[Toxicity assessments of chemical substances using primary culture of rat hepatocytes]. 1986

J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada

A primary hepatocyte culture was used as a model system to assess the toxicity of various chemical substances. Chemical substances tested in this experiment included 14 kinds of organic solvents, arsenic acid and N-nitrosodiumethylamine, most of which are known as hepatotoxic materials. Enzyme (GPT and LDH) leakage and albumin secreted from the hepatocytes to culture medium were measured to evaluate the cell damage after exposure to the chemical substances at various concentrations for 3 d. Cell counts and protein contents before and after exposure to the chemical substances were also measured during the course of these experiments. The extent of LDH leakage from hepatocytes was parallel to that of GPT leakage after exposure to the chemicals. Albumin secreted from the hepatocytes in the culture medium evidently decreased at concentrations of the chemicals which increased the enzyme leakage. Viable cell counts were significantly decreased by chemicals that increased the enzyme leakage, although the cell protein contents were not significantly affected. The minimum concentration of the chemicals at which enzyme leakage from hepatocytes was significantly increased was defined as the lowest toxic concentration (TCL0). Judging from TCL0 values, the degree of toxicity in these chemicals seems to be almost identical to the degree of in vivo hepatotoxicity reported previously. We, furthermore, observed that there is a positive correlation (r = 0.780, p less than 0.01) between PT50 calculated by the LD50 value reported previously and -Log magnitude of TCL0.(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D007770 L-Lactate Dehydrogenase A tetrameric enzyme that, along with the coenzyme NAD+, catalyzes the interconversion of LACTATE and PYRUVATE. In vertebrates, genes for three different subunits (LDH-A, LDH-B and LDH-C) exist. Lactate Dehydrogenase,Dehydrogenase, L-Lactate,Dehydrogenase, Lactate,L Lactate Dehydrogenase
D007928 Lethal Dose 50 The dose amount of poisonous or toxic substance or dose of ionizing radiation required to kill 50% of the tested population. LD50,Dose 50, Lethal
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008297 Male Males
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D002251 Carbon Tetrachloride A solvent for oils, fats, lacquers, varnishes, rubber waxes, and resins, and a starting material in the manufacturing of organic compounds. Poisoning by inhalation, ingestion or skin absorption is possible and may be fatal. (Merck Index, 11th ed) Tetrachloromethane,Tetrachloride, Carbon
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D002725 Chloroform A commonly used laboratory solvent. It was previously used as an anesthetic, but was banned from use in the U.S. due to its suspected carcinogenicity. Trichloromethane
D006586 Hexanes Six-carbon saturated hydrocarbon group of the methane series. Include isomers and derivatives. Various polyneuropathies are caused by hexane poisoning. Hexane,Isohexane,Isohexanes
D000410 Alanine Transaminase An enzyme that catalyzes the conversion of L-alanine and 2-oxoglutarate to pyruvate and L-glutamate. (From Enzyme Nomenclature, 1992) EC 2.6.1.2. Alanine Aminotransferase,Glutamic-Pyruvic Transaminase,SGPT,Alanine-2-Oxoglutarate Aminotransferase,Glutamic-Alanine Transaminase,Alanine 2 Oxoglutarate Aminotransferase,Aminotransferase, Alanine,Aminotransferase, Alanine-2-Oxoglutarate,Glutamic Alanine Transaminase,Glutamic Pyruvic Transaminase,Transaminase, Alanine,Transaminase, Glutamic-Alanine,Transaminase, Glutamic-Pyruvic

Related Publications

J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
January 1971, Journal of occupational medicine. : official publication of the Industrial Medical Association,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
June 1990, Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
February 2002, Hepatobiliary & pancreatic diseases international : HBPD INT,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
December 2002, Planta medica,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
February 2005, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
July 1982, Journal of toxicology and environmental health,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
October 2002, Toxicological sciences : an official journal of the Society of Toxicology,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
January 1985, Xenobiotica; the fate of foreign compounds in biological systems,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
June 2005, Biochemical pharmacology,
J F Fang, and Y Kitagawa, and S Ishikawa, and H Yanagisawa, and K Nakajima, and S Manabe, and O Wada
May 1985, Proceedings of the National Academy of Sciences of the United States of America,
Copied contents to your clipboard!