期刊
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
卷 322, 期 1, 页码 254-264出版社
AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
DOI: 10.1124/jpet.106.117093
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资金
- NIMH NIH HHS [T32 MH065215] Funding Source: Medline
Group II metabotropic glutamate receptors ( mGluRs), mGluR2 and mGluR3, play a number of important roles in mammalian brain and represent exciting new targets for certain central nervous system disorders. We now report synthesis and characterization of a novel family of derivatives of dihydrobenzo[ 1,4] diazepin-2-one that are selective negative allosteric modulators for group II mGluRs. These compounds inhibit both mGluR2 and mGluR3 but have no activity at group I and III mGluRs. The novel mGluR2/3 antagonists also potently block mGluR2/3- mediated inhibition of the field excitatory postsynaptic potentials at the perforant path synapse in hippocampal slices. These compounds induce a rightward shift and decrease the maximal response in the glutamate concentration-response relationship, consistent with a noncompetitive antagonist mechanism of action. Furthermore, radioligand binding studies revealed no effect on binding of the orthosteric antagonist [H-3] LY341495 [2S-2-amino-2-(1S, 2S-2-carboxycyclopropan1- yl)-3-( xanth-9-yl) propionic acid]. Site-directed mutagenesis revealed that a single point mutation in transmembrane V ( N735D), previously shown to be an important residue for potentiation activity of the mGluR2 allosteric potentiator LY487379 [ N-(4-(2-methoxyphenoxy) phenyl)- N-( 2,2,2- trifluoroethylsulfonyl) pyrid- 3- ylmethylamine], is not critical for the inhibitory activity of negative allosteric modulators of group II mGluRs. However, this single mutation in human GluR2 almost completely blocked the enhancing activity of biphenyl- indanone A, a novel allosteric potentiator of mGluR2. Our data suggest that these two positive allosteric modulators of mGluR2 may share a common binding site and that this site may be distinct from the binding site for the new negative allosteric modulators of group II mGluRs.
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