bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 1, 2023
SUMMARY
Our
movements
result
in
predictable
sensory
feedback
that
is
often
multimodal.
Based
on
deviations
between
predictions
and
actual
input,
primary
areas
of
cortex
have
been
shown
to
compute
sensorimotor
prediction
errors.
How
errors
one
modality
influence
the
computation
another
still
unclear.
To
investigate
multimodal
mouse
auditory
(ACx),
we
used
a
virtual
environment
experimentally
couple
running
both
self-generated
visual
feedback.
Using
two-photon
microscopy,
first
characterized
responses
layer
2/3
(L2/3)
neurons
sounds,
stimuli,
onsets
found
all
three
stimuli.
Probing
evoked
by
audiomotor
mismatches,
they
closely
resemble
visuomotor
mismatch
(V1).
Finally,
testing
for
cross
modal
coupling
sound
amplitude
flow
speed
running,
were
amplified
when
paired
with
concurrent
mismatches.
results
demonstrate
non-hierarchical
interactions
shape
error
cortical
L2/3.
Journal of Neuroscience,
Journal Year:
2024,
Volume and Issue:
44(11), P. e1227232024 - e1227232024
Published: Jan. 29, 2024
Neurons
in
the
mouse
auditory
cortex
are
strongly
influenced
by
behavior,
including
both
suppression
and
enhancement
of
sound-evoked
responses
during
movement.
The
comprises
multiple
fields
with
different
roles
sound
processing
distinct
connectivity
to
movement-related
centers
brain.
Here,
we
asked
whether
modulation
male
mice
might
differ
across
cortical
fields,
thereby
contributing
heterogeneity
at
single-cell
level.
We
used
wide-field
calcium
imaging
identify
cellular-resolution
two-photon
visualize
activity
layer
2/3
excitatory
neurons
within
each
field.
measured
neuron's
three
categories
(pure
tones,
chirps,
amplitude-modulated
white
noise)
as
rested
ran
on
a
non-motorized
treadmill.
found
that
individual
field
typically
respond
just
one
category.
Some
only
active
rest
others
locomotion,
those
responsive
conditions
retain
their
sound-category
tuning.
effects
locomotion
vary
level,
neural
responses,
net
modulatory
effect
is
largely
conserved
fields.
Movement-related
also
reflects
more
complex
behavioral
patterns,
instantaneous
running
speed
nonlocomotor
movements
such
grooming
postural
adjustments,
similar
patterns
seen
all
Our
findings
underscore
complexity
throughout
indicate
widespread
phenomenon.
Effective
regulation
of
energy
metabolism
is
critical
for
survival.
Metabolic
control
involves
various
nuclei
within
the
hypothalamus,
which
receive
information
about
body's
state
and
coordinate
appropriate
responses
to
maintain
homeostasis,
such
as
thermogenesis,
pancreatic
insulin
secretion,
food-seeking
behaviors.
It
has
recently
been
found
that
hippocampus,
a
brain
region
traditionally
associated
with
memory
spatial
navigation,
also
involved
in
metabolic
regulation.
Specifically,
hippocampal
sharp
wave-ripples
(SWRs),
are
high-frequency
neural
oscillations
supporting
consolidation
foraging
decisions,
have
shown
reduce
peripheral
glucose
levels.
However,
whether
SWRs
enhanced
by
recent
feeding-when
need
increases,
if
so,
feeding-dependent
modulation
communicated
other
regions
regulation-remains
unknown.
To
address
these
gaps,
we
recorded
from
dorsal
CA1
hippocampus
mice
during
sleep
sessions
before
after
consumption
meals
varying
caloric
values.
We
occurring
significantly
following
food
intake,
magnitude
enhancement
being
dependent
on
content
meal.
This
pattern
occurred
under
both
food-deprived
ad
libitum
feeding
conditions.
Moreover,
demonstrate
GABAergic
neurons
lateral
known
regulate
exhibit
robust
SWR-triggered
increase
activity.
These
findings
identify
satiety
factor
modulating
suggest
hippocampal-lateral
hypothalamic
communication
potential
mechanism
could
modulate
intake.
Effective
regulation
of
energy
metabolism
is
critical
for
survival.
Metabolic
control
involves
various
nuclei
within
the
hypothalamus,
which
receive
information
about
body’s
state
and
coordinate
appropriate
responses
to
maintain
homeostasis,
such
as
thermogenesis,
pancreatic
insulin
secretion,
food-seeking
behaviors.
It
has
recently
been
found
that
hippocampus,
a
brain
region
traditionally
associated
with
memory
spatial
navigation,
also
involved
in
metabolic
regulation.
Specifically,
hippocampal
sharp
wave
ripples
(SWRs),
are
high-frequency
neural
oscillations
supporting
consolidation
foraging
decisions,
have
shown
influence
peripheral
glucose
metabolism.
However,
whether
SWRs
enhanced
by
recent
feeding–when
need
increases,
if
so,
feeding-dependent
modulation
communicated
other
regions
regulation,
remains
unknown.
To
address
these
gaps,
we
recorded
from
dorsal
CA1
hippocampus
mice
during
sleep
sessions
before
after
consumption
meals
varying
caloric
values.
We
occurring
significantly
following
food
intake,
magnitude
enhancement
being
dependent
on
content
meal.
This
pattern
occurred
under
both
food-deprived
ad
libitum
feeding
conditions.
Moreover,
demonstrate
GABAergic
neurons
lateral
known
regulate
exhibit
robust
SWR-triggered
increase
activity.
These
findings
identify
satiety
factor
modulating
suggest
hippocampal-lateral
hypothalamic
communication
potential
mechanism
could
modulate
intake.
Our
movements
result
in
predictable
sensory
feedback
that
is
often
multimodal.
Based
on
deviations
between
predictions
and
actual
input,
primary
areas
of
cortex
have
been
shown
to
compute
sensorimotor
prediction
errors.
How
errors
one
modality
influence
the
computation
another
still
unclear.
To
investigate
multimodal
mouse
auditory
(ACx),
we
used
a
virtual
environment
experimentally
couple
running
both
self-generated
visual
feedback.
Using
two-photon
microscopy,
first
characterized
responses
layer
2/3
(L2/3)
neurons
sounds,
stimuli,
onsets
found
all
three
stimuli.
Probing
evoked
by
audiomotor
mismatches,
they
closely
resemble
visuomotor
mismatch
(V1).
Finally,
testing
for
cross
modal
coupling
sound
amplitude
flow
speed
running,
were
amplified
when
paired
with
concurrent
mismatches.
results
demonstrate
non-hierarchical
interactions
shape
error
cortical
L2/3.
Our
movements
result
in
predictable
sensory
feedback
that
is
often
multimodal.
Based
on
deviations
between
predictions
and
actual
input,
primary
areas
of
cortex
have
been
shown
to
compute
sensorimotor
prediction
errors.
How
errors
one
modality
influence
the
computation
another
still
unclear.
To
investigate
multimodal
mouse
auditory
cortex,
we
used
a
virtual
environment
experimentally
couple
running
both
self-generated
visual
feedback.
Using
two-photon
microscopy,
first
characterized
responses
layer
2/3
(L2/3)
neurons
sounds,
stimuli,
onsets
found
all
three
stimuli.
Probing
evoked
by
audiomotor
(AM)
mismatches,
they
closely
resemble
visuomotor
(VM)
mismatch
(V1).
Finally,
testing
for
cross
modal
AM
coupling
sound
amplitude
flow
speed
running,
were
amplified
when
paired
with
concurrent
VM
mismatches.
results
demonstrate
non-hierarchical
interactions
shape
error
cortical
L2/3.
Effective
regulation
of
energy
metabolism
is
critical
for
survival.
Metabolic
control
involves
various
nuclei
within
the
hypothalamus,
which
receive
information
about
body’s
state
and
coordinate
appropriate
responses
to
maintain
homeostasis,
such
as
thermogenesis,
pancreatic
insulin
secretion,
food-seeking
behaviors.
It
has
recently
been
found
that
hippocampus,
a
brain
region
traditionally
associated
with
memory
spatial
navigation,
also
involved
in
metabolic
regulation.
Specifically,
hippocampal
sharp
wave-ripples
(SWRs),
are
high-frequency
neural
oscillations
supporting
consolidation
foraging
decisions,
have
shown
reduce
peripheral
glucose
levels.
However,
whether
SWRs
enhanced
by
recent
feeding—when
need
increases,
if
so,
feeding-dependent
modulation
communicated
other
regions
regulation—remains
unknown.
To
address
these
gaps,
we
recorded
from
dorsal
CA1
hippocampus
mice
during
sleep
sessions
before
after
consumption
meals
varying
caloric
values.
We
occurring
significantly
following
food
intake,
magnitude
enhancement
being
dependent
on
content
meal.
This
pattern
occurred
under
both
food-deprived
ad
libitum
feeding
conditions.
Moreover,
demonstrate
GABAergic
neurons
lateral
known
regulate
exhibit
robust
SWR-triggered
increase
activity.
These
findings
identify
satiety
factor
modulating
suggest
hippocampal-lateral
hypothalamic
communication
potential
mechanism
could
modulate
intake.
Effective
regulation
of
energy
metabolism
is
critical
for
survival.
Metabolic
control
involves
various
nuclei
within
the
hypothalamus,
which
receive
information
about
body’s
state
and
coordinate
appropriate
responses
to
maintain
homeostasis,
such
as
thermogenesis,
pancreatic
insulin
secretion,
food-seeking
behaviors.
It
has
recently
been
found
that
hippocampus,
a
brain
region
traditionally
associated
with
memory
spatial
navigation,
also
involved
in
metabolic
regulation.
Specifically,
hippocampal
sharp
wave
ripples
(SWRs),
are
high-frequency
neural
oscillations
supporting
consolidation
foraging
decisions,
have
shown
reduce
peripheral
glucose
levels.
However,
whether
SWRs
enhanced
by
recent
feeding–
when
need
increases,
if
so,
feeding-dependent
modulation
communicated
other
regions
regulation,
remains
unknown.
To
address
these
gaps,
we
recorded
from
dorsal
CA1
hippocampus
mice
during
sleep
sessions
before
after
consumption
meals
varying
caloric
values.
We
occurring
significantly
following
food
intake,
magnitude
enhancement
being
dependent
on
content
meal.
This
pattern
occurred
under
both
food-deprived
ad
libitum
feeding
conditions.
Moreover,
demonstrate
GABAergic
neurons
lateral
known
regulate
exhibit
robust
SWR-triggered
increase
activity.
These
findings
identify
satiety
factor
modulating
suggest
hippocampal-lateral
hypothalamic
communication
potential
mechanism
could
modulate
intake.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 29, 2025
Abstract
The
ability
to
rapidly
detect
and
respond
unexpected
auditory
stimuli
is
critical
for
adaptive
behavior,
especially
during
locomotion.
Since
movement
suppresses
cortical
activity,
it
remains
unclear
how
salient
information
influences
locomotor
circuits.
In
this
work,
using
in
vivo
calcium
imaging,
electrophysiology,
chemo-
optogenetics,
we
investigate
the
path
that
relays
loud
broadband
sounds
dorsal
hippocampus
(dHPC)
modulates
theta
oscillations.
We
demonstrate
noise
accelerates
frequency
decreases
its
power,
effects
mediated
by
entorhinal
cortex
(EC)
medial
septum
(MS)
inputs
while
independent
of
primary
cortex.
Activation
cochlear
nucleus
(DCN)
neurons
projecting
pontine
reticular
(PRN)
mimics
noise-driven
hippocampal
responses,
supporting
a
brainstem-limbic
processing
route.
Furthermore,
selectively
CA1
pyramidal
neuron
interneuron
reflecting
diverse
circuit
dynamics.
Finally,
stimulus
increased
coherence
between
dHPC
prefrontal
(mPFC),
enhancing
interregional
synchronization.
These
results
highlight
mechanisms
which
DCN
filters
behaviorally
relevant
promoting
acoustic
motor
integration
locomotion,
without
direct
influence
PLoS Biology,
Journal Year:
2025,
Volume and Issue:
23(4), P. e3003087 - e3003087
Published: April 7, 2025
Active
sensation
requires
the
brain
to
interpret
external
stimuli
against
an
ongoing
estimate
of
body
position.
While
internal
estimates
position
are
often
ascribed
cerebral
cortex,
we
examined
midbrain
superior
colliculus
(SC),
due
its
close
relationship
with
sensory
periphery
as
well
higher,
motor-related
regions.
Using
high-density
electrophysiology
and
movement
tracking,
discovered
that
on-going
kinematics
whisker
motion
locomotion
speed
accurately
predict
firing
rate
mouse
SC
neurons.
Neural
activity
was
best
predicted
by
movements
occurring
either
in
past,
present,
or
future,
indicating
population
continuously
a
trajectory
self-motion.
A
combined
representation
slow
fast
whisking
features
absolute
angle
at
high
temporal
resolution.
Sensory
reafference
played
least
partial
role
shaping
this
feature
tuning.
Taken
together,
these
data
indicate
contains
joint
locomotor
is
potentially
useful
guiding
complex
orienting
involving
face
limbs.
Our
movements
result
in
predictable
sensory
feedback
that
is
often
multimodal.
Based
on
deviations
between
predictions
and
actual
input,
primary
areas
of
cortex
have
been
shown
to
compute
sensorimotor
prediction
errors.
How
errors
one
modality
influence
the
computation
another
still
unclear.
To
investigate
multimodal
mouse
auditory
(ACx),
we
used
a
virtual
environment
experimentally
couple
running
both
self-generated
visual
feedback.
Using
two-photon
microscopy,
first
characterized
responses
layer
2/3
(L2/3)
neurons
sounds,
stimuli,
onsets
found
all
three
stimuli.
Probing
evoked
by
audiomotor
mismatches,
they
closely
resemble
visuomotor
mismatch
(V1).
Finally,
testing
for
cross
modal
coupling
sound
amplitude
flow
speed
running,
were
amplified
when
paired
with
concurrent
mismatches.
results
demonstrate
non-hierarchical
interactions
shape
error
cortical
L2/3.