5-Oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid

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5-Oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-oxo-ETE) is a biologically active lipid derived from the arachidonic acid pathway. It is a potent eicosanoid that plays a significant role in inflammatory responses and immune system regulation.

Structure and Synthesis[edit | edit source]

5-Oxo-ETE is a 20-carbon polyunsaturated fatty acid with four double bonds, specifically in the 6E, 8Z, 11Z, and 14Z positions. It is synthesized from 5-hydroxyeicosatetraenoic acid (5-HETE) through the action of 5-hydroxyeicosanoid dehydrogenase (5-HEDH), an enzyme that catalyzes the oxidation of the hydroxyl group at the 5th carbon to a keto group.

Biological Function[edit | edit source]

5-Oxo-ETE is known for its role in the activation of eosinophils, a type of white blood cell involved in allergic reactions and asthma. It acts by binding to the OXE receptor, a G-protein coupled receptor, which leads to the activation and chemotaxis of eosinophils. This makes 5-oxo-ETE a significant mediator in conditions such as asthma, allergic rhinitis, and other eosinophil-associated diseases.

Pathophysiological Role[edit | edit source]

In addition to its role in eosinophil activation, 5-oxo-ETE is involved in the regulation of other immune cells, including neutrophils and monocytes. It has been implicated in the pathogenesis of various inflammatory diseases, including rheumatoid arthritis and inflammatory bowel disease.

Clinical Implications[edit | edit source]

Due to its potent effects on eosinophils and other immune cells, 5-oxo-ETE is a target for therapeutic intervention in diseases characterized by excessive inflammation and immune response. Inhibitors of 5-oxo-ETE synthesis or its receptor antagonists are being explored as potential treatments for asthma and other inflammatory conditions.

Research Directions[edit | edit source]

Ongoing research is focused on understanding the detailed mechanisms of 5-oxo-ETE action, its role in various diseases, and the development of specific inhibitors or antagonists that can modulate its activity for therapeutic purposes.

Also see[edit | edit source]



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Contributors: Prab R. Tumpati, MD