of colchicine-induced alterations are discussed.