Lysine induces lipid and protein damage and decreases reduced glutathione concentrations in brain of young rats

• Published in: International journal of developmental neuroscience 2008-11, Vol.26 (7), p.693-698
• Main Authors: Seminotti, Bianca, Leipnitz, Guilhian, Amaral, Alexandre U., Fernandes, Carolina G., Silva, Lucila de Bortoli da, Tonin, Anelise Miotti, Vargas, Carmen R., Wajner, Moacir
• Format: Article
• Language: English
• Subjects: Animals; Animals, Newborn; Antioxidants - metabolism; Brain Diseases, Metabolic - metabolism; Brain Diseases, Metabolic - physiopathology; Cerebral cortex; Cerebral Cortex - metabolism; Cerebral Cortex - physiopathology; Down-Regulation - physiology; Free Radical Scavengers - metabolism; Free Radical Scavengers - pharmacology; Glutathione - metabolism; Hyperlysinemia; Iron Carbonyl Compounds - metabolism; Lipid Peroxidation - drug effects; Lipid Peroxidation - physiology; Lysine; Lysine - metabolism; Lysine - toxicity; Nerve Degeneration - chemically induced; Nerve Degeneration - metabolism; Nerve Degeneration - physiopathology; Nerve Tissue Proteins - metabolism; Neurotoxins - metabolism; Neurotoxins - toxicity; Oxidants - metabolism; Oxidants - toxicity; Oxidative stress; Oxidative Stress - drug effects; Oxidative Stress - physiology; Rats; Rats, Wistar; Sulfhydryl Compounds - metabolism
• ISSN: 0736-5748; 1873-474X
• DOI: 10.1016/j.ijdevneu.2008.07.011

The present work investigated the in vitro effects of lysine on important parameters of oxidative stress in cerebral cortex of young rats. Our results show that lysine significantly induced lipid peroxidation, as determined by increase of thiobarbituric acid‐reactive substances and chemiluminescence levels, as well as protein oxidative damage since carbonyl formation and sulfhydryl oxidation were enhanced by this amino acid. Furthermore, the addition of free radical scavengers significantly prevented lysine‐induced lipid oxidative damage, suggesting that free radicals were involved in this effect. Lysine also significantly diminished glutathione levels in cortical supernatants, decreasing, therefore, the major brain antioxidant defense. Finally, lysine markedly oxidized a glutathione commercial solution in a medium devoid of brain supernatants, indicating that it behaved as a direct acting oxidant. The present data indicate that lysine induces oxidative stress in cerebral cortex of young rats. Therefore, it is presumed that this pathomechanism may be involved at least in part in the neurological damage found in patients affected by disorders with hyperlysinemia.