Medicina,
Journal Year:
2024,
Volume and Issue:
60(4), P. 658 - 658
Published: April 19, 2024
Background
and
Objectives.
Neurogenesis
is
an
integral
process
in
post-stroke
recovery,
involving
the
recruitment
of
proliferating
neuroblasts
from
neurogenic
niches
mammal
brain.
However,
role
neurogenesis
long-term
restoration
following
ischemic
stroke
fragmented.
Post-stroke
motor
dysfunction
includes
challenges
proper,
coordinated
use
hands
present
roughly
two-thirds
human
patients.
In
this
study,
we
investigated
chronic
behavioral
biochemical
alterations
after
transient
cerebral
ischemia
adult
male
mice.
Materials
Methods:
Twelve-week-old
C57BL/6N
mice
were
used,
fMCAo
lasting
60
min
was
induced.
At
multiple
timepoints
induction,
a
single
pellet
reaching
task
performed.
Six
months
procedure,
immunohistochemically
determined
number
(BrdU
DCX-positive)
differentiated
astrocytes
(GFAP-positive)
both
brain
hemispheres.
Results:
The
ability
impaired
one
month
to
six
induction
ischemia.
Neuroblast
proliferation
increased
ipsilateral
SVZ,
whereas
GFAP+
cell
count
elevated
hippocampal
DG
hemispheres
group
Conclusions:
Our
current
report
demonstrates
effects
on
functional
parameters
progression.
data
demonstrate
that
promotes
long-lasting
regenerative
response
hemisphere,
specifically
SVZ
regions.
Frontiers in Neuroscience,
Journal Year:
2023,
Volume and Issue:
17
Published: March 21, 2023
Stroke-induced
depression
is
a
common
complication
and
an
important
risk
factor
for
disability.
Besides
psychiatric
symptoms,
depressed
patients
may
also
exhibit
variety
of
gastrointestinal
even
take
symptoms
as
the
primary
reason
medical
treatment.
It
well
documented
that
stress
disrupt
balance
gut
microbiome
in
suffering
from
post-stroke
(PSD),
disruption
closely
related
to
severity
condition
patients.
Therefore,
maintaining
intestinal
microbiota
can
be
focus
research
on
mechanism
acupuncture
treatment
PSD.
Furthermore,
stroke
effectively
treated
with
at
all
stages
it
act
special
microecological
regulator
by
regulating
well.
In
this
article,
we
reviewed
studies
changing
after
examined
existing
problems
development
prospects
acupuncture,
microbiome,
poststroke
depression,
order
provide
new
ideas
future
research.
BMC Neurology,
Journal Year:
2023,
Volume and Issue:
23(1)
Published: June 12, 2023
Abstract
Starting
from
the
perspective
of
an
immune-privileged
site,
our
knowledge
inflammatory
processes
within
central
nervous
system
has
increased
rapidly
over
last
30
years,
leading
to
a
rather
puzzling
picture
today.
Of
particular
interest
is
emergence
disease-
and
injury-specific
responses
brain,
which
may
form
basis
for
future
therapeutic
approaches.
To
advance
this
important
topic,
we
invite
authors
contribute
research
clinical
papers
Collection
“Neuroinflammation
Brain
Disease”.
Romanian Journal of Morphology and Embryology,
Journal Year:
2025,
Volume and Issue:
65(4), P. 679 - 685
Published: Feb. 13, 2025
Non-alcoholic
fatty
liver
disease
(NAFLD)
has
emerged
as
a
silent
global
epidemic,
frequently
contributing
to
systemic
inflammation.
As
the
primary
immune
cells
of
central
nervous
system
(CNS),
microglia
undergo
morphological
changes
that
serve
critical
indicators
CNS
health.
In
this
study,
we
aimed
quantify
alterations
in
microglial
morphology
within
cortex
young
and
aged
mice
with
damage.
Our
results
demonstrated
hepatic
dysfunction
leads
significant
increase
total
branch
length
both
(285.79±68.23
μm)
animals
(268.67±69.06
μm),
compared
their
respective
controls
(164.07±33.05
μm
140.96±27.18
(p
0.0001).
Additionally,
damage
exhibited
mean
5.84±0.66
μm,
higher
than
2.63±0.19
observed
those
without
injury.
The
number
branches
decreased
from
6.6±1.2
3.1±1.5
addition,
have
shown
decrease
secondary
This
suggests
not
only
respond
CNS-specific
injuries
but
also
chronic
pathologies
like
NAFLD.
These
findings
highlight
importance
better
understanding
liver–brain
axis
order
understand
neuroimmune
consequences
diseases.
Journal of Cerebral Blood Flow & Metabolism,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
Stroke
is
a
multifaceted
disease
with
genetic
and
environmental
components
like
diet
lifestyle.
The
central
nervous
immune
systems
display
complex
interactions,
the
peripheral
response
participating
in
brain
injury
repair
mechanisms
following
stroke.
bidirectional
communication
between
injured
blood
presents
an
opportunity
to
investigate
molecular
changes
latter.
There
substantial
heterogeneity
stroke
pathogenesis,
pathophysiology,
comorbidities,
treatment
outcome.
This
captured
underscored
by
transcriptome.
current
review
highlights
role
of
human
transcriptome
architecture
for
phenotyping
different
etiologies
identifying
underlying
correlates
clinically
important
variables
outcomes.
Specific
features
can
potentially
provide
targets
clinical
translation
prioritizing
genes
pathways
evaluation
experimental
models.
We
also
propose
approach
study
patient-specific
transcriptional
uncover
combinatorial
altered
patients
that
guide
search
prevention
targets.
Deciphering
tissue
be
easily
accessed
monitored,
such
as
blood,
may
improve
trial
success.
Life,
Journal Year:
2024,
Volume and Issue:
14(9), P. 1110 - 1110
Published: Sept. 3, 2024
Post-stroke
depression
(PSD)
represents
a
significant
neuropsychiatric
complication
that
affects
between
39%
and
52%
of
stroke
survivors,
leading
to
impaired
recovery,
decreased
quality
life,
increased
mortality.
This
comprehensive
review
synthesizes
our
current
knowledge
PSD,
encompassing
its
epidemiology,
risk
factors,
underlying
neurochemical
mechanisms,
the
existing
tools
for
preclinical
investigation,
including
animal
models
behavioral
analyses.
Despite
high
prevalence
severe
impact
challenges
persist
in
accurately
modeling
complex
symptomatology
settings,
underscoring
need
robust
valid
better
understand
treat
PSD.
also
highlights
multidimensional
nature
where
both
biological
psychosocial
factors
interplay
influence
onset
course.
Further,
we
examine
efficacy
limitations
mimicking
human
PSD
condition,
along
with
tests
used
evaluate
depressive-like
behaviors
rodents.
sets
new
precedent
by
integrating
latest
findings
across
multidisciplinary
studies,
thereby
offering
unique
perspective
knowledge.
Finally,
development
more
sophisticated
closely
replicate
clinical
features
is
crucial
order
advance
translational
research
facilitate
discovery
future
effective
therapies.
Communications Biology,
Journal Year:
2025,
Volume and Issue:
8(1)
Published: Feb. 22, 2025
Abstract
Despite
known
sex
differences
in
human
synucleinopathies
such
as
Parkinson’s
disease,
the
impact
of
on
alpha-synuclein
pathology
mouse
models
has
been
largely
overlooked.
To
address
this
need,
we
examine
whole
brain
signatures
neurodegeneration
due
to
aSyn
toxicity
M83
model
using
longitudinal
magnetic
resonance
imaging
(MRI;
T1-weighted;
100
μm
3
isotropic
voxel;
-7,
30,
90
and
120
days
post-injection
[dpi];
n
≥
8
mice/group/sex/time
point).
initiate
spreading,
mice
are
inoculated
with
recombinant
preformed
fibrils
(Hu-PFF)
or
phosphate
buffered
saline
right
striatum.
We
observe
more
aggressive
neurodegenerative
profiles
over
time
for
male
Hu-PFF-injected
when
examining
voxel-wise
trajectories.
However,
at
dpi,
widespread
patterns
female
mice.
These
not
accompanied
by
any
motor
symptom
onset
between
sexes.
reached
their
humane
endpoint
sooner.
findings
suggest
that
post-motor
onset,
despite
accelerated
disease
trajectories
mice,
may
appear
sooner
(prior
symptomatology).
sex-specific
synucleinopathy
phenotypes
urgently
need
be
considered
improve
our
understanding
neuroprotective
mechanisms.
Science Advances,
Journal Year:
2025,
Volume and Issue:
11(10)
Published: March 5, 2025
Once
taken
into
consideration,
sex
differences
in
neurological
diseases
emerge
abundance:
(i)
Stroke
severity
is
significantly
higher
females
than
males,
(ii)
Alzheimer's
disease
(AD)
pathology
more
pronounced
females,
and
(iii)
conspicuous
links
with
hormonal
cycles
led
to
female-specific
diagnoses,
such
as
catamenial
migraines
epilepsy.
While
these
receive
increasing
attention
isolation,
they
likely
link
similar
processes
the
brain.
Hence,
this
review
aims
present
an
overview
of
influences
chromosomes,
hormones,
aging
on
male
female
brains
across
health
disease,
a
particular
focus
AD
stroke.
The
here
advancements
several
fields
holds
promise
fuel
future
research
lead
enriched
understanding
brain
effective
personalized
neurologic
care
for
all.
GeroScience,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 17, 2025
Abstract
An
overactive
neuroinflammatory
response
is
often
evident
in
the
elderly
and
a
significant
contributor
to
brain
tissue
damage
following
acute
ischemic
stroke.
Such
an
inflammatory
largely
mediated
by
microglial
cells
peripheral
blood
mononuclear
(PBMCs).
Classical
anti-inflammatory
agents
have
not
proved
clinically
effective
mitigating
impact
of
stroke
but
highlighted
targets
for
new
drug
development,
particular
excessive
proinflammatory
cytokine
release.
The
immunomodulatory
imide
(IMiD)
class
has
shown
potential
reducing
neuroinflammation
switching
phenotypic
expression
away
from
regenerative
one.
3-Monothiopomalidomide
(3-MP),
IMiD,
brain/plasma
concentration
ratio
0.5
0.6,
oral
bioavailability
38.5%,
monophasic
disappearance
half-life
3.2
h
administration.
3-MP
pretreatment
mitigates
lipopolysaccharide
(LPS)-induced
inflammation
cellular
human
PBMCs
and,
rat
studies,
lowers
levels
conditioned
media
plasma
brain,
respectively.
Administered
systemically
rats
challenged
with
middle
cerebral
artery
occlusion
(MCAo)
reperfusion,
post-MCAo
treatment
reduced
infarction
volume;
improved
body
asymmetry,
behavioral
measure
impact;
lowered
inflammation.
In
summary,
exerted
neuroprotective
effects
via
actions
against
MCAo-induced
injury
represents
therapeutic
that
warrants
further
investigation
as
related
disorders
associated