Our brains are constantly bombarded with sensory information. The ability to distinguish relevant information from irrelevant distractions is a critical skill, one that is impaired in many brain disorders. By studying the visual system of humans and animals, Robert Desimone has shown that when we attend to something specific, neurons in certain brain regions fire in unison – like a chorus rising above the noise – allowing the relevant information to be “heard” more efficiently by other regions of the brain.
Desimone is interested in how the brain deals with the challenge of information overload. Just as our world buzzes with distractions, the neurons in our brain are constantly bombarded with messages. Some messages contain relevant information, but many do not. By studying the visual system of humans and animals, Desimone has shown that relevant information is selectively amplified in certain brain regions, while irrelevant information is suppressed. One reason this happens is that neurons whose activity reflects the relevant information become synchronized with one another. The rhythmic activity produced by a group of synchronized neurons resembles a chorus chanting a tune that rises above the background chatter of the crowd. This synchronized chanting allows the relevant information to be ‘heard’ more efficiently by other brain regions.
Desimone’s work also suggests that the prefrontal cortex – a brain region known to be involved in planning and executive control of behavior – most likely serves as the conductor of this neural chorus. The prefrontal cortex provides a top-down signal that coordinates rhythmic activity across multiple brain regions. Desimone suspects this pattern of rhythmic activity is not just specific to attention, but could also represent a more general mechanism for communication between different parts of the brain.
Sometimes, distraction can be a good thing — a train barreling towards us should grab our attention regardless of what else we’re doing. But these kinds of “bottom-up” distractions must be balanced against the need to stay on message. If this balance is disrupted, many aspects of life may be impaired as a result. Desimone believes that altered neural synchrony may underlie many brain disorders that disrupt attention – such as attention deficit disorder, Parkinson’s disease, and schizophrenia – and that searching for ways to enhance synchrony may be a useful strategy for developing new treatments for these conditions.
Robert Desimone is director of the McGovern Institute and the Doris and Don Berkey Professor in the Department of Brain and Cognitive Sciences. Prior to joining the McGovern Institute in 2004, he was director of the Intramural Research Program at the National Institutes of Mental Health, the largest mental health research center in the world.
Honors and Awards
Member, National Academy of Sciences
Member, American Academy of Arts and Sciences
Kavli Distinguished Career Award of the Cognitive Neuroscience Society, 2020
Patricia Goldman Rakic Prize of the Brain and Behavior Research Foundation, 2020
Secretary, Society for Neuroscience, 2016-2019
Helmholtz Prize, International Neural Network Society, 2009
Fellow, Association for Psychological Science, 2007
Outstanding Mentor Award, Asian and Pacific Americans DHHS Employee Association, 2004
Recognition Award, NIH Hispanic Employees Association, 2002
Fellow, American Association for the Advancement of Science, 1999
Golden Brain Award of the Minerva Foundation, 1994
US Public Health Service Superior Service Award, 1994
Fleming Award for Scientific Achievement and Service, 1991
Troland Prize, National Academy of Sciences, 1990
The effects of visual stimulation and selective visual attention on rhythmic neuronal synchronization in macaque area V4. Fries, P, Womelsdorf T, Oostenveld R, and Desimone R. (2008).
Journal of Neuroscience 28, 4823-4835.
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Mendoza-Halliday, D, Xu, H, Azevedo, FAC, Desimone, R. Dissociable neuronal substrates of visual feature attention and working memory. Neuron. 2024; :. doi: 10.1016/j.neuron.2023.12.007. PubMed PMID:38228138 .