Research may impact development of treatments for movement
disorders such as Parkinson's and Huntington's diseases, as well as
conditions such as autism
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The basal ganglia, structures deep in the forebrain already known to
control voluntary movements, also may play a critical role in how people
form habits, both bad and good, and in influencing mood and feelings.
"This system is not just a motor system," says Ann Graybiel."We think it also strongly affects the emotional part of the brain."
Graybiel,
an investigator at the McGovern Institute of the Massachusetts
Institute of Technology and professor in MIT's department of brain and
cognitive sciences, believes that a core function of the basal ganglia
is to help humans develop habits that eventually become automatic,
including habits of thought and emotion.
"Many everyday movements
become habitual through repetition, but we also develop habits of
thought and emotion," she says."If cognitive and emotional habits are
also controlled by the basal ganglia, this may explain why damage to
these structures can lead not only to movement disorders, but also to
repetitive and intrusive thoughts, emotions and desires."
Graybiel's
research focuses on the brain's relationship to habits--how we make or
break them--and the neurobiology of the habit system. She and her team
have identified and traced neural loops that run from the outer layer of
the brain--"the thinking cap," as she calls it--to a region called the
striatum, which is part of the basal ganglia, and back again. These
loops, in fact, connect sensory signals to habitual behaviors.
Her
work ultimately could have an impact not just on such classic movement
disorders as Parkinson's and Huntington's diseases, but in other
conditions where repetitive movements commonly occur, such as Tourette
Syndrome, autism, or obsessive-compulsive disorder, the latter when
sufferers experience unwanted and repeated thoughts, feelings, ideas,
sensations or behaviors that make them feel driven to do something, for
example, repeatedly washing their hands.
Moreover, the research
could have an immediate value for trying to understand "what happens in
the brain as addiction occurs, as bad habits form, not just good
habits," she says. "There are many psychiatric and neurologic conditions
in which these same brain regions are disordered.
"These
conditions may in part be influenced by the very system we are working
on," Graybiel adds. "We are working with models of anxiety and
depression, stress and some of these movement disorders."
It turns
out that the emotional circuits of the brain have strong ties to the
striatum, she says. Graybiel's research suggests that activity in the
striatum strongly affects the emotional decisions that people make:
whether to accept a good outcome or a potentially bad one, for example,
and that there are circuits favoring good outcomes, and, surprisingly,
other circuits that favor bad ones.
"This work ties into new
research suggesting that there are brain systems for ‘good' and brain
systems for ‘bad,'" she says. "What is intriguing is that we may have
identified the circuits that decide between the two."
Recently,
Graybiel, an early National Science Foundation grantee, won the
prestigious Kavli Prize in neuroscience (along with Cornelia Isabella
Bargmann of Rockefeller University and Winfried Denk of the Max Planck
Institute for Medical Research) for their groundbreaking research
"elucidating basic neuronal mechanisms underlying perception and
decision."
These prizes recognize scientists for their seminal
advances in astrophysics, nanoscience and neuroscience, and include a
cash award of $1 million in each field.
Graybiel's lab was the
first to discover more than three decades ago that neurotransmitters in
the striatum had a precise and unique organization--compartments similar
to layers--a finding that surprised most scientists at the time.
"We
couldn't see this organization in regular old anatomy, but we found
this with chemical markers, by using stains," she says. "Imagine if you
look at a desert and everything looks plain and uniform, just all
sand. Then you put on special glasses, and all of a sudden, you could
see the chemical composition of the sands. The whole landscape looks
totally different, and that's what happened when we did this stain.
"We
now know that all over the brain, these molecules are highly ordered,"
she adds. "They are communication lines, and connections from a to b and
b to c, and these connections all work because of these chemical
communication molecules. We happened to find that the deep brain, which
looked so primitive, wasn't as primitive as people thought. We found
that if we looked at the chemicals and then at the inputs and the
outputs, everything was organized with respect to these chemical
compartments."
She and her team also determined that communication
molecules known to be related to human disorders, such as dopamine, a
key neurotransmitter, were prominently organized in this way. Dopamine
dysfunction is associated with the development of Parkinson's disease.
"As
we looked more and more, we found that we could trace connections from
the neocortex to the striatum," she says. "They were all organized in
compartments either in the compartments we called striosomes or in the
compartments that surrounded them.''
The striosomes are one of
two complementary chemical compartments within the striatum. The second
compartment is known as the matrix.
Following upon this, "the
next thing we found was that the whole thing looked like a learning
machine because of the way it all was organized," she says. "We decided
to study learning. In order to do that, we had to learn to record the
neural activity. It turns out that the system is tremendously active as
we learn habits. That's how we began."
Graybiel uses electrical
recordings, behavioral tests and gene-based approaches to study these
issues, and has seen remarkable changes in neural activity within the
striatum as animals learned new habits.
"The activity in this part
of the brain changed as the animals learned, and they were highly
correlated with the learning," she says. "We take the animals to
‘school' every day, and give them practice. They do learn habits-to run
to the right, or do something when a click occurs, until it's habitual.
As they learn, there are all these changes in the neural activity."
She
and her lab also found that these changes are coordinated with activity
patterns in the hippocampus, a brain structure involved with memory of
facts and events. Currently, she and her lab are studying new methods
to influence the activity in the striatum, and genes found in the brain
region thought to be involved in the brain's response to abusive drugs,
as well as to therapeutic drugs, such as those to treat Parkinson's.
Their
work suggests a new view of how the core brain structures involved in
Parkinson's disease are affected by dopamine depletion, and how this key
neurotransmitter might influence the ability to maintain movement and
thought.
"Hopefully, our basic science work can lead to new
therapeutic approaches to these disorders, not only in drug treatments
but also other novel treatments that affect the on-going activity of
neurons in the basal ganglia," she says. "There is nothing I would
rather do than to help in the search for new therapies to treat the
range of disorders related to the system we study, from Parkinson's
disease to OCD to addiction, and maybe, just maybe, to help the rest of
us unlearn bad habits."
-- | Marlene Cimons, National Science Foundation |
Investigators
Ann Graybiel
Related Institutions/Organizations
Massachusetts Institute of Technology
Related Awards
#8720475 Development of the Striatum
#7301547 Experimental Anatomical Study of the Oculomotor System
#8720475 Development of the Striatum
#7301547 Experimental Anatomical Study of the Oculomotor System
The National Science Foundation(NSF)
Guillermo Gonzalo Sánchez Achutegui
ayabaca@gmail.com
ayabaca@hotmail.com
ayabaca@yahoo.com
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