Nature,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 4, 2024
Abstract
Anhedonia,
the
diminished
drive
to
seek,
value,
and
learn
about
rewards,
is
a
core
feature
of
major
depressive
disorder
1–3
.
The
neural
underpinnings
anhedonia
how
this
emotional
state
drives
behaviour
remain
unclear.
Here
we
investigated
code
by
taking
advantage
fact
that
when
mice
are
exposed
traumatic
social
stress,
susceptible
animals
become
socially
withdrawn
anhedonic,
whereas
others
resilient.
By
performing
high-density
electrophysiology
record
activity
patterns
in
basolateral
amygdala
(BLA)
ventral
CA1
(vCA1),
identified
signatures
susceptibility
resilience.
When
actively
sought
BLA
resilient
showed
robust
discrimination
between
reward
choices.
contrast,
exhibited
rumination-like
signature,
which
neurons
encoded
intention
switch
or
stay
on
previously
chosen
reward.
Manipulation
vCA1
inputs
rescued
dysfunctional
dynamics,
amplified
dynamics
associated
with
resilience,
reversed
anhedonic
behaviour.
Finally,
were
at
rest,
spontaneous
greater
number
distinct
population
states.
This
allowed
us
decode
group
identity
infer
whether
mouse
had
history
stress
better
than
behavioural
outcomes
alone.
work
reveals
population-level
explain
individual
differences
responses
suggests
modulating
vCA1–BLA
can
enhance
resilience
regulating
these
dynamics.
Current Opinion in Behavioral Sciences,
Journal Year:
2024,
Volume and Issue:
59, P. 101441 - 101441
Published: Sept. 2, 2024
The
tail
of
the
striatum
(TS)
is
increasingly
recognized
as
a
unique
subdivision
striatum,
characterized
by
its
dense
sensory
inputs
and
projections
received
from
distinct
group
dopamine
neurons.
Separate
lines
research
have
functional
role
TS,
TS-projecting
neurons,
in
three
realms:
saccadic
eye
movement
towards
valuable
visual
stimuli;
tone-guided
choice
between
two
options;
defensive
responses
to
threatening
stimuli.
We
propose
framework
for
reconciling
these
diverse
roles
varied
implementations
conserved
response
salient
stimuli,
with
TS
providing
teaching
signal
promote
quick
attentional
shifts
that
facilitate
stimulus-driven
orientation
and/or
avoidance.
Neuron,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 1, 2024
Some
individuals
are
susceptible
to
chronic
stress,
and
others
more
resilient.
While
many
brain
regions
implicated
in
learning
dysregulated
after
little
is
known
about
whether
how
neural
teaching
signals
during
stress
differ
between
resilient
individuals.
Here,
we
seek
determine
if
activity
the
lateral
habenula
(LHb),
which
encodes
a
negative
signal,
differs
mice
produce
different
outcomes.
After
(but
not
before)
social
defeat
LHb
active
when
proximity
of
aggressor
strain.
During
higher
interactions,
activation
biases
toward
susceptibility.
This
manipulation
generates
persistent
widespread
increase
balance
subcortical
vs.
cortical
mice.
Taken
together,
our
results
indicate
that
heightened
produces
lasting
brainwide
behavioral
substrates
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 28, 2024
Learning
a
new
task
is
challenging
because
the
world
high
dimensional,
with
only
subset
of
features
being
reward-relevant.
What
neural
mechanisms
contribute
to
initial
acquisition,
and
why
do
some
individuals
learn
much
more
quickly
than
others?
To
address
these
questions,
we
recorded
longitudinally
from
dopamine
(DA)
axon
terminals
in
mice
learning
visual
task.
Across
striatum,
DA
responses
tracked
idiosyncratic
side-specific
trajectories.
However,
even
before
any
rewards
were
delivered,
contralateral-side-specific
present
dorsomedial
striatum
(DMS).
These
pre-existing
predicted
extent
for
contralateral
stimuli.
Moreover,
activation
improved
performance.
Thus,
conditions
projection-specific
feature-specific
signal
help
explain
individual
More
broadly,
this
work
implies
that
functional
heterogeneity
across
projections
serves
bias
target
regions
towards
about
different
subsets
features,
providing
mechanism
dimensionality
problem.
IEEE Transactions on Neural Systems and Rehabilitation Engineering,
Journal Year:
2024,
Volume and Issue:
32, P. 1314 - 1323
Published: Jan. 1, 2024
Depression
is
one
of
the
most
serious
mental
disorders
affecting
modern
human
life
and
often
caused
by
chronic
stress.
Dopamine
system
dysfunction
proposed
to
contribute
pathophysiology
stress,
especially
ventral
tegmental
area
(VTA)
which
mainly
consists
dopaminergic
neurons.
Focused
ultrasound
stimulation
(FUS)
a
promising
neuromodulation
modality
multiple
studies
have
demonstrated
effective
ultrasonic
activation
cortical,
subcortical,
related
networks.
However,
effects
FUS
on
dopamine
potential
link
stress-induced
depressive
behaviors
are
relatively
unknown.
Here,
we
measured
targeting
VTA
improvement
depression-like
behavior
evaluated
concentration
in
downstream
region
-
medial
prefrontal
cortex
(mPFC).
We
found
that
treatment
alleviated
restraint
stress
(CRS)
-induced
anhedonia
despair
behavior.
Using
an
vivo
photometry
approach,
analyzed
signal
mPFC
revealed
significant
increase
following
FUS,
positively
associated
with
also
protected
neurons
from
damage
CRS
exposure.
Thus,
these
results
significantly
rescued
depressive-like
declined
level
induced
CRS.
These
beneficial
might
be
due
protection
DA
neuron
VTA.
Our
findings
suggest
could
serve
as
new
therapeutic
strategy
for
stress-related
disorders.
Nature,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 4, 2024
Abstract
Anhedonia,
the
diminished
drive
to
seek,
value,
and
learn
about
rewards,
is
a
core
feature
of
major
depressive
disorder
1–3
.
The
neural
underpinnings
anhedonia
how
this
emotional
state
drives
behaviour
remain
unclear.
Here
we
investigated
code
by
taking
advantage
fact
that
when
mice
are
exposed
traumatic
social
stress,
susceptible
animals
become
socially
withdrawn
anhedonic,
whereas
others
resilient.
By
performing
high-density
electrophysiology
record
activity
patterns
in
basolateral
amygdala
(BLA)
ventral
CA1
(vCA1),
identified
signatures
susceptibility
resilience.
When
actively
sought
BLA
resilient
showed
robust
discrimination
between
reward
choices.
contrast,
exhibited
rumination-like
signature,
which
neurons
encoded
intention
switch
or
stay
on
previously
chosen
reward.
Manipulation
vCA1
inputs
rescued
dysfunctional
dynamics,
amplified
dynamics
associated
with
resilience,
reversed
anhedonic
behaviour.
Finally,
were
at
rest,
spontaneous
greater
number
distinct
population
states.
This
allowed
us
decode
group
identity
infer
whether
mouse
had
history
stress
better
than
behavioural
outcomes
alone.
work
reveals
population-level
explain
individual
differences
responses
suggests
modulating
vCA1–BLA
can
enhance
resilience
regulating
these
dynamics.