Detailseite
Projekt Druckansicht

Die Rolle der abnormen NMDA Rezeptor-vermittelten Transmission in spezifischen neuronalen Populationen in dem post-adoleszenten Ausbruch der Psychose

Fachliche Zuordnung Biologische Psychiatrie
Förderung Förderung von 2016 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 290792871
 
Erstellungsjahr 2022

Zusammenfassung der Projektergebnisse

A vast body of evidence supports a causal role of NMDAR-mediated glutamatergic dysfunction in triggering psychosis. However, the neuronal substrate and mechanisms are yet unknown. Previous genetic models of NMDAR hypofunction restricted to parvalbumin-positive interneurons indicate the necessity of an early postnatal impairment to trigger schizophrenia-like abnormalities, whereas the substrates of NMDAR-mediated psychosis at adolescent/adult stages are unknown. We analyzed the effect of the inducible ablation of NMDARs in ErbB4-expressing cells in mice during late adolescence using a pharmacogenetic approach. Interestingly, the tamoxifeninducible NMDAR deletion during this late developmental stage did not induce behavioral alterations resembling depression, schizophrenia or anxiety. Our data indicate that post-adolescent NMDAR deletion, even in a wider cell population than parvalbumin-positive interneurons, is not sufficient to generate behavioral abnormalities resembling psychiatric disorders. Other neuronal substrates may underlie post-adolescent NMDAR-driven psychosis. NMDAR agonists such as D-serine and rapastinel represent promising therapeutic alternatives in the treatment of psychosis with a more favourable side-effect profile than NMDAR antagonists also during neurodevelopment. Surprisingly, targeting microglia activation by minocycline aggravates perinatal neurotoxicity induced by NMDAR blockade, questioning ist uility as early intervention. Perinatal hypoxia as environmental risk factor induces long-term functional impairment of parvalbumin-positive interneurons and is influenced differentially by subunit- versus global NMDAR antagonists.

Projektbezogene Publikationen (Auswahl)

  • (2016) Minocycline exacerbates apoptotic neurodegeneration induced by the NMDA receptor antagonist MK-801 in the early postnatal mouse brain. Eur Arch Psychiatry Clin Neurosci, 266:673-677
    Inta I, Vogt MA, Vogel AS, Bettendorf M, Gass P, Inta D
    (Siehe online unter https://doi.org/10.1007/s00406-015-0649-2)
  • (2017) Modulation of NMDA receptors activity as a novel treatment option for depression: Current clinical evidence and therapeutic potential of Rapastinel (GLYX-13). Neuropsychiatr Dis Treat 13:973-980
    Vasilescu AN, Schweinfurth N, Borgwardt S, Gass P, Lang UE, Inta D, Eckart S
    (Siehe online unter https://doi.org/10.2147/NDT.S119004)
  • (2017) Puberty marks major changes in the hippocampal and cortical c-Fos activation pattern induced by NMDA receptor antagonists. Neuropharmacology 112:181-187
    Inta I, Domonkos E, Pfeiffer N, Sprengel R, Bettendorf M, Lang UE, Inta D, Gass P
    (Siehe online unter https://doi.org/10.1016/j.neuropharm.2016.03.023)
  • (2018) Altered expression of schizophrenia-related genes in mice lacking mGlu5 receptors. Eur Arch Psychiatry Clin Neurosci. 268(1):77-87
    Luoni A, Gass P, Brambilla P, Ruggeri M, Riva MA, Inta D
    (Siehe online unter https://doi.org/10.1007/s00406-016-0728-z)
  • (2018) Antagonism at the NR2B subunit of NMDA receptors induces increased connectivity of the prefrontal and subcortical regions regulating reward behavior. Psychopharmacology. 235:1055-1068
    Gass N, Becker R, Markus Sack S, Schwarz AJ, Reinwald J, Alejandro Cosa- Linan A, Zheng L, Clemm von Hohenberg C, Inta D, Meyer-Lindenberg A, Weber-Fahr W, Gass P, Sartorius A
    (Siehe online unter https://doi.org/10.1007/s00213-017-4823-2)
  • (2018) Chronic treatment with fluoxetine or clozapine of socially isolated rats prevents subsector-specific reduction of parvalbumin-immunoreactive cells in the hippocampus. Neuroscience. 371:384-394
    Filipovic D, Stanisavljevic A, Jasnic N, Bernardi R.E., Inta D, Peric I, Gass P
    (Siehe online unter https://doi.org/10.1016/j.neuroscience.2017.12.020)
  • (2018) Molecular and cellular dissection of NMDA receptor subtypes as antidepressant targets. Neurosci Biobehav Rev 84:352-358
    Lang E, Mallien AS, Vasilescu AN, Hefter D, Luoni A, Riva MA, Borgwardt S, Sprengel R, Lang UE, Gass P, Inta D
    (Siehe online unter https://doi.org/10.1016/j.neubiorev.2017.08.012)
  • (2019) Altered prepulse inhibition of the acoustic startle response in BDNF-deficient mice in a model of early postnatal hypoxia: implications for schizophrenia. Eur Arch Psychiatry Clin Neurosci,269(4):439-447
    Lima-Ojeda JM, Mallien AS, Brandwein C, Lang UE, Hefter D, Inta D
    (Siehe online unter https://doi.org/10.1007/s00406-018-0882-6)
  • (2021) Cre-Activation in ErbB4-Positive Neurons of Floxed Grin1/NMDA Receptor Mice Is Not Associated With Major Behavioral Impairment. Front Psychiatry. 12:750106
    Mallien AS, Pfeiffer N, Vogt MA, Chourbaji S, Sprengel R, Gass P, Inta D
    (Siehe online unter https://doi.org/10.3389/fpsyt.2021.750106)
  • (2021) Rapastinel alleviates the neurotoxic effect induced by NMDA receptor blockade in the early postnatal mouse brain. Eur Arch Psychiatry Clin Neurosci 271:1587-1591
    Vasilescu AN, Mallien AS, Pfeiffer N, Lange UE, Gass P, Inta D
    (Siehe online unter https://doi.org/10.1007/s00406-020-01180-5)
 
 

Zusatzinformationen

Textvergrößerung und Kontrastanpassung