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Background
Yale University School
of Medicine researchers received a $9 million grant from the National
Institute on Alcohol Abuse and Alcoholism in 2001 to help translate research
findings about alcoholism into treatment for patients. The new Center
for Translational Neuroscience of Alcoholism (CTNA) was formed to create
links between basic research advances and the development of new treatments
for alcoholism.
It was a Yale researcher, E. M. Jellinek, who pioneered the hypothesis
that alcoholism is a medical illness. Over the years, researchers have
identified ethanol targets in the brain and specific genes that show vulnerability
for alcoholism. With new imaging tools to look at brain chemicals, and
molecular genetics studies, we now have an opportunity to observe broad
clinical implications from molecular neuroscience.
CTNA is designed to
better define the biochemical and functional characteristics of a brain
circuit that appears to be involved in the vulnerability to alcoholism
and the characteristics of alcohol dependence. This circuit involves a
brain region involved in higher cognitive processes, the frontal cortex,
and emotion, the limbic system. The "translational" mission
of the Center involves the effort to use fundamental insights gained from
basic research to guide clinical research studies in people vulnerable
to developing alcoholism or suffering with alcoholism. These mechanistic
human research studies are possible because of new advances in molecular
genetics as well as in positron emission tomography (PET) and magnetic
resonance imaging (MRI) that make it feasible to study many aspects of
the structure, chemistry, and function of specific regions in the brain.
Dr. John Krystal,
CTNA Director, notes the critical nature of the collaboration between
scientists and the community in solving the urgent problems associated
with alcohol dependence. "We can only accomplish the goals of the
Center with the help of people in the community who participate in studies."
CTNA projects are actively seeking healthy individuals with and without
family histories of alcohol problems as well as heavy social drinkers
as well as people who are alcohol-dependent or heavy drinkers.
RECENT AWARD
Two Yale CTNA investigators
received the American Psychiatric Association's (APA) APIRE/Kempf Fund
Award for Research Development in Psychobiological Psychiatry at the association's
annual meeting May 5, 2005. Dr. John Krystal, CTNA Director, the Robert
L. McNeil Jr. Professor of Clinical Pharmacology and deputy chair for
research in the Department of Psychiatry at the Yale School of Medicine
and Dr. Daniel Mathalon, Pilot Investigator and assistant professor of
psychiatry, were recognized for providing new insights into the neurobiology
and treatment of cognitive impairments associated with schizophrenia.
Their award-winning research studied the interplay of glutamate and dopamine
systems in cognitive functions associated with the prefrontal cortex.
The Kempf Fund Award recognizes the senior Researcher, Krystal, for his
scientific contributions to the field of schizophrenia research and his
mentorship of an outstanding young scientist. This award also supports
the young investigator, Mathalon, with a research career development award.
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