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Researchers discover a new migraine-associated mechanism

The researchers Alba Andrés-Bilbé and Xavier Gasull, from the Faculty of Medicine and Health Sciences, the Institute of Neurosciences of the University of Barcelona (UBNeuro) and the IDIBAPS Research Group on Neurophysiology.

The researchers Alba Andrés-Bilbé and Xavier Gasull, from the Faculty of Medicine and Health Sciences, the Institute of Neurosciences of the University of Barcelona (UBNeuro) and the IDIBAPS Research Group on Neurophysiology.

Episodes of migraine are related to a higher electric irritability of sensorial neurons.

Episodes of migraine are related to a higher electric irritability of sensorial neurons.

28/03/2019

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A mutation in the gen that codes the ionic channel TRESK –involved in the control of neuron irritability- causes the dysfunction of some neurons that increase neuronal activity and induce migraine pain.

This is the main conclusion of a new study published in the journal Neuron, in which the experts Xavier Gasull and Alba Andrés-Bilbé, from the Faculty of Medicine and Health Sciences, the Institute of Neurosciences of the University of Barcelona (UBNeuro) and the IDIBAPS Research Group on Neurophysiology- have taken part. 

 

Migraine, one of the most common neurological disorders


Migraine is a neurological disorder affecting about 15 % of the population, with a genetic, environmental and hormonal basis. This pathology causes continuous and severe episodes of headache, and in some cases it also causes nausea, vomiting, and photophobia. About 80 % of the cases are considered migraine without aura, and the other 20 % are episodes in which the headaches are preceded by transitory neurological symptoms that are visual (migraine with aura).


Despite the high prevalence of this headache, “many of the genetic causes and physiopathological mechanisms are still unknown, which makes it harder to find efficient treatments”, notes Xavier Gasull.

 

 


Ionic channels: controlling neuronal irritability


Episodes of migraine are related to a higher electric irritability of sensorial neurons. Electric activity is controlled by proteins –ionic channels- that ease or inhibit the activation of neurons. The study, in particular, focuses on TRESK and TREK ionic channels, which are found in sensorial neurons and stop the excessive neuronal activation.


According to the conclusions, a mutation in the gene that codes the TRESK ionic channel leads to a dysfunctional protein, which alters the ability of the channel to reduce electric activity. At the same time, this mutation generates another altered protein affecting the physiological function of other ionic channels such as TREK1. Finding a mechanism with which the mutation creates two dysfunctional proteins –a process which may be shared with other genetic pathologies- provides new perspectives to be explored in the future.
“Paradoxically, other mutations that removed the TREK protein but did not cause migraine had been described. In the new study, we prove the combination of both factors necessary to have a higher electric activation of sensorial neuros, which causes the typical migraine pain”, notes Xavier Gasull.


The new study, coordinated by the researcher Guillaume Sandoz, from the University of Nice and the French National Centre for Scientific Research (CNRS), will open new pathways to design future therapeutic strategies to treat migraine, and is a significant progress to know the mechanisms that cause episodes of migraine with aura, which are so far unknown.
 

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