A study shows how brains are able to multitask

What’s actually going on inside our brains that allows for us to strategically focus on one task over another? Researchers at New York University published a paper in the journal Nature saying they identified one small region of the brain, the thalamic reticular nucleus (TRN),as the one that controls our ability to multitask.
 
Working as a task "switchboard", the TRN enables our brains to focus on the sensory stimulus that is most vital at any given moment. Now, with a better understanding of how the process works, researchers hope to use the information to study diseases in which multitasking or sensory overload goes awry, autism, schizophrenia, and ADHD, for example.
 
“We have identified the [TRN] as a station. That is something that hasn’t really been described in the past, says Michael Halassa, a neuroscientist at NYU who led the research. “Now we can answer questions like whether individuals with autism have a broken TRN or potentially develop drugs that target [it].”
 
The ability to multitask is a vital part of life, as it’s needed to perform everyday functions like driving, cooking, or even socializing with a group of friends. But at any given time, our brains are bombarded with a multitude of sensory information, and we’re forced to decide what’s important in that instant, focus on it, and tune out everything else. Researchers have known about this process for years, but they weren’t sure exactly how it worked because they couldn’t come up with a reliable experiment for identifying what parts of the brain were involved.
 
Back in the 1980s, Francis Crick had hypothesized that the TRN, a small, shell-shaped region located deep in the brain, helped the brain decide what sensory information to focus on and what to tune out. But at the time, he had little evidence to back that idea up.
 
Fast forward to today, and researchers at NYU were able to test Crick’s hypothesis. By putting laboratory mice through a game-like experiment, they were able to show that different neurons within the TRN regulated which senses the brain should focus on and which should be set aside.
 
The experiment involved training mice to respond to a specific sensory stimulus, either light or sound. If the mice observed and followed the correct stimulus, they received milk as a reward. At the same time, the researchers would attempt to distract the mice with the opposite stimulus (the mice trained to respond to light would be distracted with sound, for example).
 
In real time, the researchers would record electrical signals that came from the TRN neurons in the mice’s brain. They were also able to inactivate various parts of the neural network, specifically the prefrontal cortex, which seeks out certain stimulus over others.
 
When the mice were trained to pay attention to a particular sound and ignore light, the TRN neurons that control vision were highly active, meaning that they were suppressing visual signals so that the mice could focus more intensely on the sound. The opposite happened when they were trained to follow the light in order to receive their milk reward.
 
Further, when the researchers inactivated the prefrontal cortex, the area of the brain responsible for higher level functioning, using a laser beam, the TRN neural signaling went completely out of whack. This shows that the prefrontal cortex stores incoming sensory information, which the TRN then uses to suppress or not suppress certain senses, much in the same way that a switchboard works, explains Halassa.
 
Halassa and his team hope to use this new understanding of the brain’s wiring to figure out what goes wrong in certain diseases that are characterized by overstimulation, in particular autism, ADHD, and schizophrenia.
 
“One commonality in patients with these disorders is that they have a really hard time suppressing [distracting stimuli],” says Halassa.