Neuromodulatory signaling contributing to the encoding of aversion
Cheng-Hsi Wu,
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Léa Camelot,
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Salvatore Lecca
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et al.
Trends in Neurosciences,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 1, 2025
The
appropriate
and
rapid
encoding
of
stimuli
bearing
a
negative
valence
enables
behaviors
that
are
essential
for
survival.
Recent
advances
in
neuroscience
using
rodents
as
model
system
highlight
the
relevance
cell
type-specific
neuronal
activities
diverse
brain
networks
aversion,
well
their
importance
subsequent
behavioral
strategies.
Within
these
networks,
neuromodulators
influence
excitability,
adjust
fast
synaptic
neurotransmission,
affect
plasticity,
ultimately
modulating
behaviors.
In
this
review
we
first
discuss
contemporary
findings
leveraging
use
cutting-edge
neurotechnologies
to
define
aversion-related
neural
circuits.
spatial
temporal
dynamics
release
neuropeptides
upon
exposure
aversive
described
within
defined
Together,
mechanistic
insights
update
present
framework
through
which
aversion
drives
motivated
Language: Английский
Inhibitory basal ganglia nuclei differentially innervate pedunculopontine nucleus subpopulations and evoke opposite motor and valence behaviors.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 6, 2024
The
canonical
basal
ganglia
model
predicts
that
the
substantia
nigra
pars
reticulata
(SNr)
and
globus
pallidus
externa
(GPe)
will
have
specific
effects
on
locomotion:
SNr
inhibiting
locomotion
GPe
enhancing
it.
In
this
manuscript,
we
use
in
vivo
optogenetics
to
show
a
projection-defined
neural
subpopulation
within
each
structure
exerts
non-canonical
locomotion.
These
subpopulations
are
defined
by
their
projection
pedunculopontine
nucleus
(PPN)
mediate
opposing
reward.
To
understand
how
these
structures
differentially
modulate
PPN,
ex
whole-cell
recording
with
comprehensively
dissect
connections
regionally-
molecularly-defined
populations
of
PPN
neurons.
inhibits
all
subtypes,
but
most
strongly
caudal
glutamatergic
selectively
GABAergic
neurons,
avoiding
both
cholinergic
rostral
cells.
This
circuit
characterization
reveals
pathways
for
valence.
Language: Английский
Inhibitory basal ganglia nuclei differentially innervate pedunculopontine nucleus subpopulations and evoke opposite motor and valence behaviors
Published: Oct. 30, 2024
The
canonical
basal
ganglia
model
predicts
that
the
substantia
nigra
pars
reticulata
(SNr)
and
globus
pallidus
externa
(GPe)
will
have
specific
effects
on
locomotion:
SNr
inhibiting
locomotion
GPe
enhancing
it.
In
this
manuscript,
we
use
in
vivo
optogenetics
to
show
a
projection-defined
neural
subpopulation
within
each
structure
exerts
non-canonical
locomotion.
These
subpopulations
are
defined
by
their
projection
pedunculopontine
nucleus
(PPN)
mediate
opposing
reward.
To
understand
how
these
structures
differentially
modulate
PPN,
ex
whole-cell
recording
with
comprehensively
dissect
connections
regionally–
molecularly-defined
populations
of
PPN
neurons.
inhibits
all
subtypes,
but
most
strongly
caudal
glutamatergic
selectively
GABAergic
neurons,
avoiding
both
cholinergic
rostral
cells.
This
circuit
characterization
reveals
pathways
for
valence.
Language: Английский
Inhibitory basal ganglia nuclei differentially innervate pedunculopontine nucleus subpopulations and evoke opposite motor and valence behaviors
Published: Oct. 30, 2024
The
canonical
basal
ganglia
model
predicts
that
the
substantia
nigra
pars
reticulata
(SNr)
and
globus
pallidus
externa
(GPe)
will
have
specific
effects
on
locomotion:
SNr
inhibiting
locomotion
GPe
enhancing
it.
In
this
manuscript,
we
use
in
vivo
optogenetics
to
show
a
projection-defined
neural
subpopulation
within
each
structure
exerts
non-canonical
locomotion.
These
subpopulations
are
defined
by
their
projection
pedunculopontine
nucleus
(PPN)
mediate
opposing
reward.
To
understand
how
these
structures
differentially
modulate
PPN,
ex
whole-cell
recording
with
comprehensively
dissect
connections
regionally–
molecularly-defined
populations
of
PPN
neurons.
inhibits
all
subtypes,
but
most
strongly
caudal
glutamatergic
selectively
GABAergic
neurons,
avoiding
both
cholinergic
rostral
cells.
This
circuit
characterization
reveals
pathways
for
valence.
Language: Английский