Ferreira Gabriela K, Cardoso Mariane R, Jeremias Isabela C, Gonçalves Cinara L, Freitas Karolina V, Antonini Rafaela, Scaini Giselli, Rezin Gislaine T, Quevedo João, Streck Emilio L
Bioenergetics Laboratory, Center of Excellence in Applied Neurosciences of Santa Catarina (NENASC), Graduate Program in Health Sciences, Universidade do Extremo Sul Catarinense (UNESC), Criciúma, SC, Brazil.
Clinical and Experimental Pathophysiology Laboratory, Graduate Program in Health Sciences, Universidade do Sul de Santa Catarina (UNISUL), Tubarão, SC, Brazil.
Braz J Psychiatry. 2014 Sep;36(3):220-6. doi: 10.1590/1516-4446-2013-1202. Epub 2014 Mar 17.
Several studies support the hypothesis that metabolism impairment is involved in the pathophysiology of depression and that some antidepressants act by modulating brain energy metabolism. Thus, we evaluated the activity of Krebs cycle enzymes, the mitochondrial respiratory chain, and creatine kinase in the brain of rats subjected to prolonged administration of fluvoxamine.
Wistar rats received daily administration of fluvoxamine in saline (10, 30, and 60 mg/kg) for 14 days. Twelve hours after the last administration, rats were killed by decapitation and the prefrontal cortex, cerebral cortex, hippocampus, striatum, and cerebellum were rapidly isolated.
The activities of citrate synthase, malate dehydrogenase, and complexes I, II-III, and IV were decreased after prolonged administration of fluvoxamine in rats. However, the activities of complex II, succinate dehydrogenase, and creatine kinase were increased.
Alterations in activity of energy metabolism enzymes were observed in most brain areas analyzed. Thus, we suggest that the decrease in citrate synthase, malate dehydrogenase, and complexes I, II-III, and IV can be related to adverse effects of pharmacotherapy, but long-term molecular adaptations cannot be ruled out. In addition, we demonstrated that these changes varied according to brain structure or biochemical analysis and were not dose-dependent.
多项研究支持这样的假说,即代谢受损参与了抑郁症的病理生理学过程,且一些抗抑郁药通过调节脑能量代谢发挥作用。因此,我们评估了长期给予氟伏沙明的大鼠脑内三羧酸循环酶、线粒体呼吸链及肌酸激酶的活性。
将Wistar大鼠每日用含氟伏沙明的生理盐水(10、30和60mg/kg)给药,持续14天。末次给药12小时后,断头处死大鼠,迅速分离前额叶皮质、大脑皮质、海马、纹状体和小脑。
长期给予氟伏沙明后,大鼠脑内柠檬酸合酶、苹果酸脱氢酶以及复合体I、II - III和IV的活性降低。然而,复合体II、琥珀酸脱氢酶和肌酸激酶的活性增加。
在所分析的大多数脑区均观察到能量代谢酶活性的改变。因此,我们认为柠檬酸合酶、苹果酸脱氢酶以及复合体I、II - III和IV活性的降低可能与药物治疗的不良反应有关,但不能排除长期的分子适应性变化。此外,我们证明这些变化因脑结构或生化分析而异,且不具有剂量依赖性。