The disorder can present itself as a single seizure that lasts longer than 30 minutes or a series of seizures between which the person doesn’t regain consciousness. If it doesn’t stop quickly, even one episode can cause brain damage, loss of cognitive function, and memory loss.
Darwin J. Prockop, chair in genomic medicine and professor at the Texas A&M College of Medicine and co-senior author, said:
“Saving the brain from injury and disease is certainly one of the holy grails of medicine. Our paper suggests one way that this might be done, and not by a procedure that requires brain surgery or even injection into a vein: All that would be required is a nasal spray that a patient might receive in a doctor’s office.”
Researchers tested the efficiency of these exosomes in a status epilepticus model with damage from a period of acute seizures.
“What is remarkable is that the animal models were rescued from long-term effects of the seizure-induced brain injury by a nasal spray of exosomes,” Prockop says.
It was able to ease inflammation of the neurons, prevent cognitive and memory dysfunction, and stop abnormal neurogenesis in the hippocampus, a vital part of the brain responsible for memory, Ashok K. Shetty, professor of molecular and cellular medicine and co-senior author of the paper, said:
“We gave the intranasal vesicle spray twice over 24 hours, the first one at two hours after the onset of a status epilepticus episode, and such treatment was effective at reducing multiple adverse effects on the hippocampus. In fact, the vesicles were able to move to the hippocampus in six hours, and their neuroprotection was enough to prevent loss of normal cognitive and memory function as well as abnormal neurogenesis, one of the substrates involved in formation of new memories.”
Post Seizure Brain Protection
Drugs like benzodiazepines, which are tranquilizers, and hydantoins, a type of anticonvulsant, are used to stop status epilepticus episodes, but they are often unavailable—especially if the person hadn’t previously been diagnosed with epilepsy, which is the case 75 percent of the time. Further, they are ineffective perhaps as much as 30 percent of the time.
“There really hasn’t been anything noninvasive like this to stop the cascade of inflammation and abnormal neuronal wiring or epileptogenesis that occurs after a status epilepticus event,” Shetty says. “These vesicles do seem able to protect the brain after seizures, stop neuroinflammation, and prevent the development of chronic epilepsy that often results without this treatment.”
Although the findings are promising, the researchers urge caution before jumping to conclusions about a treatment for humans with seizures.
“Before this therapy can safely be tested in patients, we need to do great deal of further work,” Prockop says. “But the inflammation in the brain caused by acute seizures is similar to the inflammation seen in the late stages of other brain diseases, including Alzheimer’s disease, parkinsonism, multiple sclerosis, and traumatic injuries,” Shetty adds. “Therefore, the promise of this new therapy is enormous.”
Qianfa Long, Dinesh Upadhya, Bharathi Hattiangady, Dong-Ki Kim, Su Yeon An, Bing Shuai, Darwin J. Prockop, and Ashok K. Shetty
Intranasal MSC-derived A1-exosomes ease inflammation, and prevent abnormal neurogenesis and memory dysfunction after status epilepticus
PNAS 2017 ; published ahead of print April 10, 2017, doi:10.1073/pnas.1703920114
Image: robin_24, CC BY 2.0
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