| First Author | Kato AS | Year | 2016 |
| Journal | Nat Med | Volume | 22 |
| Issue | 12 | Pages | 1496-1501 |
| PubMed ID | 27820603 | Mgi Jnum | J:240979 |
| Mgi Id | MGI:5896898 | Doi | 10.1038/nm.4221 |
| Citation | Kato AS, et al. (2016) Forebrain-selective AMPA-receptor antagonism guided by TARP gamma-8 as an antiepileptic mechanism. Nat Med 22(12):1496-1501 |
| abstractText | Pharmacological manipulation of specific neural circuits to optimize therapeutic index is an unrealized goal in neurology and psychiatry. AMPA receptors are important for excitatory synaptic transmission, and their antagonists are antiepileptic. Although efficacious, AMPA-receptor antagonists, including perampanel (Fycompa), the only approved antagonist for epilepsy, induce dizziness and motor impairment. We hypothesized that blockade of forebrain AMPA receptors without blocking cerebellar AMPA receptors would be antiepileptic and devoid of motor impairment. Taking advantage of an AMPA receptor auxiliary protein, TARP gamma-8, which is selectively expressed in the forebrain and modulates the pharmacological properties of AMPA receptors, we discovered that LY3130481 selectively antagonized recombinant and native AMPA receptors containing gamma-8, but not gamma-2 (cerebellum) or other TARP members. Two amino acid residues unique to gamma-8 determined this selectivity. We also observed antagonism of AMPA receptors expressed in hippocampal, but not cerebellar, tissue from an patient with epilepsy. Corresponding to this selective activity, LY3130481 prevented multiple seizure types in rats and mice and without motor side effects. These findings demonstrate the first rationally discovered molecule targeting specific neural circuitries for therapeutic advantage. |
