ScienceDaily (Mar. 13, 2008) — Short-term stress lasting as little as a few 
hours can impair brain-cell communication in areas associated with learning and 
memory, University of California, Irvine researchers have found.

It has been known that severe stress lasting weeks or months can impair cell 
communication in the brain's learning and memory region, but this study 
provides the first evidence that short-term stress has the same effect.

"Stress is a constant in our lives and cannot be avoided," said Dr. Tallie Z. 
Baram, the Danette Shepard Chair in Neurological Sciences in the UC Irvine 
School of Medicine and study leader. "Our findings can play an important role 
in the current development of drugs that might prevent these undesirable 
effects and offer insights into why some people are forgetful or have 
difficulty retaining information during stressful situations."

In their study, Baram and her UC Irvine colleagues identified a novel process 
by which stress caused these effects. They found that rather than involving the 
widely known stress hormone cortisol, which circulates throughout the body, 
acute stress activated selective molecules called corticotropin releasing 
hormones, which disrupted the process by which the brain collects and stores 
memories.

Learning and memory take place at synapses, which are junctions through which 
brain cells communicate. These synapses reside on specialized branchlike 
protrusions on neurons called dendritic spines.

In rat and mouse studies, Baram's group saw that the release of CRH in the 
hippocampus, the brain's primary learning and memory center, led to the rapid 
disintegration of these dendritic spines, which in turn limited the ability of 
synapses to collect and store memories.

The researchers discovered that blocking the CRH molecules' interaction with 
their receptor molecules eliminated stress damage to dendritic spines in the 
hippocampal cells involved with learning and memory.

In addition, the authors replicated the effects of stress on dendritic spines 
by administering low levels of synthetic CRH, and watching how the spines 
retracted over minutes. "Fortunately, once we removed the CRH, the spines 
seemed to grow back," Baram said.

Baram also noted that there are compounds under development that show the 
ability to block CRH receptors, and that this study can play a role in the 
creation of therapies based on these compounds to address stress-related 
learning and memory loss.

The study appears in the March 12 edition of the Journal of Neuroscience.  
Yuncai Chen, Celine Dubé and Courtney Burgdorff of UC Irvine also participated 
in the study, which was supported by the National Institutes of Health.

Disclaimer: This article is not intended to provide medical advice, diagnosis 
or treatment. Views expressed here do not necessarily reflect those of 
ScienceDaily or its staff.



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