Abstract
Maltol (3-hydroxy-2-methyl-4-pyrone) inhibited iron-mediated lipid peroxidation, determined as the formation of thiobarbituric acid-reactive substances, but dimethylpyrone, an analogue of maltol showed no effect on the formation of lipid peroxides. NADP-isocitrate dehydrogenase, a principal enzyme generating reduced NADP, was protected by maltol but not by dimethylpyrone from the ferrous ion-mediated inactivation. Protection of NADP-isocitrate dehydrogenase can enhance the supply of NADPH required for the regeneration of reduced glutathione for scavenging reactive oxygen species. Antioxidant properties of maltol were closely related to the enhanced oxidation of ferrous ion as a prooxidant, and can be explained by the electron-deficient nature of 3-hydroxypyrone ring.
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CITATION STYLE
Murakami, K., Ito, M., Tanemura, Y., & Yoshino, M. (2001). Maltol as an antioxidant: Inhibition of lipid peroxidation and protection of NADP- Isocitrate dehydrogenase from the iron-mediated inactivation. Biomedical Research, 22(4), 183–186. https://doi.org/10.2220/biomedres.22.183
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