The role of NMDAR subtypes and charge transfer during hippocampal UP induction

被引:83
作者
Berberich, Sven
Jensen, Vidar
Hvalby, Oivind
Seeburg, Peter H.
Koehr, Georg
机构
[1] Max Planck Inst Med Res, Dept Mol Microbiol, D-69120 Heidelberg, Germany
[2] Univ Oslo, Inst Basic Med Sci, Mol Neurobiol Res Grp, N-0317 Oslo, Norway
关键词
frequency; temporal signaling; gene-targeted mouse; NVP-AAM077; Ro25-6981; CP-101,606;
D O I
10.1016/j.neuropharm.2006.07.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activation of NMDA receptors (NMDARs) is a requirement for persistent synaptic alterations, such as long-term potentiation of synaptic transmission (UP). NMDARs are composed of NR1 and NR2 subunits, and NR2 subunit-dependent gating properties of NMDAR subtypes cause dramatic differences in the timing of charge transfer. These postsynaptic temporal profiles are further influenced by the frequency of synaptic activation. Here, we investigated in the CA1 region of hippocampal slices from P28 mice, whether particular NMDAR subtypes are recruited based on NR2 subunit-specific gating following different induction protocols. For high frequency afferent stimulation (HFS), we found that genetic impairment of NR2A or pharmacological block of NR2A- or NR2B-type NMDARs can reduce field UP. In contrast, when pairing low frequency synaptic stimulation with postsynaptic depolarization (LFS pairing) in single CAI neurons, pharmacological antagonism of either subtype modestly reduced the charge transfer during LFS pairing without reducing the UP magnitude. These results indicate that HFS-triggered UP is induced by more than one NMDAR subtype, whereas a single subtype is sufficient during LFS pairing. Analysis of charge transfer during LFS pairing in 13 different conditions revealed a threshold for UP induction, which was independent of the NR2 antagonist tested. Thus, at least for LFS pairing, the amount of charge transfer, and thus Ca2+ influx, during UP induction is a factor more critical than the participation of a particular NMDAR subtype. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 86
页数:10
相关论文
共 38 条
[1]   Spatiotemporal visualization of long-term potentiation and depression in the hippocampal CA1 area [J].
Aihara, Takeshi ;
Kobayashi, Yuki ;
Tsukada, Minoru .
HIPPOCAMPUS, 2005, 15 (01) :68-78
[2]   Lack of NMDA receptor subtype selectivity for hippocampal long-term potentiation [J].
Berberich, S ;
Punnakkal, P ;
Jensen, V ;
Pawlak, V ;
Seeburg, PH ;
Hvalby, O ;
Köhr, G .
JOURNAL OF NEUROSCIENCE, 2005, 25 (29) :6907-6910
[3]   The NMDA receptor NR2B subunit: A valid therapeutic target for multiple CNS pathologies [J].
Chazot, PL .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (03) :389-396
[4]   Studies on the subtype selectivity of CP-101,606: evidence for two classes of NR2B-selective NMDA receptor antagonists [J].
Chazot, PL ;
Lawrence, S ;
Thompson, CL .
NEUROPHARMACOLOGY, 2002, 42 (03) :319-324
[5]   Requirements for LTP induction by pairing in hippocampal CA1 pyramidal cells [J].
Chen, HX ;
Otmakhov, N ;
Lisman, J .
JOURNAL OF NEUROPHYSIOLOGY, 1999, 82 (02) :526-532
[6]   NMDA receptor NR2 subunit dependence of the slow component of magnesium unblock [J].
Clarke, Richard J. ;
Johnson, Jon W. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (21) :5825-5834
[7]   Receptor trafficking and synaptic plasticity [J].
Collingridge, GL ;
Isaac, JTR ;
Wang, YT .
NATURE REVIEWS NEUROSCIENCE, 2004, 5 (12) :952-962
[8]   Bidirectional synaptic plasticity correlated with the magnitude of dendritic calcium transients above a threshold [J].
Cormier, RJ ;
Greenwood, AC ;
Connor, JA .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 85 (01) :399-406
[9]  
Cull-Candy Stuart G, 2004, Sci STKE, V2004, pre16, DOI 10.1126/stke.2552004re16
[10]  
Dingledine R, 1999, PHARMACOL REV, V51, P7