Chronic stress during pregnancy is a predictor of postpartum depression.
The study, conducted by scientists from Ohio State University, examined
the brain cells of rats that were chronically stressed during pregnancy.
The research was presented at Neuroscience 2014, the annual meeting of the Society for Neuroscience.
The aim of the research was to identify the changes in the brain that may cause the symptoms of postpartum depression, focusing on an area within the brain that controls the reward system, known as the nucleus accumbens.
"We have a suspicion that stress
during pregnancy is somehow altering the reward system in the brain,
producing anhedonia and making these depressed mothers less rewarded by
their offspring and less motivated to care for them," says senior author
Benedetta Leuner. "It's possible that the effects of stress on the
brain circuit regulating reward can lead to these symptoms."
Postpartum depression, whereby new mothers experience a long-lasting form of depression,
is a serious health problem that can have consequences for both the new
mother and her family. According to the American Psychological
Association (APA), an estimated 9-16% of new mothers develop the
condition.
Although the symptoms of postpartum depression are distinct, experts are
still uncertain as to what happens in the brain when mothers develop
this condition.
The effects of depression on the reward system
Citalopram is a commonly prescribed drug for postpartum depression. It is a selective serotonin
reuptake inhibitor (SSRI), a type of drug that promotes the amount of
serotonin in the brain, helping the organ to send and receive neural
messages, resulting in better and more stable moods.
Lead author Achikam Haim says the team found that citalopram was
effective in improving the mood of stressed mothers and completely
reversed the effects of stress in areas of the brain shown to be altered
during pregnancy.
Dr. Leuner designed a rat model of postpartum depression in order to
illustrate the changes that occurred in the brain. Depressive-like
symptoms were induced in the rats by subjecting them to chronic stress
during their pregnancy - a known predictor of postpartum depression
within humans.
The rats would go on to exhibit symptoms shared by humans with
postpartum depression. These included mood changes, deficits in
caregiving behaviors and anhedonia - an inability to experience
pleasure.
Within the nucleus accumbens, the researchers found stressed
rats had fewer dendritic spines - small protrusions on brain cells that
enable communication with other neurons - than unstressed rats. This
deficit indicated a state of reduced flexibility or ability to adapt,
referred to as reduced plasticity.
A similar result was found during research in humans that showed in
mothers with postpartum depression; the reward center did not activate
in response to hearing the sound of their child crying.
Citalopram found to reverse stress-induced brain changes
"The structural data from our work in rats can at least partially
explain that, because neurons with fewer spines, and therefore less
input, arguably have lower activation levels," Haim said.
Citalopram was then administered daily for 3 weeks to the mother rats
showing depressive-like symptoms, using mini-pumps implanted under the
skin. This treatment led to a reversal in the changes that had been
induced by chronic stress, returning the cells to their normal levels of
complexity.
Although the antidepressants
were found to be effective, the 3-week treatment timeframe is still
problematic; it could be too long a timeframe with regards to a serious
symptom of postpartum depression - poor maternal care.
Neglect that arises as a result of postpartum depression can
have a lasting impact on the health of the child, potentially leading to
an increased risk of depression and slowed cognitive and social
development.
As a result, Dr. Leuner says that they the researchers will be looking
at other neurochemical systems to target. "Fixing that impaired maternal
functioning is really what's critical in moving forward and developing
better treatment options."
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