Striatum Rhesactome Regulates Amphetamine Induced Motor Activity
A specific signaling circuit in the brain is deeply involved in motor activity, scientists from the Florida campus of The Scripps Research Institute have found.
The new findings that could have an impact the development of therapies for a number of currently untreatable brain disorders such as Parkinson’s and Huntington’s diseases.
Despite many advances, the precise signaling mechanisms that regulate motor function in the striatum, that part of the brain responsible for motor activity, remain unknown. The new study identified for the first time a protein interaction network that helps control these functions by inhibiting the signaling of dopamine, a neurotransmitter involved in regulating movement.
RasGRP1-Rhes Signaling Circuit
The study, which was led by The Scripps Research Institute’s Associate Professor Srinivasa Subramaniam, focused on amphetamine-induced activity affected by what is known as RasGRP1-Rhes signaling circuitry.
“A pair of proteins operates through a protein-protein interaction network, what we call a ‘Rhesactome’, in the striatum,” Subramaniam said. “This may have much broader implications in neurological, psychiatric and addictive disorders. Drugs that bind to either of these proteins may have therapeutic benefits for the diseases that affect this part of the brain.”
Drugs like amphetamine, which trigger dopamine release in the striatum, enhance locomotor activity. Rhes acts as a kind of brake on the amphetamine-induced locomotion.
In order for normal motor activity to occur, the RasGRP1 and other protein partners in the Rhesactome network induced by amphetamine have to block Rhes. It is the calibrated interaction of Rhes with the protein RasGRP1 that adjusts striatal control of motor functions.
In the study, the researchers succeeded in using RasGRP1 to inhibit Rhes-mediated control of striatal motor activity in animal models. Animal models that were Rhes-deficient had a much stronger active behavioral response to amphetamines.
But all that changed if RasGRP1 was depleted.
“It’s a delicate and highly complex relationship,” Subramaniam said. “Imagine that you are running. This protein complex carefully controls that motor function by modulating the effect of Rhes. That’s why you need to have the double control elements of both RasGRP1 and Rhes to fine-tune those motor functions. Our study captures this dynamic complex, so that now for the first time we can biochemically visualize it at the network level.”
What remains unknown at this point is how RasGRP1 actually modulates Rhes.
“We speculate that both transcriptional and post-transcriptional mechanisms are involved. Considering that the Rhes protein is enhanced predominantly at synaptic locations, one intriguing possibility is that RasGRP1 regulates local translation of Rhes messenger RNA at the synapse,”
said The Scripps Research Institute staff scientist Neelam Shahani, the first author of the study.