Nature Communications,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: May 4, 2021
Survival
depends
on
a
balance
between
seeking
rewards
and
avoiding
potential
threats,
but
the
neural
circuits
that
regulate
this
motivational
conflict
remain
largely
unknown.
Using
an
approach-food
vs.
avoid-predator
threat
test
in
rats,
we
identified
subpopulation
of
neurons
anterior
portion
paraventricular
thalamic
nucleus
(aPVT)
which
express
corticotrophin-releasing
factor
(CRF)
are
preferentially
recruited
during
conflict.
Inactivation
aPVTCRF
biases
animal's
response
toward
food,
whereas
activation
these
cells
recapitulates
food-seeking
suppression
observed
project
densely
to
accumbens
(NAc),
activity
pathway
reduces
food
increases
avoidance.
In
addition,
ventromedial
hypothalamus
(VMH)
as
critical
input
neurons,
demonstrated
VMH-aPVT
mediate
defensive
behaviors
exclusively
Together,
our
findings
describe
hypothalamic-thalamostriatal
circuit
suppresses
reward-seeking
behavior
under
competing
demands
threats.
Annual Review of Neuroscience,
Journal Year:
2020,
Volume and Issue:
43(1), P. 417 - 439
Published: April 7, 2020
Escape
is
one
of
the
most
studied
animal
behaviors,
and
there
a
rich
normative
theory
that
links
threat
properties
to
evasive
actions
their
timing.
The
behavioral
principles
escape
are
evolutionarily
conserved
rely
on
elementary
computational
steps
such
as
classifying
sensory
stimuli
executing
appropriate
movements.
These
common
building
blocks
general
adaptive
behaviors.
Here
we
consider
challenges
required
for
behaviors
be
implemented,
discuss
possible
algorithmic
solutions,
review
some
underlying
neural
circuits
mechanisms.
We
outline
shared
can
implemented
by
ancient
systems
generate
behavior,
which
cortical
encephalization
has
been
added
allow
increased
sophistication
flexibility
in
responding
threat.
Molecular Psychiatry,
Journal Year:
2021,
Volume and Issue:
26(7), P. 2837 - 2853
Published: March 26, 2021
Abstract
The
high
comorbidity
between
obesity
and
mental
disorders,
such
as
depression
anxiety,
often
exacerbates
metabolic
neurological
symptoms
significantly.
However,
neural
mechanisms
that
underlie
reciprocal
control
of
feeding
states
are
largely
elusive.
Here
we
report
melanocortin
4
receptor
(MC4R)
neurons
located
in
the
dorsal
bed
nucleus
stria
terminus
(dBNST)
engage
regulation
mentally
associated
weight
gain
by
receiving
GABAergic
projections
from
hypothalamic
AgRP
onto
α5-containing
GABA
A
receptors
serotonergic
afferents
5-HT
3
receptors.
Chronic
treatment
with
a
high-fat
diet
(HFD)
significantly
blunts
hyperexcitability
response
to
not
only
hunger
but
also
anxiety
depression-like
stimuli.
Such
HFD-mediated
desensitization
reduces
outputs
downstream
MC4R
dBNST
neurons,
resulting
severe
dysregulation.
Genetic
enhancement
R-α5
or
suppression
R
within
abolishes
HFD-induced
robustly
body
food
intake.
To
further
translational
insights,
revealed
combined
zonisamide
(enhancing
signaling)
granisetron
(a
selective
antagonist)
alleviates
dysfunction
yields
robust
reversal
diet-induced
reducing
total
calorie
intake
altering
preference
towards
healthy
low-fat
diet.
Our
results
unveil
mechanism
for
appetite
states,
which
culminates
novel
zonisamide-granisetron
cocktail
therapy
potential
tackling
psychosis-obesity
comorbidity.
Nature Communications,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: May 4, 2021
Survival
depends
on
a
balance
between
seeking
rewards
and
avoiding
potential
threats,
but
the
neural
circuits
that
regulate
this
motivational
conflict
remain
largely
unknown.
Using
an
approach-food
vs.
avoid-predator
threat
test
in
rats,
we
identified
subpopulation
of
neurons
anterior
portion
paraventricular
thalamic
nucleus
(aPVT)
which
express
corticotrophin-releasing
factor
(CRF)
are
preferentially
recruited
during
conflict.
Inactivation
aPVTCRF
biases
animal's
response
toward
food,
whereas
activation
these
cells
recapitulates
food-seeking
suppression
observed
project
densely
to
accumbens
(NAc),
activity
pathway
reduces
food
increases
avoidance.
In
addition,
ventromedial
hypothalamus
(VMH)
as
critical
input
neurons,
demonstrated
VMH-aPVT
mediate
defensive
behaviors
exclusively
Together,
our
findings
describe
hypothalamic-thalamostriatal
circuit
suppresses
reward-seeking
behavior
under
competing
demands
threats.