Glutamate is a Partial Agonist at GluN2A Containing NMDA Receptors

被引：0
|
作者：
Kussius, Cassandra [1 ]
Popescu, Gabriela K. [1 ]
机构：
[1] SUNY Buffalo, Buffalo, NY 14260 USA
来源：
BIOPHYSICAL JOURNAL | 2010年 / 98卷 / 03期
关键词：
D O I：
10.1016/j.bpj.2009.12.2853
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
引用
收藏
页码：525A / 525A
页数：1
相关论文
共 50 条
  • [1] GluN2A and GluN2B subunit-containing NMDA receptors in hippocampal plasticity
    Shipton, Olivia A.
    Paulsen, Ole
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2014, 369 (1633)
  • [2] GluN2A Subunit-Containing NMDA Receptors Are the Preferential Neuronal Targets of Homocysteine
    Sibarov, Dmitry A.
    Abushik, Polina A.
    Giniatullin, Rashid
    Antonov, Sergei M.
    [J]. FRONTIERS IN CELLULAR NEUROSCIENCE, 2016, 10
  • [3] GluN2A and GluN2B NMDA receptors use distinct allosteric routes
    Tian, Meilin
    Stroebel, David
    Piot, Laura
    David, Melissa
    Ye, Shixin
    Paoletti, Pierre
    [J]. NATURE COMMUNICATIONS, 2021, 12 (01)
  • [4] GluN2A and GluN2B NMDA receptors use distinct allosteric routes
    Meilin Tian
    David Stroebel
    Laura Piot
    Mélissa David
    Shixin Ye
    Pierre Paoletti
    [J]. Nature Communications, 12
  • [5] The σ-1 Receptor Interacts Directly with GluN1 But Not GluN2A in the GluN1/GluN2A NMDA Receptor
    Balasuriya, Dilshan
    Stewart, Andrew P.
    Edwardson, J. Michael
    [J]. JOURNAL OF NEUROSCIENCE, 2013, 33 (46): : 18219 - 18224
  • [6] Distinct Functional and Pharmacological Properties of Triheteromeric GluN1/GluN2A/GluN2B NMDA Receptors
    Hansen, Kasper B.
    Ogden, Kevin K.
    Yuan, Hongjie
    Traynelis, Stephen F.
    [J]. NEURON, 2014, 81 (05) : 1084 - 1096
  • [7] A single-channel mechanism for pharmacological potentiation of GluN1/GluN2A NMDA receptors
    Chopra, Divyan A.
    Sapkota, Kiran
    Irvine, Mark W.
    Fang, Guangyu
    Jane, David E.
    Monaghan, Daniel T.
    Dravid, Shashank M.
    [J]. SCIENTIFIC REPORTS, 2017, 7
  • [8] DCMQA, a caffeoylquinic acid derivative alleviates NMDA-induced neurotoxicity via modulating GluN2A and GluN2B-containing NMDA receptors in vitro
    Yang, Yue
    Gao, Huan
    Liu, Wenwu
    Jiang, Xiaowen
    Shen, Zexu
    Li, Xiang
    Ren, Tianshu
    Xu, Zihua
    Cheng, Gang
    Zhao, Qingchun
    [J]. TOXICOLOGY IN VITRO, 2020, 67
  • [9] A single-channel mechanism for pharmacological potentiation of GluN1/GluN2A NMDA receptors
    Divyan A. Chopra
    Kiran Sapkota
    Mark W. Irvine
    Guangyu Fang
    David E. Jane
    Daniel T. Monaghan
    Shashank M. Dravid
    [J]. Scientific Reports, 7
  • [10] MPX-004: A New Pharmacological Tool to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit
    Volkmann, Robert A.
    Fanger, Christopher
    Anderson, David R.
    Menniti, Frank S.
    [J]. BIOPHYSICAL JOURNAL, 2016, 110 (03) : 288A - 288A
12345