In a breakthrough, researchers including an Indian-origin scientist have discovered a novel way to turn an old brain young by flipping a single molecular switch.
The flip of a single molecular switch helps create the mature neuronal connections that allow the brain to bridge the gap between adolescent impressionability and adult stability.
Now Yale School of Medicine researchers have reversed the process, recreating a youthful brain that facilitated both learning and healing in the adult mouse.
Scientists have long known that the young and old brains are very different. Adolescent brains are more malleable or plastic, which allows them to learn languages more quickly than adults and speeds recovery from brain injuries.
The comparative rigidity of the adult brain results in part from the function of a single gene that slows the rapid change in synaptic connections between neurons.
By monitoring the synapses in living mice over weeks and months, Yale researchers have identified the key genetic switch, reported in the journal Neuron.
The Nogo Receptor 1 gene is required to suppress high levels of plasticity in the adolescent brain and create the relatively quiescent levels of plasticity in adulthood.
In mice without this gene, juvenile levels of brain plasticity persist throughout adulthood. When researchers blocked the function of this gene in old mice, they reset the old brain to adolescent levels of plasticity.
"These are the molecules the brain needs for the transition from adolescence to adulthood," said Dr Stephen Strittmatter, senior author of the paper.
"It suggests we can turn back the clock in the adult brain and recover from trauma the way kids recover," Strittmatter said in a statement.
Rehabilitation after brain injuries like strokes requires that patients re-learn tasks such as moving a hand.
Researchers including Sarah M Bhagat, Pujan R Patel and William BJ Cafferty found that adult mice lacking Nogo Receptor recovered from injury as quickly as adolescent mice and mastered new, complex motor tasks more quickly than adults with the receptor.
"This raises the potential that manipulating Nogo Receptor in humans might accelerate and magnify rehabilitation after brain injuries like strokes," said Feras Akbik, Yale doctoral student and first author of the study.
