Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1991 Apr;16(4):435-42.
doi: 10.1007/BF00965563.

Non-NMDA excitatory amino acid receptors in a subcellular fraction enriched in cerebellar glomeruli

Affiliations

Non-NMDA excitatory amino acid receptors in a subcellular fraction enriched in cerebellar glomeruli

F Viennot et al. Neurochem Res. 1991 Apr.

Abstract

In the internal granular layer of the cerebellar cortex the polysynaptic complexes called glomeruli consist mainly of homogeneous populations of glutamatergic and GABAergic synapses, both located on granule cell dendrites. A subcellular fraction enriched in glomeruli was prepared from rat cerebellum, and the distribution of the different types of NMDA and non-NMDA glutamate binding sites was studied in the membranes derived from this fraction (fraction G) as compared to that in the membranes prepared from a total cerebellar homogenate (fraction T). Cl-/Ca2+ independent [3H]glutamate binding sites were not abundant and could be reliably measured only in fraction G. Cl- dependent/Ca2+ activated [3H]glutamate binding sites were more abundant and exhibited a single KD in both fractions G and T. Quisqualate, NMDA, kainate, L-AP4 and trans-ACPD inhibited [3H]glutamate binding to different extents in the two membrane fractions. Quisqualate sensitive sites were predominant in all cases but more abundant in fraction T than in fraction G. An opposite distribution was observed for the NMDA sensitive binding sites while kainate sensitive binding sites were scarce everywhere. Trans-ACPD, a ligand presumed selective for metabotropic glutamate binding sites, displaced [3H]glutamate from fraction T but nor from fraction G, suggesting the absence of these sites from glomeruli. Similarly, no L-AP4 sensitive sites were present in fraction G while they were abundant in fraction T. Binding sites associated with ionotropic receptors of the quisqualate type were determined by measuring [3H]AMPA binding. The density of the high affinity [3H]AMPA binding sites in fraction T was twice as high as in fraction G, indicating that these sites are abundant in structures other than glomeruli.(ABSTRACT TRUNCATED AT 250 WORDS)

PubMed Disclaimer

Similar articles

Cited by

References

    1. Science. 1982 Apr 2;216(4541):78-80 - PubMed
    1. Neurosci Lett. 1986 May 15;66(2):193-8 - PubMed
    1. Neurochem Int. 1988;13(4):463-7 - PubMed
    1. Trends Pharmacol Sci. 1990 Mar;11(3):126-33 - PubMed
    1. Brain Res. 1985 Mar 11;329(1-2):319-22 - PubMed

LinkOut - more resources