A neural mechanism for exacerbation of headache by light

被引:398
作者
Noseda, Rodrigo [1 ]
Kainz, Vanessa [1 ]
Jakubowski, Moshe [1 ]
Gooley, Joshua J. [2 ]
Saper, Clifford B. [2 ,3 ]
Digre, Kathleen [4 ]
Burstein, Rami [1 ,3 ]
机构
[1] Harvard Univ, Sch Med, Dept Anesthesia, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
[4] Univ Utah, Moran Eye Ctr, Dept Neurol & Ophthalmol, Salt Lake City, UT USA
基金
美国国家卫生研究院;
关键词
RETINAL GANGLION-CELLS; CUTANEOUS ALLODYNIA; NOCICEPTIVE NEURONS; NON-CONE; NON-ROD; MELANOPSIN; STIMULATION; MIGRAINE; CORTEX; PROJECTIONS;
D O I
10.1038/nn.2475
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The perception of migraine headache, which is mediated by nociceptive signals transmitted from the cranial dura mater to the brain, is uniquely exacerbated by exposure to light. We found that exacerbation of migraine headache by light is prevalent among blind individuals who maintain non-image-forming photoregulation in the face of massive rod/cone degeneration. Using single-unit recording and neural tract tracing in the rat, we identified dura-sensitive neurons in the posterior thalamus whose activity was distinctly modulated by light and whose axons projected extensively across layers I-V of somatosensory, visual and associative cortices. The cell bodies and dendrites of such dura/light-sensitive neurons were apposed by axons originating from retinal ganglion cells (RGCs), predominantly from intrinsically photosensitive RGCs, the principle conduit of non-image-forming photoregulation. We propose that photoregulation of migraine headache is exerted by a non-image-forming retinal pathway that modulates the activity of dura-sensitive thalamocortical neurons.
引用
收藏
页码:239 / U128
页数:8
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