Involvement of NMDA receptor subtypes in cortical spreading depression in rats assessed by fMRI

被引:37
作者
Shatillo, Artem [1 ]
Salo, Raimo A. [1 ]
Giniatullin, Rashid [1 ,2 ]
Groehn, Olli H. [1 ]
机构
[1] Univ Eastern Finland, AI Virtanen Inst Mol Sci, Dept Neurobiol, Kuopio 70700, Finland
[2] Kazan Fed Univ, Neurobiol Lab, Kazan 420008, Republic Of Tat, Russia
基金
芬兰科学院;
关键词
Spreading depression; BOLD; fMRI; Glutamate; NMDA receptors; METHYL-D-ASPARTATE; CEREBRAL-BLOOD-FLOW; DIZOCILPINE MK-801; GLUTAMATE RELEASE; FUNCTIONAL MRI; MIGRAINE AURA; IFENPRODIL; ANTAGONIST; MECHANISMS; PATHOPHYSIOLOGY;
D O I
10.1016/j.neuropharm.2015.01.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cortical spreading depression (CSD) is a phenomenon implicated in migraine with aura and associated with other neurological disorders (e.g. stroke, brain trauma). Current evidence points to the essential role of NMDA receptors in CSD mechanisms. However, the roles of multiple subunits of NMDA receptors expressed in neurons, glia and blood vessels in vivo, are little explored. Using BOLD fMRI of urethane anesthetized rats as an integrative CSD readout, we tested the involvement of different NMDA receptor subtypes in CSD induction and propagation. Rats were treated with a non-selective NMDA blocker (MK-801), NR2B antagonist (ifenprodil) or a NR2A selective antagonist (TCN-201). CSD was induced during fMRI scanning by application of KCl onto the cerebral cortex and fMRI data were collected by 9.41 MRI. The non-specific NMDA antagonist MK-801 coinpletely blocked CSD, which was not observed in the NR2A group where TCN-201 did not alter the CSD features. Unexpectedly, the NR2B specific antagonist ifenprodil largely promoted the initial negative phase of the BOLD CSD response, likely due to altered neurovascular coupling. Our data suggest key roles and differential involvement of NMDA receptor subtypes in CSD generation and propagation, highlighting an important role for the NR2B subtype. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:164 / 170
页数:7
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