Abstract |
Administration of the muscarinic cholinoreceptor agonist arecoline (6 mg/kg, s.c.) to mice induced long-lasting tremor. The ability of non-competitive antagonists of ionotropic glutamate receptors to suppress the onset of tremor was studied. These antagonists, i.e., adamantane and phenylcyclohexyl derivatives, selectively blocked NMDA-type receptor channels (monocations) or both NMDA-and AMPA-type channels (dications). Both types of blocker weakened arecoline tremor, though the dose-response relationships were different for mono-and dications. The effects of dications appeared only at low blocker doses (0.0001-0.01 micromol/kg) but gradually disappeared on dose elevation. These data lead to the conclusion that the mechanism of pathogenesis of arecoline tremor predominantly involves NMDA-type receptors. Moderate blockade of AMPA-type receptors could potentiate the preventive effect of mixed-action antagonists (anti-NMDA+anti- AMPA), though predominance of blocking action against AMPA-type receptors prevented this effect.
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Authors | N Ya Lukomskaya, V V Lavrent'eva, L A Starshinova, E P Zhabko, V E Gmiro, L G Magazanik |
Journal | Neuroscience and behavioral physiology
(Neurosci Behav Physiol)
Vol. 38
Issue 4
Pg. 421-6
(May 2008)
ISSN: 0097-0549 [Print] United States |
PMID | 18401736
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cyclohexylamines
- Excitatory Amino Acid Antagonists
- Quaternary Ammonium Compounds
- Receptors, AMPA
- Receptors, N-Methyl-D-Aspartate
- Arecoline
- Adamantane
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Topics |
- Adamantane
(analogs & derivatives, pharmacology)
- Animals
- Arecoline
- Cyclohexylamines
(pharmacology)
- Excitatory Amino Acid Antagonists
(pharmacology)
- Mice
- Quaternary Ammonium Compounds
(pharmacology)
- Receptors, AMPA
(drug effects, metabolism)
- Receptors, N-Methyl-D-Aspartate
(drug effects, metabolism)
- Tremor
(chemically induced, metabolism, prevention & control)
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