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不同药理作用的抗抑郁药和心境稳定剂对呼吸链复合物及柠檬酸合酶活性的影响。

Activities of respiratory chain complexes and citrate synthase influenced by pharmacologically different antidepressants and mood stabilizers.

作者信息

Hroudova Jana, Fisar Zdenek

机构信息

Department of Psychiatry, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.

出版信息

Neuro Endocrinol Lett. 2010;31(3):336-42.

Abstract

OBJECTIVE

Mitochondrial dysfunctions, impaired bioenergetics and dysfunction of neurotrophins are included in many neurodegenerative and psychiatric diseases. We investigated in vitro effects of pharmacologically different antidepressants and mood stabilizers on mitochondrial enzymes to discover, which mitochondrial functions could be involved in pathophysiology of mood disorders.

METHODS

In vitro effects of eight pharmacologically different antidepressants (desipramine, amitriptyline, imipramine, citalopram, venlafaxine, mirtazapine, tianeptine, and moclobemide) and three mood stabilizers (lithium, valproate, and olanzapine) on the activities of mitochondrial enzymes (citrate synthase and enzymes in electron transport chain, i.e. complexes I, II, IV) were measured in crude mitochondrial fraction isolated from pig brain.

RESULTS

Most of the antidepressants and mood stabilizers inhibited the activities of respiratory electron transport chain complexes, complexes I and IV were the most affected. Statistically significant decrease of the complex I activity was caused by desipramine, amitriptyline, imipramine, citalopram, mirtazapine, valproate and olanzapine. Complex II was significantly inhibited only by amitriptyline, imipramine, citalopram and venlafaxine. Complex IV was significantly inhibited by all tested drugs except for citalopram and moclobemide. Unchanged or slightly increased citrate synthase activity was observed; significant activation of the enzyme was observed after citalopram, tianeptine and olanzapine.

CONCLUSIONS

Our results indicate that antidepressants may act generally as inhibitors of complex I and complex IV of the electron transport chain. These mitochondrial enzymes are suggested as proper candidates in searching of new biological markers of mood disorders, targets of new antidepressants or predictors of response to pharmacotherapy.

摘要

目的

线粒体功能障碍、生物能量学受损以及神经营养因子功能障碍存在于许多神经退行性疾病和精神疾病中。我们研究了药理学上不同的抗抑郁药和心境稳定剂对线粒体酶的体外作用,以发现哪些线粒体功能可能与心境障碍的病理生理学有关。

方法

在从猪脑分离的粗线粒体组分中,测定了八种药理学上不同的抗抑郁药(地昔帕明、阿米替林、丙咪嗪、西酞普兰、文拉法辛、米氮平、噻奈普汀和吗氯贝胺)和三种心境稳定剂(锂盐、丙戊酸盐和奥氮平)对线粒体酶(柠檬酸合酶以及电子传递链中的酶,即复合体I、II、IV)活性的影响。

结果

大多数抗抑郁药和心境稳定剂抑制呼吸电子传递链复合体的活性,其中复合体I和IV受影响最大。地昔帕明、阿米替林、丙咪嗪、西酞普兰、米氮平、丙戊酸盐和奥氮平导致复合体I活性有统计学意义的降低。只有阿米替林、丙咪嗪、西酞普兰和文拉法辛显著抑制复合体II。除西酞普兰和吗氯贝胺外,所有受试药物均显著抑制复合体IV。观察到柠檬酸合酶活性不变或略有增加;西酞普兰、噻奈普汀和奥氮平后观察到该酶有显著激活。

结论

我们的结果表明,抗抑郁药通常可能作为电子传递链复合体I和复合体IV的抑制剂起作用。这些线粒体酶被认为是寻找心境障碍新生物标志物、新型抗抑郁药靶点或药物治疗反应预测指标的合适候选者。

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