Journal
ATHEROSCLEROSIS
Volume 158, Issue 1, Pages 95-101Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/S0021-9150(01)00419-1
Keywords
lipid peroxidation; aldehydes; 2,4-decadienal; THP-1 human macrophages; TNF-alpha; gene expression; atherosclerosis
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Oxidized lipoproteins inhibit TNF-alpha secretion by human THP-1 macrophages due, at least in part, to aldehydes derived from the oxidation of polyunsaturated fatty acids. This study extends these findings by investigating the effect of three aldehydes (2,4-decadienal (2,4-DDE), hexanal and 4-hydroxynonenal (4-HNE)) on TNF-alpha and IL-1 beta mRNA expression. The 2,4-DDE and 4-HNE showed considerable biological activity which induced cytotoxicity on THP-1 macrophages at concentration of 50 muM. Hexanal, on the other hand, had a lower cytotoxic capacity and concentration of 1000 muM was needed for the effect to be observed. Exposure of THP-1 macrophages to aldehydes for 24 h inhibited TNF-alpha mRNA expression but increased or did not affect IL-1 beta mRNA levels. The inhibitory action of 2,4-DDE was dose dependent and began at 5 muM (46%, P < 0.001). The effect of 4-HNE was less inhibitory than 4-DDE but only when cytotoxic concentrations were used (50 muM). Very high concentrations of hexanal (200 muM) were needed to inhibit TNF-alpha expression (23%, P < 0.001). This downregulation of TNF-alpha gene expression by 2,4-DDE was parallel to a lower protein production. These data indicate that low levels of 2,4-DDE may modulate inflammatory action by inhibiting TNF-alpha mRNA gene expression and that the biological activity of 2,4-DDE may be involved in the development of atherosclerosis. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
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