Preventing excessive neurogenesis or the synthesis of nerve cells after brain injury could prevent seizures.
After a traumatic head injury the excessive burst of new brain cells that scientists have traditionally believed helped in recovery could instead lead to epileptic seizures and long-term cognitive decline, according to a new Rutgers New JerseyMedical School study. Viji Santhakumar, associate professor in the department of Pharmacology, Physiology and Neuroscience, and her colleagues, challenge the prevailing assumption by scientists in the field that excessive neurogenesis (the birth of new brain cells) after injury is advantageous.
‘The excess new neurons that grow after a head injury can lead to epileptic seizures and could contribute to cognitive decline.’
"There is an initial increase in birth of new neurons after a brain injury but within weeks, there is a dramatic decrease in the normal rate at which neurons are born, depleting brain cells that under normal circumstances should be there to replace damaged cells and repair the brain's network," said Santhakumar. In the United States an estimated 1.7milllion people sustain a TBI each year, making the condition a major cause of death and disability. Symptoms can include impaired thinking or memory, personality changes and depression and vision and hearing problems as well as epilepsy. About 80 percent of those who develop epilepsy after a brain injury have seizures within the first two years after the damage occurs.
Santhakumar said while researchers who study epilepsy have started to look more closely at how preventing excessive neurogenesis after brain injury could prevent seizures, neuroscientists have traditionally viewed the process as helpful to overall brain recovery.
Studying laboratory rats, Rutgers scientists found, however, that within a month after experimental brain injury, the number of new brain cells declined dramatically, below the numbers of new neurons that would have been detected if an injury had not occurred.
When scientists were able to prevent the excessive neurogenesis which occurs within days of the injury with a drug similar to one under trial for chemotherapy treatments, the rate of birth of new brain cells went back to normal levels and risk for seizures was reduced.
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While the regenerative capability of brain cells, in the hippocampus - the part of the brain responsible for learning and memory - slows down as part of the aging process, the Rutgers scientists determined that the process that occurred after a head injury was related to injury and not age.
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Source-Eurekalert