期刊
JOURNAL OF NEUROSCIENCE
卷 34, 期 34, 页码 11325-11338出版社
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0458-14.2014
关键词
NMDA receptor; protein synthesis; sigma-1 receptor; surface biotinylation; trafficking; Western blot
资金
- Canadian Institutes of Health Research [MOP-79360, MOP-115062]
Sigma-1 receptors (sigma-1Rs) are endoplasmic reticulum resident chaperone proteins implicated in many physiological and pathological processes in the CNS. A striking feature of sigma-1Rs is their ability to interact and modulate a large number of voltage-and ligand-gated ion channels at the plasma membrane. We have reported previously that agonists for sigma-1Rs potentiate NMDA receptor (NMDAR) currents, although the mechanism by which this occurs is still unclear. In this study, we show that in vivo administration of the selective sigma-1R agonists (+)-SKF 10,047 [2S-(2 alpha,6 alpha,11R*]-1,2,3,4,5,6-hexahydro-6,11-dimethyl-3-(2-propenyl)-2,6-methano-3-benzazocin-8-ol hydrochloride (N-allylnormetazocine) hydrochloride], PRE-084 (2-morpholin-4-ylethyl 1-phenylcyclohexane-1-carboxylate hydrochloride), and (+)-pentazocine increases the expression of GluN2A and GluN2B subunits, as well as postsynaptic density protein 95 in the rat hippocampus. We also demonstrate that sigma-1R activation leads to an increased interaction between GluN2 subunits and sigma-1Rs and mediates trafficking of NMDARs to the cell surface. These results suggest that sigma-1R may play an important role in NMDAR-mediated functions, such as learning and memory. It also opens new avenues for additional studies into a multitude of pathological conditions in which NMDARs are involved, including schizophrenia, dementia, and stroke.
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