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MUSC launches first meth addiction
center
by Mary
Helen Yarborough
Public
Relations
The National Institutes of Health (NIH) has awarded MUSC a $3-million
grant for the nation’s first Translational Research in Addiction Center
(TRAC), which will focus on the clinical neurobiology of
methamphetamine dependence.
MUSC’s TRAC was ranked the first in a nationwide competitive program
initiated by the National Institute on Drug Abuse (NIDA). The
initiative is part of the larger goal of the NIH to develop research
centers that can bridge the gap between basic preclinical science and
clinical research. The MUSC TRAC will be recruiting
methamphetamine-dependent individuals from the Lowcountry area to
participate in the study. Most of the participants will be referrals,
according to TRAC director Ronald See, Ph.D., of MUSC’s Department of
Neurosciences.
Methamphetamine abuse and dependence has rapidly become a major health
problem throughout the United States, while basic and clinical
understanding of the neurobiology and treatment of methamphetamine
addiction has lagged behind research on other abused drugs.
Drs. Ronald See,
left, and Peter Kalivas stand in front of a hand-scrawled formula used
to understand methamphetamine addiction.
The TRAC, the first such program like it in the nation, will be
directed by See along with co-investigators Peter Kalivas, Ph.D.,
chairman of the department of Neurosciences, and Robert Malcolm, M.D.,
and Kathleen Brady, M.D., Ph.D., of MUSC’s Department of Psychiatry.
The TRAC will be funded by the NIH grant over the next four years.
During this time, the investigators will develop integrated,
multidisciplinary teams to explore the neural pathways, cognitive and
behavioral dysfunctions, and potential treatments for methamphetamine
addiction.
The TRAC will employ an animal model of relapse in conjunction with a
clinical laboratory and brain imaging center in an innovative
collaboration designed to directly test hypotheses derived from the
animal model in human subjects. In turn, information derived from
methamphetamine-dependent subjects in the clinical laboratory will
inform and guide new directions in the animal model.
Importantly, neurobiological information gained from the projects will
be used to develop novel therapies that may be effective in treating
methamphetamine addiction and reducing the individual and public health
consequences of this devastating illness.
Testing medications for addiction
Certain medications that will be tested on meth addiction have
been previously used to treat other disorders. For example, Abilify, a
drug used to treat schizophrenia, may be useful in treating cocaine
addiction. By stabilizing levels of brain dopamine as opposed to
completely shutting them down, its use is less objectionable to
patients. Researchers hope that it will help quell relapse tendencies
in meth addiction, as well.
“In studying cocaine self-administration using rats, we learned
the drug blocked their relapse to cocaine-seeking,” See said. He
added that studies in the TRAC will focus on physiological and
behavioral changes in rats at all points of meth use, including
relapse. While there are similarities between addiction to meth,
alcohol and heroin, the power that meth addiction holds over the
individual is the extended length of time the high lasts and the depths
to which the person sinks during the let-down. These dynamics fuel the
desire for more meth. “But we don’t know how different [the addiction]
is from cocaine,” Kalivas said. “There may be different things
happening. We do know that there are more cognitive deficits involved
with meth. Even the brain circuitry may be differentially altered in
meth addicts.”
Kalivas said much of the project will focus on activity in the frontal
cortex, the part of the brain critically involved in decision making.
Neuroscience research has determined that the frontal cortex plays a
significant role in addiction, schizophrenia, attention deficit
hyperactivity disorder, as well as all other cognitive functions.
Interestingly, the frontal cortex does not fully develop in humans
until their early 20s. This slow development is paralleled by the
period of greatest vulnerability to addiction between the ages of 14
and 25.
The TRAC will have multiple components. The first consists of using
animal models of relapse and cognitive deficits produced by meth. These
studies will examine what happens in the pre-frontal neurocircuitry in
relationship to relapse and cognitive function.
Secondly, a clinical component led by Brady and Malcolm will focus on
human participants during the same time that the basic studies are
conducted. A virtual reality cue system will be developed to test the
reactivity of meth addicts to drug-paired cues that are associated with
periods of drug use. Measures of craving and physiological arousal will
be determined during cue reactivity, as well as assessment of cognitive
performance. In addition, brain imaging techniques will assess dynamic
changes in brain function during cue exposure.
Finally, a major goal of the TRAC will be the assessment of compounds
that may simultaneously improve cognitive performance and blunt craving
for meth in both the animal model and in humans.
“Although the TRAC is not a treatment study, per se, it will utilize
compounds to improve addicts’ ability to not think of the drug,”
Kalivas said. “MUSC is unique in that it has a team of investigators
that bridge the gap from basic research to clinical trials. Who can
best move stuff from the bench to the bedside? That is what we are
doing here at MUSC.”
For information about MUSC’s Department of Neurosciences, visit http://neurosciences.musc.edu/.
Friday, Nov. 10, 2006
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