Bioengineered,
Journal Year:
2022,
Volume and Issue:
13(4), P. 10373 - 10385
Published: April 1, 2022
As
an
endocrine
and
metabolic
disorder,
polycystic
ovarian
syndrome
(PCOS)
is
common
in
females
at
childbearing
age.
Our
work
was
intended
to
uncover
the
underlying
role
of
LINC00173
its
potential
regulatory
mechanism
PCOS
based
on
two
cell
lines
(PCOS
granulosa
cells
KGN
cells)
vivo
model
established
from
Sprague
Dawley
rats.
It
revealed
that
JAG1
expressions
were
upregulated,
while
miR-124-3p
poorly
expressed
patients
Functional
assays
showed
overexpression
repressed
proliferation
stimulated
apoptosis
cells,
downregulation
exhibited
opposite
effects.
Besides,
it
verified
upregulated
expression
via
competitively
binding
miR-124-3p.
Similarly,
abundance
inversely
related
level
PCOS.
Subsequently,
rescue
elucidated
upregulation
or
eliminated
effects
mediated
by
knockdown.
In
addition,
found
adversely
modulated
positively
LINC00173.
Moreover,
further
demonstrated
reduced
vitality
increased
induced
overexpressing
could
be
relieved
deletion.
These
findings
suggested
a
latent
regulating
factor
for
progression
modulating
miR-124-3p/JAG1
cascade.
Cell Cycle,
Journal Year:
2021,
Volume and Issue:
20(1), P. 112 - 125
Published: Jan. 2, 2021
Accumulating
data
manifest
that
long
non-coding
RNA
(lncRNAs)
are
involved
in
all
kinds
of
neurodegenerative
disorders,
consisting
the
onset
and
progression
Alzheimer's
disease
(AD).
The
study
was
for
research
mechanism
lncRNA
H19
(H19)
viability
apoptosis
PC12
cells
induced
by
Aβ25-35
a
cellular
model
AD
with
regulation
microRNA
(miR)-129
high
mobility
group
box-1
protein
(HMGB1).
An
established
using
Aβ25-35.
Aβ25-35-induced
were
transfected
si-H19
or
miR-129
mimic
to
figure
their
roles
cell
viability,apoptosis,
mitochondrial
membrane
potential
dysfunction
oxidative
stress
AD.
Luciferase
reporter
assay
RNA-pull
down
employed
verification
binding
relationship
between
targeting
HMGB1.
mouse
brain
tissues
collected.
H19,
HMGB1
detected
Aβ25-35-treated
mice.
Elevated
decreased
found
as
well
Silenced
elevated
promoted
viability,
inhibited
apoptosis,
prevented
cells.
could
specifically
bind
miR-129.
MiR-129
suppressed
expression.
This
suggests
silenced
up-regulated
accelerates
represses
stimulated
AD,
which
is
beneficial
treatment.
Frontiers in Aging Neuroscience,
Journal Year:
2021,
Volume and Issue:
13
Published: Oct. 12, 2021
Alzheimer's
disease
(AD)
is
a
progressive
and
deleterious
neurodegenerative
disease,
strongly
affecting
the
cognitive
functions
memory
of
seniors
worldwide.
Around
58%
affected
patients
live
in
low
middle-income
countries,
with
estimates
increasing
deaths
caused
by
AD
coming
decade.
multifactor
pathology.
Mitochondrial
function
declines
brain
currently
emerging
as
hallmark
this
disease.
It
has
been
considered
one
intracellular
processes
severely
compromised
AD.
Many
mitochondrial
parameters
decline
already
during
aging;
efficiency
for
energy
production,
reactive
oxygen
species
(ROS)
metabolism
de
novo
synthesis
pyrimidines,
to
reach
an
extensive
functional
failure,
concomitant
onset
conditions.
Besides
its
impact
on
functions,
characterized
loss
synapses,
extracellular
amyloid
plaques
composed
amyloid-β
peptide
(Aβ),
aggregates
hyperphosphorylated
Tau
protein,
accompanied
drastic
sleep
disorders,
sensory
alterations
pain
sensitization.
Unfortunately,
till
date,
effective
management
AD-related
disorders
early,
non-invasive
diagnostic
markers
are
yet
be
found.
MicroRNAs
(miRNAs)
small
non-coding
nucleic
acids
that
regulate
key
signaling
pathway(s)
various
About
70%
experimentally
detectable
miRNAs
expressed
where
they
neurite
outgrowth,
dendritic
spine
morphology,
synaptic
plasticity.
Increasing
studies
suggest
intimately
involved
specific
signals
formation.
This
pivotal
considering
crucial
molecules
studied
dysfunctions
increasingly
acknowledged
contributor
via
deregulating
genes
pathogenesis.
Moreover,
have
proved
control
sensitization
circadian
clock
system
affects
process.
Interestingly,
differential
expression
miRNA
panels
implies
their
potential
biomarkers.
In
review,
we
will
present
updated
analysis
role
regulating
pathologies.
We
discuss
current
challenges
against
wider
use
future
promising
capabilities
therapeutic
means
better
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
175, P. 116703 - 116703
Published: May 6, 2024
The
distinctive
role
of
Yes-associated
protein
(YAP)
in
the
nervous
system
has
attracted
widespread
attention.
This
comprehensive
review
strategically
uses
retina
as
a
vantage
point,
embarking
on
an
extensive
exploration
YAP's
multifaceted
impact
from
to
brain
development
and
pathology.
Initially,
we
explore
crucial
roles
YAP
embryonic
cerebral
development.
Our
focus
then
shifts
retinal
development,
examining
detail
regulatory
influence
pigment
epithelium
(RPE)
progenitor
cells
(RPCs),
its
significant
effects
hierarchical
structure
functionality
retina.
We
also
investigate
essential
contributions
maintaining
homeostasis,
highlighting
precise
regulation
cell
proliferation
survival.
In
terms
retinal-related
diseases,
epigenetic
connections
pathophysiological
diabetic
retinopathy
(DR),
glaucoma,
proliferative
vitreoretinopathy
(PVR).
Lastly,
broaden
our
brain,
emphasizing
research
paradigm
"retina:
window
brain."
Special
is
given
emerging
studies
disorders
such
Alzheimer's
disease
(AD)
Parkinson's
(PD),
underlining
potential
therapeutic
value
neurodegenerative
neuroinflammation.
Brain and Behavior,
Journal Year:
2024,
Volume and Issue:
14(5)
Published: May 1, 2024
Abstract
Background
Crocin
has
a
good
prospect
in
the
treatment
of
Alzheimer's
disease
(AD),
but
mechanisms
underlying
its
neuroprotective
effects
remain
elusive.
This
study
aimed
to
investigate
and
AD.
Methods
AD
mice
were
set
up
by
injecting
Aβ
25‐35
solution
into
hippocampus.
Then,
injected
intraperitoneally
with
40
mg/kg/day
for
14
days.
Following
completion
treatment,
an
open‐field
test,
Y‐maze
test
Morris
water
maze
conducted
evaluate
impact
on
spatial
learning
memory
deficiency
mice.
The
hippocampal
neuron
injury,
proinflammatory
cytokine
expressions
(IL‐1β,
IL‐6,
TNF‐α),
PI3K/AKT
signaling‐related
protein
measured
using
hematoxylin
eosin
staining,
Western
blot,
quantitative
real‐time
polymerase
chain
reaction
(qRT‐PCR)
experiments,
respectively.
Results
attenuated
‐induced
injury.
Furthermore,
blot
qRT‐PCR
results
showed
that
effectively
suppressed
inflammation
activated
pathway
Conclusion
restrained
neuroinflammation
via
activation
pathway,
thereby
ameliorating
cognitive
dysfunction
Aging and Disease,
Journal Year:
2022,
Volume and Issue:
13(1), P. 87 - 87
Published: Jan. 1, 2022
Alzheimer's
disease
(AD)
is
a
current
public
health
challenge
and
will
remain
until
the
development
of
an
effective
intervention.
However,
developing
treatment
for
requires
thorough
understanding
its
etiology,
which
currently
lacking.
Although
several
studies
have
shown
association
between
oxidative
damage
AD,
only
few
clarified
specific
mechanisms
involved.
Herein,
we
reviewed
recent
preclinical
clinical
that
indicated
significance
in
as
well
potential
antioxidants.
factors
regulate
stress
centered
our
investigation
on
apolipoprotein
E
gut
microbiome.
Apolipoprotein
E,
particularly
E-ε4,
can
impair
structural
facets
mitochondria.
This,
turn,
minimize
mitochondrial
functionality
result
progressive
build-up
free
radicals,
eventually
leading
to
stress.
Similarly,
microbiome
influence
significant
degree
via
metabolite,
trimethylamine
N-oxide.
Given
various
roles
these
two
modulating
stress,
also
discuss
possible
relationship
them
provide
future
research
directions.
International Journal of Molecular Sciences,
Journal Year:
2022,
Volume and Issue:
23(10), P. 5452 - 5452
Published: May 13, 2022
There
are
limited
neuroprotective
strategies
for
various
central
nervous
system
conditions
in
which
fast
and
sustained
management
is
essential.
Neuroprotection-based
therapeutics
have
become
an
intensively
researched
topic
the
neuroscience
field,
with
multiple
novel
promising
agents,
from
natural
products
to
mesenchymal
stem
cells,
homing
peptides,
nanoparticles-mediated
all
aiming
significantly
provide
neuroprotection
experimental
clinical
studies.
Dexmedetomidine
(DEX),
α2
agonist
commonly
used
as
anesthetic
adjuvant
sedation
opioid-sparing
medication,
stands
out
this
context
due
its
well-established
effects.
Emerging
evidence
preclinical
studies
suggested
that
DEX
could
be
protect
against
cerebral
ischemia,
traumatic
brain
injury
(TBI),
spinal
cord
injury,
neurodegenerative
diseases,
postoperative
cognitive
disorders.
MicroRNAs
(miRNAs)
regulate
gene
expression
at
a
post-transcriptional
level,
inhibiting
translation
of
mRNA
into
functional
proteins.
In
vivo
vitro
deciphered
brain-related
miRNAs
dysregulated
miRNA
profiles
after
several
disorders,
including
TBI,
ischemic
stroke,
Alzheimer's
disease,
sclerosis,
providing
emerging
new
perspectives
therapy
by
modulating
these
miRNAs.
Experimental
revealed
some
effects
mediated
miRNAs,
counteracting
mechanisms
disease
models,
such
lipopolysaccharides
induced
neuroinflammation,
β-amyloid
dysfunction,
ischemic-reperfusion
anesthesia-induced
neurotoxicity
models.
This
review
aims
outline
disorders
We
address
targeting
ameliorating
anesthetics,
reducing
improving
diseases.
Frontiers in Neuroscience,
Journal Year:
2024,
Volume and Issue:
18
Published: March 7, 2024
Background
Alzheimer’s
disease
(AD)
is
a
common,
refractory,
progressive
neurodegenerative
disorder
in
which
cognitive
and
memory
deficits
are
highly
correlated
with
abnormalities
hippocampal
brain
regions.
There
still
lack
of
hippocampus-related
markers
for
AD
diagnosis
prevention.
Methods
Differently
expressed
genes
were
identified
the
gene
expression
profile
GSE293789
region.
Enrichment
analyses
GO,
KEGG,
GSEA
used
to
identify
biological
pathways
involved
DEGs
AD-related
group.
WGCNA
was
modules
that
associated
samples.
The
intersecting
extracted
top
ten
ranked
hub
identified.
Finally
GES48350
as
validation
cohort
predict
diagnostic
efficacy
genes.
Results
From
GSE293789,
225
identified,
mainly
calcium
response,
glutamatergic
synapses,
calcium-dependent
phospholipid-binding
response.
analysis
yielded
dark
green
bright
yellow
modular
most
relevant
AD.
these
two
modules,
176
extracted,
taken
be
intersected
DEGs,
yielding
51
Then
10
them:
HSPA1B,
HSPB1,
HSPA1A,
DNAJB1,
HSPB8,
ANXA2,
ANXA1,
SOX9,
YAP1,
AHNAK.
Validation
found
have
excellent
performance.
Conclusion
Ten
hippocampus
contributing
further
understanding
development
targets
therapeutic