Mechanisms of initiation of cortical spreading depression

The Journal of Headache and Pain

Research

Maral Zarin Zadeh¹  Angelita Tottene¹  Marina Vitale¹  Daniela Pietrobon²  KC Brennan³ 

[1] Department of Biomedical Sciences, University of Padova, 35131, Padova, Italy;Department of Biomedical Sciences, University of Padova, 35131, Padova, Italy;Padova Neuroscience Center (PNC), University of Padova, 35131, Padova, Italy;Department of Neurology, University of Utah School of Medicine, 84108, Salt Lake City, UT, USA;

关键词: Migraine;    Cortical spreading depression;    Spreading depolarization;    Cerebral cortex;    Glutamate NMDA receptors;    Voltage-gated calcium channels;   

DOI  :  10.1186/s10194-023-01643-9

 received in 2023-06-17, accepted in 2023-07-31,  发布年份 2023

来源: Springer

【 摘 要 】

BackgroundThere is increasing evidence from human and animal studies that cortical spreading depression (CSD) is the neurophysiological correlate of migraine aura and a trigger of migraine pain mechanisms. The mechanisms of initiation of CSD in the brain of migraineurs remain unknown, and the mechanisms of initiation of experimentally induced CSD in normally metabolizing brain tissue remain incompletely understood and controversial. Here, we investigated the mechanisms of CSD initiation by focal application of KCl in mouse cerebral cortex slices.MethodsHigh KCl puffs of increasing duration up to the threshold duration eliciting a CSD were applied on layer 2/3 whilst the membrane potential of a pyramidal neuron located very close to the site of KCl application and the intrinsic optic signal were simultaneously recorded. This was done before and after the application of a specific blocker of either NMDA or AMPA glutamate receptors (NMDARs, AMPARs) or voltage-gated Ca2+ (CaV) channels. If the drug blocked CSD, stimuli up to 12–15 times the threshold were applied.ResultsBlocking either NMDARs with MK-801 or CaV channels with Ni2+ completely inhibited CSD initiation by both CSD threshold and largely suprathreshold KCl stimuli. Inhibiting AMPARs with NBQX was without effect on the CSD threshold and velocity. Analysis of the CSD subthreshold and threshold neuronal depolarizations in control conditions and in the presence of MK-801 or Ni2+ revealed that the mechanism underlying ignition of CSD by a threshold stimulus (and not by a just subthreshold stimulus) is the CaV-dependent activation of a threshold level of NMDARs (and/or of channels whose opening depends on the latter). The delay of several seconds with which this occurs underlies the delay of CSD initiation relative to the rapid neuronal depolarization produced by KCl.ConclusionsBoth NMDARs and CaV channels are necessary for CSD initiation, which is not determined by the extracellular K+ or neuronal depolarization levels per se, but requires the CaV-dependent activation of a threshold level of NMDARs. This occurs with a delay of several seconds relative to the rapid depolarization produced by the KCl stimulus. Our data give insights into potential mechanisms of CSD initiation in migraine.

【 授权许可】

CC BY   
© Springer-Verlag Italia S.r.l., part of Springer Nature 2023

【 图 表 】

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