bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2021,
Номер
unknown
Опубликована: Май 29, 2021
Abstract
Spontaneous
correlated
activity
is
a
universal
hallmark
of
immature
neural
circuits.
However,
the
cellular
dynamics
and
intrinsic
mechanisms
underlying
network
burstiness
in
intact
developing
brain
are
largely
unknown.
Here,
we
use
two-photon
Ca
2+
imaging
to
comprehensively
map
developmental
trajectories
spontaneous
hippocampal
area
CA1
vivo
.
We
unexpectedly
find
that
peaks
after
emergence
effective
synaptic
inhibition
second
postnatal
week.
demonstrate
enhanced
reflects
an
increased
functional
coupling
individual
neurons
local
population
activity.
pairwise
neuronal
correlations
low,
bursts
(NBs)
recruit
pyramidal
cells
virtually
random
manner.
Using
dynamic
systems
modeling
approach,
reconcile
these
experimental
findings
identify
bi-stability
as
potential
regime
at
this
age.
Our
analyses
reveal
important
role
input
characteristics
instability
for
NB
generation.
Collectively,
our
data
suggest
mechanism,
whereby
performs
extensive
input-discrimination
learning
prior
onset
environmental
exploration.
CNS Drugs,
Год журнала:
2023,
Номер
37(9), С. 755 - 779
Опубликована: Авг. 21, 2023
γ-Aminobutyric
acid
(GABA)
is
the
most
prevalent
inhibitory
neurotransmitter
in
mammalian
brain
and
has
been
found
to
play
an
important
role
pathogenesis
or
expression
of
many
neurological
diseases,
including
epilepsy.
Although
GABA
can
act
on
different
receptor
subtypes,
component
system
that
critical
modulation
seizure
activity
Journal of Neurochemistry,
Год журнала:
2023,
Номер
165(1), С. 6 - 28
Опубликована: Янв. 22, 2023
Abstract
Epilepsy
is
a
common
neurological
disorder
associated
with
alterations
of
excitation‐inhibition
balance
within
brain
neuronal
networks.
GABA
A
receptor
neurotransmission
the
most
prevalent
form
inhibitory
and
strongly
implicated
in
both
pathophysiology
treatment
epilepsy,
serving
as
primary
target
for
antiseizure
medications
over
century.
It
now
established
that
exerts
multifaceted
influence
through
an
array
subtypes
extends
far
beyond
simply
negating
excitatory
activity.
As
role
circuits
elaborated,
this
will
enable
development
precision
therapies
correct
network
dysfunction
underlying
epileptic
pathology.
image
Abstract
Early
environments
can
have
significant
and
lasting
effects
on
brain,
body,
behavior
across
the
lifecourse.
Here,
we
address
current
research
efforts
to
understand
how
experiences
impact
neurodevelopment
with
a
new
perspective
integrating
two
well‐known
conceptual
frameworks
–
Developmental
Origins
of
Health
Disease
(DOHaD)
sensitive/critical
period
frameworks.
Specifically,
consider
prenatal
characterized
in
DOHaD
model
key
neurobiological
mechanisms
periods
for
adapting
learning
from
postnatal
environment.
We
draw
both
animal
human
summarize
state
knowledge
particular
substance
exposures
(psychoactive
substances
heavy
metals)
nutritional
profiles
(protein‐energy
malnutrition
iron
deficiency)
each
differentially
brain
circuits'
excitation/GABAergic
inhibition
balance
myelination.
Finally,
highlight
directions
that
emerge
this
integrated
framework,
including
testing
alter
timing
identifying
potential
promotional/buffering
periods.
hope
integrative
framework
considering
influences
neuroplasticity
will
stimulate
early
consequences
our
brains,
behavior,
health.
Protein
homeostasis
(proteostasis)
deficiency
is
an
important
contributing
factor
to
neurological
and
metabolic
diseases.
However,
how
the
proteostasis
network
orchestrates
folding
assembly
of
multi-subunit
membrane
proteins
poorly
understood.
Previous
proteomics
studies
identified
Hsp47
(Gene:
SERPINH1
),
a
heat
shock
protein
in
endoplasmic
reticulum
lumen,
as
most
enriched
interacting
chaperone
for
gamma-aminobutyric
acid
type
A
(GABA
)
receptors.
Here,
we
show
that
enhances
functional
surface
expression
GABA
receptors
rat
neurons
human
HEK293T
cells.
Furthermore,
molecular
mechanism
study
demonstrates
acts
after
BiP
HSPA5
preferentially
binds
folded
conformation
without
inducing
unfolded
response
Therefore,
promotes
subunit-subunit
interaction,
receptor
process,
anterograde
trafficking
Overexpressing
sufficient
correct
function
epilepsy-associated
variants
also
other
Cys-loop
receptors,
including
nicotinic
acetylcholine
serotonin
3
addition
its
known
collagen
chaperone,
this
work
establishes
plays
critical
general
role
maturation
neuroreceptors.
Elevated
blood
glucose
levels,
or
hyperglycemia,
can
increase
brain
excitability
and
amyloid-β
(Aβ)
release,
offering
a
mechanistic
link
between
type
2
diabetes
Alzheimer's
disease
(AD).
Since
the
cellular
mechanisms
governing
this
relationship
are
poorly
understood,
we
explored
whether
ATP-sensitive
potassium
(KATP)
channels,
which
couple
changes
in
energy
availability
with
excitability,
play
role
AD
pathogenesis.
First,
demonstrate
that
KATP
channel
subunits
Kir6.2/KCNJ11
SUR1/ABCC8
were
expressed
on
excitatory
inhibitory
neurons
human
brain,
cortical
expression
of
KCNJ11
ABCC8
changed
pathology
humans
mice.
Next,
eliminating
neuronal
activity
uncoupled
metabolism,
Aβ
potentially
novel
mouse
model
cerebral
amyloidosis
ablation
(i.e.,
amyloid
precursor
protein
[APP]/PS1
Kir6.2–/–
mouse).
Using
both
acute
chronic
paradigms,
Kir6.2-KATP
channels
metabolic
sensors
regulate
hyperglycemia-dependent
increases
interstitial
fluid
levels
Aβ,
amyloidogenic
processing
APP,
plaque
formation,
may
be
dependent
lactate
release.
These
studies
identify
new
for
suggest
pharmacological
manipulation
holds
therapeutic
promise
reducing
patients
prediabetes.
Frontiers in Neurology,
Год журнала:
2023,
Номер
14
Опубликована: Апрель 17, 2023
The
SCN1A
gene
is
strongly
associated
with
epilepsy
and
plays
a
central
role
for
supporting
cortical
excitation-inhibition
balance
through
the
expression
of
Na
V
1.1
within
inhibitory
interneurons.
phenotype
disorders
has
been
conceptualized
as
driven
primarily
by
impaired
interneuron
function
that
predisposes
to
disinhibition
hyperexcitability.
However,
recent
studies
have
identified
gain-of-function
variants
epilepsy,
presence
cellular
synaptic
changes
in
mouse
models
point
toward
homeostatic
adaptations
complex
network
remodeling.
These
findings
highlight
need
understand
microcircuit-scale
dysfunction
contextualize
genetic
disease
mechanisms.
Targeting
restoration
microcircuit
properties
may
be
fruitful
strategy
development
novel
therapies.
Brain Sciences,
Год журнала:
2025,
Номер
15(3), С. 284 - 284
Опубликована: Март 7, 2025
Background:
Childhood
is
a
crucial
period
for
brain
development,
and
short-term
juvenile
stress
has
demonstrated
long-lasting
effects
on
cognitive
cellular
functions
in
the
hippocampus.
However,
influence
of
such
brain’s
overall
network
remains
unclear.
Methods:
In
this
study,
we
employed
functional
magnetic
resonance
imaging
(fMRI)
to
explore
transient
wild
male
rats.
Pregnant
rats
were
purchased
housed
specific
pathogen-free
(SPF)
environment,
with
pups
separated
by
sex
postnatal
day
21
(PD21).
From
PD27
PD29,
subjected
stress,
which
included
forced
swimming,
elevated
platform
exposure,
restraint
stress.
Following
all
animals
carefully
maintained
scanned
at
42
days
age
(PD42)
using
fMRI.
Structural
analysis
was
performed
voxel-based
morphometry
(VBM)
assess
changes
gray
matter
volume,
while
activity
evaluated
through
regional
homogeneity
(ReHo)
voxel-wise
connectivity.
Results:
The
results
showed
significant
reductions
volume
several
regions
group,
including
periaqueductal
(PAG),
entorhinal
cortex
(Ent),
dentate
gyrus
(DG).
terms
activity,
cortical
regions,
particularly
primary
somatosensory
areas,
exhibited
decreased
whereas
increased
observed
PAG,
DG,
medulla.
Furthermore,
connectivity
revealed
reduction
between
DG
cortex,
DG-PAG
significantly
enhanced.
Conclusions:
These
findings
suggest
that
leads
profound
alterations
both
structure
function,
potentially
disrupting
emotional
regulation
memory
processing
affecting
development
key
regions.
International Journal of Oncology,
Год журнала:
2022,
Номер
61(3)
Опубликована: Июль 11, 2022
An
increasing
body
of
evidence
has
become
available
to
reveal
the
synaptic
and
functional
integration
glioma
into
brain
network,
facilitating
tumor
progression.
The
novel
discovery
glioma‑neuronal
interactions
fundamentally
challenged
our
understanding
this
refractory
disease.
present
review
aimed
provide
an
overview
how
neuronal
activities
function
through
synapses,
neurotransmitters,
ion
channels,
gap
junctions,
microtubes
molecules
establish
communications
with
glioma,
as
well
a
simplified
explanation
reciprocal
effects
crosstalk
on
pathophysiology.
In
addition,
current
state
therapeutic
avenues
targeting
critical
factors
involved
in
glioma‑euronal
is
discussed
clinical
trial
data
for
further
investigation
provided.
Finally,
newly
emerging
technologies,
including
immunomodulation,
neural
stem
cell‑based
delivery
system,
optogenetics
techniques
co‑culture
neuron
organoids
are
proposed,
which
may
pave
way
towards
gaining
deeper
insight
both
mechanisms
associated
neuron‑
glioma‑communicating
networks
development
strategies
target
currently
lethal
tumor.
Frontiers in Neural Circuits,
Год журнала:
2023,
Номер
17
Опубликована: Март 30, 2023
Neural
circuits
are
characterized
as
interconnecting
neuron
networks
connected
by
synapses.
Some
kinds
of
gene
expression
and/or
functional
changes
neurons
and
synaptic
connections
may
result
in
aberrant
neural
circuits,
which
has
been
recognized
one
crucial
pathological
mechanism
for
the
onset
many
neurological
diseases.
Gradual
advances
single-cell
sequencing
approaches
with
strong
technological
advantages,
exemplified
high
throughput
increased
resolution
live
cells,
have
enabled
it
to
assist
us
understanding
neuronal
diversity
across
diverse
brain
regions
further
transformed
our
knowledge
cellular
building
blocks
through
revealing
numerous
molecular
signatures.
Currently
published
transcriptomic
studies
elucidated
various
subpopulations
well
their
distribution
prefrontal
cortex,
hippocampus,
hypothalamus,
dorsal
root
ganglion,
etc.
Better
characterization
region-specific
shed
light
on
new
mechanisms
involved
selecting
potential
targets
prevention
treatment
specific
disorders
based
established
roles.
Given
populations
different
regions,
we
aim
give
a
brief
sketch
current
progress
circuit
complexity
according
locations.
With
special
focus
application
sequencing,
thereby
summarize
relevant
findings.
Considering
importance
spatial
context
connectivity
also
discuss
few
results
obtained
transcriptomics.
Taken
together,
these
data
lay
mechanistic
basis
identification
components,
links
signatures
anatomical
connectivity,
morphology,
physiology.
Furthermore,
comprehensive
subtypes,
distributions,
patterns
via
is
critical
properties
how
they
generate
region-dependent
interactions
context.