Removal Of Molecule in Brain Found to Improve Memory Formation Dramatically

Monday, November 17, 2014

Fragile X Related Protein 1

 Neuroscience
A new study has identified new player in brain function and memoryWhen the scientists removed a molecule from the brains of mice, they found memory-creation molecules flourished. 




R esearchers have identified a molecule that regulates brain processing and found that when it is removed, brain function and memory recall is improved.

The study was published in the latest issue of Cell Reports, and has implications for neurodevelopmental and neurodegenerative diseases, such as autism spectral disorders and Alzheimer’s disease.

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“Previous research has shown that production of new molecules is necessary for storing memories in the brain; if you block the production of these molecules, new memory formation does not take place,” says RI-MUHC neuroscientist, Dr. Keith Murai, the study’s senior author and Associate Professor in the Department of Neurology and Neurosurgery at McGill University. “Our findings show that the brain has a key protein that limits the production of molecules necessary for memory formation. When this brake-protein is suppressed, the brain is able to store more information.”

"Our findings show that the brain has a key protein that limits the production of molecules necessary for memory formation. When this brake-protein is suppressed, the brain is able to store more information."


Murai and his colleagues used a mouse model to study how changes in brain cell connections produce new memories.  They showed that a protein, FXR1P (Fragile X Related Protein 1), was responsible for suppressing the production of molecules required for building new memories.

When FXR1P was removed from certain parts of the brain, new molecules were produced that strengthened connections between brain cells and this correlated with improved memory and recall in the mice.

“The role of FXR1P was a surprising result,” says Dr. Murai. “Previous to our work, no-one had identified a role for this regulator in the brain. Our findings have provided fundamental knowledge about how the brain processes information. We’ve identified a new pathway that directly regulates how information is handled and this could have relevance for understanding and treating brain diseases.”

“Future research in this area could be very interesting,” he adds. “If we can identify compounds that control the braking potential of FXR1P, we may be able to alter the amount of brain activity or plasticity. For example, in autism, one may want to decrease certain brain activity and in Alzheimer’s disease, we may want to enhance the activity."

 Apart from the benefits to medicine research like this may, one day extend basic human capabilities.  Murai says, "By manipulating FXR1P, we may eventually be able to adjust memory formation and retrieval, thus improving the quality of life of people suffering from brain diseases.”


SOURCE  McGill University

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