Alpha-lipoic acid affects the oxidative stress in various brain structures in mice with methionine and choline deficiency

• Published in: Experimental biology and medicine (Maywood, N.J.) N.J.), 2015-04, Vol.240 (4), p.418-425
• Main Authors: Veskovic, Milena, Mladenovic, Dusan, Jorgacevic, Bojan, Stevanovic, Ivana, de Luka, Silvio, Radosavljevic, Tatjana
• Format: Article
• Language: English
• Subjects: Animals; Brain - metabolism; Catalase - metabolism; Cerebral Cortex - drug effects; Cerebral Cortex - metabolism; Choline Deficiency - metabolism; Corpus Striatum - drug effects; Corpus Striatum - metabolism; Disease Models, Animal; Glutathione - metabolism; Hippocampus - drug effects; Hippocampus - metabolism; Hypothalamus - drug effects; Hypothalamus - metabolism; Lipid Peroxidation - drug effects; Male; Malondialdehyde - metabolism; Methionine - deficiency; Methionine - metabolism; Mice; Mice, Inbred C57BL; Nitric Oxide - metabolism; Original Research; Oxidative Stress - drug effects; Superoxide Dismutase - metabolism; Thioctic Acid - pharmacology
• ISSN: 1535-3702; 1535-3699
• DOI: 10.1177/1535370214549521

Deficiency in methionine or choline can induce oxidative stress in various organs such as liver, kidney, heart, and brain. This study was to examine the effects of alpha-lipoic acid (LA) on oxidative stress induced by methionine and choline deficiency (MCD) in several brain structures. Male mice C57BL/6 (n = 28) were divided into four groups: (1) control – continuously fed with standard chow; (2) LA – fed with standard chow and receiving LA; (3) MCD2 – fed with MCD diet for two weeks, and (4) MCD2+LA – fed with MCD diet for two weeks and receiving LA (100 mg/kg/day intraperitonealy [i.p.]). Brain tissue (cortex, hypothalamus, striatum and hippocampus) was taken for determination of oxidative stress parameters. MCD diet induced a significant increase in malondialdehyde and NOx concentration in all brain regions, while LA restored their content to normal values. Similar to this, in MCD2 group, activity of total SOD, MnSOD, and Cu/ZnSOD was reduced by MCD diet, while LA treatment improved their activities in all brain structures. Besides, in MCD2 group a decrease in catalase activity in cortex and GSH content in hypothalamus was evident, while LA treatment induced an increase in catalase activity in cortex and striatum and GSH content in hypothalamus. LA treatment can significantly reduce lipid peroxidation and nitrosative stress, caused by MCD diet, in all brain regions by restoring antioxidant enzymes activities, predominantly total SOD, MnSOD, and Cu/ZnSOD, and to a lesser extent by modulating catalase activity and GSH content. LA supplementation may be used in order to prevent brain oxidative injury induced by methionine and choline deficiency.