PAIN Group, Brain Imaging Center, McLean Hospital, Harvard Medical School, Belmont, MA 02478, USA.
Hum Brain Mapp. 2012 Jan;33(1):75-88. doi: 10.1002/hbm.21194. Epub 2011 Feb 17.
The pathway that underlies exacerbation of migraine headache by light has not been elucidated in the human brain but has recently been reported in a rodent model. We employ diffusion weighted imaging and probabilistic tractography to map connectivity of direct pathways from the optic nerve to the pulvinar implicated with whole-body allodynia during migraine. Nine healthy subjects were recruited to the study and underwent scanning on a 3T magnet. We were able to define well-known image-forming (optic nerve -> lateral geniculate -> visual cortex) as well as a less known nonimage forming visual pathway from the optic chiasm to the pulvinar, and from the pulvinar to several associative cortical brain regions. Such pathway may allow photic signals to converge on a thalamic region we described recently to be selectively activated during migraine headache. Consistent with physiological and anatomical studies in rats, the data provide an anatomical substrate for exacerbation of migraine headache by light in the human.
光引发偏头痛加剧的途径在人类大脑中尚未阐明,但最近在啮齿动物模型中已有报道。我们采用弥散加权成像和概率追踪技术,对偏头痛期间全身感觉过敏时视神经至丘脑中直接通路的连接进行了映射。9 名健康受试者被招募到该研究中,并在 3T 磁体上进行了扫描。我们能够很好地定义了众所周知的成像通路(视神经->外侧膝状体->视觉皮层),以及一条不太为人知的非成像视觉通路,从视交叉到丘脑中,以及从丘脑中到几个相关的大脑皮层区域。这种通路可能允许光信号汇聚到我们最近描述的一个丘脑区域,该区域在偏头痛发作期间被选择性激活。与大鼠的生理和解剖研究一致,这些数据为人类中光引发偏头痛加剧提供了解剖学基础。