GENE KNOCKOUT SCORES A FEARLESS MOUSE

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute of Mental Health (NIMH)
http://www.nimh.nih.gov/
National Institute of Neurological Disorders and Stroke (NINDS)
http://www.ninds.nih.gov/
National Institute on Drug Abuse (NIDA)
http://www.nida.nih.gov/

FOR IMMEDIATE RELEASE: Tuesday, November 22, 2005 

CONTACT: Jules Asher, NIMH press office, 301-443-4536, NIMHpress@xxxxxxx
 
GENE KNOCKOUT SCORES A FEARLESS MOUSE

Knocking out a gene in the brain's fear hub creates mice unperturbed by
situations that would normally trigger instinctive or learned fear
responses, researchers funded in part by the National Institutes of
Health have discovered. The findings may lead to improved treatments for
anxiety disorders
(http://www.nimh.nih.gov/healthinformation/anxietymenu.cfm), they
suggest.

The scientific team, led by National Institute of Mental Health (NIMH)
grantee and Nobel Laureate Dr. Eric Kandel, Columbia University, Dr.
Vadim Bolshakov, Harvard University, a grantee of the National Institute
of Neurological Disorders and Stroke (NINDS) and the National Institute
on Drug Abuse (NIDA), and Dr. Gleb Shumyatsky, Rutgers University,
report on their study in the November 18, 2005 issue of "Cell".

Fear memories are so essential for survival that they are easily formed
and rarely lost. The workings of fear circuitry, centered in the
amygdala, an almond-shaped structure deep in the brain, are well
understood. But relatively little is known about fear's molecular basis,
note the researchers.

The gene in the current study codes for stathmin, a protein that appears
to be critical for the amygdala to rearrange connections and form fear
memories. Stathmin normally controls this process by regulating the
supply of microtubules, building materials that amygdala cells use to
make structural adaptations that encode the memories. Runaway production
of these building materials stymied construction of fear memories in a
mouse strain molecularly engineered to lack stathmin, the researchers
found.

They first showed that circuitry on the side of the amygdala known to be
critical for fear learning is rich in stathmin. They then demonstrated
that a cellular process critical for memory formation, long-term
potentiation, is impaired there in stathmin knockout mice, due to the
excess production of microtubules.

Compared to control animals, the stathmin knockout mice showed less
anxiety (freezing) when they heard a tone that had previously been
associated with a shock, indicating less learned fear. The knockout mice
also were more prone to explore novel open space and maze environments,
a reflection of less innate fear.

"Stathmin knockout mice can be used as a model of anxiety states of
mental disorders with innate and learned fear components," propose the
researchers. "As a corollary, these animal models could be used to
develop new anti-anxiety agents."

This and related studies with other knockout mouse models suggest that
subclasses of anxiety disorders will ultimately emerge, "each of which
is likely to have a unique molecular signature and require distinctive
pharmacological approaches," they add.

"Whether stathmin is similarly expressed and pivotal for anxiety in the
human amygdala remains to be confirmed," noted NIMH director Dr. Thomas
Insel. "Yet, this surprising discovery in the mouse hints at the
potential for new treatment strategies likely still hidden in the vast
uncharted territory of brain genetics."

Also participating in the study: Shuichi Takizawa, Jamie Joseph, Rutgers
University; Gael Malleret Stanislav Zakharenko, Svetlana Vronskaya, DeQi
Yin, Columbia University; Keith Tully, Evgeny Tsvetkov, Harvard
University; Ulrich Schubart, Albert Einstein College of Medicine.

In addition to the NIH, the research was also supported by NARSAD, NAAR,
The Cure Autism Now Foundation, the New Jersey Governor's council on
Autism, the G. Harold and Leila Y. Mathers Charitable Foundation, the
Whitehall Foundation, and the Esther A. & Joseph Klingenstein Fund.

NIMH, NINDS and NIDA are parts of the National Institutes of Health
(NIH), the Federal Government's primary agency for biomedical and
behavioral research. NIH is a component of the U.S. Department of Health
and Human Services.
The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U. S. Department of Health and Human Services. It is
the primary Federal agency for conducting and supporting basic,
clinical, and translational medical research, and it investigates the
causes, treatments, and cures for both common and rare diseases. For
more information about NIH and its programs, visit http://www.nih.gov.
  
##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/nov2005/nimh-22.htm.

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