Abstract

This review describes the subjective experience of visual aura in migraine, outlines theoretical models of this phenomenon, and explores how these may be linked to neurochemical, electrophysiological, and psychophysical differences in sensory processing that have been reported in migraine with aura. Reaction–diffusion models have been used to model the hallucinations thought to arise from cortical spreading depolarisation and depression in migraine aura. One aim of this review is to make the underlying principles of these models accessible to a general readership. Cortical spreading depolarisation and depression in these models depends on the balance of the diffusion rate between excitation and inhibition and the occurrence of a large spike in activity to initiate spontaneous pattern formation. We review experimental evidence, including recordings of brain activity made during the aura and attack phase, self-reported triggers of migraine, and psychophysical studies of visual processing in migraine with aura, and how these might relate to mechanisms of excitability that make some people susceptible to aura. Increased cortical excitability, increased neural noise, and fluctuations in oscillatory activity across the migraine cycle are all factors that are likely to contribute to the occurrence of migraine aura. There remain many outstanding questions relating to the current limitations of both models and experimental evidence. Nevertheless, reaction–diffusion models, by providing an integrative theoretical framework, support the generation of testable experimental hypotheses to guide future research.

Highlights

  • Migraine is a debilitating disorder, yet there is little cross-discipline consensus as to its cause

  • We outline reaction–diffusion models in general terms and how these have been used as models of cortical dynamics of the visual brain. We review their role in explaining the hallucinatory experience of migraine aura and the factors that make networks of neurons more susceptible to hallucination in migraine with aura

  • Direct links to electrophysiology are difficult due to the lack of experimental data during the attack; neural oscillations may be a fruitful area of investigation as these relate to functional connectivity of the network and the excitability of the brain, which may relate to the terms of the models

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Summary

Introduction

Migraine is a debilitating disorder, yet there is little cross-discipline consensus as to its cause. Of interest in the current review are those reporting migraine with aura (MA). These individuals fulfil the International Headache Society diagnostic criteria for migraine, but experience hallucinations around the time of the onset of the headache. The majority of those with MA do not experience the hallucinations on every attack—79% of those with MA experience attacks without aura [1]. Migraine aura is thought to be linked to a spreading wave of hyper-excitation (spreading depolarisation) across the brain’s surface followed by a period of reduced blood-flow (hypoperfusion) and suppressed neural activity (spreading depression) [2]. The phenomenology of cortical spreading depolarisation and cortical spreading depression provides an insight into the probable mechanisms underlying migraine aura

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