Physiological Research,
Journal Year:
2025,
Volume and Issue:
1/2025, P. 1 - 17
Published: March 10, 2025
Alzheimer's
disease
(AD),
a
leading
cause
of
dementia
worldwide,
is
multifactorial
neurodegenerative
disorder
characterized
by
amyloid-beta
plaques,
tauopathy,
neuronal
loss,
neuro-inflammation,
brain
atrophy,
and
cognitive
deficits.
AD
manifests
as
familial
early-onset
(FAD)
with
specific
gene
mutations
or
sporadic
late-onset
(LOAD)
caused
various
genetic
environmental
factors.
Numerous
transgenic
rodent
models
have
been
developed
to
understand
pathology
development
progression.
The
TgF344-AD
rat
model
double
that
carries
two
human
mutations:
APP
the
Swedish
mutation
PSEN-1
Δ
exon
9
mutations.
This
exhibits
complete
repertoire
in
an
age-dependent
manner.
review
summarizes
multidisciplinary
research
insights
gained
from
studying
rats
context
pathology.
We
explore
neuropathological
findings;
electrophysiological
assessments
revealing
disrupted
synaptic
transmission,
reduced
spatial
coding,
network-level
dysfunctions,
altered
sleep
architecture;
behavioral
studies
highlighting
impaired
memory;
alterations
excitatory-inhibitory
systems;
molecular
physiological
changes
emphasizing
their
age-related
effects.
Additionally,
impact
interventions
studied
compiled,
underscoring
role
bridging
gaps
understanding
pathogenesis.
offers
significant
potential
identifying
biomarkers
for
early
detection
therapeutic
interventions,
providing
robust
platform
advancing
translational
research.
Theranostics,
Journal Year:
2023,
Volume and Issue:
13(10), P. 3434 - 3450
Published: Jan. 1, 2023
Background:
Alzheimer's
disease
(AD),
one
of
the
most
common
forms
dementia,
is
a
widely
studied
neurodegenerative
characterized
by
Aβ
accumulation
and
tau
hyperphosphorylation.
Currently,
there
no
effective
cure
available
for
AD.The
astrocyte
AQP4
polarized
distribution-mediated
glymphatic
system
essential
abnormal
clearance
potential
therapeutic
target
AD.However,
role
exercise
on
distribution
association
between
phenotype
polarization
are
poorly
understood.Methods:
Using
streptozotocin
(STZ)-induced
sporadic
AD
rat
model,
we
investigated
effects
high-intensity
interval
training
pathologies.The
Branes
maze
task
was
conducted
to
measure
spatial
learning
memory.Immunofluorescence
staining
NeuN
with
TUNEL,
Fluoro-Jade
C,
relative
neuronal
damage
markers
applied
apoptosis,
neurodegeneration,
damage.Sholl
analysis
carried
out
analyze
morphology
microglia.Line-scan
analysis,
3D
rendering,
orthogonal
view
were
colocalization.Western
blot
enzyme-linked
immunosorbent
assay
(ELISA)
examine
Aβ,
respectively.An
APP/PS1
transgenic
mice
model
used
confirm
key
findings.Results:
High-intensity
(HIIT)
alleviates
cognitive
dysfunction
in
STZ-induced
AD-like
models
provides
neuroprotection
against
damage,
loss.Additionally,
HIIT
improved
drainage
from
cortex
hippocampus
via
kidney.Further
mechanistic
studies
support
that
beneficial
might
be
due,
part,
glial
cells
neurotoxic
towards
neuroprotective
phenotype.Furthermore,
an
intriguing
finding
our
study
strongly
correlated
phenotype.We
found
A2
exhibited
more
evident
than
A1
phenotype.
Conclusion:Our
findings
indicate
ameliorates
disease-like
pathology
regulating
phenotype-associated
polarization.These
changes
promote
p-tau
brain
tissue
through
kidney.
Translational Neurodegeneration,
Journal Year:
2023,
Volume and Issue:
12(1)
Published: May 12, 2023
Abstract
Neurological
conditions,
including
cognitive
impairment
and
Alzheimer’s
disease
(AD),
impose
a
huge
burden
on
society,
affecting
millions
of
people
globally.
In
addition
to
genetic
factors,
recent
studies
indicate
that
environmental
experiential
factors
may
contribute
the
pathogenesis
these
diseases.
Early
life
adversity
(ELA)
has
profound
impact
brain
function
health
later
in
life.
rodent
models,
exposure
ELA
results
specific
deficits
aggravated
AD
pathology.
Extensive
concerns
have
been
raised
regarding
higher
risk
developing
impairments
with
history
ELA.
this
review,
we
scrutinize
findings
from
human
animal
focusing
connection
AD.
These
discoveries
suggest
ELA,
especially
at
early
postnatal
stages,
increases
susceptibility
terms
mechanisms,
could
lead
dysregulation
hypothalamus-pituitary-adrenal
axis,
altered
gut
microbiome,
persistent
inflammation,
oligodendrocyte
dysfunction,
hypomyelination,
aberrant
adult
hippocampal
neurogenesis.
Crosstalks
among
events
synergistically
Additionally,
discuss
several
interventions
alleviate
adverse
consequences
Further
investigation
into
crucial
area
will
help
improve
management
reduce
related
neurological
conditions.
Aging and Disease,
Journal Year:
2023,
Volume and Issue:
unknown, P. 0 - 0
Published: Jan. 1, 2023
Alzheimer’s
disease,
one
of
the
most
common
forms
dementia,
is
characterized
by
a
slow
progression
cognitive
impairment
and
neuronal
loss.
Currently,
approved
treatments
for
AD
are
hindered
various
side
effects
limited
efficacy.
Despite
considerable
research,
practical
have
not
been
developed.
Increasing
evidence
shows
that
glial
cells,
especially
microglia
astrocytes,
essential
in
initiation
AD.
During
progression,
activated
resident
increases
ability
resting
astrocytes
to
transform
into
reactive
promoting
neurodegeneration.
Extensive
clinical
molecular
studies
show
involvement
astrocyte-mediated
neuroinflammation
pathology,
indicating
may
be
potential
therapeutic
targets
This
review
will
summarize
significant
recent
advances
pathogenesis
three
parts.
First,
we
typical
pathological
changes
discuss
terms
function
phenotypic
changes.
Second,
describe
astrocytes’
physiological
role
These
roles
include
inflammatory
response,
“eat
me”
“don’t
eat
signals,
Aβ
seeding,
propagation,
clearance,
synapse
loss,
synaptic
pruning,
remyelination,
demyelination.
Last,
pharmacological
non-pharmacological
therapies
targeting
We
conclude
development
Therefore,
understanding
new
critical
future
trials.
Moreover,
pharmacological,
with
specific
investigating
damage
repair,
promising
research
direction
regarding
treatment
prevention.
Translational Neurodegeneration,
Journal Year:
2023,
Volume and Issue:
12(1)
Published: Nov. 14, 2023
Abstract
Oligodendrocyte
progenitor
cells
(OPCs)
play
pivotal
roles
in
myelin
formation
and
phagocytosis,
communicating
with
neighboring
contributing
to
the
integrity
of
blood–brain
barrier
(BBB).
However,
under
pathological
circumstances
Alzheimer’s
disease
(AD),
brain’s
microenvironment
undergoes
detrimental
changes
that
significantly
impact
OPCs
their
functions.
Starting
OPC
functions,
we
delve
into
transformation
myelin-producing
oligodendrocytes,
intricate
signaling
interactions
other
central
nervous
system
(CNS),
fascinating
process
which
influences
function
affects
CNS
homeostasis.
Moreover,
discuss
essential
role
BBB
highlight
critical
contribution
forming
CNS-protective
barriers.
In
context
AD,
deterioration
local
brain
is
discussed,
mainly
focusing
on
neuroinflammation,
oxidative
stress,
accumulation
toxic
proteins.
The
disturb
delicate
balance
brain,
impacting
regenerative
capacity
compromising
integrity.
Under
conditions,
experience
significant
alterations
migration
proliferation,
leading
impaired
differentiation
a
reduced
ability
produce
mature
oligodendrocytes.
degeneration
become
increasingly
active
progressive
neurodegeneration.
Finally,
summarize
current
therapeutic
approaches
targeting
AD.
Strategies
revitalize
senescence,
modulate
pathways
enhance
differentiation,
explore
potential
avenues
are
promising
alleviating
AD
function.
conclusion,
this
review
highlights
indispensable
involvement
pathogenesis
interplay
between
underscores
complexity
neurodegenerative
diseases.
Insights
from
studying
conditions
provide
foundation
for
innovative
strategies
fostering
Future
research
will
advance
our
understanding
management
diseases,
ultimately
offering
hope
effective
treatments
improved
quality
life
those
affected
by
related
disorders.
Translational Psychiatry,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 11, 2025
Repeated
closed-head
injuries
(rCHI)
from
activities
like
contact
sports,
falls,
military
combat,
and
traffic
accidents
pose
a
serious
risk
due
to
their
cumulative
impact
on
the
brain.
Often,
rCHI
is
not
diagnosed
until
symptoms
of
irreversible
brain
damage
appear,
highlighting
need
for
preventive
measures.
This
study
assessed
prophylactic
efficacy
remote
photobiomodulation
(PBM)
targeted
at
lungs
against
rCHI-induced
injury
associated
behavioral
deficits.
Utilizing
"Marmarou"
weight-drop
model,
was
induced
in
rats
days
0,
5,
10.
Remote
PBM,
employing
an
808
nm
continuous
wave
laser,
administered
daily
2-min
sessions
per
lung
side
over
20
days.
Behavioral
deficits
were
through
three-chamber
social
interaction,
forced
swim,
grip
strength,
open
field,
elevated
plus
maze,
Barnes
maze
tests.
Immunofluorescence
staining
3D
reconstruction
evaluated
neuronal
damage,
apoptosis,
degeneration,
morphology
microglia
astrocytes,
as
well
astrocyte
microglia-mediated
excessive
synapse
elimination.
Additionally,
16S
rDNA
amplicon
sequencing
analyzed
changes
microbiome
following
PBM
treatment.
Results
demonstrated
that
significantly
improved
depressive-like
behaviors,
motor
dysfunction,
interaction
impairment
while
enhancing
strength
reducing
degeneration
by
rCHI.
Analysis
revealed
enrichment
lipopolysaccharide
(LPS)
biosynthesis
pathways,
suggesting
potential
link
neuroprotection.
Furthermore,
mitigated
hyperactivation
cortical
astrocytes
reduced
synaptic
phagocytosis
these
cells,
its
strategy
with
neuroprotective
effects.
Nutrients,
Journal Year:
2022,
Volume and Issue:
14(20), P. 4298 - 4298
Published: Oct. 14, 2022
Alzheimer’s
disease
(AD),
an
age-related
neurodegenerative
disorder,
is
currently
incurable.
Imbalanced
amyloid-beta
(Aβ)
generation
and
clearance
are
thought
to
play
a
pivotal
role
in
the
pathogenesis
of
AD.
Historically,
strategies
targeting
Aβ
have
typically
focused
on
central
clearance,
but
with
limited
clinical
success.
Recently,
contribution
peripheral
systems,
particularly
liver,
has
sparked
increased
interest.
In
addition,
AD
presents
pathological
features
similar
those
metabolic
syndrome,
critical
involvement
brain
energy
disturbances
this
been
recognized.
More
importantly,
liver
may
be
key
regulator
these
abnormalities,
far
beyond
our
past
understanding.
Here,
we
review
recent
animal
findings
indicating
that
dysfunction
represents
early
event
pathophysiology.
We
further
propose
compromised
by
aberrant
hepatic
physiological
processes
contribute
neurodegeneration.
The
synthesis
product,
fibroblast
growth
factor
21
(FGF21),
management
also
discussed.
A
deeper
understanding
communication
between
lead
new
opportunities
for
diagnosis
treatment
Aging Cell,
Journal Year:
2023,
Volume and Issue:
22(7)
Published: April 24, 2023
Alzheimer's
disease
(AD),
a
prevalent
form
of
dementia,
is
characterized
by
the
decline
cognitive
abilities
with
age.
Available
treatment
options
for
AD
are
limited,
making
it
significant
public
health
concern.
Recent
research
suggests
that
metabolic
dysfunction
plays
role
in
development
AD.
In
addition,
insulin
therapy
has
been
shown
to
improve
memory
patients
decline.
this
study,
we
report
first
examination
body
composition,
peripheral
sensitivity,
and
glucose
tolerance
relation
behavioral
assessments
learning,
memory,
anxiety
TgF344-AD
rat
model
Results
from
tests
show
female
rats
exhibit
impaired
clearance
reduced
sensitivity
at
both
9
12
months
age,
while
males
display
no
differences
even
improved
months.
Morris
Water
Maze
assessment
learning
reveal
male
impairments
only
Furthermore,
results
open
field
elevated
plus
maze
suggest
increased
age;
however,
were
detected
or
Overall,
our
findings
metabolism,
commonly
associated
type
2
diabetes,
occur
before
simultaneously
sexually
dimorphic
manner
model.
Aging and Disease,
Journal Year:
2023,
Volume and Issue:
15(2), P. 698 - 698
Published: Aug. 2, 2023
Cellular
senescence
is
an
irreversible
and
multifaceted
process
inducing
tissue
dysfunction
organismal
aging,
thus
the
clearance
of
senescent
cells
can
prevent
or
delay
onset
aging-related
pathologies.
Herein,
we
developed
augmented
photothermal
therapy
strategy
integrated
with
antibody
against
β2-microglobulin
(aB2MG)
immune
adjuvant
imiquimod
(R837)
to
effectively
accelerate
cell
apoptosis
under
a
near-infrared
light.
With
this
strategy,
designed
CroR@aB2MG
enables
targeting
application
concomitantly,
initiation
subsequently,
finally
realization
protective
effects
senescence.
Our
results
showed
that
photo-induced
heating
effect
caused
quickly
undergo
synchronous
response
accelerated
in
vitro
vivo.
Therefore,
photoactivated
speedy
clearing
may
provide
efficient
way
for
treatment
senescence-related
diseases
by
eliminating
biomaterials.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(10), P. 8625 - 8625
Published: May 11, 2023
Rare
ginsenosides
are
the
major
components
of
red
ginseng.
However,
there
has
been
little
research
into
relationship
between
structure
and
their
anti-inflammatory
activity.
In
this
work,
BV-2
cells
induced
by
lipopolysaccharide
(LPS)
or
nigericin,
activity
eight
rare
ginsenosides,
target
proteins
expression
AD
were
compared.
addition,
Morris
water
maze
test,
HE
staining,
thioflavins
urine
metabonomics
used
to
evaluate
effect
Rh4
on
mice.
Our
results
showed
that
configuration
influences
ginsenosides.
Ginsenosides
Rk1,
Rg5,
Rk3,
have
significant
compared
S-Rh1,
R-Rh1,
S-Rg3,
R-Rg3.
S-Rh1
S-Rg3
more
pronounced
than
R-Rh1
R-Rg3,
respectively.
Furthermore,
two
pairs
stereoisomeric
can
significantly
reduce
level
NLRP3,
caspase-1,
ASC
in
cells.
Interestingly,
improve
learning
ability
mice,
cognitive
impairment,
hippocampal
neuronal
apoptosis
Aβ
deposition,
regulate
AD-related
pathways
such
as
tricarboxylic
acid
cycle
sphingolipid
metabolism.
findings
conclude
with
a
double
bond
those
without,
20(S)-ginsenosides
excellent
20(R)-ginsenosides.