Antioxidants and Redox Signaling,
Journal Year:
2023,
Volume and Issue:
39(10-12), P. 708 - 727
Published: July 14, 2023
Significance:
Redox
signaling
through
mitochondrial
reactive
oxygen
species
(mtROS)
has
a
key
role
in
several
mechanisms
of
regulated
cell
death
(RCD),
necroptosis,
ferroptosis,
pyroptosis,
and
apoptosis,
thereby
decisively
contributing
to
inflammatory
disorders.
The
mtROS
apoptosis
been
extensively
addressed,
but
their
involvement
necrotic-like
RCD
just
started
being
elucidated,
providing
novel
insights
into
the
pathophysiology
acute
inflammation.
Recent
Advances:
p53
together
with
drive
necroptosis
inflammation
downregulation
sulfiredoxin
peroxiredoxin
3.
Mitochondrial
hydroorotate
dehydrogenase
is
redox
system
regulation
ferroptosis.
In
addition,
noncanonical
pathway,
which
generates
Ragulator-Rag
complex
acts
via
mTORC1
promote
gasdermin
D
oligomerization,
triggers
pyroptosis.
Critical
Issues:
trigger
positive
feedback
loops
leading
lytic
conjunction
necrosome,
inflammasome,
glutathione
depletion,
peroxidase
4
deficiency.
Future
Directions:
precise
mechanism
membrane
rupture
ferroptosis
contribution
disorders
are
still
unclear,
will
need
further
research.
antioxidants
may
provide
promising
therapeutic
approaches
toward
However,
establishing
doses
windows
action
be
required
optimize
potential,
avoid
potential
adverse
side
effects
linked
blockade
beneficial
adaptive
signaling.
Antioxid.
Signal.
39,
708-727.
Cell Death and Disease,
Journal Year:
2022,
Volume and Issue:
13(6)
Published: June 6, 2022
Abstract
Compelling
evidences
have
revealed
the
emerging
role
of
ferroptosis
in
pathophysiological
process
acute
lung
injury
(ALI),
but
its
modulation
is
not
clear.
Here,
we
identified
that
STAT6
acted
as
a
critical
regulator
epithelium
during
ALI.
Firstly,
expression
and
activity
were
increased
ALI
mice
models
caused
by
crystalline
silica
(CS),
LPS
X-ray
exposure.
Followed
confirming
contribution
above
with
ferrostatin-1
deferoxamine
intervention,
bioinformatic
analyses
was
negatively
correlated
ferroptosis.
Consistently,
epithelium-specific
depletion
or
knockdown
cultured
epithelial
cells
exacerbated
While
overexpression
attenuated
Mechanistically,
SLC7A11
typical
ferroptosis-related
gene
regulated
P53.
CREB-binding
protein
(CBP)
acetyltransferase
P53
acetylation,
showing
valuable
regulation
on
targets’
transcription.
Herein,
found
regulates
through
competitively
binding
CBP,
which
inhibits
acetylation
transcriptionally
restores
expression.
Finally,
pulmonary-specific
decreased
CS
induced
injury.
Our
findings
pivotal
ferroptosis,
may
be
potential
therapeutic
target
for
treatment
Cells,
Journal Year:
2022,
Volume and Issue:
11(13), P. 2040 - 2040
Published: June 27, 2022
Ferroptosis,
which
has
been
widely
associated
with
many
diseases,
is
an
iron-dependent
regulated
cell
death
characterized
by
intracellular
lipid
peroxide
accumulation.
It
exhibits
morphological,
biochemical,
and
genetic
characteristics
that
are
unique
in
comparison
to
other
types
of
death.
The
course
ferroptosis
can
be
accurately
the
metabolism
iron,
lipids,
amino
acids,
various
signal
pathways.
In
this
review,
we
summarize
basic
ferroptosis,
its
regulation,
as
well
relationship
between
chronic
diseases
such
cancer,
nervous
system
metabolic
inflammatory
bowel
diseases.
Finally,
describe
regulatory
effects
food-borne
active
ingredients
on
ferroptosis.
Frontiers in Pharmacology,
Journal Year:
2021,
Volume and Issue:
12
Published: Aug. 2, 2021
Acute
lung
injury
(ALI),
a
common
and
critical
illness
with
high
morbidity
mortality,
is
caused
by
multiple
causes.
It
has
been
confirmed
that
oxidative
stress
plays
an
important
role
in
the
development
of
ALI.
Ferroptosis,
newly
discovered
programmed
cell
death
2012,
characterized
iron-dependent
lipid
peroxidation
involved
many
diseases.
To
date,
compelling
evidence
reveals
emerging
ferroptosis
pathophysiological
process
Here,
we
review
pathogenesis
ALI
its
therapeutic
potential
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: March 9, 2023
Acute
lung
injury
(ALI)
is
a
life-threatening
disease
with
high
incidence
and
mortality
rates.
Urolithin
A
(UA)
pomegranate
intestinal
flora
metabolite
anti-inflammatory,
antioxidant,
anti-aging
properties.
Ferroptosis
critical
factor
in
lipopolysaccharide
(LPS)-induced
acute
(ALI).
However,
the
link
between
UA
ferroptosis
unknown.
The
purpose
of
this
research
was
to
look
into
role
regulating
LPS-induced
ALI.
current
study
used
LPS
injure
two
models,
one
BEAS-2B
cell
model
ALI
mouse
model.
effectively
alleviated
compared
group
by
lowering
vivo
wet/dry
weight
ratio,
reactive
oxygen
species,
malondialdehyde
production,
as
well
superoxide
dismutase,
catalase,
glutathione
depletion.
Furthermore,
increasing
GPX4
SLC7A11
expression
decreasing
Fe2+
levels,
histopathological
damage,
inflammatory
cytokine
secretion,
levels
can
be
significantly
reduced.
Keap1-Nrf2/HO-1
pathway
upregulated
UA,
which
inhibited
ferroptosis.
ML385
UA's
protective
effect
against
These
findings
suggested
that
could
novel
potential
therapeutic
target
for