Cited 18 times in
Trafficking patterns of NMDA and GABAA receptors in a Mg2+-free cultured hippocampal neuron model of status epilepticus
DC Field | Value | Language |
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dc.contributor.author | 김영환 | - |
dc.contributor.author | 김원주 | - |
dc.contributor.author | 정승수 | - |
dc.contributor.author | 조양제 | - |
dc.contributor.author | 허경 | - |
dc.date.accessioned | 2018-07-20T08:05:16Z | - |
dc.date.available | 2018-07-20T08:05:16Z | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 0920-1211 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/160823 | - |
dc.description.abstract | An altered pattern of receptor trafficking is one of the pathophysiologic mechanisms of status epilepticus (SE). The gradual internalization of GABAA receptors (GABARs) occurs in both in vitro and in vivo models of SE and is thought to be a cause of decreased GABAergic inhibition. Unlike GABARs, little is known about alterations in NMDA receptor (NMDAR) trafficking during SE, even though increased activity of NMDARs is indispensable for the induction and maintenance of SE. Therefore, we aimed to simultaneously investigate the changes in the trafficking patterns of GABARs and NMDARs in an in vitro cultured hippocampal neuron model of SE. For induction of epileptiform discharges, hippocampal neurons were exposed to external medium without Mg2+. Biotinylation assay and immunofluorescence staining for GABAR β2,3 and NMDAR NR1 subunits were performed to quantify and visualize surface GABARs and NMDARs, respectively. The frequency of spontaneous action potentials increased more than 4-fold after Mg2+-free induction. The level of surface GABARs decreased over time after Mg2+-free induction, dropping to approximately 50% of control levels an hour after Mg2+-free induction. By contrast, the trafficking of NMDARs to the surface was enhanced after a slight time lag, increasing by 30% of control levels an hour after Mg2+-free induction. Our data showed the changes of both NMDAR and GABAR trafficking during prolonged SE induced by a Mg2+-free extracellular environment and confirmed that this in vitro SE model is suitable for examining alterations in the receptor trafficking pattern by prolonged seizure activity. These results suggest that targeting of surface NMDAR could be a promising method in controlling benzodiazepine-resistant SE. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier Science Publishers | - |
dc.relation.isPartOf | EPILEPSY RESEARCH | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Action Potentials/physiology | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Biotinylation | - |
dc.subject.MESH | Cell Membrane/metabolism | - |
dc.subject.MESH | Cell Membrane/pathology | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Fluorescent Antibody Technique | - |
dc.subject.MESH | Hippocampus/metabolism* | - |
dc.subject.MESH | Hippocampus/pathology | - |
dc.subject.MESH | Magnesium Deficiency | - |
dc.subject.MESH | Neurons/metabolism* | - |
dc.subject.MESH | Neurons/pathology | - |
dc.subject.MESH | Patch-Clamp Techniques | - |
dc.subject.MESH | Protein Transport | - |
dc.subject.MESH | Rats, Sprague-Dawley | - |
dc.subject.MESH | Receptors, GABA-A/metabolism* | - |
dc.subject.MESH | Receptors, N-Methyl-D-Aspartate/metabolism* | - |
dc.subject.MESH | Status Epilepticus/metabolism* | - |
dc.subject.MESH | Status Epilepticus/pathology | - |
dc.title | Trafficking patterns of NMDA and GABAA receptors in a Mg2+-free cultured hippocampal neuron model of status epilepticus | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Physiology | - |
dc.contributor.googleauthor | Yang-Je Cho | - |
dc.contributor.googleauthor | Hyunjeong Kim | - |
dc.contributor.googleauthor | Won-Joo Kim | - |
dc.contributor.googleauthor | Seungsoo Chung | - |
dc.contributor.googleauthor | Young-Hwan Kim | - |
dc.contributor.googleauthor | Inja Cho | - |
dc.contributor.googleauthor | Byung In Lee | - |
dc.contributor.googleauthor | Kyoung Heo | - |
dc.identifier.doi | 10.1016/j.eplepsyres.2017.08.003 | - |
dc.contributor.localId | A00732 | - |
dc.contributor.localId | A00771 | - |
dc.contributor.localId | A03643 | - |
dc.contributor.localId | A03851 | - |
dc.contributor.localId | A04341 | - |
dc.relation.journalcode | J00796 | - |
dc.identifier.eissn | 1872-6844 | - |
dc.identifier.pmid | 28858777 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0920121116302777 | - |
dc.subject.keyword | Epileptiform activity | - |
dc.subject.keyword | GABA(A) receptor | - |
dc.subject.keyword | Low Mg(2+) solution | - |
dc.subject.keyword | NMDA receptor | - |
dc.subject.keyword | Receptor trafficking | - |
dc.subject.keyword | Status epilepticus | - |
dc.contributor.alternativeName | Kim, Young Hwan | - |
dc.contributor.alternativeName | Kim, Won Joo | - |
dc.contributor.alternativeName | Chung, Seung Soo | - |
dc.contributor.alternativeName | Cho, Yang Je | - |
dc.contributor.alternativeName | Heo, Kyoung | - |
dc.contributor.affiliatedAuthor | Kim, Young Hwan | - |
dc.contributor.affiliatedAuthor | Kim, Won Joo | - |
dc.contributor.affiliatedAuthor | Chung, Seung Soo | - |
dc.contributor.affiliatedAuthor | Cho, Yang Je | - |
dc.contributor.affiliatedAuthor | Heo, Kyoung | - |
dc.citation.volume | 136 | - |
dc.citation.startPage | 143 | - |
dc.citation.endPage | 148 | - |
dc.identifier.bibliographicCitation | EPILEPSY RESEARCH, Vol.136 : 143-148, 2017 | - |
dc.identifier.rimsid | 60707 | - |
dc.type.rims | ART | - |
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