Tamoxifen has an anti-manic effect but not protect the brain against oxidative stress in an animal model of mania induced by ouabain

被引:5
|
作者
Dal-Pont, Gustavo C. [1 ]
Resende, Wilson R. [1 ]
Bianchini, Guilherme [1 ]
Gava, Fernanda F. [1 ]
Peterle, Bruna R. [1 ]
Trajano, Kerolen S. [1 ]
Varela, Roger B. [1 ]
Quevedo, Joao [1 ,2 ,3 ,4 ]
Valvassori, Samira S. [1 ]
机构
[1] Univ Southern Santa Catarina UNESC, Grad Program Hlth Sci, Translat Psychiat Lab, Criciuma, SC, Brazil
[2] Univ Texas Hlth Sci Ctr Houston, UTHlth, Ctr Excellence Mood Disorders, Dept Psychiat & Behav Sci,McGovern Med Sch, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Neurosci Grad Program, UTHlth, Grad Sch Biomed Sci, Houston, TX 77030 USA
[4] Univ Texas Hlth Sci Ctr Houston, UTHlth, Translat Psychiat Program, Dept Psychiat & Behav Sci,McGovern Med Sch, Houston, DC USA
关键词
Bipolar disorder; Tamoxifen; Mania; Oxidative stress; Ouabain; Lithium; KINASE-C INHIBITION; BIPOLAR DISORDER; LITHIUM; VALPROATE; MARKERS; RATS; EFFICACY; BEHAVIOR; ENZYMES; MARCKS;
D O I
10.1016/j.jpsychires.2019.03.020
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Studies have suggested the involvement of oxidative stress in the physiopathology of bipolar disorder. Preclinical data have shown that PKC inhibitors may act as mood-stabilizing agents and protect the brain in animal models of mania. The present study aimed to evaluate the effects of Lithium (Li) or tamoxifen (TMX) on behavioral changes and oxidative stress parameters in an animal model of mania induced by ouabain (OUA). Wistar rats received a single intracerebroventricular (ICV) injection of OUA or artificial cerebrospinal fluid (ACSF). From the day following ICV injection, the rats were treated for seven days with intraperitoneal injections of saline, Li or TMX twice a day. On the 7th day after OUA injection, locomotor activity was measured using the open-field test, and the oxidative stress parameters were evaluated in the hippocampus and frontal cortex of rats. The results showed that OUA induced hyperactivity in rats, which is considered a manic-like behavior. Also, OUA increased lipid peroxidation and oxidative damage to proteins, as well as causing alterations to antioxidant enzymes in the frontal cortex and hippocampus of rats. The Li or TMX treatment reversed the manic-like behavior induced by OUA. Besides, Li, but not TMX, reversed the oxidative damage caused by OUA. These results suggest that the manic-like effects induced by OUA and the antimanic effects of TMX seem not to be related to the oxidative stress.
引用
收藏
页码:181 / 189
页数:9
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