Cortical spreading depression and gene regulation: Relevance to migraine

被引:81
作者
Choudhuri, R
Cui, L
Yong, C
Bowyer, S
Klein, RM
Welch, KMA
Berman, NEJ
机构
[1] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66160 USA
[3] Henry Ford Hosp, Dept Neurol, Detroit, MI 48202 USA
关键词
D O I
10.1002/ana.10158
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cortical spreading depression (CSD) may be the underlying mechanism of migraine aura. The role of CSD in initiating a migraine headache remains to be determined, but it might involve specific changes in gene expression in the brain. To examine these changes, four episodes of CSD at 5-minute intervals were induced in the mouse brain by application of 300mM KCl, and gene expression was examined 2 hours later using cDNA array and reverse transcriptase-polymerase chain reaction. Controls consisted of groups that received anesthesia only, attachment of recording electrodes only, and application of 0.9% NaCl. Of the over 1,180 genes examined in our experiments, those consistently regulated by CSD included vasoactive peptides; the vasodilator atrial natriuretic peptide was induced by CSD, while the vasoconstrictor neuropeptide Y was downregulated. Other genes specifically regulated by CSD were involved in oxidative stress responses (major prion protein, glutathione-S-transferase-5, and apolipoprotein E). L-type calcium channel mRNA was upregulated. In summary, CSD regulates genes that are intrinsic to its propagation, that identify accompanying vascular responses as a potential source of pain, and that protect against its potential pathological consequences. We believe these observations have strong relevance to the mechanisms of migraine and its outcomes.
引用
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页码:499 / 506
页数:8
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