Electrical synapses in the brain offer new avenue for epilepsy research and possible treatment

Dr. Philippe Coulon thinks electrical signals directly exchanged between brain cells may hold promise as a potential target for absence epilepsy treatments.

A child with absence epilepsy may be in the middle of doing something—she could be dancing, studying, talking—when all of a sudden she stares off into space for a few moments. Then, as quickly as she drifted off, the child snaps back into whatever she was doing, unaware that the episode occurred.

That brief moment of disconnect from reality is called an absence seizure, and according to the Epilepsy Society, childhood absence epilepsy accounts for 2-8% of all epilepsy diagnoses. Most cases of childhood absence epilepsy end after puberty, but about 30% of cases continue into adulthood or lead to other forms of epilepsy, says Dr. Philippe Coulon, a neuroscientist at Seattle Children’s Research Institute.

“Some kids can have hundreds of these brief seizures a day,” said Coulon. “I can only imagine how hard it is for them to function and have a normal childhood.”

In a study published in the Journal of Physiology, Coulon and his colleagues suggest that electrical signals directly exchanged between brain cells may hold promise as a potential target for absence epilepsy treatments.

“This research is important in helping us understand how epilepsies work, how they manifest and what possibilities there are in treating them,” Coulon said. “There has been a debate about whether the cortex or the thalamus is the origin of absence seizures. This research once again shows that the thalamus is an important contributor.”

How brain cells communicate

Brain cells use chemicals and electricity to communicate and send signals to each other. In people with epilepsy, the communication between brain cells becomes abnormal, disrupted or excessive and this can lead to seizures.

Drugs to treat epilepsy target brain cells to reduce or stop the abnormal activity. Coulon studies electrical synapses, which are not as well-understood as chemical synapses, but are also modifiable and can be targeted. Existing epilepsy drugs target ion channels or chemical synapses to reduce the signaling between brain cells.

Animation of a Neuron
This 3D animation shows neurons directly connected by electrical synapses in the studied region of the rat brain.

“It’s not fully understood what function electrical synapses serve in the brain, but we believe they may play a role in the control of consciousness and attention,” Coulon said. “They could act like a resonance feedback system that enables stable rhythms in the brain, and they may connect neuronal networks to create very fast information transfer,” he said.

Coulon, Dr. Denise Kohmann and their colleagues describe in the study how electrical synapses in epileptic animal models behave differently than in healthy animals: Electrical synapses in epileptic animals weakened when the cells were active, a process called neuroplasticity. When they blocked these electrical synapses, it was effective in reducing epileptic activity. They focused on an area of the brain important for selective attention, sleep and alertness.

Next steps in the research

Coulon now wants to determine if the observed plasticity exists in other parts of the brain besides the thalamus and whether blocking electrical synapses is effective in halting epileptic activity in other brain regions. Coulon says that while current epilepsy drugs focus either on changing neuronal activity or on changing the chemical signaling between neurons, there may also be effective ways to target electrical synapses.

“If we can verify that these direct electrical links between neurons play a role in the development of epileptic seizures, this could lead to new lines of research for treatments and new classes of drugs to consider,” he said.

This research was funded by Innovative Medical Research in Muenster, Germany.

Resources

  • Study, Journal of Physiology
  • Dr. Philippe Coulon, Seattle Children’s Research Institute
  • Seattle Children’s Epilepsy Program