GABAPENTIN PREVENTS CORTICAL SPREADING DEPOLARIZATION-INDUCED DISINHIBITION

被引:9
作者
Mesgari, Masoud [1 ]
Krueger, Johanna [1 ]
Riemer, Christopher Theo [1 ]
Ghadiri, Maryam Khaleghi [2 ]
Kovac, Stjepana [3 ]
Gorji, Ali [1 ,2 ,3 ,4 ,5 ]
机构
[1] Westfal Wilhelms Univ Munster, Epilepsy Res Ctr, Munster, Germany
[2] Westfal Wilhelms Univ Munster, Dept Neurosurg, Munster, Germany
[3] Westfal Wilhelms Univ Munster, Dept Neurol, Munster, Germany
[4] Khatam Alanbia Hosp, Shefa Neurosci Res Ctr, Tehran, Iran
[5] Mashhad Univ Med Sci, Dept Neurosci, Mashhad, Iran
基金
美国国家科学基金会;
关键词
anticonvulsive; seizure; epilepsy; stroke; spreading depolarization; LONG-TERM POTENTIATION; IN-VITRO; ALPHA(2)DELTA SUBUNITS; SYNAPTIC-TRANSMISSION; PYRAMIDAL NEURONS; CEREBRAL-CORTEX; DEPRESSION; CONDUCTANCE; INHIBITION; RECEPTORS;
D O I
10.1016/j.neuroscience.2017.08.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cortical spreading depolarization (CSD) has an important role in brain diseases such as stroke, subarachnoid hemorrhage, migraine with aura, and epilepsy. Several anti-epileptic drugs (AEDs) are used to treat paroxysmal brain diseases and are thus known to suppress CSD. One of these AEDs is gabapentin (GBP) which has been traditionally used for treatment of some CSD-related neurological diseases. We applied intra- and extracellular recordings to investigate the effect of CSD on inhibitory post synaptic potentials (IPSPs) and synaptic properties of rodent neocortex after application of GBP. Application of GBP after CSD increased the amplitude of IPSPs. In addition, GBP inhibited induction of long-term potentiation after CSD. These data support an effect of GBP on GABA-mediated inhibition in the late hyperexcitable phase of CSD. Modulations of synaptic properties and post-CSD GABAergic function are likely GBP's mechanisms of action in CSD-related disorders. These mechanisms could be targeted for further drug discovery in CSD-related diseases. (C) 2017 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
相关论文
共 31 条
  • [1] Alles SR, 2016, NEUROSCIENTIST
  • [2] Spreading depression enhances human neocortical excitability in vitro
    Berger, M.
    Speckmann, E-J
    Pape, H. C.
    Gorji, A.
    [J]. CEPHALALGIA, 2008, 28 (05) : 558 - 562
  • [3] THALAMIC AFFERENT ACTIVATION OF SUPRAGRANULAR LAYERS IN AUDITORY CORTEX IN VITRO: A VOLTAGE SENSITIVE DYE STUDY
    Broicher, T.
    Bidmon, H-J.
    Kamuf, B.
    Coulon, P.
    Gorji, A.
    Pape, H-C.
    Speckmann, E-J.
    Budde, T.
    [J]. NEUROSCIENCE, 2010, 165 (02) : 371 - 385
  • [4] Antiepileptic drugs in migraine: from clinical aspects to cellular mechanisms
    Calabresi, Paolo
    Galletti, Francesca
    Rossi, Cristiana
    Sarchielli, Paola
    Cupini, Letizia M.
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (04) : 188 - 195
  • [5] Adenylyl cyclase subtype 1 is essential for late-phase long term potentiation and spatial propagation of synaptic responses in the anterior cingulate cortex of adult mice
    Chen, Tao
    O'Den, Gerile
    Song, Qian
    Koga, Kohei
    Zhang, Ming-Ming
    Zhuo, Min
    [J]. MOLECULAR PAIN, 2014, 10
  • [6] Gabapentin increases a tonic inhibitory conductance in hippocampal pyramidal neurons
    Cheng, Victor Y.
    Bonin, Robert P.
    Chiu, Mary W.
    Newell, J. Glen
    MacDonald, John F.
    Orser, Beverley A.
    [J]. ANESTHESIOLOGY, 2006, 105 (02) : 325 - 333
  • [7] Auditory thalamocortical synaptic transmission in vitro
    Cruikshank, SJ
    Rose, HJ
    Metherate, R
    [J]. JOURNAL OF NEUROPHYSIOLOGY, 2002, 87 (01) : 361 - 384
  • [8] The α2δ subunits of voltage-gated calcium channels
    Dolphin, Annette C.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2013, 1828 (07): : 1541 - 1549
  • [9] Ca2+ channel α2δ ligands:: novel modulators of neurotransmission
    Dooley, David J.
    Taylor, Charles P.
    Donevan, Sean
    Feltner, Douglas
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (02) : 75 - 82
  • [10] The Stroke-Migraine Depolarization Continuum
    Dreier, Jens P.
    Reiffurth, Clemens
    [J]. NEURON, 2015, 86 (04) : 902 - 922