Volume 92, Issue 4 pp. 337-343
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Unchanged balance between levels of mRNA encoding AMPA glutamate receptor subtypes following global cerebral ischemia in the rat.

L. Frank

L. Frank

Histology, Health Care Discovery, Novo Nordisk A/S (Denmark)

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N. H. Diemer

N. H. Diemer

Institute of Neuropathology, University of Copenhagen, Denmark

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F. Kaiser

F. Kaiser

Neuropharmacology, Health Care Discovery, Novo Nordisk A/S (Denmark)

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M. Sheardown

M. Sheardown

Neuropharmacology, Health Care Discovery, Novo Nordisk A/S (Denmark)

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J. S. Rasmussen

J. S. Rasmussen

Molecular Biology, Health Care Discovery, Novo Nordisk A/S (Denmark)

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P. Kristensen

Corresponding Author

P. Kristensen

Histology, Health Care Discovery, Novo Nordisk A/S (Denmark)

Peter Kristensen, Histology, Health Care Discovery, Novo Nordisk A/S, Novo Alle, Bld. 6A., DK–2880 Bagsvzrd, DenmarkSearch for more papers by this author
First published: October 1995
Citations: 26

Abstract

Transient global ischemia leads to glutamate mediated delayed neuronal death in the CAI but not in the CA3 region of the rat hippocampus, and changes in AMPA receptor subunit composition has been proposed to cause a difference in excitatory input to the CAI and CA3 regions. In situ hybridization with riboprobes for AMPA receptor subtype GluR1–4 mRNA was performed on sections from the brain of sham operated and ischemic rats in two models (neck cuff and 4-vessel occlusion combined with hypotension) with identical results: the content of the GluR1–3 mRNA species was down regulated in the hippocampal regions CAI and CA3 but only weak changes were observed in the dentate gyrus. The down regulation observed in CA1 was non-selective among GluR1–3, i.e. all GluR mRNA species showed approximately the same degree of down regulation. A change in calcium permeability of the AMPA channels mediated by a shift in channel sub-unit composition and corroborating an increased calcium influx is thus not supported by these findings.

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