Antibiotics,
Journal Year:
2022,
Volume and Issue:
11(12), P. 1767 - 1767
Published: Dec. 7, 2022
In
order
to
develop
properly,
the
brain
requires
intricate
interconnection
of
genetic
factors
and
pre-and
postnatal
environmental
events.
The
gut-brain
axis
has
recently
raised
considerable
interest
for
its
involvement
in
regulating
development
functioning
brain.
Consequently,
alterations
gut
microbiota
composition,
due
antibiotic
administration,
could
favor
onset
neurodevelopmental
disorders.
Literature
data
suggest
that
modulation
is
often
altered
individuals
affected
by
It
been
shown
animal
studies
metabolites
released
an
imbalanced
axis,
leads
function
deficits
social
behavior.
Here,
we
report
potential
effects
before
after
birth,
relation
risk
developing
We
also
review
role
probiotics
treating
gastrointestinal
disorders
associated
with
dysbiosis
their
possible
effect
ameliorating
disorder
symptoms.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(6), P. 5487 - 5487
Published: March 13, 2023
Autism
spectrum
disorder
(ASD)
is
a
neurodevelopmental
(NDD)
characterized
by
impairments
in
social
communication,
repetitive
behaviors,
restricted
interests,
and
hyperesthesia/hypesthesia
caused
genetic
and/or
environmental
factors.
In
recent
years,
inflammation
oxidative
stress
have
been
implicated
the
pathogenesis
of
ASD.
this
review,
we
discuss
pathophysiology
ASD,
particularly
focusing
on
maternal
immune
activation
(MIA).
MIA
one
common
risk
factors
for
onset
ASD
during
pregnancy.
It
induces
an
reaction
pregnant
mother’s
body,
resulting
further
placenta
fetal
brain.
These
negative
cause
developing
brain
subsequently
behavioral
symptoms
offspring.
addition,
also
effects
anti-inflammatory
drugs
antioxidants
basic
studies
animals
clinical
Our
review
provides
latest
findings
new
insights
into
involvements
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(5), P. 1886 - 1886
Published: Feb. 22, 2025
Pediatric
stroke,
a
significant
cause
of
long-term
neurological
deficits
in
children,
often
arises
from
disruptions
within
neurovascular
unit
(NVU)
components.
The
NVU,
dynamic
ensemble
astrocytes,
endothelial
cells,
pericytes,
and
microglia,
is
vital
for
maintaining
cerebral
homeostasis
regulating
vascular
brain
development.
Its
structural
integrity,
particularly
at
the
blood-brain
barrier
(BBB),
depends
on
intercellular
junctions
basement
membrane,
which
together
restrict
paracellular
transport
shield
systemic
insults.
Dysfunction
this
intricate
system
increasingly
linked
to
pediatric
stroke
related
cerebrovascular
conditions.
Mutations
disrupting
cell
adhesion
or
pericyte-endothelial
interactions
can
compromise
BBB
stability,
leading
pathological
outcomes
such
as
intraventricular
hemorrhage
germinal
matrix,
hallmark
immaturity.
Additionally,
inflammation,
ferroptosis,
necroptosis,
autophagy
are
key
cellular
processes
influencing
damage
repair.
Excessive
activation
these
mechanisms
exacerbate
NVU
injury,
whereas
targeted
therapeutic
modulation
offers
potential
pathways
mitigate
support
recovery.
This
review
explores
molecular
underlying
dysfunction,
disruption,
subsequent
injury
stroke.
Understanding
interplay
between
genetic
mutations,
environmental
stressors,
dynamics
provides
new
insights
into
pathogenesis.
susceptibility
matrix
rupture
further
emphasizes
critical
role
integrity
early
Targeting
inflammatory
death
presents
promising
strategies
preserve
function
improve
affected
neonates.
Acta Physiologica,
Journal Year:
2025,
Volume and Issue:
241(4)
Published: March 5, 2025
Silencing
of
DEP-domain
containing
mTOR-interacting
protein
(DEPTOR),
an
endogenous
inhibitor
the
mammalian
target
rapamycin
(mTOR)
pathway,
increases
mTOR
signaling
and
System
A/L
amino
acid
transport
activity
in
cultured
primary
human
trophoblast
cells.
However,
there
is
no
evidence
supporting
regulatory
role
DEPTOR
placental
function
vivo.
We
hypothesized
that
trophoblast-specific
Deptor
knockdown
(KD)
mice
signaling,
transport,
enhances
fetal
growth.
generated
DeptorKD
transgenic
mice,
at
embryonic
day
18.5,
placentas
were
analyzed
to
confirm
efficiency,
specificity,
pathway
levels.
Trophoblast
plasma
membrane
(TPM)
expression
also
determined.
examined
relationship
between
birthweight
levels
collected
term
from
appropriate
for
gestational
age
(AGA)
large
(LGA)
pregnancies.
Reducing
RNA
increased
transporter
expression/activity,
growth
mice.
Similarly,
LGA
displayed
decreased
levels,
inversely
correlated
BMI.
This
first
report
showing
sufficient
activate
a
master
regulator
function,
which
TPM
A
L
activity.
propose
mechanistically
linked
Furthermore,
modulation
may
represent
promising
approach
improve
outcomes
pregnancies
characterized
by
abnormal
Biology,
Journal Year:
2024,
Volume and Issue:
13(2), P. 126 - 126
Published: Feb. 17, 2024
Neurodevelopmental
disorders
(NDDs)
comprise
a
diverse
group
of
diseases,
including
developmental
delay,
autism
spectrum
disorder
(ASD),
intellectual
disability
(ID),
and
attention-deficit/hyperactivity
(ADHD).
NDDs
are
caused
by
aberrant
brain
development
due
to
genetic
environmental
factors.
To
establish
specific
curative
therapeutic
approaches,
it
is
indispensable
gain
precise
mechanistic
insight
into
the
cellular
molecular
pathogenesis
NDDs.
Mutations
European Journal of Neuroscience,
Journal Year:
2024,
Volume and Issue:
60(2), P. 3858 - 3890
Published: May 30, 2024
Abstract
Patients
with
neurodevelopmental
disorders,
such
as
autism
spectrum
disorder,
often
display
abnormal
circadian
rhythms.
The
role
of
the
system
in
these
disorders
has
gained
considerable
attention
over
last
decades.
Yet,
it
remains
largely
unknown
how
disruptions
occur
and
to
what
extent
they
contribute
disorders'
development.
In
this
review,
we
examine
dysregulation
observed
patients
animal
models
disorders.
Second,
explore
whether
rhythm
constitute
a
risk
factor
for
from
studies
humans
model
organisms.
Lastly,
focus
on
impact
psychiatric
medications
rhythms
potential
benefits
chronotherapy.
literature
reveals
that
altered
sleep–wake
cycles
melatonin
rhythms/levels
heterogeneous
manner,
organisms
used
study
appear
support
dysfunction
may
be
an
inherent
characteristic
Furthermore,
pre‐clinical
clinical
evidence
indicates
disruption
at
environmental
genetic
levels
behavioural
changes
Finally,
suggest
medications,
particularly
those
prescribed
attention‐deficit/hyperactivity
disorder
schizophrenia,
can
have
direct
effects
chronotherapy
leveraged
offset
some
side
effects.
This
review
highlights
is
likely
core
pathological
feature
further
research
required
elucidate
relationship.
Frontiers in Neuroscience,
Journal Year:
2024,
Volume and Issue:
18
Published: Jan. 25, 2024
The
growth
arrest
and
DNA
damage
inducible
protein
45
(GADD45)
family
comprises
stress-induced
nuclear
proteins
that
interact
with
demethylases
to
facilitate
demethylation,
thereby
regulating
diverse
cellular
processes
including
oxidative
stress,
repair,
apoptosis,
proliferation,
differentiation,
inflammation,
neuroplasticity
by
modulating
the
expression
patterns
of
specific
genes.
Widely
expressed
in
central
nervous
system,
GADD45
plays
a
pivotal
role
various
neurological
disorders,
rendering
it
potential
therapeutic
target
for
system
diseases.
This
review
presented
comprehensive
overview
mechanisms
action
associated
each
member
(GADD45α,
GADD45β,
GADD45γ)
neurodevelopmental,
neurodegenerative,
neuropsychiatric
while
also
explored
strategies
harness
these
intervention
treatment.
Future
research
should
prioritize
development
effective
modulators
targeting
clinical
trials
aimed
at
treating
Open Medicine,
Journal Year:
2023,
Volume and Issue:
18(1)
Published: Jan. 1, 2023
Abstract
Today,
in
the
modern
world,
people
are
often
exposed
to
electromagnetic
waves,
which
can
have
undesirable
effects
on
cell
components
that
lead
differentiation
and
abnormalities
proliferation,
deoxyribonucleic
acid
(DNA)
damage,
chromosomal
abnormalities,
cancers,
birth
defects.
This
study
aimed
investigate
effect
of
waves
fetal
childhood
abnormalities.
PubMed,
Scopus,
Web
Science,
ProQuest,
Cochrane
Library,
Google
Scholar
were
searched
1
January
2023.
The
Cochran’s
Q
-test
I
2
statistics
applied
assess
heterogeneity,
a
random-effects
model
was
used
estimate
pooled
odds
ratio
(OR),
standardized
mean
difference
(SMD),
for
different
outcomes,
meta-regression
method
utilized
factors
affecting
heterogeneity
between
studies.
A
total
14
studies
included
analysis,
outcomes
investigated
were:
change
gene
expression,
oxidant
parameters,
antioxidant
DNA
damage
parameters
umbilical
cord
blood
fetus
developmental
disorders,
development
disorders.
Totally,
events
more
common
parents
who
been
EMFs
compared
those
not
(SMD
95%
confidence
interval
[CI],
0.25
[0.15–0.35];
,
91%).
Moreover,
disorders
(OR,
1.34;
CI,
1.17–1.52;
0%);
cancer
1.14;
1.05–1.23;
60.1%);
2.10;
1.00–3.21;
changes
expression
(mean
[MD],
1.02;
0.67–1.37;
93%);
(MD,
0.94;
0.70–1.18;
61.3%);
1.01;
0.17–1.86;
91.6%)
than
not.
According
meta-regression,
publication
year
has
significant
(coefficient:
0.033;
0.009–0.057).
Maternal
exposure
fields,
especially
first
trimester
pregnancy,
due
high
level
stem
cells
their
sensitivity
this
radiation,
biochemical
examined
shown
increased
oxidative
stress
reactions,
protein
embryonic
In
addition,
parental
ionizing
non-ionizing
radiation
enhancement
cell-based
cancers
such
as
speech
problems
childhood.