AMN 082, an agonist of mGluR7, exhibits mixed anti- and proconvulsant effects in developing rats
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19154087
DOI
10.33549/physiolres.931671
PII: 1671
Knihovny.cz E-resources
- MeSH
- Excitatory Amino Acid Agonists toxicity MeSH
- Anticonvulsants toxicity MeSH
- Benzhydryl Compounds toxicity MeSH
- Rats MeSH
- Disease Models, Animal MeSH
- Pentylenetetrazole MeSH
- Motor Activity drug effects MeSH
- Rats, Wistar MeSH
- Reaction Time MeSH
- Receptors, Metabotropic Glutamate agonists metabolism MeSH
- Aging MeSH
- Age Factors MeSH
- Dose-Response Relationship, Drug MeSH
- Seizures chemically induced metabolism prevention & control MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Excitatory Amino Acid Agonists MeSH
- Anticonvulsants MeSH
- Benzhydryl Compounds MeSH
- metabotropic glutamate receptor 7 MeSH Browser
- N,N'-dibenzhydrylethane-1,2-diamine dihydrochloride MeSH Browser
- Pentylenetetrazole MeSH
- Receptors, Metabotropic Glutamate MeSH
Metabotropic glutamate receptors (mGluRs) represent a potential therapeutic target. Possible anticonvulsant action of AMN 082, an agonist of mGluR7 subtype, was studied in immature rats using pentylenetetrazol (PTZ)-induced seizures as a model. Five age groups of rats (7-, 12-, 18-, 25-day-old and adult animals) were pretreated with AMN 082 in doses of 0.5, 1, 2, and 5 mg/kg i.p. and 30 min later PTZ was administered (100 mg/kg s.c.). Controls received saline instead of the agonist. AMN 082 did not exhibit clear anticonvulsant action with the exception of suppression of the tonic phase of generalized tonic-clonic seizures (GTCS) in 12-day-old rats. Shorter latencies of GTCS after AMN 082 pretreatment indicate a proconvulsant action. Involuntary movements (mostly tremor) appeared after AMN 082 before PTZ administration, therefore we performed another experimental series with AMN 082 only (1, 2, 5, and 10 mg/kg i.p.). During 60-min observation period tremor appeared in all age groups; sensitivity to this action decreased with age from the 2 mg/kg dose in 7- and 12-day-old rats to the 10 mg/kg dose in adult rats. Mixed anti- and proconvulsant actions of AMN 082 together with unwanted motor effects makes clinical use of this drug highly improbable.
References provided by Crossref.org