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Overview

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by Felix C.

Describe the pathophysiology.

  • The pathophysiology of migraine is not fully understood.

  • Various factors are thought to contribute to the development and severity of migraines.

    • Activation of meningeal nociceptors

      • Dilatation of intracranial blood vessels → activation of meningeal nociceptors

      • Activation of the trigeminovascular pathway: activation of trigeminal neurons → release of vasoactive neuropeptides such as substance P or calcitonin gene-related peptide (CGRP) → vasodilatation and release of proinflammatory molecules (histamine, bradykinin, serotonin, prostaglandins) → neurogenic inflammation → activation of meningeal nociceptors [6]

      • Cortical spreading depression: excitation and inhibition of the cerebral cortex → changes in cortical enzymatic activity (proinflammatory molecules) → neurogenic inflammation → activation of meningeal nociceptors [7]

    • Dysregulation of pain sensitization in the trigeminal system (CN V): cortical spreading depression → dysregulation of trigeminovascular neurons → neurogenic inflammation → hypersensitization → nausea, loss of appetite, yawning, fatigue, anxiety, depression [8]

    • Genetic predisposition: in individuals with migraine, the brain does not have the ability to habituate itself to external stimuli (e.g., stress, hormonal changes) → hyperexcitable brain [7]

    • Activation of the autonomic nervous system: external physiological and emotional stimulation (e.g., hormonal changes, stress) → hypothalamic response to the change in homeostasis → hypothalamic neurons influence the autonomic nervous system → shift toward a parasympathetic tone → constriction and dilatation of intracranial, especially the meningeal, blood vessels [7]

Vasodilatation is now considered an epiphenomenon rather than the primary cause of migraine headache.

Author

Felix C.

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