Subject(s)
Alkylating Agents/toxicity , Carcinogens, Environmental/toxicity , Methylnitrosourea/toxicity , Alkylating Agents/chemistry , Alkylating Agents/poisoning , Animals , Carcinogenicity Tests , Carcinogens, Environmental/chemistry , Carcinogens, Environmental/poisoning , Environmental Exposure/adverse effects , Environmental Exposure/legislation & jurisprudence , Environmental Exposure/standards , Government Regulation , Guidelines as Topic , Guinea Pigs , Humans , Methylnitrosourea/chemistry , Methylnitrosourea/poisoning , Mice , Molecular Structure , Occupational Exposure/adverse effects , Occupational Exposure/legislation & jurisprudence , Occupational Exposure/standards , RatsABSTRACT
The investigations were performed on oligodendroglial cells isolated from the cerebral white matter of Wistar rats treated intravenously with a 3% solution of MNU at a dose of 60 mg/kg body weight. The oligodendroglial fraction showed a decrease of the sphingomyelin, phosphatidylserine and phosphoinositides content. The observed changes correlated with alterations of the lipid spectrum found in the myelin fraction of MNU intoxicated rats. This would indicate that MNU acting in the central nervous system affects in a similar way the lipid metabolism of both components of the oligodendroglia-myelin system.
Subject(s)
Brain Diseases/chemically induced , Lipids/analysis , Methylnitrosourea/poisoning , Neuroglia/analysis , Nitrosourea Compounds/poisoning , Oligodendroglia/analysis , Animals , Nerve Tissue Proteins/analysis , Oligodendroglia/drug effects , Rats , Rats, Inbred StrainsSubject(s)
Brain Chemistry , Fatty Acids/analysis , Methylnitrosourea/poisoning , Myelin Sheath/analysis , Nitrosourea Compounds/poisoning , Phospholipids/analysis , Animals , Cholesterol Esters/analysis , Female , Male , Phosphatidylcholines/analysis , Plasmalogens/analysis , Rats , Sphingomyelins/analysisABSTRACT
The repair of potential lethal damages was investigated in the LL cell line induced by some chemicals. Three different chemical compounds were used. An inhibitor of DNA synthesis--hydroxyurea, an alkylating agent--methylnitrosourea, and an antibiotic intercalating in DNA--actinomycin D. It was shown that damages induced by hydroxyurea could be repaired. Unlike, the repair of damages induced by methylnitrosourea and actinomycin D was not observed.