Effects of mGluR5 and mGluR1 antagonists on anxiety-like behavior and learning in developing rats
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
19505510
DOI
10.1016/j.bbr.2009.05.032
PII: S0166-4328(09)00346-5
Knihovny.cz E-resources
- MeSH
- Excitatory Amino Acid Antagonists administration & dosage pharmacology MeSH
- Anti-Anxiety Agents administration & dosage pharmacology MeSH
- Time Factors MeSH
- Indans administration & dosage pharmacology MeSH
- Rats MeSH
- Receptor, Metabotropic Glutamate 5 MeSH
- Random Allocation MeSH
- Neuropsychological Tests MeSH
- Motor Activity drug effects MeSH
- Rats, Wistar MeSH
- Pyridines administration & dosage pharmacology MeSH
- Receptors, Metabotropic Glutamate antagonists & inhibitors MeSH
- Aging * MeSH
- Learning drug effects MeSH
- Anxiety drug therapy MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 1-aminoindan-1,5-dicarboxylic acid MeSH Browser
- 6-methyl-2-(phenylethynyl)pyridine MeSH Browser
- Excitatory Amino Acid Antagonists MeSH
- Anti-Anxiety Agents MeSH
- Grm5 protein, rat MeSH Browser
- Indans MeSH
- metabotropic glutamate receptor type 1 MeSH Browser
- Receptor, Metabotropic Glutamate 5 MeSH
- Pyridines MeSH
- Receptors, Metabotropic Glutamate MeSH
Antagonists of group I metabotropic receptors exhibit anxiolytic action in adult rats. In immature animals we demonstrated anticonvulsant action of MPEP and AIDA, antagonists of group 5 and group 1, respectively. However, there are no developmental data on anxiolytic-like and learning actions of both compounds. This study investigated whether the anticonvulsant dose range of MPEP and AIDA affects anxiety-like behavior and learning ability in immature rats. Animals at 12, 18 and 25 postnatal (P) days received MPEP in doses of 10, 20 or 40 mg/kg i.p., AIDA in doses of 10 or 20 mg/kg i.p. In P18 and P25 rats anxiety-like behavior and locomotor activity were tested in the light-dark box and open-field test at 15 (1st session) and 60 (2nd session) minutes after drug administration. Learning ability of P12, P18, and P25 animals was examined in the homing response test 15 min after drug administration. Both antagonists exhibited anxiolytic-like action in the 1st session, effects in the 2nd session were less marked. In the open-field test both antagonists increased locomotion only in P18 animals. Age-dependent changes were found in the homing response test, the return latency being longer only in P12 animals. While MPEP in doses of 20- and 40-mg/kg in P12 and 40-mg/kg in P18 rats prolonged the homing response, AIDA did not affect the homing behavior. Both MPEP and AIDA exert anxiolytic-like effect also in immature rats. Except for the youngest animals no changes in learning ability in the homing response test were found.
References provided by Crossref.org
The outcome of early life status epilepticus-lessons from laboratory animals
Consequences of early postnatal benzodiazepines exposure in rats. I. Cognitive-like behavior