TRUST-BUILDING HORMONE SHORT-CIRCUITS FEAR IN HUMANS

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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/

FOR IMMEDIATE RELEASE: Wednesday, December 7, 2005 

CONTACT: Jules Asher, NIMH Press Office, 301-443-4536, NIMHpress@xxxxxxx

 
TRUST-BUILDING HORMONE SHORT-CIRCUITS FEAR IN HUMANS 

A brain chemical recently found to boost trust appears to work by
reducing activity and weakening connections in fear-processing
circuitry, a brain imaging study at the National Institutes of Health's
(NIH) National Institute of Mental Health (NIMH) has discovered. Scans
of the hormone oxytocin's effect on human brain function reveal that it
quells the brain's fear hub, the amygdala, and its brainstem relay
stations in response to fearful stimuli. The work at NIMH and a
collaborating site in Germany suggests new approaches to treating
diseases thought to involve amygdala dysfunction and social fear, such
as social phobia, autism, and possibly schizophrenia, report Andreas
Meyer-Lindenberg, M.D., Ph.D., NIMH Genes Cognition and Psychosis
Program, and colleagues, in the December 7, 2005 issue of the "Journal
of Neuroscience". 

"Studies in animals, pioneered by now NIMH director Dr. Thomas Insel,
have shown that oxytocin plays a key role in complex emotional and
social behaviors, such as attachment, social recognition and aggression"
noted NIH Director Elias Zerhouni, M.D.. "Now, for the first time, we
can literally see these same mechanisms at work in the human brain." 

"The observed changes in the amygdala are exciting as they suggest that
a long-acting analogue of oxytocin could have therapeutic value in
disorders characterized by social avoidance," added Insel. 

Inspired by Swiss scientists who last summer reported1 that oxytocin
increased trust in humans, Meyer-Lindenberg and colleagues quickly
mounted a brain imaging study that would explore how this works at the
level of brain circuitry. British researchers had earlier linked
increased amygdala activity to decreased trustworthiness2. Having just
discovered "decreased amygdala activity"
(http://www.nimh.nih.gov/press/williamspathway.cfm ) in response to
social stimuli in people with a rare genetic brain disorder that
rendered them overly trusting of others, Meyer-Lindenberg hypothesized
that oxytocin boosts trust by suppressing the amygdala and its
fear-processing networks. 

To test this idea, he asked 15 healthy men to sniff oxytocin or a
placebo prior to undergoing a functional magnetic resonance imaging
(fMRI) scan, which reveals what parts of the brain that are activated by
particular activities. While in the scanner, the men performed "tasks
known to activate the amygdale"
(http://www.nimh.nih.gov/Press/pramygdala.cfm )-- matching angry or
fearful faces and threatening scenes. 

As expected, the threatening pictures triggered strong activation of the
amygdala during the placebo scan, but markedly less activity following
oxytocin. The difference was especially pronounced in response to
threatening faces, suggesting a pivotal role for oxytocin in regulating
social fear. In addition, oxytocin dampened the amygdala's communication
with sites in the upper brainstem that telegraph the fear response. The
results mirrored findings in rats3, reported earlier this year by
European scientists. 

"Because increased amygdala activation has been associated with social
fear in social phobia, genetic risk for anxiety and depression, and
possibly with social fear in autism assessed during faces processing,
this dual mode of action of oxytocin in humans suggests a potentially
powerful treatment approach toward socially relevant fear," suggest the
researchers. 

People with autism characteristically avert their gaze from faces. A
fMRI study4 reported earlier this year by NIMH grantee Richard Davidson,
Ph.D., University of Wisconsin, and colleagues, found over-activation of
the amygdala in people with autism when they were looking at faces.
Meyer-Lindenberg said future studies may test oxytocin as a treatment
for such social anxiety symptoms in children with autism. 

"Future research may also examine how oxytocin affects the amygdala in
women, the mode of action of related hormones such as vasopressin, and
how genetic variants in these hormones and their receptors affect brain
function," he added. 

Also participating in the research were: Peter Kirsch, Christin
Esslinger, Daniela Mier, Stefanie Lis, Harald Gruppe, Bernd Gallhofer,
Justus-Liebig University, Giessen, Germany; Qiang Chen, Sarina
Siddhanti, Venkata Mattay, NIMH Genes Cognition and Psychosis Program. 

To view a photo that depicts functional magnetic resonance imaging data
(red) superimposed on structural MRI scans, please visit
http://www.nih.gov/news/pr/dec2005/nimh-07.htm. Frightful faces
triggered a dramatic reduction in amygdala activity in subjects who had
sniffed oxytocin, suggesting that oxytocin mediates social fear and
trust via the amygdala and related circuitry. (Source: NIMH Genes,
Cognition and Psychosis Program) 

NIMH is part 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.
 
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.
  
##

------------------------------------------------
1 Kosfeld M, Heinrichs M, Zak PJ, Fischbacher U, Fehr E. "Oxytocin
increases trust in humans". "Nature". 2005 Jun 2;435(7042):673-6. 

2 Winston JS, Strange BA, O'Doherty J, Dolan RJ. "Automatic and
intentional brain responses during evaluation of trustworthiness of
faces". "Nat Neurosci". 2002 Mar;5(3):277-83. "

3 Huber D, Veinante P, Stoop R. "Vasopressin and oxytocin excite
distinct neuronal populations in the central amygdala". "Science". 2005
Apr 8;308(5719):245-8. 

4 Dalton KM, Nacewicz BM, Johnstone T, Schaefer HS, Gernsbacher MA,
Goldsmith HH, Alexander AL, Davidson RJ. "Gaze fixation and the neural
circuitry of face processing in autism". "Nat Neurosci". 2005
Apr;8(4):519-26. Epub 2005 Mar 6. 
------------------------------------------------
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/dec2005/nimh-07.htm.

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