Abstract
Primary cultures of rat skin fibroblasts were used as a model system to investigate the biological effects of the lipid peroxidation product malonaldehyde (MA). Acetaldehyde (AA) was used as a reference compound. Cells exposed to 103 M MA for 120 h exhibited altered morphology, cytoplasmic vacuolization, karyorrhexis, micro‐and multinucleation, and a marked reduction in mitotic index and DNA‐, RNA‐, and protein‐synthesizing capacity. At 104 M, MA also caused mitotic aberrations, micronucleation, and a reduction in mitotic index and DNA synthesis. At 105 and 106 M, MA induced only the formation of small and irregular nuclei. Acetaldehyde at 103 M had similar but less severe effects on nuclear morphology, mitotic index, and macromolecule synthesis. At 104 M AA, only mitotic aberrations and nuclear changes were observed. At 105 and 106 M, AA exerted no apparent effects on either the structure or anabolic activity of the cells. With respect to antimitotic activity, MA was approximately 10 times as toxic as AA.

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