University at Buffalo scientists have discovered a tiny piece of a critical receptor that fuels the brain as a promising new drug target for Alzheimer's and other neurodegenerative diseases.
"This is the first time that this site has been shown to be useful as a drug target," says Gabriela K. Popescu, Ph.D., associate professor of biochemistry in UB's School of Medicine and Biomedical Sciences and senior author on the study. The research on the NMDA (N-methyl-D-aspartate) receptor was published online October 11 in Nature Communications.
"If we could find a drug that attaches itself to this site and locks together NMDA receptor subunits, that would be huge for fighting disability from stroke, Alzheimer's, and other neurodegenerative diseases," Popescu said.
The research focuses on the brain's receptors for the neurotransmitter, glutamate, which is implicated in these diseases as well as in other conditions, such as glaucoma. The two main glutamate receptors in the brain are NMDA and AMPA receptors, both of which play critical roles in human learning and memory. Both types of receptors are made of four subunits and within each receptor these subunits are organized in pairs called dimers.
Because these receptors are similar in structure, scientists had assumed that they function in much the same way.
"But when we altered the dimer interface, the site where two subunits come together within each pair, we found that the NMDA receptor works just the opposite of the way that the AMPA receptor works," Popescu said. "Cementing this interface in AMPA receptors leads to more activity, whereas we found just the opposite to be true in NMDA receptors."
By locking the subunits together, the UB researchers were able to achieve a marked reduction in NMDA activity and, subsequently, a marked reduction in the amount of calcium that enters neurons in response to the neurotransmitter glutamate. Calcium overload due to overactive NMDA receptors is what eventually kills off neurons, Popescu said, leading to the symptoms that occur after a stroke, and in Alzheimer's and other neurodegenerative diseases.
"The fact that by cross-linking the subunits, we could so dramatically reduce NMDA receptor activation demonstrates, for the first time, the tantalizing possibility that we may be able to develop new therapies that can much more effectively treat, or even one day prevent, some of these devastating diseases, like Alzheimer's and stroke," Popescu says.
And, because each type of NMDA receptor has a slightly different dimer interface, Popescu says, this finding represents a new opportunity for rationally designing drugs that would preferentially inhibit only a select population of NMDA receptors in the brain, thus reducing the possibility of side effects.
Currently, the Alzheimer's drug called Namenda, one of the only existing pharmaceuticals that inhibit the NMDA receptor, targets a different site within the receptor.
"If a new drug could be developed to target the dimer interface, which we discovered to be inhibitory, it would allow more specific effects than current drugs," Popescu said. "That's because at this particular interface, the interactions between these subunit interfaces are more precise than those currently being targeted."
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