Effects of MK-801 on the expression of serine racemase and d-amino acid oxidase mRNAs and on the D-serine levels in rat brain
- PMID: 17109841
- DOI: 10.1016/j.ejphar.2006.09.062
Effects of MK-801 on the expression of serine racemase and d-amino acid oxidase mRNAs and on the D-serine levels in rat brain
Abstract
We have investigated the acute effects of the increasing doses of non-competitive N-methyl-d-aspartate receptor antagonist MK-801 (0.2-1.6 mg/kg) on the expression of serine racemase and d-amino acid oxidase (DAO) mRNAs in several brain areas of rats. We have also evaluated the effects of the chronic administration of MK-801 (0.4 mg/kg) on the gene expression of serine racemase and DAO and on the d-serine concentrations. A dose-dependent augmentation of the expression of serine racemase mRNA was seen in most brain areas at both 1 and 4 h after the administration. In contrast, a drastic decline in the expression of DAO mRNA was observed in most brain areas 1 h after the MK-801 administration, whereas a dose-dependent elevation in the expression of DAO mRNA was observed in most brain areas 4 h after the administration. The chronic MK-801 administration produced a significant increase in the expression of serine racemase mRNA in almost all brain areas, whereas no significant changes were found in the level of DAO mRNA in most brain areas. In addition, the chronic administration caused a slight but significant elevation in the concentrations of d-serine in the cortex and striatum. These present findings indicate that increasing the serine racemase mRNA and no changes in the DAO mRNA after the chronic administration could contribute to the elevation of the d-serine level in the forebrain, and that serine racemase and DAO could play an important role in the regulation of N-methyl-d-aspartate receptors via the d-serine metabolism.
Similar articles
-
Acute treatment with morphine augments the expression of serine racemase and D-amino acid oxidase mRNAs in rat brain.Eur J Pharmacol. 2005 Nov 21;525(1-3):94-7. doi: 10.1016/j.ejphar.2005.09.001. Epub 2005 Oct 27. Eur J Pharmacol. 2005. PMID: 16256980
-
MK-801 upregulates the expression of d-amino acid oxidase mRNA in rat brain.Brain Res Mol Brain Res. 2004 Nov 24;131(1-2):141-4. doi: 10.1016/j.molbrainres.2004.08.017. Brain Res Mol Brain Res. 2004. PMID: 15530664
-
Distribution and MK-801-induced expression of serine racemase mRNA in rat brain by real-time quantitative PCR.Brain Res Mol Brain Res. 2004 Sep 10;128(1):90-4. doi: 10.1016/j.molbrainres.2004.06.015. Brain Res Mol Brain Res. 2004. PMID: 15337321
-
D-amino acids in the brain: the biochemistry of brain serine racemase.FEBS J. 2008 Jul;275(14):3538-45. doi: 10.1111/j.1742-4658.2008.06517.x. FEBS J. 2008. PMID: 18564178 Review.
-
[Endogenous D-serine in mammalian brains].Nihon Shinkei Seishin Yakurigaku Zasshi. 2000 Feb;20(1):33-9. Nihon Shinkei Seishin Yakurigaku Zasshi. 2000. PMID: 10890022 Review. Japanese.
Cited by
-
D-amino acid oxidase is expressed in the ventral tegmental area and modulates cortical dopamine.Front Synaptic Neurosci. 2014 May 2;6:11. doi: 10.3389/fnsyn.2014.00011. eCollection 2014. Front Synaptic Neurosci. 2014. PMID: 24822045 Free PMC article.
-
Serine racemase is associated with schizophrenia susceptibility in humans and in a mouse model.Hum Mol Genet. 2009 Sep 1;18(17):3227-43. doi: 10.1093/hmg/ddp261. Epub 2009 May 30. Hum Mol Genet. 2009. PMID: 19483194 Free PMC article.
-
The neurobiology of D-amino acid oxidase and its involvement in schizophrenia.Mol Psychiatry. 2010 Feb;15(2):122-37. doi: 10.1038/mp.2009.99. Epub 2009 Sep 29. Mol Psychiatry. 2010. PMID: 19786963 Free PMC article. Review.
-
Effects of antipsychotic drugs on MK-801-induced attentional and motivational deficits in rats.Neuropharmacology. 2009 Mar;56(4):788-97. doi: 10.1016/j.neuropharm.2009.01.004. Neuropharmacology. 2009. PMID: 19705572 Free PMC article.
-
Effect of Vaccinium macrocarpon on MK-801-induced psychosis in mice.Indian J Pharmacol. 2018 Sep-Oct;50(5):227-235. doi: 10.4103/ijp.IJP_74_17. Indian J Pharmacol. 2018. PMID: 30636825 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases