Psychopharmacology & biological narcology,
Год журнала:
2024,
Номер
15(3), С. 237 - 244
Опубликована: Окт. 26, 2024
In
the
brain,
main
inducers
of
neuroinflammation
are
proinflammatory
cytokines,
chemokines,
reactive
oxygen
species
and
other
mediators
produced
by
microglia,
astrocytes
endothelial
cells.
Chronic
neuroinflammatory
conditions
manifested
infiltration
peripheral
immune
cells
through
blood-brain
barrier
cause
tissue
damage
in
central
nervous
system,
promoting
glial
activation
increasing
permeability
barrier.
According
to
a
number
studies,
one
regulators
these
processes
is
small
non-coding
RNA,
or
microRNA,
which
can
either
contribute
disease
progression
or,
conversely,
reflect
an
attempt
system
prevent
excessive
restore
homeostasis.
Studying
role
microRNA.
miR-30a-5p
among
others,
shed
light
on
pathogenetic
mechanisms
underlying
neurological
diseases
lead
discovery
new
therapeutic
agents.
this
review,
we
discuss
regulation
pro-
anti-inflammatory
cytokine
gene
expression,
possible
its
action,
use
as
potential
target
for
pharmacological
correction
pathological
system.
Medicine in Omics,
Год журнала:
2024,
Номер
11, С. 100039 - 100039
Опубликована: Май 21, 2024
Over
the
last
few
years,
development
of
so-called
omics
technologies
has
greatly
contributed
to
discovery
new
biomarkers
and
targets,
embracing
various
fields
from
diagnostics
therapy
contributing
meliorate
advance
precision
personalized
medicine.
In
addition
classic
omics,
including
genomics,
transcriptomics,
proteomics,
metabolomics,
newer-generation
their
platforms,
such
as
microbiomics
nutrigenomics,
are
emerging.
parallel,
use
liquid
biopsies,
optimal
biological
samples,
consisting
in
fluids
(i.e.
blood,
saliva,
urine)
easy
collect,
whose
components
(cells,
nucleic
acids,
exosome)
can
be
analysed
using
throughput
techniques,
is
becoming
an
attractive,
because
enables
extrapolation
big
data
via
multi-omics
technologies.
Here,
we
report
a
brief
description
discussion
technologies,
by
evidencing
applications
eventual
limitations.
This
review
offers
a
comprehensive
of
the
signals
and
paramount
role
neuroinflammation
plays
in
neurodegenerative
diseases
such
as
Alzheimer's,
Parkinson's,
Huntington's,
amyotrophic
lateral
sclerosis.
The
study
explores
sophisticated
interactions
between
microglial,
astrocytic,
dendritic
cells
how
affects
long-term
neuronal
damage
dysfunction.
There
are
specific
pathways
related
to
mentioned
inflammatory
processes,
including
Janus
kinases/signal
transducer
activator
transcriptions,
nuclear
factor-κB,
mitogen-activated
protein
kinases
pathways.
Neuroinflammation
is
argued
be
double-edged
sword,
being
not
only
protective
agent
that
prevents
further
neuron
but
also
causative
factor
more
cell
injury
development.
concept
contrasting
inflammation
with
neuroprotection
advocates
for
use
therapeutic
techniques
seek
modulate
neuroinflammatory
responses
part
neurodegeneration
treatment.
recent
research
findings
integrated
established
knowledge
help
present
image
neuroinflammation's
impact
on
its
implications
future
therapy.
Molecular Neurodegeneration,
Год журнала:
2024,
Номер
19(1)
Опубликована: Окт. 10, 2024
Blood-based
biomarkers
are
gaining
grounds
for
the
detection
of
Alzheimer's
disease
(AD)
and
related
disorders
(ADRDs).
However,
two
key
obstacles
remain:
lack
methods
multi-analyte
assessments
need
pathophysiological
processes
like
neuroinflammation,
vascular,
synaptic
dysfunction.
A
novel
proteomic
method
pre-selected
analytes,
based
on
proximity
extension
technology,
was
recently
introduced.
Referred
to
as
NULISAseq
CNS
panel,
assay
simultaneously
measures
~
120
analytes
neurodegenerative
diseases,
including
those
linked
both
core
(i.e.,
tau
amyloid-beta
(Aβ))
non-core
AD
processes.
This
study
aimed
evaluate
technical
clinical
performance
this
targeted
panel.
FARMAKOEKONOMIKA Modern Pharmacoeconomics and Pharmacoepidemiology,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 25, 2025
Background.
Nitric
monooxide
(NO)
is
a
signaling
molecule
that
plays
an
important
role
in
many
physiological
processes,
including
the
regulation
of
vascular
tone,
neurotransmission,
immunity,
mitochondrial
respiration,
and
skeletal
muscle
contractility.
Certain
molecules,
which
are
micronutrients
or
active
ingredients
number
drugs,
improve
biosynthesis
secretion
NO.
Objective:
systematization
information
on
impact
various
molecules
modulation
NO
levels
normal
pathological
conditions.
Material
methods.
An
array
all
currently
available
publications
fundamental
clinical
studies
effects
was
studied.
By
query
“nitric
oxide”
PubMed/MEDLINE
database
biomedical
198,480
articles
were
detected,
by
oxide
AND
endothelium”
27,869
found
(with
peak
2005).
After
loading
this
sample,
systematic
analysis
these
performed
using
topological
metric
approaches.
Results.
This
paper
presents
results
issue,
allowed
us
to
identify
at
least
123
that,
one
way
another,
modulate
body.
Molecules
metabolism
can
be
conditionally
divided
into
four
groups:
(1)
macro-
micronutrients;
(2)
components
natural
extracts;
(3)
medicines;
(4)
affect
nitric
through
reparation
glycocalyx
damage.
Of
above
variety
endothelium
biosynthesis,
sulodexide
stands
out
(by
its
effect
glycocalyx).
Conclusion.
The
use
(a
mixture
glycosaminoglycans
with
high
degree
pharmaceutical
standardization)
promising
areas
therapy
for
endothelial
dysfunction
restoration
glycocalyx,
accompanied
biosynthesis.
Journal of Neural Transmission,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 3, 2025
Abstract
While
diagnostic
criteria
have
been
established
and
validated
for
most
neurodegenerative
diseases,
the
considerable
overlap
between
individual
nosological
entities
remains
a
significant
challenge.
Increasing
evidence
suggests
that
neurodegeneration
is
often
initiated
by
inflammation
within
central
nervous
system.
The
identification
of
could
serve
as
first
signal
pathophysiological
process.
As
such,
biological
markers
(“biomarkers”)
neuroinflammation
are
critically
important.
This
study
aimed
to
assess
presence
levels
inflammatory
biomarkers
in
three
diseases:
Lewy
body
diseases
(LBD),
multiple
system
atrophy
(MSA),
4-repeat
tauopathies
(4RT).
A
total
83
LBD,
24
MSA,
31
4RT
patients
were
included,
with
control
subjects
comparison.
Six
immune-related
proteins
analysed
cerebrospinal
fluid
(CSF)
blood
serum
(serum):
C3
complement,
C4
haptoglobin,
transferrin,
orosomucoid,
β2
microglobulin
(β2M).
ANCOVA
statistical
analysis
revealed
significantly
lower
several
LBD
(CSF:
orosomucoid;
Serum:
β2M)
MSA
orosomucoid)
compared
controls.
Significant
differences
also
observed
synucleinopathy
patient
groups
(LBD
MSA)
complement.
Additionally,
CSF/serum
quotients
transferrin
complement
(LBD)
disease
relative
These
findings
suggest
processes
may
play
role
pathophysiology
proteinopathies,
warranting
further
research
confirm
these
associations.
potential
would
then
represent
promising
step
forward
field.
Frontiers in Cellular Neuroscience,
Год журнала:
2025,
Номер
19
Опубликована: Апрель 23, 2025
Major
depressive
disorder
(MDD)
is
one
of
the
most
common
mental
health
conditions,
characterized
by
pervasive
and
persistent
low
mood,
self-esteem,
a
loss
interest
or
pleasure
in
activities
that
are
typically
enjoyable.
Despite
decades
research
into
etiology
pathophysiological
mechanisms
depression,
therapeutic
outcomes
for
many
individuals
remain
less
than
expected.
A
promising
new
area
focuses
on
stress-induced
neuroinflammatory
processes,
such
as
excessive
activation
crosstalk
microglia
astrocytes
central
nervous
system
under
stress,
well
elevated
levels
pro-inflammatory
cytokines,
which
closely
linked
to
onset
progression
depression.
This
review
summarizes
through
neuroinflammation
induces
promotes
development
also
highlights
effective
roles
small
molecules
with
anti-inflammatory
activity
treatment
MDD.
Understanding
specific
further
impacts
using
technologies
single-cell
RNA
sequencing
elucidate
subtypes
interactions
great
importance
developing
more
strategies
Frontiers in Neuroscience,
Год журнала:
2025,
Номер
19
Опубликована: Апрель 30, 2025
Increased
extracellular
free
water
(FW)
is
considered
to
provide
better
pathophysiological
information
than
conventional
diffusion
tensor
imaging
(DTI)
metrics.
The
cholinergic
brain
network
a
key
hub
for
cognitive
function,
and
microstructural
changes
detected
by
in
this
system
may
be
associated
with
impairment
Alzheimer's
disease
(AD).
However,
the
specific
impact
of
FW
on
domains
across
AD
continuum
their
diagnostic
value
remain
unclear.
Here,
we
investigated
basal
forebrain
alterations
based
water-corrected
healthy
controls
(n
=
36),
amnestic
mild
(aMCI;
n
31),
group
33).
subregions
were
divided
into
Broca
diagonal
band
(Ch1-3)
Meynert
nucleus
(Ch4).
performance
was
measured
using
Montreal
Cognitive
Assessment
(MoCA).
Additionally,
evaluated
fraction
(FWf)
within
system.
FWf
bilateral
Ch1-3
Ch4
regions
increased
age,
significantly
higher
aMCI
(p
<
0.001).
In
AD,
correlated
total
MoCA
score
(R
-0.42,
p
0.015),
especially
visual
spatial/executive
-0.47,
0.006)
orientation
deficits
-0.38,
0.029).
No
significant
correlations
found
group.
ROC
curve
analysis
showed
that
had
high
efficacy
versus
HC
(AUC
0.958,
95%
CI
0.909-1.00),
moderate
0.795,
0.685-0.905)
0.719,
0.589-0.850).
captures
damage
entire
continuum.
These
occur
early
but
selectively
affect
domain-specific
cognition
later
stages
possibly
through
dysfunction.
Our
results
highlight
potential
as
biomarker
decline.
Background:
White
matter
hyperintensities
(WMHs)
are
common
neuroimaging
markers
of
cerebral
small
vessel
disease
(CSVD)
and
strongly
associated
with
cognitive
impairment.
While
hypoperfusion
neuroinflammation
recognized
as
major
contributors
to
WMH
pathology,
the
interplay
between
inflammatory
biomarkers
blood
flow
(CBF)
remains
poorly
understood.
Soluble
triggering
receptor
expressed
on
myeloid
cells
2
(sTREM2),
a
marker
microglial
activation,
may
play
dual
role
in
vascular
dysfunction.
Methods:
A
total
138
participants
aged
50–80
years
were
enrolled,
including
75
individuals
group
63
healthy
control
(HC)
group.
All
subjects
underwent
magnetic
resonance
imaging
(MRI)
arterial
spin
labeling(ASL)
for
CBF
quantification
neuropsychological
assessments.
Serum
sTREM2
levels
measured.
Group
comparisons,
logistic
regression,
partial
correlation
analyses
performed
explore
associations
among
sTREM2,
CBF,
performance.
Results:
Compared
HC
group,
serum
significantly
elevated
(P
=
0.036),
gray
matter(GM)
was
lower
0.038).
Logistic
regression
identified
(OR
1.041,
P
0.006)
age
1.081,
0.018)
independent
risk
factors
WMHs.
Partial
revealed
positive
association
controls,
but
negative
Additionally,
GM
positively
correlated
global
scores
(MMSE,
MoCA)
executive
function
(Stroop
Test
C)
Conclusion:
Our
findings
suggest
that
higher
reduced
brain
perfusion
be
closely
linked
presence
progression
white
decline.
Notably,
direction
relationship
appears
vary
by
status,
indicating
possible
shift
from
compensatory
harmful
inflammation.
These
results
highlight
clinical
value
combining
identifying
at
vessel-related
impairment
provide
useful
targets
early
intervention
monitoring.