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Attenuation of Oxidative and Nitrosative Stress in Cortical Area Associates With Antidepressant-Like Effects of Tropisetron in Male Mice Following Social Isolation Stress Publisher Pubmed



Hajmirzaian A1, 2 ; Amiri S2, 3 ; Aminikhoei H1, 2 ; Rahimibalaei M4 ; Kordjazy N1, 2 ; Olson CO3 ; Rastegar M3 ; Naserzadeh P5 ; Marzban H4 ; Dehpour AR1, 2 ; Hosseini MJ6, 7 ; Samiei E1 ; Mehr SE1, 2
Authors
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Authors Affiliations
  1. 1. Experimental Medicine Research Center, Tehran University of Medical Sciences, P.O. Box: 13145-784, Tehran, Iran
  2. 2. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, P.O. Box: 13145-784, Tehran, Iran
  3. 3. Department of Biochemistry and Medical Genetics, College of Medicine, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada
  4. 4. Department of Human Anatomy and Cell Science, Faculty of Medicine, University of Manitoba, BMSB, 745 Bannatyne Avenue, Winnipeg, R3E 0J9, MB, Canada
  5. 5. Faculty of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Zanjan Applied Pharmacology Research Center, Zanjan University of Medical sciences, Zanjan, Iran
  7. 7. Department of Pharmacology and Toxicology, School of Pharmacy, Zanjan University of Medical Sciences, P.O. Box: 45139-56184, Zanjan, Iran

Source: Brain Research Bulletin Published:2016


Abstract

Tropisetron, a 5-HT3 receptor antagonist widely used as an antiemetic, has been reported to have positive effects on mood disorders. Adolescence is a critical period during the development of brain, where exposure to chronic stress during this time is highly associated with the development of depression. In this study, we showed that 4 weeks of juvenile social isolation stress (SIS) provoked depressive-like behaviors in male mice, which was associated with disruption of mitochondrial function and nitric oxide overproduction in the cortical areas. In this study, tropisetron (5 mg/kg) reversed the negative behavioral effects of SIS in male mice. We found that the effects of tropisetron were mediated through mitigating the negative activity of inducible nitric oxide synthase (iNOS) on mitochondrial activity. Administration of aminoguanidine (specific iNOS inhibitor, 20 mg/kg) augmented the protective effects of tropisetron (1 mg/kg) on SIS. Furthermore, l-arginine (nitric oxide precursor, 100 mg/kg) abolished the positive effects of tropisetron. These results have increased our knowledge on the pivotal role of mitochondrial function in the pathophysiology of depression, and highlighted the role of 5-HT3 receptors in psychosocial stress response during adolescence. Finally, we observed that tropisetron alleviated the mitochondrial dysfunction through decreased nitrergic system activity in the cerebral cortex. © 2016 Elsevier Inc.
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