4-Hydroxynonenal

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4-Hydroxynonenal


4-Hydroxynonenal (4-HNE) is a highly reactive aldehyde produced as a byproduct of lipid peroxidation, a process that occurs when free radicals steal electrons from the lipids in cell membranes. This process results in cell damage and is implicated in several diseases, including cardiovascular disease, cancer, and neurodegenerative diseases.

Production and Metabolism[edit | edit source]

4-HNE is produced from the peroxidation of polyunsaturated fatty acids (PUFAs), particularly those containing a double bond at the sixth carbon from the methyl end, such as arachidonic acid and linoleic acid. The process of lipid peroxidation is initiated by the abstraction of a hydrogen atom from the bis-allylic position of PUFAs by a free radical. This results in the formation of a lipid radical, which reacts with molecular oxygen to form a lipid peroxyl radical. The lipid peroxyl radical can then react with another PUFA to form a lipid hydroperoxide and a new lipid radical, propagating the chain reaction.

4-HNE is metabolized and detoxified in the body through three main pathways: reduction to 1,4-dihydroxy-2-nonene (DHN) by alcohol dehydrogenase, oxidation to 4-hydroxy-2-nonenoic acid (HNA) by aldehyde dehydrogenase, and conjugation with glutathione (GSH) by glutathione S-transferase.

Biological Effects[edit | edit source]

4-HNE is not merely a toxic byproduct of lipid peroxidation but also plays a role in cell signaling. It can form Michael adducts with proteins, altering their function and potentially leading to cell damage or death. However, at low levels, 4-HNE can also activate signaling pathways that lead to cell survival and adaptation to oxidative stress.

4-HNE has been implicated in several diseases. It is elevated in the brains of patients with Alzheimer's disease and Parkinson's disease, suggesting a role in neurodegeneration. It is also elevated in the blood of patients with cardiovascular disease and in the tumors of cancer patients.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD