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Published on: July 9, 2016
Contribution of metabotropic glutamate receptor mGluR4 to L-2-[3H]amino-4-phosphonobutyrate binding in mouse brain
1Department of Molecular Pharmacology, Novo Nordisk A/S, Måløv, Denmark.
Abstract:
The binding of L-2-[3H]amino-4-phosphonobutyrate ([3H]L-AP4) was examined in brain sections of wild-type mice and mice lacking the mGluR4 subtype of metabotropic glutamate receptors (mGluRs). Very high relative densities of [3H]L-AP4 binding were observed in the molecular layer of the cerebellar cortex, the nucleus basalis, the outer layer of the superior colliculus, and the substantia nigra. In mGluR4 knock-out mice, very low levels of binding were observed in these regions. The moderate levels of binding observed with wild-type mice in the molecular layer of the hippocampal dentate gyrus and in the thalamus were absent in mGluR4 knock-out mice. In contrast, the moderate levels observed in most of the cerebral cortex, caudate putamen, and globus pallidus were not different in mGluR4 knock-out mice compared with wild-type. In these regions, mGluR8 is likely to be labeled by [3H]L-AP4 because mGluR8 is expressed in such brain regions and, like mGluR4, has high affinity for L-AP4. We conclude that mGluR4 contributes substantially to the high-affinity binding site for [3H]L-AP4 in several regions of mouse brain, including cerebellar cortex, nucleus basalis, thalamus, superior colliculus, substantia nigra, and hippocampal dentate gyrus.
Insights
Metabotropic glutamate receptor 4 (mGluR4) significantly contributes to L-2-[3H]amino-4-phosphonobutyrate ([3H]L-AP4) binding in key mouse brain regions. This receptor is crucial for high-affinity binding sites in the cerebellum and other areas.
Area of Science:
- Neuroscience
- Receptor Pharmacology
Background:
- Metabotropic glutamate receptors (mGluRs) are involved in neurotransmission.
- [3H]L-AP4 is a ligand used to study glutamate receptor binding.
- The role of mGluR4 in [3H]L-AP4 binding was not fully elucidated.
Purpose of the Study:
- To investigate the contribution of mGluR4 to [3H]L-AP4 binding in the mouse brain.
- To identify brain regions where mGluR4 is the primary binding site for [3H]L-AP4.
Main Methods:
- Radioligand binding assays using [3H]L-AP4.
- Comparison of binding in wild-type and mGluR4 knock-out mice.
- Analysis of binding distribution across various brain sections.
Main Results:
- High [3H]L-AP4 binding was observed in the cerebellar cortex, nucleus basalis, superior colliculus, and substantia nigra of wild-type mice.
- These binding levels were significantly reduced in mGluR4 knock-out mice.
- Binding in the hippocampus and thalamus was also dependent on mGluR4, while binding in the cerebral cortex and basal ganglia was not.
Conclusions:
- mGluR4 plays a substantial role in high-affinity [3H]L-AP4 binding in several brain regions.
- mGluR8 may account for [3H]L-AP4 binding in regions lacking mGluR4.
- This study clarifies the receptor distribution of [3H]L-AP4 binding sites in the mouse brain.

