Antioxidant treatment ameliorates experimental diabetes-induced depressive-like behaviour and reduces oxidative stress in brain and pancreas

• Published in: Diabetes/metabolism research and reviews Vol. 32; no. 3; pp. 278 - 288
• Main Authors: Réus, Gislaine Z., dos Santos, Maria Augusta B., Abelaira, Helena M., Titus, Stephanie E., Carlessi, Anelise S., Matias, Beatriz I., Bruchchen, Livia, Florentino, Drielly, Vieira, Andriele, Petronilho, Fabricia, Ceretta, Luciane B., Zugno, Alexandra I., Quevedo, João
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.03.2016; Wiley Subscription Services, Inc
• Subjects: Acetylcysteine - pharmacology; Animals; antioxidants; Antioxidants - pharmacology; Behavior, Animal - drug effects; Brain - drug effects; Brain - metabolism; Brain - pathology; deferoxamine; Deferoxamine - pharmacology; Depressive Disorder - metabolism; Depressive Disorder - pathology; Depressive Disorder - prevention & control; diabetes; Diabetes Mellitus, Experimental - drug therapy; Diabetes Mellitus, Experimental - pathology; Diabetes Mellitus, Experimental - psychology; Free Radical Scavengers - pharmacology; Lipid Peroxidation - drug effects; major depressive disorder; Male; N-acetylcysteine; oxidative stress; Oxidative Stress - drug effects; Pancreas - drug effects; Pancreas - metabolism; Pancreas - pathology; Rats; Rats, Wistar; Siderophores - pharmacology; deferoxamine; major depressive disorder; antioxidants; diabetes; oxidative stress; N-acetylcysteine
• ISSN: 1520-7552; 1520-7560
• DOI: 10.1002/dmrr.2732

Studies have shown a relationship between diabetes mellitus (DM) and the development of major depressive disorder. Alterations in oxidative stress are associated with the pathophysiology of both diabetes mellitus and major depressive disorder. This study aimed to evaluate the effects of antioxidants N‐acetylcysteine and deferoxamine on behaviour and oxidative stress parameters in diabetic rats. To this aim, after induction of diabetes by a single dose of alloxan, Wistar rats were treated with N‐acetylcysteine or deferoxamine for 14 days, and then depressive‐like behaviour was evaluated. Oxidative stress parameters were assessed in the prefrontal cortex, hippocampus, amygdala, nucleus accumbens and pancreas. Diabetic rats displayed depressive‐like behaviour, and treatment with N‐acetylcysteine reversed this alteration. Carbonyl protein levels were increased in the prefrontal cortex, hippocampus and pancreas of diabetic rats, and both N‐acetylcysteine and deferoxamine reversed these alterations. Lipid damage was increased in the prefrontal cortex, hippocampus, amygdala and pancreas; however, treatment with N‐acetylcysteine or deferoxamine reversed lipid damage only in the hippocampus and pancreas. Superoxide dismutase activity was decreased in the amygdala, nucleus accumbens and pancreas of diabetic rats. In diabetic rats, there was a decrease in catalase enzyme activity in the prefrontal cortex, amygdala, nucleus accumbens and pancreas, but an increase in the hippocampus. Treatment with antioxidants did not have an effect on the activity of antioxidant enzymes. In conclusion, animal model of diabetes produced depressive‐like behaviour and oxidative stress in the brain and periphery. Treatment with antioxidants could be a viable alternative to treat behavioural and biochemical alterations induced by diabetes. Copyright © 2015 John Wiley & Sons, Ltd.