LY395756 promotes NR2B expression via activation of AKT/CREB signaling in the juvenile methylazoxymethanol mice model of schizophrenia

• Published in: Brain and behavior Vol. 12; no. 2; pp. e2466 - n/a
• Main Authors: Li, Meng‐lin, Peng, Yuan, An, Ying, Li, Guo‐yan, Lan, Yue
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.02.2022; John Wiley and Sons Inc; Wiley
• Subjects: Amino Acids, Dicarboxylic; Animal cognition; Animals; Bridged Bicyclo Compounds; Cognitive ability; CREB; Cyclic AMP Response Element-Binding Protein - metabolism; Disease Models, Animal; Drug dosages; Fluorides; Laboratory animals; LY395756; Methylazoxymethanol Acetate - analogs & derivatives; Mice; NR2B; Original; Phosphorylation; Proteins; Proto-Oncogene Proteins c-akt - metabolism; Receptors, N-Methyl-D-Aspartate - metabolism; Schizophrenia; Schizophrenia - chemically induced; Signal Transduction; Beijing China; United States > US; China; NR2B; LY395756; CREB; schizophrenia
• ISSN: 2162-3279; 2162-3279
• DOI: 10.1002/brb3.2466

Introduction Synaptic N‐methyl‐d‐aspartate receptor subtype 2B(NR2B) is significantly reduced in prefrontal cortex (PFC) in the neurodevelopmental methylazoxymethanol (MAM) model of schizophrenia (SCZ). Recent research has shown that LY395756 can effectively restore NR2B levels and improve cognitive performance in juvenile MAM mice model. However, the underlying mechanisms of these beneficial effects remain unclear. Materials and methods Juvenile MAM mice model of SCZ is used in our study. Synaptic membrane protein levels were examined by western blotting under different treatment conditions. Interaction of cAMP‐response element binding protein (CREB) and the promoter of NR2B was detected by the chromatin immunoprecipitation (ChIP) assay. Further examination of signaling pathway that mediates NR2B expression was also investigated by western blotting. Results In the PFC of the juvenile MAM mice schizophrenia model, CREB was found to directly bind with the promoter of NR2B. LY395756 activated the phosphorylation of AKT. Phosphorylated AKT subsequently induced the phosphorylation of CREB, and the activated CREB promoted the expression of NR2B. Subsequent experiments showed that the dephosphorylation of CREB induced by protein phosphatase 1 (PP1) can inhibit NR2B levels. Taken together, these findings support that the AKT/CREB signaling pathway is essential for the promoting effect of LY395756 on synaptic NR2B in PFC in juvenile MAM mice SCZ model. Conclusions Our investigation has identified a novel mechanism by which LY395756 increases NR2B expression in juvenile MAM mice SCZ model. The AKT/CREB signaling pathway warrants further research as a potential direction for clinical treatment of SCZ. Our investigation has identified a novel mechanism by which LY395756 increases NR2B expression in juvenile MAM mice SCZ model. The AKT/CREB signaling pathway warrants further research as a potential direction for clinical treatment of SCZ.