| Literature DB >> 31020389 |
Peiqiang Liu1, Danxue Qin1, Xi Huang1,2, Huiying Chen1, Wenhua Ye1, Xiaoyu Lin1, Jiping Su3.
Abstract
The purpose of this study was to observe the regulatory effects of GABAA (γ-aminobutyric acid A) receptor on the N-methyl-D-aspartate (NMDA) receptor during excitotoxicity in spiral ganglion neurons in the rat cochlea induced by sodium salicylate (SS). Western blot illustrated SS decreased the expression of NMDA receptor 2B subunit (NR2B) surface protein through affecting GABAA receptor, but the total protein content did not significantly change. Y1472 and S1480 are important phosphorylation sites in NR2B, SS downregulated the Fyn-dependent phosphorylation of Y1472 in a manner not related to the CK2 (Casein Kinase 2) dependent phosphorylation of S1480, thus regulating the surface distribution and internalization of NMDA receptor through GABAA receptor. These results suggest that the modified pattern of dynamic balance between excitation and inhibition by coactivation of the GABAA receptor can attenuate the excitatory NMDA receptor under the action of SS, via inhibiting the Fyn-dependent phosphorylation of Y1472.Entities:
Keywords: GABAAR; NMDAR; Neurotoxicity; Sodium salicylate; Spiral ganglion neurons
Year: 2019 PMID: 31020389 DOI: 10.1007/s00359-019-01339-z
Source DB: PubMed Journal: J Comp Physiol A Neuroethol Sens Neural Behav Physiol ISSN: 0340-7594 Impact factor: 1.836