Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6271918 | Neuroscience | 2015 | 10 Pages |
â¢GLYX-13 produces antidepressant-like effects for ⩾1 week following a single dose.â¢GLYX-13 facilitates learning and memory for ⩾1 week following a single dose.â¢GLYX-13 enhances hippocampal metaplasticity 24 h - 2 weeks following a single dose.â¢Repeat doses of GLYX-13 maintained the metaplasticity effects for at least 8 weeks.â¢GLYX-13 increased the number of mature dendritic spines 24 h after a single dose.
Rapastinel (GLYX-13) is an N-methyl-d-aspartate receptor (NMDAR) modulator that has characteristics of a glycine site partial agonist. Rapastinel is a robust cognitive enhancer and facilitates hippocampal long-term potentiation (LTP) of synaptic transmission in slices. In human clinical trials, rapastinel has been shown to produce marked antidepressant properties that last for at least one week following a single dose. The long-lasting antidepressant effect of a single dose of rapastinel (3Â mg/kg IV) was assessed in rats using the Porsolt, open field and ultrasonic vocalization assays. Cognitive enhancement was examined using the Morris water maze, positive emotional learning, and contextual fear extinction tests. LTP was assessed in hippocampal slices. Dendritic spine morphology was measured in the dentate gyrus and the medial prefrontal cortex. Significant antidepressant-like or cognitive enhancing effects were observed that lasted for at least one week in each model. Rapastinel facilitated LTP 1Â day-2Â weeks but not 4Â weeks post-dosing. Biweekly dosing with rapastinel sustained this effect for at least 8Â weeks. A single dose of rapastinel increased the proportion of whole-cell NMDAR current contributed by NR2B-containing NMDARs in the hippocampus 1Â week post-dosing, that returned to baseline by 4Â weeks post-dosing. The NMDAR antagonist 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) blocked the antidepressant-like effect of rapastinel 1Â week post dosing. A single injection of rapastinel also increased mature spine density in both brain regions 24Â h post-dosing. These data demonstrate that rapastinel produces its long-lasting antidepressant effects via triggering NMDAR-dependent processes that lead to increased sensitivity to LTP that persist for up to two weeks. These data also suggest that these processes led to the alterations in dendritic spine morphologies associated with the maintenance of long-term changes in synaptic plasticity associated with learning and memory.