Abstract
This review focuses on HDL function in modulating LDL oxidation and LDL-induced inflammation. Dysfunctional HDL has been identified in animal models and humans with chronic inflammatory diseases including atherosclerosis. The loss of antiinflammatory function correlated with a loss of function in reverse cholesterol transport. In animal models and perhaps in humans, dysfunctional HDL can be improved by apoA-I mimetic peptides that bind oxidized lipids with high affinity. Copyright ©2009 by the American Society for Biochemistry and Molecular Biology, Inc.
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Navab, M., Reddy, S. T., Van Lenten, B. J., Anantharamaiah, G. M., & Fogelman, A. M. (2009, April). The role of dysfunctional HDL in atherosclerosis. Journal of Lipid Research. https://doi.org/10.1194/jlr.R800036-JLR200
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