Converging evidence on D-amino acid oxidase-dependent enhancement of hippocampal firing activity and passive avoidance learning in rats.

BACKGROUND N-methyl-D-aspartate (NMDA) receptor activation requires the binding of a co-agonist on the glycine-binding site. D-serine is the main endogeneous co-agonist of NMDA receptors, and its availability significantly depends on the activity of the metabolic enzyme D-amino acid oxidase (DAAO). Inhibition of DAAO increases the brain levels of D-serine, and modulates a variety of physiological functions including cognitive behavior. METHODS Here, we examined the effects of a novel 4‑hydroxypyridazin-3(2H)‑one derivative DAAO inhibitor, Compound 30 (CPD30) on passive avoidance learning and on neuronal firing activity in rats. RESULTS D-serine administration was applied as reference, which increased cognitive performance and enhanced hippocampal firing activity and responsiveness to NMDA after both local and systemic application. Similarly to D-serine, CPD30 (0.1 mg/kg) effectively reversed MK-801 induced memory impairment in the passive avoidance test. Furthermore, local iontophoretic application of CPD30 in the vicinity of hippocampal pyramidal neurons significantly increased firing rate, and enhanced their responses to locally applied NMDA. Compound 30 also enhanced hippocampal firing activity after systemic administration. In 0.1-1.0 mg/kg doses, CPD30 increased spontaneous and NMDA-evoked firing activity of the neurons. Effects of CPD30 on NMDA-responsiveness emerged faster (at 10 min post-injection) when 1.0 mg/kg dose was applied compared to the onset of the effects of 0.1 mg/kg CPD30 (at 30 min post-injection). CONCLUSIONS The present results confirm that the inhibition of DAAO enzyme is an effective strategy for cognitive enhancement. Our findings further facilitate the understanding of the cellular mechanisms underlying the behavioral effects of DAAO inhibition in the mammalian brain.