Effect of acute administration of ketamine and imipramine on Creatine kinase activity in the brain of rats

被引:24
作者
Assis, Lara C. [1 ]
Rezin, Gislaine T. [1 ]
Comim, Clarissa M. [2 ]
Valvassori, Samira S. [2 ]
Jeremias, Isabela C. [1 ]
Zugno, Alexandra I. [2 ]
Quevedo, Joao [2 ]
Streck, Emilio L. [1 ]
机构
[1] Univ Extremo Sul Catarinense, Postgrad Program Hlth Sci, Expt Physiopathol Lab, BR-88806000 Criciuma, SC, Brazil
[2] Univ Extremo Sul Catarinense, Postgrad Program Hlth Sci, Neurosci Lab, BR-88806000 Criciuma, SC, Brazil
关键词
Imipramine; Creatine kinase; Depression; Brain; Rats; MAJOR DEPRESSIVE DISORDER; FORCED SWIMMING TEST; NMDA RECEPTORS; ANIMAL-MODEL; MITOCHONDRIAL DYSFUNCTION; NITRIC-OXIDE; ANTAGONISTS; METABOLISM; DISEASE; STRESS;
D O I
10.1590/S1516-44462009000300010
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Clinical findings suggest that ketamine may be used for the treatment of major depression. The present study aimed to compare behavioral effects and brain Creatine kinase activity in specific brain regions after administration of ketamine and imipramine in rats. Method: Rats were acutely given ketamine or imipramine and antidepressant-like activity was assessed by the forced swimming test; Creatine kinase activity was measured in different regions of the brain. Results: The results showed that ketamine (10 and 15mg/kg) and imipramine (20 and 30mg/kg) reduced immobility time when compared to saline group. We also observed that ketamine (10 and 15mg/kg) and imipramine (20 and 30mg/kg) increased Creatine kinase activity in striatum and cerebral cortex. Ketamine at the highest dose (15mg/kg) and imipramine (20 and 30mg/kg) increased Creatine kinase activity in cerebellum and prefrontal cortex. On the other hand, hippocampus was not affected. Conclusion: Considering that metabolism impairment is probably involved in the pathophysiology of depressive disorders, the modulation of energy metabolism (like increase in Creatine kinase activity) by antidepressants could be an important mechanism of action of these drugs.
引用
收藏
页码:247 / 252
页数:6
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