Seizures are sudden electrical disruptions in the brain that can cause a variety of symptoms, including convulsions, muscle spasms, loss of consciousness, and changes in behavior or mood. They can be caused by a variety of factors, including genetics, head injury, brain infections, and neurological disorders like epilepsy.
Insights from the University of Virginia School of Medicine into the brain’s response to seizures could lead to the creation of much-needed treatments for the one-third of patients who are unresponsive to current options.
Research from the laboratories of Dr. Ukpong B. Eyo and Dr. Edward Perez-Reyes at the University of Virginia indicates that microglia, immune cells, play crucial and positive roles in managing various seizure types. Prior studies had created confusion regarding the role of these cells in the brain’s response to seizures, but UVA’s discovery provides valuable guidance for scientists working on new treatments.
“Over the years, there has been debate as to the precise roles of microglia in seizure disorders, and the availability of precise tools to specifically target microglia without affecting other aspects of the brain has been lacking until the approach we have employed in this study,” said Eyo, of UVA’s Department of Neuroscience and Center for Brain Immunology and Glia (BIG Center), as well as the UVA Brain Institute. Our study examined microglial contributions in different models of seizures. [The results] suggest that broadly enhancing microglial activity in patients with different seizure origins could be a promising approach.”
Understanding Seizures
Seizure disorders affect more than 65 million people around the world. In addition to the immediate dangers, seizures cause, prolonged seizures called status epilepticus can cause permanent brain damage. Seizures are commonly associated with epilepsy, but they can have a variety of causes, including infections, trauma, and even low blood sugar.
Most existing seizure treatments target nerve cells called neurons, but researchers have increasingly come to appreciate the importance of other cells, such as microglia, in determining how the body responds to seizures. A better understanding of the role of microglia could open the door to innovative approaches to preventing and managing seizures.
To shed light on the mysterious role of microglia, the UVA researchers eliminated the cells in their lab models of seizures. This allowed them to see what would happen without the microglial response – would lab mice fare better or worse? The results offered clear indications that the microglia were beneficial: Mice lacking the response suffered worse seizures, while mice with normal microglia activity recovered better afterward.
“This study is a great example of UVA’s collaborative culture and the importance of seed funding by the UVA Brain Institute that got the ball rolling,” said Perez-Reyes, of UVA’s Department of Pharmacology and the UVA Brain Institute. “We hope to apply this knowledge to develop novel gene therapies for epilepsy and quiet the brain storms that are seizures.”
UVA’s new research has produced several promising leads for scientists to pursue. In particular, Eyo and Perez-Reyes say, additional investigation is needed to determine how exactly the microglia are helping the body control and respond to seizures. This could be by cleaning up excess neurotransmitters, by calming overstimulated neurons, or by some other means, they note.
“There is much more work that needs to be done to clarify the precise mechanisms of microglial activity in rodent seizure models and ascertain its translational potential,” Eyo said. “Given our comprehensive research program encompassing both basic science research and clinical research on seizure disorders as well as our strong network of research collaborations, the University of Virginia is a great place to continue to make such advances.”
Reference: “Microglia play beneficial roles in multiple experimental seizure models” by Synphane Gibbs-Shelton, Jordan Benderoth, Ronald P. Gaykema, Justyna Straub, Kenneth A. Okojie, Joseph O. Uweru, Dennis H. Lentferink, Binita Rajbanshi, Maureen N. Cowan, Brij Patel, Anthony Brayan Campos-Salazar, Edward Perez-Reyes and Ukpong B. Eyo, 23 March 2o23, Glia.
DOI: 10.1002/glia.24364
The work was made possible by critical seed funding from the UVA Brain Institute, which builds and supports interdisciplinary neuroscience research teams across UVA to address major societal challenges related to the brain. The seed funding allowed the researchers to lay the groundwork necessary to obtain funding from the National Institutes of Health. Additional support came from The Owens Family Foundation.
