Arachidonic acid (AA) and other 20 or 22-carbon polyunsaturated
fatty acids (PUFAs) are precursors of lipid mediators of
inflammation known as eicosanoids. These mediators are critical in
disease processes and in regulating normal cell function.
Remodeling is important in maintaining homeostasis and in
regulating cell function by dictating how PUFAs are converted to
lipid mediators of inflammation. Thus, PUFA remodeling is a
critical process in the biosynthesis of a multitude of mediators,
and understanding this process will unravel better therapeutic
targets for controlling inflammatory diseases such as asthma and
Alzheimer s disease.
AA metabolism is described in an integrated context linking the
remodeling processes with the biosynthesis of mediators and
diseases. By following the movement of the substrate (AA), the
volume describes how upstream biosynthetic pathways influence the
formation of lipid mediators of inflammation, showing the metabolic
interrelationship between all AA-derived mediators."
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