Frontiers in Aging Neuroscience,
Journal Year:
2023,
Volume and Issue:
14
Published: April 26, 2023
Microglia,
characterized
by
responding
to
damage,
regulating
the
secretion
of
soluble
inflammatory
mediators,
and
engulfing
specific
segments
in
central
nervous
system
(CNS),
function
as
key
immune
cells
CNS.
Emerging
evidence
suggests
that
microglia
coordinate
responses
CNS
play
a
pivotal
role
pathogenesis
age-related
neurodegenerative
diseases
(NDDs).
Remarkably,
autophagy
participates
regulation
subcellular
substances,
which
includes
degradation
misfolded
proteins
other
harmful
constituents
produced
neurons.
Therefore,
regulates
neuronal
homeostasis
maintenance
process
neuroinflammation.
In
this
review,
we
aimed
at
highlighting
NDDs.
Besides
mechanistic
co-interaction
between
different
kinds
NDDs,
also
emphasized
potential
therapeutic
agents
approaches
could
be
utilized
onset
progression
these
through
modulating
autophagy,
including
promising
nanomedicines.
Our
review
provides
valuable
reference
for
subsequent
studies
focusing
on
treatments
disorders.
The
exploration
development
nanomedicines
greatly
enhances
current
understanding
Journal of Neuroinflammation,
Journal Year:
2023,
Volume and Issue:
20(1)
Published: March 11, 2023
Microglial
activation-mediated
neuroinflammation
is
one
of
the
essential
pathogenic
mechanisms
sepsis-associated
encephalopathy
(SAE).
Mounting
evidence
suggests
that
high
mobility
group
box-1
protein
(HMGB1)
plays
a
pivotal
role
in
and
SAE,
yet
mechanism
by
which
HMGB1
induces
cognitive
impairment
SAE
remains
unclear.
Therefore,
this
study
aimed
to
investigate
underlying
SAE.An
model
was
established
cecal
ligation
puncture
(CLP);
animals
sham
underwent
cecum
exposure
alone
without
perforation.
Mice
inflachromene
(ICM)
were
continuously
injected
with
ICM
intraperitoneally
at
daily
dose
10
mg/kg
for
9
days
starting
1
h
before
CLP
operation.
The
open
field,
novel
object
recognition,
Y
maze
tests
performed
on
14-18
after
surgery
assess
locomotor
activity
function.
secretion,
state
microglia,
neuronal
measured
immunofluorescence.
Golgi
staining
detect
changes
morphology
dendritic
spine
density.
In
vitro
electrophysiology
long-term
potentiation
(LTP)
CA1
hippocampus.
vivo
neural
oscillation
hippocampus.CLP-induced
accompanied
increased
secretion
microglial
activation.
phagocytic
capacity
microglia
enhanced,
resulting
aberrant
pruning
excitatory
synapses
loss
reduced
activity,
impaired
LTP,
decreased
theta
Inhibiting
treatment
reversed
these
changes.HMGB1
activation,
synaptic
pruning,
neuron
dysfunction
an
animal
leading
impairment.
These
results
suggest
might
be
target
treatment.
CNS Neuroscience & Therapeutics,
Journal Year:
2021,
Volume and Issue:
28(2), P. 247 - 258
Published: Nov. 27, 2021
Fisetin,
the
effective
ingredient
of
traditional
Chinese
medicine
named
Cotinus
coggygria,
is
recommended
to
be
active
therapeutic
in
many
disorders.
However,
its
role
sepsis-associated
encephalopathy
(SAE)
remains
unclarified.Cecal
ligation
and
puncture
(CLP)
operation
was
performed
establish
a
rat
model
SAE.
Rats
were
grouped
according
surgery
fisetin
administration.
Cognitive
impairment
assessed
by
Morris
water
maze
test.
Disruption
blood-brain
barrier
(BBB)
integrity
detected
Evan's
blue
staining.
The
mitophagy,
reactive
oxygen
species
(ROS)
generation,
NLRP3
inflammasome
activation,
pro-inflammatory
cytokines
levels
measured
through
western
blot
double
immunofluorescence
labeling.
A
transmission
electron
microscope
applied
for
observation
mitochondrial
autophagosomes.Rats
CLP
group
presented
increased
expression
IL-1R1,
pNF-κB,
TNF-α,
iNOS
microglial
cells,
indicating
severe
inflammation
central
nervous
system
(CNS).
Nevertheless,
there
no
increase
BBB
permeability.
Meanwhile,
activated
cerebral
microvascular
endothelial
cells
(CMECs),
with
an
elevation
caspase-1
IL-1β
secretion
into
CNS.
In
addition,
we
found
significantly
improved
cognitive
dysfunction
rats
Neuroprotective
effects
might
associated
inhibition
neuroinflammation,
represented
decreased
microglia.
Furthermore,
induced
scavenged
ROS,
blocked
activation
CMECs,
as
evidenced
reduced
release
CNS.Collectively,
fisetin-blocked
via
promoting
mitophagy
CMECs
may
suppress
CNS,
reduce
contribute
amelioration
impairment.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Oct. 24, 2022
Neuroinflammation
is
the
fundamental
immune
response
against
multiple
factors
in
central
nervous
system
and
characterized
by
production
of
inflammatory
mediators,
activated
microglia
astrocytes,
recruitment
innate
adaptive
cells
to
sites,
that
contributes
pathological
process
related
brain
diseases,
such
as
Alzheimer’s
disease,
Parkinson’s
depression,
stroke.
Flavonoids,
a
species
important
natural
compounds,
have
been
widely
revealed
alleviate
neuroinflammation
inhibiting
pro-inflammatory
elevating
secretion
anti-inflammatory
factors,
modulating
polarization
astrocyte,
mainly
via
suppressing
activation
NLRP3
inflammasome,
well
NF-κB,
MAPK,
JAK/STAT
pathways,
promoting
Nrf2,
AMPK,
BDNF/CREB,
Wnt/β-Catenin,
PI3k/Akt
signals
SIRT1-mediated
HMGB1
deacetylation.
This
review
will
provide
latest
comprehensive
knowledge
on
therapeutic
benefits
mechanisms
flavonoids
neuroinflammation,
might
be
developed
into
food
supplements
or
lead
compounds
for
neuroinflammation-associated
disorders.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
178, P. 117180 - 117180
Published: July 27, 2024
Sepsis
and
septic
shock
are
critical
medical
conditions
characterized
by
a
systemic
inflammatory
response
to
infection,
significantly
contributing
global
mortality
rates.
The
progression
multiple
organ
dysfunction
syndrome
(MODS)
represents
the
most
severe
complication
of
sepsis
markedly
increases
clinical
mortality.
Central
pathophysiology
sepsis,
endothelial
cells
play
crucial
role
in
regulating
microcirculation
maintaining
barrier
integrity
across
various
organs
tissues.
Recent
studies
have
underscored
pivotal
function
development
sepsis-induced
MODS.
This
review
aims
provide
comprehensive
overview
MODS,
with
specific
focus
on
dysfunction.
It
also
compiles
compelling
evidence
regarding
potential
small
molecules
that
could
attenuate
subsequent
multi-organ
damage
modulating
function.
Thus,
this
serves
as
an
essential
resource
for
practitioners
involved
diagnosing,
managing,
providing
intensive
care
associated
injuries,
emphasizing
importance
targeting
enhance
outcomes
patients.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
174, P. 116453 - 116453
Published: March 20, 2024
Sepsis-associated
encephalopathy
(SAE),
a
common
neurological
complication
of
sepsis,
is
heterogenous
complex
clinical
syndrome
caused
by
the
dysfunctional
response
host
to
infection.
This
leads
excess
mortality
and
morbidity
worldwide.
Despite
relevance
with
high
incidence,
there
lack
understanding
for
its
both
acute/chronic
pathogenesis
therapeutic
management.
A
better
molecular
mechanisms
behind
SAE
may
provide
tools
enhance
efficacy.
Mounting
evidence
indicates
that
some
types
non-apoptotic
regulated
cell
death
(RCD),
such
as
ferroptosis,
pyroptosis,
autophagy,
contribute
SAE.
Targeting
these
RCD
meaningful
targets
future
treatments
against
review
summarizes
core
mechanism
which
We
focus
on
emerging
compounds
can
inhibit
delineate
their
beneficial
pharmacological
effects
Within
this
we
suggest
inhibition
serve
potential
strategy
Cell Death Discovery,
Journal Year:
2024,
Volume and Issue:
10(1)
Published: Feb. 19, 2024
Abstract
Mitochondria
produce
adenosine
triphosphate
and
potentially
contribute
to
proinflammatory
responses
cell
death.
Mitophagy,
as
a
conservative
phenomenon,
scavenges
waste
mitochondria
their
components
in
the
cell.
Recent
studies
suggest
that
severe
infections
develop
alongside
mitochondrial
dysfunction
mitophagy
abnormalities.
Restoring
protects
against
excessive
inflammation
multiple
organ
failure
sepsis.
Here,
we
review
normal
process,
its
interaction
with
invading
microorganisms
immune
system,
summarize
mechanism
of
during
infection.
We
highlight
critical
role
preventing
Journal of Advanced Research,
Journal Year:
2024,
Volume and Issue:
65, P. 297 - 327
Published: May 14, 2024
Autophagy
is
an
evolutionarily
conserved
turnover
process
for
intracellular
substances
in
eukaryotes,
relying
on
lysosomal
(in
animals)
or
vacuolar
yeast
and
plants)
mechanisms.
In
the
past
two
decades,
emerging
evidence
suggests
that,
under
specific
conditions,
autophagy
can
target
particular
macromolecules
organelles
degradation,
a
termed
selective
autophagy.
Recently,
accumulating
studies
have
demonstrated
that
abnormality
of
closely
associated
with
occurrence
progression
many
human
diseases,
including
neurodegenerative
cancers,
metabolic
cardiovascular
diseases.
This
review
aims
at
systematically
comprehensively
introducing
its
role
various
while
unravelling
molecular
mechanisms
By
providing
theoretical
basis
development
related
small-molecule
drugs
as
well
treating
this
seeks
to
contribute
understanding
therapeutic
potential.
review,
we
introduce
dissect
major
categories
been
discovered.
We
also
focus
recent
advances
underlying
both
classical
non-classical
Moreover,
current
situation
targeting
different
types
further
summarized,
valuable
insights
into
discovery
more
candidate
future.
On
other
hand,
reveal
clinically
relevant
implementations
are
potentially
autophagy,
such
predictive
approaches
treatments
tailored
individual
patients.
Phytomedicine,
Journal Year:
2024,
Volume and Issue:
130, P. 155725 - 155725
Published: May 12, 2024
Bidirectional
communication
between
the
gut
microbiota
and
brain
may
play
an
essential
role
in
cognitive
dysfunction
associated
with
chronic
sleep
deprivation(CSD).
Salvia
miltiorrhiza
Bunge
(Danshen,
DS),
a
famous
Chinese
medicine
functional
tea,
is
extensively
used
to
protect
learning
memory
capacities,
although
mechanism
of
action
remains
unknown.
Oxidative Medicine and Cellular Longevity,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 28
Published: May 14, 2022
Mitochondria
play
a
critical
role
in
neuron
viability
or
death
as
it
regulates
energy
metabolism
and
cell
pathways.
They
are
essential
for
cellular
metabolism,
reactive
oxygen
species
production,
apoptosis,
Ca++
homeostasis,
aging,
regeneration.
Mitophagy
mitochondrial
dynamics
thus
processes
the
quality
control
of
mitochondria.
Improvements
several
fundamental
features
biology
susceptible
neurons
AD
brains
putative
underlying
mechanisms
such
changes
have
made
significant
progress.
AD’s
etiology
has
been
reported
by
malfunction
oxidative
damage.
According
to
recent
articles,
continual
fusion
fission
balance
mitochondria
is
vital
their
normal
function
maintenance.
As
result,
shape
inextricably
linked.
This
study
examines
evidence
suggesting
that
dysfunction
plays
early
impact
on
pathology.
Furthermore,
roles
discussed
with
link
between
autophagy
also
explored.
In
addition,
research
mitophagy
this
review.
It
goes
into
how
these
flaws
affect
control.
advanced
therapy
techniques
lifestyle
adjustments
lead
improved
management
demonstrated,
hence
improving
conditions
contribute
AD.