Activities of respiratory chain complexes and citrate synthase influenced by pharmacologically different antidepressants and mood stabilizers
Language English Country Sweden Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
20588251
PII: NEL310310A03
Knihovny.cz E-resources
- MeSH
- Antidepressive Agents pharmacology MeSH
- Antipsychotic Agents pharmacology MeSH
- Benzodiazepines pharmacology MeSH
- Citrate (si)-Synthase metabolism MeSH
- Valproic Acid pharmacology MeSH
- Mitochondria drug effects MeSH
- Cerebral Cortex drug effects metabolism MeSH
- Olanzapine MeSH
- Swine MeSH
- Electron Transport Complex I metabolism MeSH
- Electron Transport Complex III metabolism MeSH
- Electron Transport Complex IV metabolism MeSH
- Lithium Compounds pharmacology MeSH
- In Vitro Techniques MeSH
- Electron Transport drug effects MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Antidepressive Agents MeSH
- Antipsychotic Agents MeSH
- Benzodiazepines MeSH
- Citrate (si)-Synthase MeSH
- Valproic Acid MeSH
- Olanzapine MeSH
- Electron Transport Complex I MeSH
- Electron Transport Complex III MeSH
- Electron Transport Complex IV MeSH
- Lithium Compounds MeSH
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.
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