July/August 2008
Rethinking Thought
A theory that Christopher Moore, PhD '98, kept under his hat for more than a decade could change the way neuroscientists understand the dynamics of perception.
By Katherine Bourzac, SM '04
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Credit: Dana Smith
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Christopher Moore was teaching a group of doctors about
functional magnetic resonance imaging (fMRI) 13 years ago when it dawned on him
that he didn't really believe what he was saying. A common brain-scanning
technique, fMRI allows doctors and researchers to see local changes in blood
flow, indicating where information processing is most active. Moore, who was at
MIT working on his PhD in neuroscience at the time, told the doctors that blood
was rushing to those areas to resupply hungry neurons with the oxygen and sugar
their work was consuming. But it seemed to Moore that metabolism alone couldn't account
for the volume of blood showing up in the scans. "This makes no sense," he
thought. "There must be something else going on beyond just metabolism."
The more he pondered the fMRI signal, the more it seemed to
him that blood was not merely feeding neurons but directly helping neurons
process information. He wasn't yet in a position to test his hypothesis, but he
knew that if he could prove it, it could change neuroscience. Now, new research
suggests that he may have been right.
Because different regions of the brain are responsible for
different kinds of information processing, the sensitivity of their
circuitry--even the sensitivity of individual neurons--changes in response to new
stimuli. That's what makes it possible for us to react to the world around
us--to come up with a witty riposte or hit a fastball, as the occasion demands. Moore thinks that
increases and decreases in blood flow contribute to these shifts in
sensitivity; that blood and neurons work hand in hand to produce perception and
cognition. Given that neuroscientists have always attributed information
processing to neurons alone, the notion that blood helps us think is radical.
It also has practical implications. If Moore is right, many brain disorders might be
treatable in new ways. Drugs or devices that control blood flow, for instance,
could be used to control problems, such as epileptic seizures, that can result
when neurons become oversensitive.
To test whether blood modulates the sensitivity of neurons, Moore had to find a way
to experimentally alter blood flow within single small vessels of the brain in
living animals, and then to watch what happens in individual cells. Such fine
control over blood flow in the brain had never previously been achieved. But
this spring, Moore, an assistant professor in the Department of Brain and
Cognitive Sciences and a principal investigator at the McGovern Institute for
Brain Research, teamed up with assistant professor Edward Boyden, a neurotechnology
whiz in the Media Lab, to tackle the challenge. They've embarked on a series of
technically sophisticated experiments that are letting Moore test his 13-year-old hypothesis at
last.
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