Journal of Applied Toxicology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 31, 2024
ABSTRACT
Acute
myocardial
infarction
(AMI)
remains
a
leading
cause
of
death
among
patients
with
cardiovascular
diseases.
Percutaneous
coronary
intervention
(PCI)
has
been
the
preferred
clinical
treatment
for
AMI
due
to
its
safety
and
efficiency.
However,
research
indicates
that
rapid
restoration
oxygen
supply
following
PCI
can
lead
secondary
injury,
termed
ischemia–reperfusion
injury
(MIRI),
posing
grave
threat
patient
survival.
Despite
ongoing
efforts,
mechanisms
underlying
MIRI
are
not
yet
fully
elucidated.
Among
them,
oxidative
stress
inflammation
stand
out
as
critical
pathophysiological
mechanisms,
playing
significant
roles
in
MIRI.
Natural
compounds
have
shown
strong
therapeutic
potential
their
high
efficacy,
availability,
low
side
effects.
Many
current
studies
indicate
natural
mitigate
by
reducing
inflammatory
responses.
Therefore,
this
paper
reviews
during
role
intervening
these
processes,
aiming
provide
basis
reference
future
development
drugs
treating
Heliyon,
Journal Year:
2025,
Volume and Issue:
11(3), P. e41654 - e41654
Published: Jan. 8, 2025
The
importance
of
nanocomposites
constantly
attains
attention
because
their
unique
properties
all
across
the
fields
especially
in
medical
perspectives.
study
green-synthesized
has
grown
to
be
extremely
fascinating
field
research.
Nanocomposites
are
more
promising
than
mono-metallic
nanoparticles
they
exhibit
synergistic
effects.
This
review
encapsulates
current
development
formulation
plant-mediated
by
using
several
plant
species
and
impact
secondary
metabolites
on
biocompatible
functioning.
Phyto-synthesis
produces
diverse
nanomaterials
with
biocompatibility,
environment-friendliness,
vivo
actions,
characterized
varying
sizes,
shapes,
biochemical
nature.
process
is
advantageous
conventional
physical
chemical
procedures.
New
studies
have
been
conducted
determine
biomedical
efficacy
against
various
diseases.
Unfortunately,
there
inadequate
investigation
into
green-assisted
nanocomposites.
Incorporating
phytosynthesized
therapeutic
interventions
not
only
enhances
healing
processes
but
also
augments
host's
immune
defenses
infections.
highlights
phytosynthesis
applications,
including
antibacterial,
antidiabetic,
antiviral,
antioxidant,
antifungal,
anti-cancer,
other
as
well
toxicity.
explores
mechanistic
action
achieve
designated
tasks.
Biogenic
for
multimodal
imaging
potential
exchange
methods
materials
Well-designed
utilized
innovative
theranostic
agents
subsequent
objective
efficiently
diagnosing
treating
a
variety
human
disorders.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(45), P. 61565 - 61582
Published: Nov. 1, 2024
Myocardial
ischemia/reperfusion
(MI/R)
injury,
a
major
contributor
to
poor
prognosis
in
patients
with
acute
myocardial
infarction,
currently
lacks
effective
therapeutic
strategies
clinical
practice.
The
long
noncoding
RNA
(lncRNA)
Oip5-as1
can
regulate
various
cellular
processes,
such
as
cell
proliferation,
differentiation,
and
survival.
may
have
potential
target
for
MI/R
injury
its
upregulated
expression
has
been
associated
reduced
infarct
size
improved
cardiac
function
animal
models,
although
how
effectively
safely
overexpress
vivo
remains
unclear.
Lipid
nanoparticles
(LNPs)
are
versatile
technology
targeted
drug
delivery
numerous
applications.
Herein,
we
aimed
assess
the
efficacy
safety
of
LNPs
coloaded
cardiomyocyte-specific
binding
peptide
(LNP@Oip5-as1@CMP)
murine
model
injury.
To
achieve
this,
LNP@Oip5-as1@CMP
was
synthesized
via
ethanol
injection
method.
structural
components
were
physicochemically
analyzed.
A
hypoxia/reoxygenation
(H/R)
HL-1
cells
coronary
artery
ligation
mice
used
simulate
Our
results
demonstrated
that
designed
cardiomyocyte
targeting
efficient
successfully
synthesized.
In
cells,
treatment
significantly
mitochondrial
apoptosis
caused
by
H/R
model,
intravenous
administration
decreased
function.
Mechanistic
investigations
revealed
inhibited
p53
signaling
pathway.
However,
cardioprotective
effects
abrogated
administrating
Nutlin-3a,
activator.
Furthermore,
no
signs
organ
damage
detected
after
injection.
study
reveals
mitigating
These
findings
pave
way
advanced
treatments
cardiovascular
diseases,
emphasizing
promise
lncRNA-based
therapies.
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
209, P. 107466 - 107466
Published: Oct. 15, 2024
Myocardial
ischemia
causes
extensive
damage,
further
exacerbated
by
reperfusion,
a
phenomenon
called
myocardial
ischemia/reperfusion
injury
(MIRI).
Nowadays,
the
pathological
mechanisms
of
MIRI
have
received
attention.
Oxidative
stress,
multiple
programmed
cell
deaths,
inflammation
and
others
are
all
essential
contributing
to
MIRI.
Mitochondria
energy
supply
centers
cells.
Numerous
studies
found
that
abnormal
mitochondrial
function
is
an
"culprit"
MIRI,
mitophagy
mediated
phosphatase
tensin
homolog
(PTEN)-induced
kinase
1
(PINK1)/Parkin
signaling
pathway
integral
part
maintaining
function.
Therefore,
exploring
association
between
PINK1/Parkin
pathway-mediated
crucial.
This
review
will
mainly
summarize
crucial
role
in
MIR-induced
several
various
potential
interventions
affect
mitophagy,
thus
ameliorating
Phytotherapy Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 9, 2025
ABSTRACT
Ischemia
reperfusion‐induced
myocardial
injury
is
a
prominent
pathological
feature
in
patients
with
coronary
artery
disease,
contributing
to
significant
mortality
and
morbidity
rates.
Mangiferin
(MGF),
the
main
active
ingredient
extracted
from
Anemarrhena
asphodeloides
Bge
,
has
anti‐inflammatory,
anti‐oxidation,
anti‐diabetes,
anti‐tumor
effects.
The
present
study
confirmed
that
GAS6/Axl
pathway
was
identified
as
promising
novel
target
for
treatment
of
ischemia
reperfusion
(IR)
injury.
However,
whether
MGF
exerts
anti‐myocardial
through
still
unclear.
In
this
study,
BALB/c
male
mice
HL‐1
cardiomyocytes
were
used
construct
model
IR
hypoxia‐reoxygenation
(HR)
(or
H
2
O
)
vivo
vitro,
respectively.
significantly
improved
cardiac
function
indicators,
structure,
enzymes,
mitochondrial
function,
together
reduced
oxidative
stress
apoptosis
IR‐injured
mice.
increased
cell
viability,
inhibited
release
LDH,
apoptosis,
both
HR
‐injured
cells.
particular,
signaling
plays
an
important
role
process.
Additionally,
we
also
demonstrated
GAS6
gene
knockout
reversed
protective
effect
against
cardiomyocytes.
effects
by
activating
pathway,
providing
theoretical
basis
potential
cardioprotective
drug
clinical
setting
International Journal of Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
55(3)
Published: Jan. 24, 2025
Regulator
of
G‑protein
signaling
12
(RGS12)
is
a
regulatory
factor
that
involved
in
various
physiological
processes.
However,
the
role
RGS12
myocardial
ischemia/reperfusion
injury
(MIRI)
currently
remains
unclear.
The
present
study
established
mouse
model
MIRI
by
ligating
left
main
coronary
artery
followed
reperfusion.
In
addition,
HL‑1
cells
were
cultured
hypoxic
and
serum‑free
medium,
reoxygenation
to
establish
an
in
vitro
cell
hypoxia/reoxygenation
(H/R).
Adenoviruses
targeting
subsequently
used
either
overexpress
or
silence
expression.
was
highly
expressed
both
tissues
mice
with
subjected
H/R.
results
from
experiments
demonstrated
knockdown
reduced
oxidative
stress
under
pathological
environment,
as
indicated
decreased
reactive
oxygen
species
(ROS)
levels
malondialdehyde
activity
increased
activities
superoxide
dismutase
catalase.
Furthermore,
underwent
H/R
stimulation
exhibited
ferroptosis,
whereas
reversed
these
changes.
These
showed
post‑RGS12
silencing
Fe2+
lipid
ROS
decreased,
expression
glutathione
peroxidase
4
cystine
transporter
solute
carrier
family
7
member
11
mitochondrial
structure
improved
preventing
loss
crest.
Mechanistically,
nuclear
erythroid
2‑related
2
(Nrf2)
pathway
anti‑ferroptosis
anti‑oxidative
capacities
activated
knockdown.
Conversely,
overexpression
exerted
opposite
effects
vivo
vitro.
Notably,
it
penehyclidine
hydrochloride
(PHC),
known
block
process,
vivo
vitro,
inhibited
therapeutic
PHC
on
MIRI.
conclusion,
RGS12,
target
PHC,
potentially
enhanced
progression
promoting
this
effect
may
involve
regulation
Nrf2
pathway.
Redox Report,
Journal Year:
2025,
Volume and Issue:
30(1)
Published: Jan. 27, 2025
Myocardial
ischemia-reperfusion
injury
(MIRI)
is
a
highly
complex
disease
with
high
morbidity
and
mortality.
Studying
the
molecular
mechanism
of
MIRI
discovering
new
targets
are
crucial
for
future
treatment
MIRI.
We
constructed
rat
model
hypoxia/reoxygenation
(H/R)
cardiomyocytes
model.
RT-PCR
Western
blot
were
used
to
investigate
expression
fat
mass
obesity-associated
(FTO)
gene.
Electrocardiogram,
echocardiography,
triphenyltetrazolium
chloride
(TTC)
staining
hematoxylin-eosin
(HE)
assess
effect
FTO
overexpression.
The
generation
reactive
oxygen
species
(ROS)
levels
superoxide
dismutase
(SOD2),
mitochondrial
transcription
factor
(TFAM)
cytochrome
c
oxidase
I
(COXI)
detected
oxidative
stress
biogenesis.
RNA
immunoprecipitation
(RIP)
pulldown
assays
identify
interaction
PGC-1a.
m6A
dot
blot,
methylated
PCR
(MeRIP-PCR)
stability
analysis
analyze
regulation
methylation
PGC-1a
by
FTO.
was
downregulated
in
rats
H/R
induced
cardiomyocytes.
Overexpression
inhibited
ROS
level
increased
SOD2,
TFAM
COXI
vitro
vivo.
In
addition,
identified
as
downstream
target
enhanced
mRNA
through
removing
modification.
Our
study
revealed
role
regulates
biogenesis
via
MIRI,
which
may
provide
approach
mitigating
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(3), P. 303 - 303
Published: Feb. 22, 2025
Objective:
To
investigate
the
effect
and
underlying
mechanism
of
α-cyperone
in
inhibiting
pyroptosis
rat
aortic
endothelial
cells
(RAECs).
Methods:
Molecular
docking
technology
was
used
to
predict
potential
binding
affinity
pyroptosis-related
proteins.
A
model
established
RAECs
using
serum
containing
10%
LPS,
with
administered
as
a
preventive
treatment
for
9
h.
Cell
viability
membrane
integrity
were
assessed
propidium
iodide
(PI)
staining
CCK-8
assay.
The
release
IL-1β
IL-18
quantified
by
ELISA.
Western
blot
RT-qPCR
performed
evaluate
expression
levels
NLRP3,
ASC,
caspase-1
p20,
N-GSDMD.
Additionally,
RNA
sequencing
analysis
conducted
identify
differentially
expressed
genes
related
LPS-induced
following
treatment,
key
differential
validated
blot.
Results:
reveals
that
exhibits
strong
targets.
α-Cyperone
significantly
improves
cell
(p
<
0.001),
reduces
downregulates
mRNA
protein
caspase-1,
GSDMD
0.001).
indicates
primarily
modulates
gene
through
PI3K/AKT
signaling
pathway.
validation
further
confirmed
effectively
inhibited
phosphorylated
total
PI3K
AKT
Conclusions:
alleviates
morphological
damage
RAEC
model,
suppresses
proinflammatory
cytokines
IL-18,
potentially
inhibits
NLRP3/caspase-1/GSDMD
activation
pathway,
thereby
attenuating
RAECs.