@article {Parsons1264, author = {Chris G. Parsons and Wojciech Danysz and G{\"u}nter Quack and Sabine Hartmann and Bianke Lorenz and Christine Wollenburg and Leokadia Baran and Edmund Przegalinski and Wojciech Kostowski and Pawel Krzascik and Boris Chizh and P. Max. Headley}, title = {Novel Systemically Active Antagonists of the Glycine Site of the N-Methyl-d-aspartate Receptor: Electrophysiological, Biochemical and Behavioral Characterization}, volume = {283}, number = {3}, pages = {1264--1275}, year = {1997}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {A series of novel tricyclic pyrido-phthalazine-dione derivatives was tested for antagonistic effects at the strychnine-insensitive modulatory site of the N-methyl-d-aspartate (NMDA) receptor (glycineB). All compounds displaced [3H]MDL-105,519 binding to rat cortical membranes with IC50 values of between 90 nM and 3.6 μM. In patch-clamp experiments, steady-state inward current responses of cultured hippocampal neurons to NMDA (200 μM, glycine 1 μM) were antagonized by these same compounds with IC50 values of 0.14 to 13.8 μM. The antagonism observed was typical for glycineBantagonists, i.e., they induced desensitization and their effects were not use or voltage dependent. Moreover, increasing concentrations of glycine were able to decrease their apparent potency. Much higher concentrations (\>100 μM) were required to antagonize α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-induced currents. They were potent, systemically active NMDA receptor antagonists in vivo against responses of single neurons in the rat spinal cord to microelectrophoretic application of NMDA with ID50 values in the low milligram per kilogram i.v. range. They also inhibited pentylenetetrazol-, NMDA- and maximal electroshock-induced convulsions in mice with ED50 values ranging from 8 to 100 mg/kg i.p. The duration of anticonvulsive action was rather short but was prolonged by the organic acid transport inhibitor probenecid (200 mg/kg). The agents tested represent a novel class of systemically active glycineB antagonists with greatly improved bioavailability. The American Society for Pharmacology and Experimental Therapeutics}, issn = {0022-3565}, URL = {https://jpet.aspetjournals.org/content/283/3/1264}, eprint = {https://jpet.aspetjournals.org/content/283/3/1264.full.pdf}, journal = {Journal of Pharmacology and Experimental Therapeutics} }