Biosensors,
Год журнала:
2025,
Номер
15(2), С. 85 - 85
Опубликована: Фев. 4, 2025
Alzheimer’s
disease
(AD)
is
a
prevalent
neurodegenerative
disorder
and
significant
cause
of
dementia
in
elderly
individuals,
with
growing
prevalence
our
aging
population.
Extracellular
amyloid-β
peptides
(Aβ),
intracellular
tau
proteins,
their
phosphorylated
forms
have
gained
prominence
as
critical
biomarkers
for
early
precise
diagnosis
AD,
correlating
progression
response
to
therapy.
The
high
costs
invasiveness
conventional
diagnostic
methods,
such
positron
emission
tomography
(PET)
magnetic
resonance
imaging
(MRI),
limit
suitability
large-scale
or
routine
screening.
However,
electrochemical
(EC)
analysis
methods
made
progress
detection
due
sensitivity,
excellent
specificity,
portability,
cost-effectiveness.
This
article
reviews
the
EC
biosensing
technologies,
focusing
on
protein
blood
(a
low-invasive,
accessible
medium).
then
discusses
various
sensing
platforms,
including
fabrication
processes,
(LOD),
clinical
potential
show
role
these
sensors
transformers
changing
face
AD
diagnostics.
International Journal of Molecular Sciences,
Год журнала:
2022,
Номер
23(9), С. 4999 - 4999
Опубликована: Апрель 30, 2022
Neurodegenerative
diseases
and
depression
are
multifactorial
disorders
with
a
complex
poorly
understood
physiopathology.
Astrocytes
play
key
role
in
the
functioning
of
neurons
norm
pathology.
Stress
is
an
important
factor
for
development
brain
disorders.
Here,
we
review
data
on
effects
stress
astrocyte
function
evidence
involvement
dysfunction
Alzheimer’s
disease
(AD).
Stressful
life
events
risk
depression;
meanwhile,
AD.
Clinical
indicate
atrophic
changes
same
areas
brain,
hippocampus
prefrontal
cortex
(PFC),
both
pathologies.
These
regions
regulating
response
most
vulnerable
to
action
glucocorticoids.
PFC
astrocytes
critically
involved
depression.
alters
can
result
pyroptotic
death
not
only
neurons,
but
also
astrocytes.
BDNF-TrkB
system
plays
normalizing
response,
appears
be
Astrocytes,
being
target
glucocorticoids,
promising
treatment
stress-dependent
Molecular Neurodegeneration,
Год журнала:
2023,
Номер
18(1)
Опубликована: Апрель 20, 2023
Understanding
and
treating
Alzheimer's
disease
(AD)
has
been
a
remarkable
challenge
for
both
scientists
physicians.
Although
the
amyloid-beta
tau
protein
hypothesis
have
largely
explained
key
pathological
features
of
disease,
mechanisms
by
which
such
proteins
accumulate
lead
to
progression
are
still
unknown.
Such
lack
understanding
disrupts
development
disease-modifying
interventions,
leaving
therapeutic
gap
that
remains
unsolved.
Nonetheless,
recent
discoveries
glymphatic
pathway
meningeal
lymphatic
system
as
components
driving
central
solute
clearance
revealed
another
mechanism
underlying
AD
pathogenesis.
In
this
regard,
narrative
review
integrates
systems
essential
involved
in
Moreover,
it
discusses
emerging
evidence
suggesting
nutritional
supplementation,
non-invasive
brain
stimulation,
traditional
Chinese
medicine
can
improve
pathophysiology
increasing
and/or
function.
Given
physical
exercise
is
well-regarded
preventive
pro-cognitive
intervention
dementia,
we
summarize
mediating
effects
AD.
Targeting
these
holds
promise
more
effective
treatment
strategies.
Aging and Disease,
Год журнала:
2024,
Номер
unknown, С. 0 - 0
Опубликована: Янв. 1, 2024
Alzheimer's
disease
(AD)
is
a
age-related
neurodegenerative
and
major
public
health
concern
both
in
Texas,
US
Worldwide.
This
mainly
characterized
by
amyloid-beta
(Aβ)
phosphorylated
Tau
(p-Tau)
accumulation
the
brains
of
patients
with
AD
increasing
evidence
suggests
that
these
are
key
biomarkers
AD.
Both
Aβ
p-tau
can
be
detected
through
various
imaging
techniques
(such
as
positron
emission
tomography,
PET)
cerebrospinal
fluid
(CSF)
analysis.
The
presence
individuals,
who
asymptomatic
or
have
mild
cognitive
impairment
indicate
an
increased
risk
developing
future.
Furthermore,
combination
often
used
for
more
accurate
diagnosis
prediction
progression.
Along
being
disease,
it
associated
other
chronic
conditions
such
cardiovascular
obesity,
depression,
diabetes
because
studies
shown
comorbid
make
people
vulnerable
to
In
first
part
this
review,
we
discuss
biofluid-based
Aβ,
p-Tau
&
plasma
could
alternative
sensitive
technique
diagnose
second
part,
underlying
molecular
mechanisms
linked
how
they
affect
clinical
care.
Abstract
Alzheimer’s
Disease
(ad)
is
the
most
common
cause
of
dementia,
and
in
addition
to
cognitive
decline,
it
directly
contributes
physical
frailty,
falls,
incontinence,
institutionalisation
polypharmacy
older
adults.
Increasing
availability
clinically
validated
biomarkers
including
cerebrospinal
fluid
positron
emission
tomography
assess
both
amyloid
tau
pathology
has
led
a
reconceptualisation
ad
as
clinical–biological
diagnosis,
rather
than
one
based
purely
on
clinical
phenotype.
However,
co-pathology
frequent
adults
which
influence
accuracy
biomarker
interpretation.
Importantly,
some
with
positive
or
pathological
may
never
experience
impairment
dementia.
These
strides
towards
achieving
an
accurate
diagnosis
are
occurring
alongside
recent
phase
3
trial
results
reporting
statistically
significant
effects
anti-amyloid
Disease-Modifying
Therapies
(DMTs)
disease
severity
early
ad.
real-world
benefit
these
DMTs
not
clear
concerns
remain
regarding
how
will
translate
populations,
potential
adverse
(including
amyloid-related
imaging
abnormalities),
can
be
severe
healthcare
systems
readiness
afford
deliver
appropriate
populations.
Here,
we
review
advances
diagnostic
classification
future
treatment
living
Advocating
for
access
more
must
done
so
holistic
gerontologically
attuned
fashion,
geriatricians
advocating
enhanced
multi-component
multi-disciplinary
care
all
This
includes
those
across
spectrum
potentially
ineligible
emerging
DMTs.
Frontiers in Neuroscience,
Год журнала:
2024,
Номер
18
Опубликована: Фев. 19, 2024
Alzheimer’s
disease
(AD)
is
a
prevalent
neurodegenerative
that
has
become
one
of
the
main
factors
affecting
human
health.
It
serious
impacts
on
individuals,
families,
and
society.
With
development
population
aging,
incidence
AD
will
further
increase
worldwide.
Emerging
evidence
suggests
many
physiological
metabolic
processes,
such
as
lipid
metabolism,
are
implicated
in
pathogenesis
AD.
Bile
acids,
undertakers
play
an
important
role
occurrence
disease.
Tauroursodeoxycholic
acid,
endogenous
bile
been
proven
to
possess
therapeutic
effects
different
diseases,
including
This
review
tries
find
relationship
between
acid
metabolism
AD,
well
explore
potential
taurocursodeoxycholic
for
this
The
mechanisms
may
include
reducing
deposition
Amyloid-β
protein,
regulating
apoptotic
pathways,
preventing
tau
hyperphosphorylation
aggregation,
protecting
neuronal
synapses,
exhibiting
anti-inflammatory
properties,
improving
disorders.
objective
study
shed
light
use
tauroursodeoxycholic
preparations
prevention
treatment
with
aim
identifying
effective
targets
clarifying
various
involved
JAMA Ophthalmology,
Год журнала:
2024,
Номер
142(2), С. 108 - 108
Опубликована: Янв. 4, 2024
Age-related
macular
degeneration
(AMD)
is
a
serious
and
common
ophthalmologic
disorder
that
hypothesized
to
result,
in
part,
from
inflammatory
reactions
the
macula.
Alzheimer
disease
(AD)
treatment,
acetylcholinesterase
inhibitors
(AChEIs),
have
anti-inflammatory
effects
it
remains
unclear
if
they
modify
risk
of
AMD.
Regenerative Therapy,
Год журнала:
2024,
Номер
26, С. 599 - 610
Опубликована: Июнь 1, 2024
Mesenchymal
stem
cells
(MSCs)
have
gained
attention
as
a
promising
therapeutic
approach
in
both
preclinical
and
clinical
osteoarthritis
(OA)
settings.
Various
joint
cell
types,
such
chondrocytes,
synovial
fibroblasts,
osteoblasts,
tenocytes,
can
produce
release
extracellular
vesicles
(EVs),
which
subsequently
influence
the
biological
activities
of
recipient
cells.
Recently,
derived
from
mesenchymal
(MSC-EVs)
shown
potential
to
modulate
various
physiological
pathological
processes
through
modulation
cellular
differentiation,
immune
responses,
tissue
repair.
This
review
explores
roles
MSC-EVs
OA
rheumatoid
arthritis,
cardiovascular
disease,
age-related
macular
degeneration,
Alzheimer's
other
degenerative
diseases.
Notably,
we
provide
comprehensive
summary
exosome
biogenesis,
microRNA
composition,
mechanisms
intercellular
transfer,
their
evolving
role
highlight
exosome-based
treatments
avenues.
Frontiers in Medicine,
Год журнала:
2024,
Номер
11
Опубликована: Дек. 16, 2024
Alzheimer's
disease
(AD)
is
a
chronic,
progressive
neurodegenerative
disorder
characterized
by
cognitive
decline,
memory
loss,
and
impaired
reasoning.
It
the
leading
cause
of
dementia
in
older
adults,
marked
pathological
accumulation
amyloid-beta
plaques
neurofibrillary
tangles.
These
changes
lead
to
widespread
neuronal
damage,
significantly
impacting
daily
functioning
quality
life.
Alzheimer s Research & Therapy,
Год журнала:
2025,
Номер
17(1)
Опубликована: Янв. 13, 2025
The
imbalance
of
glutamate
(Glu)
and
gamma-aminobutyric
acid
(GABA)
neurotransmitter
system
plays
a
crucial
role
in
the
pathogenesis
Alzheimer's
disease
(AD).
Riluzole
is
Glu
modulator
originally
approved
for
amyotrophic
lateral
sclerosis
that
has
shown
potential
neuroprotective
effects
various
neurodegenerative
disorders.
However,
whether
riluzole
can
improve
GABA
homeostasis
AD
brain
its
related
mechanism
action
remain
unknown.
This
study
utilized
chemical
exchange
saturation
transfer
(CEST)
imaging
combined
with
proton
magnetic
resonance
spectroscopy
(1H-MRS)
to
monitor
dynamic
changes
riluzole-treated
mice,
aiming
evaluate
efficacy
treatment.
GluCEST,
GABACEST
1H-MRS
were
used
longitudinally
levels
3xTg
mice
treated
(12.5
mg/kg/day)
or
vehicle
20
weeks.
Magnetic
measurements
performed
at
baseline,
6,
12,
weeks
post-treatment.
Cognitive
performance
was
assessed
using
Morris
Water
Maze
(MWM)
10,
At
endpoint,
immunohistochemistry,
Nissl
staining,
Western
blot
pathology,
neuronal
survival,
protein
expression.
consistently
revealed
higher
compared
untreated
controls,
which
associated
improvements
spatial
learning
memory.
cognitive
significantly
correlated
increased
GluCEST
signals
levels.
Immunohistochemistry
staining
demonstrated
treatment
reduced
amyloid-beta
(Aβ)
deposition,
tau
hyperphosphorylation,
GFAP-positive
astrocyte
activation,
prevented
loss.
Moreover,
upregulated
expression
excitatory
amino
transporter
2
(EAAT2),
glutamic
decarboxylase
65/67
(GAD65/67),
glutamine
synthetase
(GS),
suggesting
enhanced
metabolism.
CEST
effectiveness
modulating
Glu-
GABA-related
improving
function
potentially
through
regulating
key
proteins
involved
These
findings
suggest
as
therapeutic
agent
highlight
utility
multimodal
MR
monitoring
response
exploring
mechanisms.