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Molecular effects of the psychotropic NMDA receptor antagonist MK-801 in the rat entorhinal cortex: Increases in AP-1 DNA binding activity and expression of Fos and Jun family members
Kontkanen O.; Lakso M.; Koponen E.; Wong G.; Castren E.
2000
Source PublicationAnnals of the New York Academy of Sciences
Volume911
Pages73-82
AbstractNoncompetitive NMDA receptor antagonists such as phencyclidine and MK-801 produce psychotropic symptoms that closely resemble schizophrenic psychosis and induce the expression of immediate early genes in limbic cortical areas. We are concentrating on analyzing molecular and physiological effects that these drugs produce in the entorhinal cortex and on the potential connection between these effects and the psychotic symptoms. We show here that MK-801 increases the DNA binding activity of the activator protein-1 (AP-1) complex in the entorhinal cortex. We also observed increased expression of mRNAs for Fos and Jun transcription factor family members c-Fos, FosB, Fra-2, and JunB, as well as Fos family proteins in the entorhinal cortex after MK-801 administration. This suggests that the activated AP-1 complex consists of these transcription factors. Genes regulated by the AP-1 complex in the entorhinal cortex might he involved in the pathophysiology of psychotic behavior and are potential targets for new antipsychotic drugs.
URLView the original
Language英語English
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Document TypeConference paper
CollectionFaculty of Health Sciences
AffiliationItä-Suomen yliopisto
Recommended Citation
GB/T 7714
Kontkanen O.,Lakso M.,Koponen E.,et al. Molecular effects of the psychotropic NMDA receptor antagonist MK-801 in the rat entorhinal cortex: Increases in AP-1 DNA binding activity and expression of Fos and Jun family members[C], 2000, 73-82.
APA Kontkanen O.., Lakso M.., Koponen E.., Wong G.., & Castren E. (2000). Molecular effects of the psychotropic NMDA receptor antagonist MK-801 in the rat entorhinal cortex: Increases in AP-1 DNA binding activity and expression of Fos and Jun family members. Annals of the New York Academy of Sciences, 911, 73-82.
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