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pubmed-article:7808219pubmed:abstractTextDifferent NMDA receptor subunits have been recently cloned. The present paper describes the developmental profile of expression of the NR-1 subunit and three NR-2 subunits (A, B, C) in the rat central nervous system. A sensitive RNase protection assay was employed to determine simultaneously the mRNA levels of these receptor subunits. We found low levels of NR-1 mRNA (comprising all different splicing isoforms) in newborn rats with a progressive increase of its expression in the following 2-3 weeks. NR-2 subunits can be regarded as 'modulatory' since their expression can produce differences in the properties of NMDA receptors. More than one NR-2 subunits can be expressed in the same brain region. NR-2A and NR-2C are concomitantly expressed in the cerebellum and during development their mRNAs increase with a similar profile from low levels in P-8 rats to maximal expression in P-21 animals. NR-2A and NR-2B are concomitantly expressed in several brain regions with a different ontogenetic profile. In the hippocampus NR-2B mRNA increases rapidly during the first week of life as compared to the NR-2A subunits which at this time is expressed to low levels indicating that NR-2B will probably be dominant in determining the NMDA properties during the first period of life. Our data can provide a molecular correlate with properties of NMDA receptors such as voltage dependent Mg2+ block and deactivation kinetics which undergo significant changes during development and have been shown to depend upon the NR-2 subunit co-expressed with the common NR-1 subunit in various brain regions.lld:pubmed
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pubmed-article:7808219pubmed:pagination209-16lld:pubmed
pubmed-article:7808219pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7808219pubmed:articleTitleRegulation of NMDA receptor subunit mRNA expression in the rat brain during postnatal development.lld:pubmed
pubmed-article:7808219pubmed:affiliationDIBIT, San Raffaele Hospital, Milan, Italy.lld:pubmed
pubmed-article:7808219pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7808219pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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