Osteoarthritis
(OA)
is
a
common
bone
and
joint
disease
characterized
by
degeneration.
The
imbalance
between
the
synthesis
breakdown
of
chondrocytes
major
contributing
factor
to
OA.
A
potential
treatment
for
OA
could
involve
targeting
degenerative
changes
in
cartilage
tissue
degradation.
Previous
studies
have
shown
close
relationship
autophagy
regulation
chondrocyte
breakdown.
Activation
has
been
found
alleviate
degeneration
tissue.
Currently,
primary
focus
osteoarthritis
symptom
relief,
as
there
no
effective
medication
halt
progression.
In
previous
studies,
luteolin,
flavonoid
Chinese
herbal
medicine,
activate
reduce
expression
MMP1
ADAMTS-5.
this
study,
an
vitro
model
was
created
using
stimulated
IL-1β,
different
concentrations
luteolin
were
used
treatment.
Treatment
with
significantly
increased
levels
factors
Aggrecan
Collagen
II,
while
decreasing
decomposition
MMP-13
Furthermore,
when
inhibited
Chloroquine,
imbalances
anabolic
catabolic
activities
induced
IL-1β
reversed.
vivo
knee
medial
meniscal
instability
(DMM),
administered
therapeutic
schedule.
After
12
weeks,
tissues
mice
collected
analysis.
Immunofluorescence
immunohistochemical
staining
showed
decrease
level
P62
increase
Beclin-1
tissues.
Additionally,
wear
joints
relieved
safranin
O
fast
green
staining.
findings
our
study
highlight
significant
role
effectively
reversing
IL-1β.
Our
results
strongly
indicate
that
be
developed
novel
agent
osteoarthritis,
offering
promising
prospects
future
drug
development.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: Nov. 16, 2024
Chemotherapy
remains
a
primary
approach
to
cancer
treatment,
widely
applied
in
bladder
(BC).
However,
the
various
side
effects
and
resistance
associated
with
chemotherapeutic
drugs
pose
significant
challenges
BC
therapy,
prompting
interest
natural
compounds
like
luteolin.
Studies
focus
on
its
key
biological
processes
involved
BC,
including
metastasis,
apoptosis,
autophagy.
This
study
investigated
regulation
of
mRNA
expression
genes
apoptosis
(BCL2,
P53),
autophagy
(ULK1,
ATG12),
metastasis
(MMP2,
MMP9)
malignant
cells
treated
was
an
vitro
experimental
study.
EJ138
were
concentrations
luteolin,
impact
cell
viability,
proliferation,
gene
assessed.The
cytotoxic
effect
luteolin
evaluated
using
MTT
assay
after
24-
48-hour
treatments
different
concentrations.
Flow
cytometry
performed
examine
luteolin's
anti-proliferative
effect,
RT-PCR
used
analyze
BCL2,
P53,
ULK1,
ATG12,
MMP2,
MMP9
genes.
results
confirmed
that
reduced
proliferation
rate
cells.
indicated
increased
death
following
treatment.
findings
demonstrated
upregulated
ATG12
while
downregulating
BCL2
expression.
treatment
did
not
significantly
alter
MMP2
levels.
These
indicate
exerts
by
dysregulating
Therefore,
shows
potential
as
effective
anti-cancer
agent
for
therapy.
Osteoarthritis
(OA)
is
a
common
bone
and
joint
disease
characterized
by
degeneration.
The
imbalance
between
the
synthesis
breakdown
of
chondrocytes
major
contributing
factor
to
OA.
A
potential
treatment
for
OA
could
involve
targeting
degenerative
changes
in
cartilage
tissue
degradation.
Previous
studies
have
shown
close
relationship
autophagy
regulation
chondrocyte
breakdown.
Activation
has
been
found
alleviate
degeneration
tissue.
Currently,
primary
focus
osteoarthritis
symptom
relief,
as
there
no
effective
medication
halt
progression.
In
previous
studies,
luteolin,
flavonoid
Chinese
herbal
medicine,
activate
reduce
expression
MMP1
ADAMTS-5.
this
study,
an
vitro
model
was
created
using
stimulated
IL-1β,
different
concentrations
luteolin
were
used
treatment.
Treatment
with
significantly
increased
levels
factors
Aggrecan
Collagen
II,
while
decreasing
decomposition
MMP-13
Furthermore,
when
inhibited
Chloroquine,
imbalances
anabolic
catabolic
activities
induced
IL-1β
reversed.
vivo
knee
medial
meniscal
instability
(DMM),
administered
therapeutic
schedule.
After
12
weeks,
tissues
mice
collected
analysis.
Immunofluorescence
immunohistochemical
staining
showed
decrease
level
P62
increase
Beclin-1
tissues.
Additionally,
wear
joints
relieved
safranin
O
fast
green
staining.
findings
our
study
highlight
significant
role
effectively
reversing
IL-1β.
Our
results
strongly
indicate
that
be
developed
novel
agent
osteoarthritis,
offering
promising
prospects
future
drug
development.