Back to Search
Start Over
Compensatory molecular and functional mechanisms in nervous system of the Grm1(crv4) mouse lacking the mGlu1 receptor: a model for motor coordination deficits.
Compensatory molecular and functional mechanisms in nervous system of the Grm1(crv4) mouse lacking the mGlu1 receptor: a model for motor coordination deficits.
- Source :
-
Cerebral cortex (New York, N.Y. : 1991) [Cereb Cortex] 2013 Sep; Vol. 23 (9), pp. 2179-89. Date of Electronic Publication: 2012 Jul 12. - Publication Year :
- 2013
-
Abstract
- The metabotropic glutamate type 1 (mGlu1) and type 5 (mGlu5) receptors, the only members of group I mGlu receptors, are implicated in synaptic plasticity and mechanisms of feedback control of glutamate release. They exhibit nearly complementary distributions throughout the central nervous system, well evident in the cerebellum, where mGlu1 receptor is most intensely expressed while mGlu5 receptor is not. Despite their different distribution, they show a similar subcellular localization and use common transducing pathways. We recently described the Grm1(crv4) mouse with motor coordination deficits and renal anomalies caused by a spontaneous mutation inactivating the mGlu1 receptor. To define the neuropathological mechanisms in these mice, we evaluated expression and function of the mGlu5 receptor in cerebral and cerebellar cortices. Western blot and immunofluorescence analyses showed mGlu5 receptor overexpression. Quantitative reverse transcriptase-polymerase chain reaction results indicated that the up-regulation is already evident at RNA level. Functional studies confirmed an enhanced glutamate release from cortical cerebral and cerebellar synaptosomes when compared with wild-type that is abolished by the mGlu5 receptor-specific inhibitor, 2-methyl-6-(phenylethynyl) pyridine hydrochloride (MPEP). Finally, acute MPEP treatment of Grm1(crv4/crv4) mice induced an evident although incomplete improvement of motor coordination, suggesting that mGlu5 receptors enhanced activity worsens, instead of improving, the motor-coordination defects in the Grm1(crv4/crv4) mice.
- Subjects :
- Animals
Brain metabolism
Disease Models, Animal
Excitatory Amino Acid Antagonists pharmacology
Female
Glutamic Acid metabolism
Male
Mice
Mice, Inbred BALB C
Mutation
Pyridines pharmacology
Receptor, Metabotropic Glutamate 5 antagonists & inhibitors
Receptor, Metabotropic Glutamate 5 metabolism
Synaptosomes physiology
Brain physiopathology
Movement Disorders physiopathology
Receptor, Metabotropic Glutamate 5 physiology
Receptors, Metabotropic Glutamate deficiency
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2199
- Volume :
- 23
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Cerebral cortex (New York, N.Y. : 1991)
- Publication Type :
- Academic Journal
- Accession number :
- 22791805
- Full Text :
- https://doi.org/10.1093/cercor/bhs200