Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
173, P. 116363 - 116363
Published: March 12, 2024
Ferroptosis,
a
novel
form
of
regulated
cell
death
characterized
by
dependence
on
iron
and
lipid
peroxidation,
has
been
implicated
in
wide
range
clinical
conditions
including
neurological
diseases,
cardiovascular
disorders,
acute
kidney
failure,
various
types
cancer.
Therefore,
it
is
critical
to
suppress
cancer
progression
proliferation.
Ferroptosis
can
be
triggered
cells
some
normal
synthetic
substances,
such
as
erastin,
Ras-selective
lethal
small
molecule-3,
or
pharmaceuticals.
Natural
bioactive
compounds
are
traditional
drug
discovery
tools,
have
therapeutically
used
dietary
additives
pharmaceutical
agents
against
malignancies.
The
fact
that
natural
products
multiple
targets
minimal
side
effects
led
notable
advances
anticancer
research.
Research
indicated
ferroptosis
also
induced
during
treatment.
In
this
review,
we
focused
the
most
recent
developments
emerging
molecular
processes
significance
To
provide
new
perspectives
future
development
ferroptosis-related
medications,
summary
implications
phytochemicals
triggering
through
ROS
production
ferritinophagy
induction
variety
Antioxidants,
Journal Year:
2024,
Volume and Issue:
13(3), P. 298 - 298
Published: Feb. 28, 2024
Ferroptosis
is
a
type
of
programmed
cell
death
that
differs
from
apoptosis,
autophagy,
and
necrosis
related
to
several
physio-pathological
processes,
including
tumorigenesis,
neurodegeneration,
senescence,
blood
diseases,
kidney
disorders,
ischemia–reperfusion
injuries.
linked
iron
accumulation,
eliciting
dysfunction
antioxidant
systems,
which
favor
the
production
lipid
peroxides,
membrane
damage,
ultimately,
death.
Thus,
signaling
pathways
evoking
ferroptosis
are
strongly
associated
with
those
protecting
cells
against
excess
and/or
lipid-derived
ROS.
Here,
we
discuss
interaction
between
metabolic
particular
focus
on
transcription
factors
implicated
in
regulation
ferroptosis,
either
as
triggers
peroxidation
or
defense
pathways.
Chinese Medicine,
Journal Year:
2025,
Volume and Issue:
20(1)
Published: Jan. 3, 2025
Abstract
Background
Magnolia
kobus
DC
(MO),
as
a
plant
medicine,
has
been
reported
to
have
various
physiological
activities,
including
neuroprotective,
anti-inflammatory,
and
anti-diabetic
effects.
However,
vascular
protective
effects
of
MO
remain
incompletely
understood.
In
this
study,
we
evaluated
the
effect
against
ferroptosis
in
carotid
artery
ligation
(CAL)-induced
neointimal
hyperplasia
mouse
model
aortic
thoracic
smooth
muscle
A7r5
cells.
Methods
This
study
was
conducted
estimate
by
systematically
measuring
histopathological
analysis
western
blot
CAL
animal
model.
vitro
were
estimating
cell
viability,
reactive
oxygen
species
(ROS)
content,
glutathione
(GSH)
levels,
lipid
peroxidation,
mitochondrial
morphological
change,
proliferation,
migration,
analysis,
qRT-PCR
erastin
(Era)-induced
Results
intake
significantly
improved
formation,
inhibited
(VSMC)
phenotypes,
ameliorated
antioxidant
system
tissues.
addition,
treatment
effectively
Era-induced
ferroptotic
cytotoxicity,
cellular
death,
ROS
production,
migration
status.
also
suppressed
proliferation
considerably
regulated
abnormal
mechanisms
related
changes,
VSMC
phenotype
switching,
scavenging
Conclusion
potential
for
use
functional
food
supplement,
nutraceutical,
or
medicinal
food,
with
on
health
regulating
phenotypic
switching.
Frontiers in Aging Neuroscience,
Journal Year:
2022,
Volume and Issue:
14
Published: June 28, 2022
Neurodegenerative
diseases
are
a
diverse
class
of
attributed
to
chronic
progressive
neuronal
degeneration
and
synaptic
loss
in
the
brain
and/or
spinal
cord,
including
Alzheimer’s
disease,
Parkinson’s
Huntington’s
amyotrophic
lateral
sclerosis
multiple
sclerosis.
The
pathogenesis
neurodegenerative
is
complex
diverse,
often
involving
mitochondrial
dysfunction,
neuroinflammation,
epigenetic
changes.
However,
has
not
been
fully
elucidated.
Recently,
accumulating
evidence
revealed
that
ferroptosis,
newly
discovered
iron-dependent
lipid
peroxidation-driven
type
programmed
cell
death,
provides
another
explanation
for
occurrence
progression
diseases.
Here,
we
provide
an
overview
process
regulation
mechanisms
summarize
current
research
progresses
support
contribution
ferroptosis
A
comprehensive
understanding
emerging
roles
will
shed
light
on
development
novel
therapeutic
technologies
strategies
slowing
down
these
Biomedicine & Pharmacotherapy,
Journal Year:
2022,
Volume and Issue:
154, P. 113611 - 113611
Published: Sept. 5, 2022
Cerebrovascular
diseases,
such
as
ischemic
stroke,
pose
serious
medical
challenges
worldwide
due
to
their
high
morbidity
and
mortality
limitations
in
clinical
treatment
strategies.
Studies
have
shown
that
reactive
oxygen
species
(ROS)-mediated
inflammation,
excitotoxicity,
programmed
cell
death
of
each
neurovascular
unit
during
post-stroke
hypoxia
reperfusion
play
an
important
role
the
pathological
cascade.
Ferroptosis,
a
characterized
by
iron-regulated
accumulation
lipid
peroxidation,
is
caused
abnormal
metabolism
lipids,
glutathione
(GSH),
iron,
can
accelerate
acute
central
nervous
system
injury.
Recent
studies
gradually
uncovered
process
ferroptosis
stroke.
Some
drugs
iron
chelators,
ferrostatin-1
(Fer-1)
liproxstatin-1
(Lip-1)
protect
nerves
after
injury
stroke
inhibiting
ferroptosis.
In
addition,
combined
with
our
previous
on
mediated
natural
compounds
this
review
summarized
progress
regulation
mechanism
chemical
components
herbal
recent
years,
order
provide
reference
information
for
future
research
lead
development
inhibitors.
Oxidative Medicine and Cellular Longevity,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 14
Published: Aug. 10, 2022
Coronary
heart
disease
(CHD)
is
closely
related
to
oxidative
stress
and
inflammatory
response
the
most
common
cardiovascular
(CVD).
Iron
an
essential
mineral
that
participates
in
many
physiological
biochemical
reactions
human
body.
Meanwhile,
on
negative
side,
iron
has
active
redox
capacity,
which
leads
accumulation
of
reactive
oxygen
species
(ROS)
lipid
peroxidation.
There
growing
evidence
disordered
metabolism
involved
CHD’s
pathological
progression.
And
result
associated
with
overload-induced
programmed
cell
death,
often
called
ferroptosis.
That
features
iron-dependent
Ferroptosis
may
play
a
crucial
role
development
CHD,
targeting
ferroptosis
be
promising
option
for
treating
CHD.
Here,
we
review
mechanisms
cardiomyocytes
(CMs)
explain
correlation
between
highlight
specific
roles
main
progression