Activities of respiratory chain complexes and citrate synthase influenced by pharmacologically different antidepressants and mood stabilizers
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
20588251
PII: NEL310310A03
Knihovny.cz E-zdroje
- MeSH
- antidepresiva farmakologie MeSH
- antipsychotika farmakologie MeSH
- benzodiazepiny farmakologie MeSH
- citrátsynthasa metabolismus MeSH
- kyselina valproová farmakologie MeSH
- mitochondrie účinky léků MeSH
- mozková kůra účinky léků metabolismus MeSH
- olanzapin MeSH
- prasata MeSH
- respirační komplex I metabolismus MeSH
- respirační komplex III metabolismus MeSH
- respirační komplex IV metabolismus MeSH
- sloučeniny lithia farmakologie MeSH
- techniky in vitro MeSH
- transport elektronů účinky léků MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- antidepresiva MeSH
- antipsychotika MeSH
- benzodiazepiny MeSH
- citrátsynthasa MeSH
- kyselina valproová MeSH
- olanzapin MeSH
- respirační komplex I MeSH
- respirační komplex III MeSH
- respirační komplex IV MeSH
- sloučeniny lithia 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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