The effect of tryptophan depletion on the action of haloperidol in MK-801-treated rats
Language English Country Netherlands Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
15464096
DOI
10.1016/j.ejphar.2004.08.034
PII: S0014-2999(04)00946-X
Knihovny.cz E-resources
- MeSH
- Dizocilpine Maleate pharmacology MeSH
- Haloperidol pharmacology MeSH
- Rats MeSH
- Cerebral Cortex drug effects metabolism MeSH
- Motor Activity drug effects physiology MeSH
- Rats, Wistar MeSH
- Serotonin metabolism MeSH
- Tryptophan deficiency genetics MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Dizocilpine Maleate MeSH
- Haloperidol MeSH
- Serotonin MeSH
- Tryptophan MeSH
We investigated the effect of tryptophan depletion (tryptophan-free mixture) on locomotor activity in an animal model of schizophrenia, induced by acute administration of 5R,10S-(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5,10-imine hydrogen maleate (MK-801), and the influence of the tryptophan-free mixture on the action of the typical antipsychotic haloperidol. Male rats were pre-treated with haloperidol 60 min after receiving the tryptophan-free mixture (or water). We measured total distance travelled in an open field during a 90-min period. Administration of the tryptophan-free mixture resulted in decreased levels of tryptophan, serotonin and its metabolite 5-hydroxyindolacetic acid in the frontal cortex. Serotonin depletion increased the total distance travelled by MK-801-treated rats, modified the inhibitory effect of haloperidol and normalized the locomotor activity pattern in the model of schizophrenia-like behaviour. The effect of the tryptophan-free mixture combined with the classical antipsychotic haloperidol in MK-801-treated rats indicates the possibly important role of the serotonergic system in the action of antipsychotics.
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