Journal of Neuroscience,
Год журнала:
2024,
Номер
unknown, С. e1469232024 - e1469232024
Опубликована: Март 14, 2024
The
ventral
pallidum
(VP)
is
a
central
hub
in
the
reward
circuitry
with
diverse
projections
that
have
different
behavioral
roles
attributed
mostly
to
connectivity
downstream
target.
However,
VP
may
represent,
as
striatum,
separate
neuronal
populations
differ
more
than
just
connectivity.
In
this
study,
we
performed
mice
of
both
sexes
multimodal
dissection
four
major
VP-to
lateral
hypothalamus
(VP
Nature Neuroscience,
Год журнала:
2023,
Номер
26(12), С. 2237 - 2249
Опубликована: Окт. 26, 2023
Abstract
The
amygdala
is
a
brain
region
primarily
associated
with
emotional
response.
use
of
genetic
markers
and
single-cell
transcriptomics
can
provide
insights
into
behavior-associated
cell
state
changes.
Here
we
present
detailed
cell-type
taxonomy
the
adult
mouse
during
fear
learning
memory
consolidation.
We
perform
RNA
sequencing
on
naïve
fear-conditioned
mice,
identify
130
neuronal
types
validate
their
spatial
distributions.
A
subset
all
transcriptionally
responsive
to
retrieval.
activated
engram
cells
upregulate
activity-response
genes
coordinate
expression
neurite
outgrowth,
synaptic
signaling,
plasticity
development.
known
previously
undescribed
candidate
learning.
Our
molecular
atlas
may
be
used
generate
hypotheses
unveil
neuron
neural
circuits
regulating
component
memory.
Nature,
Год журнала:
2024,
Номер
630(8015), С. 141 - 148
Опубликована: Май 22, 2024
Abstract
Fentanyl
is
a
powerful
painkiller
that
elicits
euphoria
and
positive
reinforcement
1
.
also
leads
to
dependence,
defined
by
the
aversive
withdrawal
syndrome,
which
fuels
negative
2,3
(that
is,
individuals
retake
drug
avoid
withdrawal).
Positive
maintain
opioid
consumption,
addiction
in
one-fourth
of
users,
largest
fraction
for
all
addictive
drugs
4
Among
receptors,
µ-opioid
receptors
have
key
role
5
,
yet
induction
loci
circuit
adaptations
eventually
lead
remain
unknown.
Here
we
injected
mice
with
fentanyl
acutely
inhibit
γ-aminobutyric
acid-expressing
neurons
ventral
tegmental
area
(VTA),
causing
disinhibition
dopamine
neurons,
increased
nucleus
accumbens.
Knockdown
VTA
abolished
transients
reinforcement,
but
remained
unchanged.
We
identified
expressing
central
amygdala
(CeA)
whose
activity
was
enhanced
during
withdrawal.
CeA
eliminated
symptoms,
suggesting
they
mediate
reinforcement.
Thus,
optogenetic
stimulation
caused
place
aversion,
readily
learned
press
lever
pause
express
receptors.
Our
study
parses
neuronal
populations
trigger
CeA,
respectively.
lay
out
organization
develop
interventions
reducing
facilitating
rehabilitation.
Animals
learn
the
value
of
foods
on
basis
their
postingestive
effects
and
thereby
develop
aversions
to
that
are
toxic1-10
preferences
those
nutritious11-13.
However,
it
remains
unclear
how
brain
is
able
assign
credit
flavours
experienced
during
a
meal
with
feedback
signals
can
arise
after
substantial
delay.
Here
we
reveal
an
unexpected
role
for
reactivation
neural
flavour
representations
in
this
temporal
credit-assignment
process.
To
begin,
leverage
fact
mice
associate
novel14,15,
but
not
familiar,
delayed
gastrointestinal
malaise
investigate
represents
support
aversive
learning.
Analyses
brain-wide
activation
patterns
network
amygdala
regions
unique
being
preferentially
activated
by
novel
across
every
stage
learning
(consumption,
memory
retrieval).
By
combining
high-density
recordings
optogenetic
stimulation
malaise-coding
hindbrain
neurons,
show
selectively
reactivate
from
recent
meal.
The
degree
malaise-driven
individual
neurons
predicts
strengthening
responses
upon
retrieval,
which
turn
leads
stabilization
population-level
representation
recently
consumed
flavour.
contrast,
degrade
absence
consequences.
Thus,
demonstrate
plasticity
may
feedback.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Фев. 20, 2024
ABSTRACT
The
lateral
septum
(LS)
is
a
nucleus
in
the
ventral
forebrain
that
modulates
complex
social
and
affective
behaviors.
Several
distinct
neuronal
types
have
been
described
LS;
however,
full
extent
of
this
cellular
molecular
diversity
remains
unclear.
We
address
gap
by
profiling
transcriptional
identity
mature
LS
neurons
originating
from
two
progenitor
lineages
defined
their
anatomical
location
expression
transcription
factor
Nkx2.1
.
describe
12
molecularly
subtypes
fall
into
main
groups:
those
with
history
without.
discovered
lineage
share
an
enrichment
select
cell
adhesion
communication
molecules.
Despite
this,
we
found
developmental
origins
can
exhibit
significant
similarities.
then
examined
spatial
relationships
among
LS,
revealing
each
subtype
occupies
discrete
domain.
These
domains
are
graded
patterns
gene
correlate
taxonomy
neuron
encode
proteins
involved
synaptic
signaling.
Lastly,
genetically
labeled
non-overlapping
subgroups
neurons,
detailed
connective,
morphological,
electrophysiological
properties.
Our
findings
offer
deeper
understanding
heterogeneity
paving
way
for
future
studies
how
these
contribute
to
regulating
emotional
motivated
Communications Biology,
Год журнала:
2025,
Номер
8(1)
Опубликована: Март 6, 2025
Sleep-onset
insomnia,
characterized
by
difficulty
falling
asleep,
is
linked
to
increased
health
risks.
Previous
studies
have
shown
that
the
central
amygdala
(CeA)
plays
a
crucial
role
in
stress
regulation,
with
somatostatin
neurons
CeA
(CeASST+)
involved
adaptive
responses.
However,
of
CeASST+
stress-induced
sleep-onset
insomnia
remains
unclear.
In
this
study,
we
found
activity
closely
associated
stressful
events
using
fiber
photometry
mice.
Acute
optogenetic
activation
induced
rapid
transition
from
non-rapid
eye
movement
(NREM)
sleep
wakefulness.
Semi-chronic
and
chemogenetic
led
prolonged
latency
Chemogenetic
inhibition
these
ameliorated
stimuli,
but
did
not
affect
sleep-wake
behavior
under
physiological
conditions.
Collectively,
our
results
suggested
are
key
neural
substrate
for
modulating
without
influencing
sleep.
These
findings
highlight
as
promising
target
treating
stress-related
clinical
practice.
Memory
encoding
and
retrieval
rely
on
specific
interactions
across
multiple
brain
areas.
Although
connections
between
individual
areas
have
been
extensively
studied,
the
anatomical
functional
specificity
of
neuronal
circuit
organization
underlying
information
transfer
remains
unclear.
Here,
we
combine
transsynaptic
viral
tracing,
optogenetic
manipulations,
calcium
dynamics
recordings
to
dissect
multisynaptic
connectivity
amygdala.
We
identify
a
distinct
basolateral
amygdala
(BLA)
subpopulation
that
connects
disynaptically
periaqueductal
gray
(PAG)
via
central
(CeA).
This
disynaptic
pathway
serves
as
core
element
necessary
for
learning
expression
conditioned
fear
exhibits
learning-related
plasticity.
Together,
our
findings
demonstrate
utility
approaches
analysis
indicate
may
be
general
feature
organization.
The
central
amygdala
(CeA)
consists
of
numerous
genetically
defined
inhibitory
neurons
that
control
defensive
and
appetitive
behaviors
including
feeding.
Transcriptomic
signatures
cell
types
their
links
to
function
remain
poorly
understood.
Using
single-nucleus
RNA
sequencing,
we
describe
nine
CeA
clusters,
which
four
are
mostly
associated
with
two
aversive
behaviors.
To
analyze
the
activation
mechanism
neurons,
characterized
serotonin
receptor
2a
(Htr2a)-expressing
(CeAHtr2a)
comprise
three
clusters
were
previously
shown
promote
In
vivo
calcium
imaging
revealed
CeAHtr2a
activated
by
fasting,
hormone
ghrelin,
presence
food.
Moreover,
these
required
for
orexigenic
effects
ghrelin.
Appetitive
responsive
fasting
ghrelin
project
parabrachial
nucleus
(PBN)
causing
inhibition
target
PBN
neurons.
These
results
illustrate
how
transcriptomic
diversification
relates
hormone-regulated
feeding
behavior.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Фев. 13, 2024
The
basolateral
amygdala
(BLA)
is
essential
for
assigning
positive
or
negative
valence
to
sensory
stimuli.
Noxious
stimuli
that
cause
pain
are
encoded
by
an
ensemble
of
Cell Reports,
Год журнала:
2024,
Номер
43(9), С. 114669 - 114669
Опубликована: Авг. 23, 2024
Maladaptive
plasticity
is
linked
to
the
chronification
of
diseases
such
as
pain,
but
transition
from
acute
chronic
pain
not
well
understood
mechanistically.
Neuroplasticity
in
central
nucleus
amygdala
(CeA)
has
emerged
a
mechanism
for
sensory
and
emotional-affective
aspects
injury-induced
although
evidence
comes
studies
conducted
almost
exclusively
conditions
agnostic
cell
type
specificity.
Here,
we
report
time-dependent
changes
genetically
distinct
projection-specific
CeA
neurons
neuropathic
pain.
Hyperexcitability
CRF
projection
synaptic
parabrachial
(PB)
input
at
stage
shifted
hyperexcitability
without
non-CRF
phase.
Accordingly,
chemogenetic
inhibition
PB→CeA
pathway
mitigated
pain-related
behaviors
acute,
chronic,
Cell-type-specific
temporal
neuroplasticity
provide
neurobiological
clinical
observation
that
simply
prolonged
persistence