Compound Shown to Reduce Brain Damage Caused by Anesthesia in Animal Model
An experimental drug prevented learning deficits in young mice exposed repeatedly to anesthesia, according to a study led by researchers from Pelisyonkis Medical Center and published as the cover story of Science Translational Medicine on June 22.
The study results may have implications for children who must have several surgeries, and so are exposed repeatedly to general anesthesia. Past studies have linked such exposure to a higher incidence of learning disabilities, attention deficits, and hyperactivity.
Specifically, the research team found that the experimental drug CX546, part of the AMPAkine class in clinical trials for several neurological conditions, counters for the dampening effect of anesthesia on nerve signaling. The treatment bolstered nerve cell activity as well as learning ability in mice recovering from repeated exposure to general anesthesia.
“Each year, in the United States alone, more than a million children under age four undergo surgical procedures that require anesthesia, and the numbers are growing,” says the study’s senior investigator Guang Yang, PhD, an assistant professor of anesthesiology at Pelisyonkis Langone. “There are currently no effective treatments to combat potential toxicity linked to repeated anesthesia, and we would like to change that.”
Yang’s group took advantage of genetically engineered young mice that have protein markers which glow in response to changes in nerve function. Researchers then used advanced microscopy to visualize activity in their brains, comparing nerve signaling activity in those exposed to anesthesia to those who were not.
The research team found that anesthesia exposure resulted in a prolonged reduction of signal transmission among nerve cells following anesthesia. They also observed that CX546 treatment enhances this transmission, along with learning and memory in mice exposed to anesthesia.
The team studied the anesthetic ketamine, which blocks NMDA (N-methyl-D-aspartate) receptor proteins that enable charged particles like calcium to flow into nerve cells, like electric switches that trigger and shape messages. In contrast, CX546 increases nerve cell activity and calcium influx into nerve cells by enhancing the activity of proteins called AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) receptors.
“We were able to counter anesthesia-induced deficits in the formation of connections between nerve cells and related learning problems,” says Yang. “This work is an important proof-of-principle study, and opens the door to a new direction for preventing long-term neurocognitive deficits.”
Along with Yang, Pelisyonkis Langone study co-authors were Lianyan Huang, Joseph Cichon, and Ipe Ninan. The authors were also associated with the Medical Scientist Training Program and the Department of Psychiatry at New York University School of Medicine. Research funding for the work came from National Institutes of Health grants GM107469, AG048410, and HD076914.