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Pharmacol Toxicol ; 92(3): 143-7, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12753430

ABSTRACT

Kainic acid induces seizures and neurotoxicity in rats, produces changes in brain serotonin (5-HT), dopamine and noradrenaline metabolites among other changes in neurotransmitters. In this work, we investigated the changes in 5-HT turnover in brain regions from 84 rats intraperitoneally injected with kainic acid and a specific behavioural change, the body and head shakes, exerted by this neurotoxin in the presence of 5-HT receptor antagonists. Kainic acid produced an increase in 5-hydroxyindoleacetic acid levels in frontal cortex (212%; 180%), striatum (177%; 116%), amygdala (202%; 337%) and hippocampus (43%; 70 %) at 2 and 24 hr as compared with controls, respectively. Serotonin turnover was increased in amygdala (157%) and frontal cortex (169%) at 2 hr; whereas 24 hr after kainic acid administration, increases were observed in amygdala (207%), and frontal cortex (178%). Kainic acid also produced an increase in the frequency of head and body shakes when administered alone or together with pargyline, a monoamine oxidase inhibitor; whereas the administration of 5-HT receptor antagonists such as ketanserin and methiothepin, decreased this behaviour 54% and 50% as compared with kainic acid alone, respectively. These results suggest an active participation of 5-HT neurotransmission on the excitotoxic action of kainic acid in the brain.


Subject(s)
Behavior, Animal/drug effects , Brain/drug effects , Excitatory Amino Acid Agonists/toxicity , Kainic Acid/toxicity , Serotonin/metabolism , Amygdala/drug effects , Amygdala/metabolism , Animals , Brain/metabolism , Cerebral Cortex/drug effects , Cerebral Cortex/metabolism , Corpus Striatum/drug effects , Corpus Striatum/metabolism , Excitatory Amino Acid Agonists/metabolism , Hippocampus/drug effects , Hippocampus/metabolism , Injections, Intraperitoneal , Kainic Acid/metabolism , Ketanserin/pharmacology , Male , Methiothepin/pharmacology , Rats , Rats, Wistar , Seizures/chemically induced , Seizures/metabolism , Serotonin Antagonists/pharmacology
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