International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(22), С. 16497 - 16497
Опубликована: Ноя. 18, 2023
Cardiovascular
diseases,
especially
ischemic
heart
disease,
as
a
leading
cause
of
failure
(HF)
and
mortality,
will
not
reduce
over
the
coming
decades
despite
progress
in
pharmacotherapy,
interventional
cardiology,
surgery.
Although
patients
surviving
acute
myocardial
infarction
live
longer,
alteration
function
later
lead
to
HF.
Its
rising
incidence
represents
danger,
among
elderly,
with
data
showing
more
unfavorable
results
females
than
males.
Experiments
revealed
an
infarct-sparing
effect
"preconditioning"
(IPC)
most
robust
form
innate
cardioprotection
based
on
heart's
adaptation
moderate
stress,
increasing
its
resistance
severe
insults.
However,
translation
clinical
practice
is
limited
by
technical
requirements
time.
Novel
forms
adaptive
interventions,
such
"remote"
IPC,
have
already
been
applied
patients,
albeit
different
effectiveness.
Cardiac
tolerance
can
also
be
increased
other
noninvasive
approaches,
hypoxia-
or
exercise-induced
preconditioning.
their
molecular
mechanisms
are
yet
fully
understood,
some
modalities
appear
promising
novel
strategies
for
fighting
HF
through
targeting
numerous
mechanisms.
In
this
review,
we
discuss
injury
repair,
well
interventions
that
potential
used
treatment
patients.
Phytomedicine,
Год журнала:
2024,
Номер
132, С. 155791 - 155791
Опубликована: Май 29, 2024
Gastric
mucosal
injury
is
a
chronic
and
progressive
stomach
disease
that
can
be
caused
by
nonsteroidal
anti-inflammatory
drugs
(NSAIDs).
Therefore,
there
an
urgent
need
to
find
safe
effective
prevent
gastric
due
NSAIDs.
Cinnamaldehyde
(CA)
bioactive
compound
extracted
from
the
rhizome
of
cinnamon
has
various
pharmacological
functions,
including
anti-inflammatory,
analgesic,
antiapoptotic,
antioxidant
activities.
However,
potential
effect
CA
on
remains
unknown.
Aims:
Angiogenesis
is
an
important
repair
mechanism
for
myocardial
infarction.
Neuroligin-3
(NLGN3)
can
promote
angiogenesis
by
activating
Gαi1/3-Akt
signaling
following
ischemic
brain
injury.
This
study
investigated
the
role
of
NLGN3
in
infarction
(MI).
Journal for Research in Applied Sciences and Biotechnology,
Год журнала:
2025,
Номер
4(1), С. 132 - 141
Опубликована: Фев. 28, 2025
Chronic
renal
disease
is
defined
as
the
presence
of
kidney
damage
or
impaired
function
over
a
period
at
least
three
months,
regardless
origin
condition.
Numerous
factors,
including
oxidative
stress,
inflammation,
and
cell
death,
are
frequently
responsible
for
acute
chronic
injury,
which
significant
issue
in
field
global
health.
Because
crucial
functions
that
they
play,
NF-κB
PI3K/Akt
signaling
pathways
potential
therapeutic
targets.
These
pathogenic
processes
mediated
by
these
pathways.
cinnamonaldehyde,
naturally
occurring
bioactive
component,
has
demonstrated
encouraging
nephroprotective
properties.
properties
attributed
to
fact
it
contains
anti-inflammatory,
antioxidant,
anti-apoptotic
The
purpose
this
review
investigate
molecular
role
cinnamaldehyde
preventing
modulating
Within
article,
we
examine
involved
highlight
treatment
disease.
Although
preclinical
studies
have
protective
effects,
additional
research,
clinical
trials,
required
validate
its
safety,
effectiveness,
uses
management
illness
people.
Biomedicines,
Год журнала:
2025,
Номер
13(4), С. 938 - 938
Опубликована: Апрель 11, 2025
Objectives:
Jasminoidin
(JA)
and
ursodeoxycholic
acid
(UA)
have
been
shown
to
exert
synergistic
effects
on
cerebral
ischemia
(CI)
therapy,
but
the
underlying
mechanisms
remain
be
elucidated.
Objective:
To
elucidate
involved
in
combined
use
of
JA
UA
(JU)
for
CI
therapy
using
a
driver-induced
modular
screening
(DiMS)
strategy.
Methods:
Network
proximity
topology-based
approaches
were
used
identify
modules
driver
genes
from
an
anti-ischemic
microarray
dataset
(ArrayExpress,
E-TABM-662).
A
middle
artery
occlusion/reperfusion
(MCAO/R)
model
was
established
30
Sprague
Dawley
rats,
divided
into
sham,
vehicle,
(25
mg/mL),
(7
JU
(JA:UA
=
1:1)
groups.
After
90
minutes
ischemia,
infarct
volume
neurological
deficit
scores
evaluated.
Western
blotting
performed
24
h
after
administration
validate
key
protein
changes.
Results:
Six,
eleven,
four
drug-responsive
On_modules
identified
JA,
UA,
JU,
respectively.
Three
(Sy-modules,
JU-Mod-7,
8,
10)
12
(e.g.,
NRF1,
FN1,
CUL3)
identified,
mainly
involving
PI3K-Akt
MAPK
pathways
regulation
actin
cytoskeleton.
synergistically
reduced
score
(2.5,
p
<
0.05)
MCAO/R
rats.
In
vivo
studies
demonstrated
that
suppressed
expression
CUL3,
ITGA4,
while
it
increased
NRF1.
Conclusions:
acts
CI–reperfusion
injury
by
regulating
NRF1
inducing
PI3K-Akt,
MAPK,
cytoskeleton
pathways.
DiMS
provides
new
approach
uncover
combination
therapies.
PLoS ONE,
Год журнала:
2024,
Номер
19(7), С. e0305058 - e0305058
Опубликована: Июль 2, 2024
Objectives
Astragaloside
IV
(AS-IV)
is
a
natural
triterpenoid
saponin
compound
with
variety
of
pharmacological
effects,
and
several
studies
have
clarified
its
anti-inflammatory
which
may
make
it
an
effective
alternative
treatment
against
inflammation.
In
the
study,
we
aimed
to
investigate
whether
AS-IV
could
attenuate
inflammatory
response
acute
lung
injury
mechanisms.
Methods
Different
doses
(20mg·kg
-1
,
40mg·kg
80mg·kg
)
were
administered
ALI
rat
model,
followed
by
collection
serum
broncho
alveolar
lavage
fluid
(BALF)
for
examination
response,
HE
staining
colon
tissues,
interpretation
potential
molecular
mechanisms
quantitative
real-time
PCR
(qRT-PCR),
Western
blotting
(WB).
addition,
fecal
samples
from
rats
collected
analyzed
16S
rRNA
sequencing.
Results
decreased
levels
TNF-α,
IL-6,
IL-1β
in
BALF
mice
Acute
(ALI).
Lung
histopathology
confirmed
that
alleviated
infiltration,
tissue
edema,
structural
changes.
qRT-PCR
WB
showed
mainly
improved
inflammation
inhibiting
expression
PI3K,
AKT
mTOR
mRNA,
disorder
intestinal
microflora
increasing
number
beneficial
bacteria
reducing
harmful
bacteria.
Conclusion
reduces
factors
PI3K/AKT/mTOR
pathway
optimizes
composition
gut
AIL
rats.
Biomedicine & Pharmacotherapy,
Год журнала:
2023,
Номер
167, С. 115452 - 115452
Опубликована: Сен. 8, 2023
In
this
study,
86
new
seco-lupane
triterpenoid
derivatives
were
designed,
synthesized,
and
characterized,
their
protective
activities
against
ischemia-reperfusion
injury
investigated
in
vitro
vivo.
Structure-activity
relationship
studies
revealed
that
most
target
compounds
could
protect
cardiomyocytes
hypoxia/reoxygenation-induced
vitro,
with
compound
85
being
the
active
exhibiting
more
potent
activity
than
clinical
first-line
drugs.
Furthermore,
all
thiophene
exhibited
stronger
furan,
pyridine,
pyrazine
derivatives,
gradually
increased
extension
of
alkyl
chain
changed
substituent.
The
data
from
in-vitro
in-vivo
experiments
protected
mitochondria
damage
by
inhibiting
excessive
production
oxidative
stressors,
such
as
intracellular
ROS,
which
turn
inhibited
apoptosis
necrotize
reduced
infarct
size,
thereby
protecting
normal
cardiac
function.
It
was
associated
enhanced
activation
PI3K/AKT-mediated
HIF-1α
signaling
pathway.
Therefore,
acts
an
stress
inhibitor,
blocks
ROS
production,
protects
cells
myocardial
ischemia/reperfusion
(MI/R)
injury,
represents
effective
drug
for
treating
MI/R
injury.