Gene Therapy Turns Elk-voles Into Stork-voles!!!
(If we at Brin-L made headers like The National
Enquirer... :D )

But this is quite fascinating (and maybe a little bit
disturbing):

http://my.webmd.com/content/Article/89/100115.htm?printing=true
"...researchers say they've found a gene that appears
to have a profound effect on the social behavior of
animals.  The gene, known as the vasopressin receptor,
is located in the brain's reward center and may also
be involved in drug addiction.  Researchers say the
findings may help explain the neurobiology behind
romantic love as well as disorders such as autism that
affect how people form social bonds.

"In the study, researchers used a harmless virus to
transfer the gene from monogamous male prairie voles,
who are known to form lifelong bonds with a single
mate, into the brain of meadow voles, who mate with
multiple partners and lack vasopressin receptors in
their brain's reward center.  A few days later, the
meadow voles had vasopressin receptors levels similar
to those found in the prairie voles. 

"Researchers paired the animals with sexually
receptive mates and allowed them a day to get to know
each other before the males were given a fidelity
test.  Each vole was allowed to wander between his
first partner and a new potential mate. The study
showed that both the prairie voles and the genetically
modified meadow moles huddled close to their original
partner while the untreated meadow voles behaved like
loners and spent time by themselves...

"...Researchers say previous research has shown that
these vasopressin receptors may play a role in social
disorders, such as autism, that make it difficult to
form social bonds.  Studies in humans have also
suggested that the same brain pathways involved in
forming romantic relationships may also be involved in
drug addiction.  "The brain process of bonding with
one's partner may be similar to becoming addicted to
drugs: both activate reward circuits in the brain,"
says researcher Miranda Lim, a postdoctoral fellow at
Emory University, in a news release. 

"Pair bonding in humans is a much more complex process
than in moles, and researchers say social, economic,
historic, and individual differences all play a role. 
"Our study, however, provides evidence, in a
comparatively simple animal model, that changes in the
activity of a single gene profoundly can change a
fundamental social behavior of animals within a
species," says researcher Larry J. Young, PhD, of
Emory University's School of Medicine..." 


Here is a 2001 technical article from the same group
on the same subject (article much longer):
http://www.jneurosci.org/cgi/content/full/21/18/7392
"...In addition, males overexpressing the V1aR in the
ventral pallidal region, but not control males, formed
strong partner preferences after an overnight
cohabitation, without mating, with a female. These
data demonstrate a role for ventral pallidal V1aR in
affiliation and social attachment and provide a
potential molecular mechanism for species differences
in social organization....A second [caveat] is the
possibility that regions other than the ventral
pallidum are involved in the AVP-dependent regulation
of social behavior and pair bonding. V1aRs are also
found in the amygdala, thalamus, cingulate cortex, and
olfactory bulb. Although our results do not rule out
an involvement of these areas, they do demonstrate
that increased levels of V1aR in the ventral pallidum
facilitate partner-preference formation....The V1aR-VP
males exhibited a strong partner preference after the
17 hr cohabitation without mating. It is important to
note that in previous studies from our group, male
prairie voles that cohabitated with a female for 24 hr
did form partner preferences if mating occurred, but
typically did not if mating did not occur (Insel and
Hulihan, 1995; Insel et al., 1995). Thus, it seems
that by increasing the density of V1aR in the ventral
pallidum, the amount of social stimulation required to
form a partner preference was decreased....

"...This striatopallidal system is an important
neurobiological substrate for the rewarding and
reinforcing properties of natural stimuli and
psychostimulants (McBride et al., 1999). Infusion of
psychostimulants directly into the ventral pallidum
leads to the development a conditioned place
preference for the environment in which the injections
were experienced (Gong et al., 1996). Given the
abundance of V1aR in the prairie vole ventral pallidum
and its role in conditioned place preference, we
hypothesize that AVP released during social
interactions or mating activates V1aR in the ventral
pallidum. Activation of this reward circuitry then
reinforces this behavior, leading to an increase in
social interactions. In a mating pair, the
reinforcement is powerful enough to lead to a
conditioned partner preference in the monogamous
prairie vole and thereby initiates the formation of a
pair bond. The lack of V1aR in the ventral pallidum of
nonmonogamous vole species may explain their inability
to form partner preferences after mating. There are
most certainly other genetic, neurochemical, or
anatomical differences between monogamous and
nonmonogamous species that contribute to their diverse
social behavior; however, the viral vector approach
provides an opportunity to test this hypothesis....

"...The role of AVP in facilitating pair bonding in
the male prairie vole is remarkably parallel to that
of oxytocin in the female prairie vole. In the female
it is oxytocin, not vasopressin, that facilitates the
formation of the pair bond with the mate (Insel and
Hulihan, 1995). Oxytocin antagonist infused into the
nucleus accumbens prevents partner-preference
formation in the female (Young et al., 2001). In
addition, prairie voles have much higher
concentrations of oxytocin receptors in the nucleus
accumbens than do nonmonogamous vole species (Insel
and Shapiro, 1992). Dopamine D2 receptor antagonists
infused into the nucleus accumbens also prevent
partner-preference formation (Gingrich et al., 2000).
Thus it appears that pair bonding is facilitated in a
sex-specific manner, by two different neuropeptide
systems acting at two separate points in a common
neural circuit.

"Our results are consistent with the hypothesis that
the striatopallidal reward circuitry facilitates
certain aspects of affiliation and social attachment,
implying common neural pathways for social attachment
and the reinforcing effects of drugs of abuse
(Panksepp, 1998). A recent functional magnetic
resonance imaging study examined the pattern of brain
activation and deactivation in human subjects as they
viewed photographs of individuals with whom they
reported to be romantically in love. The regions of
activation were strikingly similar to those activated
in studies of cocaine- and µ opioid agonist-induced
euphoria..."


A more readable overview for those who don't care what
a palladium is - or think it only has something to do
with computers:  ;)
http://www.americanscientist.org/template/AssetDetail/assetid/14756#18144
http://makeashorterlink.com/?R23025898

Debbi
who is glad that the vole her cat brought home last
week was likely a mountain vole, lest she have to
think of the partner left behind...


                
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