Frontiers in Pharmacology,
Год журнала:
2022,
Номер
13
Опубликована: Май 20, 2022
Stroke
is
one
of
the
leading
causes
mortality,
and
survivors
experience
serious
neurological
motor
behavioral
deficiencies.
Following
a
cerebral
ischemic
event,
substantial
alterations
in
both
cellular
molecular
activities
occur
because
ischemia/reperfusion
injury.
Wnt
signaling
an
evolutionarily
conserved
pathway
that
has
been
manifested
to
play
key
role
embryo
development
function
maintenance
adults.
Overactivation
previously
investigated
cancer-based
research
studies.
Recently,
abnormal
activity
observed
stroke,
which
accompanied
by
massive
blood–brain
barrier
(BBB)
disruption,
neuronal
apoptosis,
neuroinflammation
within
central
nervous
system
(CNS).
Significant
therapeutic
effects
were
after
reactivating
adynamic
canonical
different
cell
types.
To
better
understand
potential
as
novel
target
for
we
reviewed
pathogenesis
stroke
types,
including
endothelial
cells,
neurons,
oligodendrocytes,
microglia.
A
comprehensive
understanding
among
cells
may
help
evaluate
its
value
strategies
based
on
activation
can
ameliorate
complications
improve
functional
rehabilitation
stroke.
Stroke,
Год журнала:
2022,
Номер
53(5), С. 1473 - 1486
Опубликована: Апрель 7, 2022
Maintaining
blood-brain
barrier
(BBB)
integrity
is
crucial
for
the
homeostasis
of
central
nervous
system.
Structurally
comprising
BBB,
brain
endothelial
cells
interact
with
pericytes,
astrocytes,
neurons,
microglia,
and
perivascular
macrophages
in
neurovascular
unit.
Brain
ischemia
unleashes
a
profound
neuroinflammatory
response
to
remove
damaged
tissue
prepare
repair.
However,
intense
neuroinflammation
occurring
during
acute
phase
stroke
associated
BBB
breakdown,
neuronal
injury,
worse
neurological
outcomes.
Here,
we
critically
discuss
role
ischemic
pathology,
focusing
on
interactions
between
system
peripheral
immune
responses.
We
highlight
inflammation-driven
injury
mechanisms
stroke,
including
oxidative
stress,
increased
MMP
(matrix
metalloproteinase)
production,
microglial
activation,
infiltration
into
tissue.
provide
an
updated
overview
imaging
techniques
vivo
detection
permeability,
leukocyte
infiltration,
upregulation
cell
adhesion
molecules
following
injury.
possibility
clinical
implementation
modalities
assess
stroke-associated
potential
image-guided
diagnosis
treatment.
summarize
results
from
several
studies
evaluating
efficacy
anti-inflammatory
interventions
stroke.
Although
convincing
preclinical
evidence
suggests
that
promising
target
thus
far,
translating
these
setting
has
proved
difficult.
Due
dual
inflammation
progression
damage,
more
research
needed
mechanistically
understand
when
begins
transition
This
could
have
important
implications
treatment
by
informing
time-
context-specific
therapeutic
interventions.
Cerebrovascular
diseases
are
a
leading
cause
of
death
and
neurologic
disability.
Further
understanding
disease
mechanisms
therapeutic
strategies
requires
deeper
knowledge
cerebrovascular
cells
in
humans.
We
profiled
transcriptomes
181,388
to
define
cell
atlas
the
adult
human
cerebrovasculature,
including
endothelial
molecular
signatures
with
arteriovenous
segmentation
expanded
perivascular
diversity.
By
leveraging
this
reference,
we
investigated
cellular
perturbations
brain
malformations,
which
stroke
young
people,
identified
pathologic
transformations
abnormal
vascular
patterning
ontology
vascularly
derived
inflammation.
illustrate
interplay
between
immune
that
contributes
hemorrhage
catalog
opportunities
for
targeting
angiogenic
inflammatory
programs
malformations.
Abstract
Alzheimer’s
disease
(AD)
is
a
genetically
complex
and
heterogeneous
disorder
with
multifaceted
neuropathological
features,
including
β-amyloid
plaques,
neurofibrillary
tangles,
neuroinflammation.
Over
the
past
decade,
emerging
evidence
has
implicated
both
beneficial
pathological
roles
for
innate
immune
genes
cells,
peripheral
cells
such
as
T
which
can
infiltrate
brain
either
ameliorate
or
exacerbate
AD
neuropathogenesis.
These
findings
support
neuroimmune
axis
of
AD,
in
interplay
adaptive
systems
inside
outside
critically
impacts
etiology
pathogenesis
AD.
In
this
review,
we
discuss
complexities
neuropathology
at
levels
genetics
cellular
physiology,
highlighting
signaling
pathways
associated
risk
interactions
among
brain.
We
emphasize
role
mechanisms
by
monocytes,
influence
neuropathology,
microglial
clearance
amyloid-β
peptide,
key
component
plaque
cores,
pro-inflammatory
cytotoxic
activity
microglia,
astrogliosis,
their
vasculature.
Finally,
review
challenges
outlook
establishing
immune-based
therapies
treating
preventing
Hypertension,
Год журнала:
2022,
Номер
80(1), С. 22 - 34
Опубликована: Окт. 5, 2022
Hypertension
affects
a
significant
proportion
of
the
adult
and
aging
population
represents
an
important
risk
factor
for
vascular
cognitive
impairment
late-life
dementia.
Chronic
high
blood
pressure
continuously
challenges
structural
functional
integrity
cerebral
vasculature,
leading
to
microvascular
rarefaction
dysfunction,
neurovascular
uncoupling
that
typically
impairs
supply.
disrupts
blood-brain
barrier
integrity,
promotes
neuroinflammation,
may
contribute
amyloid
deposition
Alzheimer
pathology.
The
mechanisms
underlying
these
harmful
effects
are
still
focus
investigation,
but
studies
in
animal
models
have
provided
molecular
cellular
mechanistic
insights.
Remaining
questions
relate
whether
adequate
treatment
hypertension
prevent
deterioration
function,
threshold
treatment,
most
effective
antihypertensive
drugs.
Recent
advances
biology,
advanced
brain
imaging,
detection
subtle
behavioral
phenotypes
begun
provide
insights
into
critical
issues.
Importantly,
parallel
analysis
parameters
humans
is
feasible,
making
it
possible
foster
translational
advancements.
In
this
review,
we
evaluation
evidence
available
experimental
examine
progress
made
identify
remaining
gaps
knowledge.
Advanced Drug Delivery Reviews,
Год журнала:
2023,
Номер
197, С. 114822 - 114822
Опубликована: Апрель 21, 2023
Central
nervous
system
(CNS)
disorders
affect
as
many
1.5
billion
people
globally.
The
limited
delivery
of
most
imaging
and
therapeutic
agents
into
the
brain
is
a
major
challenge
for
treatment
CNS
disorders.
With
advent
nanotechnologies,
controlled
drugs
with
nanoparticles
holds
great
promise
in
overcoming
blood-brain
barrier
(BBB)
improving
efficacy.
In
recent
years,
magnetic
iron
oxide
(MIONPs)
have
stood
out
promising
theranostic
nanoplatform
drug
they
possess
unique
physical
properties
biodegradable
characteristics.
this
review,
we
summarize
advances
MIONP-based
platforms
diseases.
We
firstly
introduce
methods
synthesis
surface
functionalization
MIONPs
emphasis
on
inclusion
biocompatible
polymers
that
allow
addition
tailored
physicochemical
properties.
then
discuss
vivo
applications
using
MIONPs.
Finally,
present
perspective
remaining
challenges
possible
future
directions
systems.
Molecular Neurodegeneration,
Год журнала:
2023,
Номер
18(1)
Опубликована: Июль 11, 2023
Abstract
Vascular
cognitive
impairment
and
dementia
(VCID)
is
commonly
caused
by
vascular
injuries
in
cerebral
large
small
vessels
a
key
driver
of
age-related
decline.
Severe
VCID
includes
post-stroke
dementia,
subcortical
ischemic
multi-infarct
mixed
dementia.
While
acknowledged
as
the
second
most
common
form
after
Alzheimer’s
disease
(AD)
accounting
for
20%
cases,
AD
frequently
coexist.
In
VCID,
vessel
(cSVD)
often
affects
arterioles,
capillaries,
venules,
where
arteriolosclerosis
amyloid
angiopathy
(CAA)
are
major
pathologies.
White
matter
hyperintensities,
recent
infarcts,
lacunes
presumed
origin,
enlarged
perivascular
space,
microbleeds,
brain
atrophy
neuroimaging
hallmarks
cSVD.
The
current
primary
approach
to
cSVD
treatment
control
risk
factors
such
hypertension,
dyslipidemia,
diabetes,
smoking.
However,
causal
therapeutic
strategies
have
not
been
established
partly
due
heterogeneous
pathogenesis
this
review,
we
summarize
pathophysiology
discuss
probable
etiological
pathways
focusing
on
hypoperfusion/hypoxia,
blood–brain
barriers
(BBB)
dysregulation,
fluid
drainage
disturbances,
inflammation
define
potential
diagnostic
targets
Nature Methods,
Год журнала:
2022,
Номер
19(8), С. 1004 - 1012
Опубликована: Авг. 1, 2022
The
advent
of
neuroimaging
has
increased
our
understanding
brain
function.
While
most
brain-wide
functional
imaging
modalities
exploit
neurovascular
coupling
to
map
activity
at
millimeter
resolutions,
the
recording
responses
microscopic
scale
in
mammals
remains
privilege
invasive
electrophysiological
or
optical
approaches,
but
is
mostly
restricted
either
cortical
surface
vicinity
implanted
sensors.
Ultrasound
localization
microscopy
(ULM)
achieved
transcranial
cerebrovascular
flow,
up
micrometre
scales,
by
localizing
intravenously
injected
microbubbles;
however,
long
acquisition
time
required
detect
microbubbles
within
vessels
so
far
ULM
application
mainly
microvasculature
structural
imaging.
Here
we
show
how
can
be
modified
quantify
hyperemia
dynamically
during
activation
reaching
a
6.5-µm
spatial
and
1-s
temporal
resolution
deep
regions
rat
brain.