Animal model of mania induced by ouabain: Evidence of oxidative stress in submitochondrial particles of the rat brain

被引:58
作者
Riegel, Rafael E. [1 ,2 ]
Valvassori, Samira S. [1 ,2 ]
Elias, Guilherme [1 ,2 ]
Reus, Gislaine Z. [1 ,2 ]
Steckert, Amanda V. [2 ,3 ]
de Souza, Bruna [2 ,3 ]
Petronilho, Fabricia [2 ,3 ]
Gavioli, Elaine C. [1 ,2 ]
Dal-Pizzol, Felipe [2 ,3 ]
Quevedo, Joao [1 ,2 ]
机构
[1] Univ Extremo Sul Catarinense, Lab Neurociencias, BR-88806000 Criciuma, SC, Brazil
[2] Univ Extremo Sul Catarinense, Inst Nacl Ciencia & Tecnol Translac Med, PPGCS, Unidade Acad Ciencias Saude UNASAU, BR-88806000 Criciuma, SC, Brazil
[3] Univ Extremo Sul Catarinense, Lab Fisiopatol Expt, BR-88806000 Criciuma, SC, Brazil
关键词
Bipolar disorder; Ouabain; Mitochondrial dysfunction; Oxidative stress; Mania; Rat; TEMPORAL-LOBE STRUCTURES; BIPOLAR DISORDER; MITOCHONDRIAL DYSFUNCTION; HYDROGEN-PEROXIDE; SCHIZOPHRENIA; EXPRESSION; PLASTICITY; TARGETS; ILLNESS; MRI;
D O I
10.1016/j.neuint.2009.05.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The intracerebroventricular (ICV) administration of ouabain (a Na+/K+-ATPase inhibitor) in rats has been suggested to mimic some symptoms of human bipolar mania. Clinical studies have shown that bipolar disorder may be related to mitochondrial dysfunction. Herein, we investigated the behavioral and biochemical effects induced by the ICV administration of ouabain in rats. To achieve this aim, the effects of ouabain injection immediately after and 7 days following a single ICV administration (at concentrations of 10(-2) and 10(-3) M) on locomotion was measured using the open-field test. Additionally, thiobarbituric acid reactive substances (TBARSs) and superoxide production were measured in submitochondrial particles of the prefrontal cortex, hippocampus, striatum and amygdala. Our findings demonstrated that ouabain at 10(-2) and 10(-3) M induced hyperlocomotion in rats, and this response remained up to 7 days following a single ICV injection. In addition, we observed that the persistent increase in the rat spontaneous locomotion is associated with increased TBARS levels and superoxide generation in submitochondrial particles in the prefrontal cortex, striatum and amygdala. In conclusion, ouabain-induced mania-like behavior may provide a useful animal model to test the hypothesis of the involvement of oxidative stress in bipolar disorder. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:491 / 495
页数:5
相关论文
共 43 条
[1]
Adleman Nancy E, 2004, Expert Rev Neurother, V4, P69, DOI 10.1586/14737175.4.1.69
[2]
An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia [J].
Altshuler, LL ;
Bartzokis, G ;
Grieder, T ;
Curran, J ;
Jimenez, T ;
Leight, K ;
Wilkins, J ;
Gerner, R ;
Mintz, J .
BIOLOGICAL PSYCHIATRY, 2000, 48 (02) :147-162
[3]
Suicide risk and treatments for patients with bipolar disorder [J].
Baldessarini, RJ ;
Tondo, L .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (11) :1517-1519
[4]
BOVERIS A, 1984, METHOD ENZYMOL, V105, P429
[5]
CELLULAR PRODUCTION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CHANCE, B ;
OSHINO, N .
BIOCHEMICAL JOURNAL, 1972, 128 (03) :617-&
[6]
MRI investigation of temporal lobe structures in bipolar patients [J].
Brambilla, P ;
Harenski, K ;
Nicoletti, M ;
Sassi, RB ;
Mallinger, AG ;
Frank, E ;
Kupfer, DJ ;
Keshavan, MS ;
Soares, JC .
JOURNAL OF PSYCHIATRIC RESEARCH, 2003, 37 (04) :287-295
[7]
Mitochondrial involvement in brain function and dysfunction: Relevance to aging, neurodegenerative disorders and longevity [J].
Calabrese, V ;
Scapagnini, G ;
Stella, AMG ;
Bates, TE ;
Clark, JB .
NEUROCHEMICAL RESEARCH, 2001, 26 (06) :739-764
[8]
N-acetyl aspartate:: A marker for neuronal loss or mitochondrial dysfunction [J].
Clark, JB .
DEVELOPMENTAL NEUROSCIENCE, 1998, 20 (4-5) :271-276
[9]
Open field is more sensitive than automated activity monitor in documenting ouabain-induced hyperlocomotion in the development of an animal model for bipolar illness [J].
Decker, S ;
Grider, G ;
Cobb, M ;
Li, XP ;
Huff, MO ;
El-Mallakh, RS ;
Levy, RS .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2000, 24 (03) :455-462
[10]
Einat H, 2003, J NEUROSCI, V23, P7311