Molecular Therapy — Nucleic Acids,
Journal Year:
2024,
Volume and Issue:
35(1), P. 102136 - 102136
Published: Feb. 2, 2024
Autism
is
a
widespread
neurodevelopmental
disorder.
Although
the
research
on
autism
spectrum
disorders
has
been
increasing
in
past
decade,
there
still
no
specific
answer
to
its
mechanism
of
action
and
treatment.
As
pro-inflammatory
microRNA,
miR-301a
abnormally
expressed
various
psychiatric
diseases
including
autism.
Here,
we
show
that
deletion
inhibition
exhibited
two
distinct
abnormal
behavioral
phenotypes
mice.
We
observed
mice
impaired
learning/memory,
enhanced
anxiety.
On
contrary,
effectively
reduced
maternal
immune
activation
(MIA)-induced
autism-like
behaviors
further
demonstrated
bound
3′UTR
region
SOCS3,
led
upregulation
SOCS3
hippocampus.
The
last
result
reduction
inflammatory
response
by
inhibiting
phosphorylation
AKT
STAT3,
expression
level
IL-17A
poly(I:C)-induced
features
obtained
data
revealed
as
critical
participant
partial
behavior
phenotypes,
which
may
exhibit
divergent
role
between
gene
knockout
knockdown.
Our
findings
ascertain
negatively
regulates
MIA-induced
could
present
new
therapeutic
target
for
ameliorating
abnormalities
Antioxidants,
Journal Year:
2021,
Volume and Issue:
11(1), P. 87 - 87
Published: Dec. 30, 2021
Allicin
(diallylthiosulfinate)
is
a
defense
molecule
produced
by
cellular
contents
of
garlic
(Allium
sativum
L.).
On
tissue
damage,
the
non-proteinogenic
amino
acid
alliin
(S-allylcysteine
sulfoxide)
converted
to
allicin
in
an
enzyme-mediated
process
catalysed
alliinase.
hydrophobic
nature,
can
efficiently
cross
membranes
and
behaves
as
reactive
sulfur
species
(RSS)
inside
cells.
It
physiologically
active
with
ability
oxidise
thiol
groups
glutathione
between
cysteine
residues
proteins.
has
shown
anticancer,
antimicrobial,
antioxidant
properties
also
serves
efficient
therapeutic
agent
against
cardiovascular
diseases.
In
this
context,
present
review
describes
antioxidant,
neuroprotective
that
ameliorate
cognitive
abilities
case
neurodegenerative
neuropsychological
disorders.
As
fights
oxygen
(ROS)
downregulation
NOX
(NADPH
oxidizing)
enzymes,
it
directly
interact
reduce
levels
different
types
ROS
variety
peroxidases.
Most
actions
are
mediated
via
redox-dependent
pathways.
inhibits
neuroinflammation
suppressing
production,
inhibition
TLR4/MyD88/NF-κB,
P38
JNK
inhibitor
cholinesterase
(AChE)
butyrylcholinesterase
(BuChE)
be
applied
manage
Alzheimer’s
disease,
helps
maintain
balance
neurotransmitters
autism
spectrum
disorder
(ASD)
attention
deficit
hyperactive
syndrome
(ADHD).
acute
traumatic
spinal
cord
injury
(SCI)
protects
neuron
damage
regulating
inflammation,
apoptosis
promoting
expression
Nrf2
(nuclear
factor
erythroid
2-related
2).
Metal
induced
neurodegeneration
attenuated
patients
suffering
from
neurological
diseases
ameliorates
administration.
Autism Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
ABSTRACT
Alzheimer's
disease
and
related
dementias
(ADRD)
are
burdensome
lethal
conditions
that
have
been
hypothesized
to
be
autism
through
shared
genetic
etiologies
environmental
risk
factors.
Our
objective
was
use
longitudinal
Medicaid
Medicare
data
describe
the
epidemiology
of
ADRD
in
publicly
insured
autistic
adults.
We
used
all
claims
encounters
from
2011
2019
identify
ADRD.
calculated
prevalence,
incidence,
age
at
onset,
created
survival
curves.
There
were
90,229
adults
≥
30
years
enrolled
for
least
1
year
and/or
267
cases.
Prevalence
2.09%
(95%
CI:
1.99%,
2.20%)
8.11%
7.92%,
8.30%)
2019.
Mean
onset
59.3
(SD:
14.2).
among
men
58.3
13.8)
61.0
females.
Incidence
higher
with
intellectual
disability
no
difference
by
sex.
is
a
prevalent
condition
middle‐
older‐aged
identified
system.
Understanding
diagnostic
process
phenotype
will
important
improve
identification
treatment.
Frontiers in Psychiatry,
Journal Year:
2022,
Volume and Issue:
13
Published: April 15, 2022
Autism
spectrum
disorder
(ASD)
is
a
complex
neurodevelopmental
condition
characterized
by
restrictive
and
repetitive
behaviors,
alongside
deficits
in
social
interaction
communication.
The
etiology
of
ASD
largely
unknown
but
strongly
linked
to
genetic
variants
neuronal
cell
adhesion
molecules
(CAMs),
cell-surface
proteins
that
have
important
roles
neurodevelopment.
A
combination
environmental
factors
are
believed
contribute
pathogenesis.
Inflammation
has
been
identified
as
one
these
factors,
demonstrated
through
the
presence
proinflammatory
cytokines,
maternal
immune
activation,
activation
glial
cells
brains.
Glial
main
source
cytokines
within
brain
and,
therefore,
their
activity
vital
mediating
inflammation
central
nervous
system.
However,
it
unclear
whether
aforementioned
CAMs
involved
modulating
neuroimmune
signaling
or
behavior.
This
review
aims
address
unexplored
role
may
play
inflammatory
cascades
underpin
neuroinflammation
ASD,
primarily
focusing
on
Notch,
nuclear
factor-κB
(NF-κB),
mitogen-activated
protein
kinase
(MAPK)
cascades.
We
will
also
evaluate
available
evidence
how
influence
associated
with
inflammation.
when
considering
impact
responses
development.
In
particular,
neural
CAM1
(NCAM1)
can
regulate
NF-κB
transcription
neurons,
directly
altering
signaling.
Additionally,
NCAM1
contactin-1
appear
mediate
astrocyte
oligodendrocyte
precursor
proliferation
which
alter
response.
Importantly,
although
this
highlights
limited
information
available,
there
CAM
regulatory
warrants
further
investigation
into
other
family
members
would
advance
our
understanding
pathology.
MedComm,
Journal Year:
2024,
Volume and Issue:
5(8)
Published: Aug. 1, 2024
Abstract
Posttranslational
modifications
play
a
crucial
role
in
governing
cellular
functions
and
protein
behavior.
Researchers
have
implicated
dysregulated
posttranslational
misfolding,
which
results
cytotoxicity,
particularly
neurodegenerative
diseases
such
as
Alzheimer
disease,
Parkinson
Huntington
disease.
These
aberrant
cause
proteins
to
gather
certain
parts
of
the
brain
that
are
linked
development
diseases.
This
leads
neuronal
dysfunction
start
disease
symptoms.
Cognitive
decline
neurological
impairments
commonly
manifest
patients,
underscoring
urgency
comprehending
modifications’
impact
on
function
for
targeted
therapeutic
interventions.
review
elucidates
critical
link
between
specific
modifications,
focusing
Tau,
APP,
α‐synuclein,
Huntingtin
protein,
Parkin,
DJ‐1,
Drp1.
By
delineating
prominent
within
underscores
significance
understanding
interplay
among
these
modifications.
Emphasizing
10
key
abnormal
this
study
aims
provide
comprehensive
framework
investigating
holistically.
The
insights
presented
herein
shed
light
potential
avenues
aimed
at
modulating
mitigate
aggregation
retard
progression.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(1), P. 349 - 349
Published: Jan. 3, 2025
Abamectin
is
an
insecticide,
miticide
and
nematicide
that
has
been
extensively
used
in
agriculture
for
many
years.
The
excessive
use
of
abamectin
inevitably
pollutes
water
soil
might
even
cause
adverse
effects
on
aquatic
biota.
However,
it
currently
unclear
how
exposure
causes
neurotoxicity
organisms.
Herein,
the
early
neural
system
development
was
assessed
zebrafish
embryos
following
exposure.
After
treatment
with
a
concentration
gradient
(0.055,
0.0825,
0.11
mg/L),
survival
rate,
average
heart
pericardial
edema
area
yolk
sac
were
all
documented
(96
hpf).
It
found
after
exposure,
embryonic
brain
impaired,
motor
behaviors
also
affected.
fluorescence
intensity
reduced
transgenic
(Eno2:
GFP).
activities
acetylcholinesterase
(AChE)
ATPase
decreased,
expression
neurodevelopment-related
genes,
such
as
sox10,
gap43,
grin1b,
abat,
gad1b,
grin2b,
nestin
glsa,
inhibited
embryo
abamectin.
Furthermore,
reactive
oxygen
species
(ROS)
triggered
upon
to
along
accumulation
ROS,
eventually
resulting
neuroapoptosis
developing
brain.
In
conclusion,
neurodevelopmental
toxicity
caused
by
oxidative
stress-induced
apoptosis
IGI Global eBooks,
Journal Year:
2025,
Volume and Issue:
unknown, P. 183 - 196
Published: Jan. 31, 2025
Autism
Spectrum
Disorder
(ASD)
and
dementia
are
two
distinct
neurological
conditions
that
affect
millions
of
individuals
worldwide.
While
they
primarily
diagnosed
in
different
age
groups—ASD
being
usually
early
childhood
commonly
older
adults—there
intriguing
similarities
their
neurological,
cognitive,
behavioral
profiles.
Understanding
these
shared
traits
enriches
the
existing
knowledge
each
condition
enhances
diagnostic
therapeutic
approaches.
This
chapter
explores
autism
dementia,
shedding
light
on
implications
for
clinical
practice.
Journal of Alzheimer s Disease Reports,
Journal Year:
2025,
Volume and Issue:
9
Published: Jan. 1, 2025
Background
Recently,
microRNAs
(miRNAs)
have
attracted
significant
interest
as
predictive
biomarkers
for
various
types
of
dementia,
including
Alzheimer's
disease
(AD),
vascular
dementia
(VaD),
with
Lewy
bodies
(DLB),
normal
pressure
hydrocephalus
(NPH),
and
mild
cognitive
impairment
(MCI).
Machine
learning
(ML)
methods
enable
the
integration
miRNAs
into
highly
accurate
models
dementia.
Objective
To
investigate
differential
expression
across
subtypes
compared
to
controls
(NC)
analyze
their
enriched
biological
pathways.
Additionally,
evaluate
use
these
in
binary
multiclass
ML
prediction
both
overall
sex-specific
datasets.
Methods
Using
data
comprising
1685
Japanese
individuals
(GSE120584
GSE167559),
we
performed
analysis
identify
associated
five
groups
Pathway
enrichment
analyses
were
conducted
further
miRNAs.
classifiers
used
create
Results
We
identified
novel
differentially
expressed
miRNA
distinguishing
NC
from
subtypes.
Incorporating
resulted
up
a
27%
improvement
risk
prediction.
highlighted
neuronal
eye
pathways
risk.
Sex-specific
revealed
unique
males
females,
miR-128-1-5
protective
factor
AD,
VaD,
DLB,
miR-4488
female
highlighting
distinct
potential
therapeutic
targets
each
sex.
Conclusions
Our
findings
support
existing
etiology
research
introduce
new
biomarkers.
Neuroscience & Biobehavioral Reviews,
Journal Year:
2023,
Volume and Issue:
146, P. 105048 - 105048
Published: Jan. 18, 2023
Steeper
delay
discounting
(i.e.,
the
extent
to
which
future
rewards
are
perceived
as
less
valuable
than
immediate
ones)
has
been
proposed
a
transdiagnostic
process
across
different
health
conditions,
in
particular
psychiatric
disorders.
Impulsive
decision-making
is
hallmark
of
neurodegenerative
conditions
but
little
known
about
domain
conditions.
We
reviewed
studies
on
patients
with
Parkinson's
disease
(PD)
and
dementia
(Alzheimer's
/
AD
or
frontotemporal
FTD).
that
could
be
an
early
marker
process.
developed
idea
altered
associated
overlapping
distinct
neurocognitive
mechanisms
diseases:
dopaminergic-related
disorders
reward
processing
PD,
memory/projection
deficits
due
medial
temporal
atrophy
AD,
modified
orbitofrontal
FTD.
Neurodegeneration
provide
framework
decipher
neuropsychological
value-based
decision-making.
Further,
become
interest
clinical
practice,
for
differential
diagnosis.