2-nonenal--(trans)-isomer has been researched along with 2-pentenal* in 2 studies
2 other study(ies) available for 2-nonenal--(trans)-isomer and 2-pentenal
Article | Year |
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In vivo absorption, metabolism, and urinary excretion of alpha,beta-unsaturated aldehydes in experimental animals. Relevance to the development of cardiovascular diseases by the dietary ingestion of thermally stressed polyunsaturate-rich culinary oils.
Thermal stressing of polyunsaturated fatty acid (PUFA)- rich culinary oils according to routine frying or cooking practices generates high levels of cytotoxic aldehydic products (predominantly trans-2-alkenals, trans,trans-alka-2,4-dienals, cis,trans-alka-2, 4-dienals, and n-alkanals), species arising from the fragmentation of conjugated hydroperoxydiene precursors. In this investigation we demonstrate that typical trans-2-alkenal compounds known to be produced from the thermally induced autoxidation of PUFAs are readily absorbed from the gut into the systemic circulation in vivo, metabolized (primarily via the addition of glutathione across their electrophilic carbon-carbon double bonds), and excreted in the urine as C-3 mercapturate conjugates in rats. Since such aldehydic products are damaging to human health, the results obtained from our investigations indicate that the dietary ingestion of thermally, autoxidatively stressed PUFA-rich culinary oils promotes the induction, development, and progression of cardiovascular diseases. Topics: Aldehydes; Animals; Arteriosclerosis; Cardiovascular Diseases; Fatty Acids; Glutathione; Lipid Peroxidation; Lipoproteins, LDL; Magnetic Resonance Spectroscopy; Male; Oils; Rats; Rats, Wistar; Receptors, LDL | 1998 |
Mutation induction in Chinese hamster lung V79 cells by five alk-2-enals produced by lipid peroxidation.
Five alk-2-enals--pent-2-enal, hex-2-enal, hept-2-enal, oct-2-enal and non-2-enal--produced by lipid peroxidation were tested for mutagenic activity in V79 Chinese hamster cells. At concentrations ranging from 0.003 to 0.3 mM all 5 alk-2-enals induced a dose-dependent increase in the frequency of 6-thioguanine-resistant mutants, and their mutagenic potency was found to increase with the length of the carbon chain. In contrast, only hept-2-enal produced a statistically significant increase in the number of mutations to ouabain resistance. Topics: Aldehydes; Animals; Cell Line; Lipid Peroxidation; Mutagenicity Tests; Mutation | 1990 |