HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Migraine and the Mu-opioidergic system-Can we directly modulate it? Evidence from neuroimaging studies.

Abstract
Migraine is a chronic trigeminal pain condition that affects the daily lives of a large part of our population. Its debilitating headache attacks, with increased sensitivity to multiple forms of stimuli, force many patients to rely on over the counter analgesics and resort to abuse of prescription medications, particularly opioid agonists. In the latter case, the indiscriminate medication-driven activation of the opioid system can lead to undesired side effects, such as the augmentation of hyperalgesia and allodynia, as well as the chronification of the attacks. However, we still lack information regarding the impact of migraine attacks and their relief on the function of μ-opioid receptor (μOR) mediated neurotransmission, the primary target of opioid medications. This line of inquiry is of particular importance as this neurotransmitter system is arguably the brain's most important endogenous mechanism involved in pain regulation, and understanding this endogenous mechanism is crucial in determining the effectiveness of opioid medications. Recently, new advances in molecular neuroimaging and neuromodulation have provided important information that can elucidate, in vivo, the role of the endogenous opioid system in migraine suffering and relief.
AuthorsAlexandre F DaSilva, Thiago D Nascimento, Marcos F DosSantos, Jon-Kar Zubieta
JournalCurrent pain and headache reports (Curr Pain Headache Rep) Vol. 18 Issue 7 Pg. 429 (Jul 2014) ISSN: 1534-3081 [Electronic] United States
PMID24842566 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Analgesics, Opioid
  • Neurotransmitter Agents
  • Receptors, Opioid, mu
Topics
  • Analgesics, Opioid (therapeutic use)
  • Humans
  • Magnetic Resonance Imaging
  • Migraine Disorders (drug therapy, physiopathology)
  • Neuroimaging
  • Neurotransmitter Agents (therapeutic use)
  • Pain (drug therapy, physiopathology)
  • Positron-Emission Tomography
  • Receptors, Opioid, mu (drug effects)
  • Synaptic Transmission (drug effects)
  • Treatment Outcome

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: