Key result
L-4F reduces oxidized fatty acids and preserves HDL anti-inflammatory function in mice.
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To determine in vivo if L-4F differentially alters plasma levels of oxidized fatty acids resulting in more antiinflammatory HDL. Injecting L-4F into apoE null mice resulted in a significant reduction in plasma levels of 15-HETE, 5- HETE, 13-HODE and 9-HODE. In contrast, plasma levels of 20-HETE were not reduced and plasma levels of 14,15-EET, which are derived from the cytochrome P450 pathway, were elevated after injection of L-4F. Injection of 13(S)-HPODE into wild-type C57BL/6J mice caused an increase in plasma levels of 13-HODE and 9-HODE and was accompanied by a significant loss in the anti-inflammatory properties of HDL. The response of atherosclerosis resistant C3H/HeJ mice to injection of 13(S)-HPODE was similar but much more blunted. Injection of L-4F at a site different from that at which the 13(S)-HPODE was injected resulted in significantly lower plasma levels of 13-HODE and 9-HODE and significantly less loss of HDL anti-inflammatory properties in both strains. i) L-4F differentially alters plasma levels of oxidized fatty acids in vivo. ii) The resistance of the C3H/HeJ strain to atherosclerosis may in part be mediated by a reduced reaction of this strain to these potent lipid oxidants. L-4F differentially alters plasma levels of oxidized fatty acids in mice and the resistance of C3H/HeJ mice to atherosclerosis may be mediated by a reduced reaction of this strain to these potent lipid oxidants.
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Imaizumi et al. (2010) studied Atherosclerosis. L-4F (apoA-I mimetic peptide) vs. 13(S)-HPODE injection alone was evaluated on Plasma levels of oxidized fatty acids (15-HETE, 5-HETE, 13-HODE, 9-HODE, 20-HETE, 14,15-EET) and HDL anti-inflammatory properties. L-4F injection in mice significantly reduced plasma 15-HETE, 5-HETE, 13-HODE, and 9-HODE levels, elevated 14,15-EET, and preserved HDL anti-inflammatory properties after 13(S)-HPODE challenge.
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