Discovery that depressed monkeys and humans show similar central nervous system characteristics may improve testing of possible therapies for depression
The discovery that depressed female monkeys
and humans show similar clinical and central nervous system characteristics
may improve testing of possible therapies for depression, according
to an article in the April issue of the Archives of General Psychiatry.
“Brain scans of depressed female monkeys
revealed the same underlying neurobiological changes that are found
in the brains of depressed people,” said Carol A. Shively, PhD,
from Wake Forest University School of Medicine. “This is further
evidence that these animal models can help researchers understand
depression, develop new treatments and test their effectiveness.”
The positron emission tomography (PET) scans
looked at the 5-HT1a serotonin receptor in 11 areas of the brain.
A tracer that binds to the serotonin receptor was injected into
a vein of each subject. The regions with tracer binding showed as
a bright yellow color during the scan. The depressed monkeys had
lower serotonin receptor binding in all areas of the brain examined,
consistent with previous studies in depressed people.
This supports earlier studies showing that
depressed female monkeys have similar physical characteristics to
women who are depressed, including low activity levels, disruptions
in hormones and higher heart rates.
“Even though women are twice as likely as
men to experience clinical depression and are at increased risk
for depression during premenstrual, postpartum and perimenopausal
times in their lives, we have never had any female animal models
of depression,” said Shively, a professor of comparative medicine.
“Monkeys offer a special opportunity for research because they are
among the few animals that have menstrual cycles and complex cognitive
function.”
In addition, the animals have never been
exposed to psychotropic medications, alcohol, tobacco or illegal
drugs. Monkey models can be used to develop new treatments and test
their effectiveness, Shively said, through observing behavior and
using brain scans to reveal if treatments or medications are actually
working.
“Another way we’d like to see the model used
is to investigate the cognitive aspects of depression,” Shively
said. “The way that many of our pharmaceutical products got onto
the market was that they were tested on rodents. But when they were
used by humans, we found side effects that caused cognitive dysfunction
like lack of concentration. Depressed people do not need more cognitive
dysfunction. This animal model could be used to test treatments
that alleviate cognitive problems associated with depression rather
than making them worse.”
Shively pointed out that there are very few
places in the country that have both a primate center and an imaging
center that made this study possible. “This research cannot be done
without having both centers here.”
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