偏头痛进展的神经生物学

Q2 Medicine Neurobiology of Pain Pub Date : 2022-08-01 DOI:10.1016/j.ynpai.2022.100094
Wanakorn Rattanawong , Alan Rapoport , Anan Srikiatkhachorn
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引用次数: 7

摘要

慢性偏头痛是最具破坏性的头痛疾病之一。人口中估计患病率为1.4-2.2%。可能导致偏头痛进展的因素包括偏头痛发作的频率高、药物过度使用、共病疼痛综合征和肥胖。一些研究表明,慢性偏头痛会导致大脑的解剖和生理发生重大变化。尽管对导致这种进展的病理生理过程没有明确的解释,但某些特征,如感觉敏感性增加、皮肤异常性痛、习惯化受损,确定了神经元的高兴奋性是可能的机制。在这篇综述中,我们描述了导致这种超兴奋性的两种主要机制。第一种是由三叉神经伤害性激活引起的持续致敏。这个过程导致了与疼痛和非疼痛行为相关的几个大脑网络的变化。第二种机制是内源性脑干抑制控制减少,从而增加三叉神经概念系统和大脑皮层神经元的兴奋性。疼痛基质连通性的增加,包括下丘脑过度活跃和血清素能系统的减弱,可能导致偏头痛的慢性化。
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Neurobiology of migraine progression

Chronic migraine is one of the most devastating headache disorders. The estimated prevalence is 1.4–2.2% in the population. The factors which may predispose to the process of migraine progression include high frequency of migraine attacks, medication overuse, comorbid pain syndromes, and obesity. Several studies showed that chronic migraine results in the substantial anatomical and physiological changes in the brain. Despite no clear explanation regarding the pathophysiologic process leading to the progression, certain features such as increased sensory sensitivity, cutaneous allodynia, impaired habituation, identify the neuronal hyperexcitability as the plausible mechanism. In this review, we describe two main mechanisms which can lead to this hyperexcitability. The first is persistent sensitization caused by repetitive and prolonged trigeminal nociceptive activation. This process results in changes in several brain networks related to both pain and non-pain behaviours. The second mechanism is the decrease in endogenous brainstem inhibitory control, hence increasing the excitability of neurons in the trigeminal noceptive system and cerebral cortex. The combination of increased pain matrix connectivity, including hypothalamic hyperactivity and a weak serotonergic system, may contribute to migraine chronification.

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来源期刊
Neurobiology of Pain
Neurobiology of Pain Medicine-Anesthesiology and Pain Medicine
CiteScore
4.40
自引率
0.00%
发文量
29
审稿时长
54 days
期刊最新文献
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