Abstract
Postoperative cognitive dysfunction may be associated with the toxic products of lipid peroxidation, such as the α,β-unsaturated aldehyde acrolein, which accumulates in aging. We previously identified an acrolein-mediated, serotonin-derived melanoid product, or SDM. This study further characterizes this putative novel neuromelanin, which is not made from catecholamines. In addition to its strong protein-binding properties, we observed that SDM binds Fe2+ readily and exhibits complex redox characteristics. SDM may exist as a two-dimensional network of polymers that coalesce into larger entities exhibiting electroactive properties. These observations suggest that SDM may contribute to the decline in cognition due to focal degeneration from SDM-mediated free-radical production. We know that inhalational anesthetics sequester acrolein, which is toxic to neurons, and we propose that the local increase in acrolein depletes serotonin levels and enhances neuronal vulnerability through the production of neuromelanin-like structures, such as SDM.
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This study was supported in part by research funds from Kansas City University of Medicine and Biosciences and the Department of Anesthesiology, University of Missouri, Kansas City/Saint Luke’s Hospital, Kansas City, Missouri.
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Murphy, M.M., Miller, E.D., Fibuch, E.E. et al. Redox Mechanism of Neurotoxicity by a Serotonin–Acrolein Polymeric Melanoid. Neurotox Res 19, 353–360 (2011). https://doi.org/10.1007/s12640-010-9173-3
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DOI: https://doi.org/10.1007/s12640-010-9173-3