Regenerative Therapy,
Год журнала:
2024,
Номер
26, С. 27 - 32
Опубликована: Май 17, 2024
We
aimed
to
examine
whether
heparin-binding
epidermal
growth
factor-like
factor
(HB-EGF)
affects
the
lung
fibrosis
process
through
activation
of
p38
protein
in
mitogen-activated
kinases
(MAPK)
signaling
pathway,
as
well
expression
downstream
inflammatory
factors.
British Journal of Pharmacology,
Год журнала:
2024,
Номер
181(17), С. 3215 - 3231
Опубликована: Май 13, 2024
Nicorandil,
a
selective
opener
of
potassium
channels,
used
to
treat
angina,
has
drawn
attention
for
its
potential
in
mitigating
lung
injury,
positioning
it
as
promising
therapeutic
approach
drug-induced
toxicity.
This
study
aimed
explore
the
protective
role
nicorandil
arsenic
trioxide
(ATO)-induced
injury
and
elucidate
underlying
mechanistic
pathways.
Naunyn-Schmiedeberg s Archives of Pharmacology,
Год журнала:
2024,
Номер
397(10), С. 7981 - 7994
Опубликована: Май 18, 2024
Abstract
The
defect
in
the
hepatobiliary
transport
system
results
an
impairment
of
bile
flow,
leading
to
accumulation
toxic
compounds
with
subsequent
liver
disorders.
Vincamine,
a
plant
indole
alkaloid
that
is
utilized
as
dietary
supplement,
has
been
known
for
its
promising
pharmacological
activities.
For
first
time,
present
study
was
planned
estimate,
at
molecular
level,
potentiality
vincamine
against
alfa-naphthyl
isothiocyanate
(ANIT)-induced
hepatic
cholestasis.
Liver
function
tests
were
analyzed.
Hepatic
activity
SOD
and
levels
GSH
MDA
assessed.
contents
bax,
bcl2,
NF-kB,
PPARγ,
catalase,
heme-oxygenase-1,
NTCP,
BSEP
evaluated
using
ELISA.
mRNA
IL-1β,
IL-6,
TNFα,
PDGF,
klf6,
PPARγ
,
P53
examined
qRT-PCR.
PI3K,
Akt
cleaved
caspase-3
proteins
assessed
western
blotting.
Histopathological
analyses
performed
hematoxylin
&
eosin
staining.
ANIT-induced
cholestasis
elevated
tests,
including
AST,
ALT,
GGT,
ALP,
total
bilirubin.
ANIT
reduced
protein
expression
NTCP
transporters.
It
induced
inflammatory
genes,
IL-1β
PDGF
NF-kB
genetic
level
suppressed
anti-inflammatory
klf6
.
Also,
antioxidant
markers
during
induction
such
GSH,
SOD,
heme-oxygenase-1
PI3K/Akt
pathway,
while
elevated.
Furthermore,
gene,
bax
caspase
3
activated,
bcl2
inhibited.
histopathological
analysis
showed
degeneration
hepatocytes
cellular
infiltrates.
However,
treatment
modulated
all
these
markers.
improved
tests.
inhibited
activated
pathway.
Additionally,
it
proteins.
More
interestingly,
better
outcomes
on
alterations
by
ANIT.
Vincamine
alleviated
dysfunction
intrahepatic
through
efficacies
modulation
NF-kB/PDGF/klf6/PPARγ
pathways.
Biomolecules,
Год журнала:
2024,
Номер
14(6), С. 689 - 689
Опубликована: Июнь 13, 2024
Reactive
oxygen
species
(ROSs)
are
byproducts
of
normal
cellular
metabolism
and
play
pivotal
roles
in
various
physiological
processes.
Disruptions
the
balance
between
ROS
levels
body’s
antioxidant
defenses
can
lead
to
development
numerous
diseases.
Glutathione
peroxidase
3
(GPX3),
a
key
component
system,
is
an
oxidoreductase
enzyme.
GPX3
mitigates
oxidative
damage
by
catalyzing
conversion
hydrogen
peroxide
into
water.
Beyond
its
function,
vital
regulating
metabolism,
modulating
cell
growth,
inducing
apoptosis
facilitating
signal
transduction.
It
also
serves
as
significant
tumor
suppressor
cancers.
Recent
studies
have
revealed
aberrant
expression
several
non-neoplastic
diseases,
associating
it
with
multiple
pathological
This
review
synthesizes
current
understanding
regulation,
highlighting
extensive
noncancerous
Additionally,
this
paper
evaluates
potential
diagnostic
biomarker
explores
emerging
therapeutic
strategies
targeting
enzyme,
offering
avenues
for
future
clinical
treatment
conditions.
Frontiers in Immunology,
Год журнала:
2025,
Номер
15
Опубликована: Янв. 17, 2025
Growing
evidence
indicates
an
association
between
circulating
immune
cell
phenotypes
and
idiopathic
pulmonary
fibrosis
(IPF).
Although
studies
have
attempted
to
elucidate
the
causal
relationship
two,
further
clarification
of
specific
mechanisms
linkages
is
warranted.
We
aimed
conduct
a
two-sample
Mendelian
randomization
(MR)
analysis
with
transcriptomics
data
cells
IPF
explore
potential
biomarkers.
first
explored
bidirectional
using
MR
analysis.
Genome-wide
for
phenotype
were
obtained
from
publicly
available
databases.
A
standardized
instrumental
variable
screening
process
was
used
select
single
nucleotide
polymorphisms
(SNPs)
inclusion
in
MR.
Five
methods
represented
by
IVW
assess
effects.
Subsequently,
SNP-nearest
genes
combined
subjected
multiple
bioinformatics
analyses
such
as
TIMER,
WGCNA,
functional
enrichment
analysis,
protein-protein
interaction
ROC
identify
Finally,
single-cell
RNA
sequencing
(scRNA-seq)
validate
our
findings
The
study
identified
27
causally
associated
IPF,
which
20
decreased
risk
developing
7
increased
risk.
CTSB
(AUC=0.98),
IL10
(AUC=0.83),
AGER
(AUC=0.87)
promising
biomarkers
IPF.
Single
showed
differences
CD14+
CD16+
monocytes,
monocytes
Granulocyte-monocyte
progenito
group
healthy
control
group.
three
hub
highly
expressed
subsets
patients.
It
underscores
feasibility
Our
demonstrates
associations
through
genetic
identifies
CTSB,
IL10,
These
provide
guidance
future
clinical
basic
research.
Pharmaceuticals,
Год журнала:
2024,
Номер
17(5), С. 584 - 584
Опубликована: Май 2, 2024
Pulmonary
fibrosis
(PF)
is
a
disease
characterised
by
diffuse
nonspecific
alveolar
inflammation
with
interstitial
fibrosis,
which
clinically
manifests
as
dyspnoea
and
significant
decline
in
lung
function.
Many
studies
have
shown
that
the
epithelial–mesenchymal
transition
(EMT)
plays
pivotal
role
pathogenesis
of
pulmonary
fibrosis.
Based
on
our
previous
findings,
hypericin
(Hyp)
can
effectively
inhibit
process
EMT
to
attenuate
Therefore,
series
hyperoside
derivatives
were
synthesised
via
modifying
structure
hyperoside,
subsequently
evaluated
for
A549
cytotoxicity.
Among
these,
pre-screening
eight
inhibits
EMT.
In
this
study,
we
efficacy
Z6,
most
promising
derivative,
reversing
TGF-β1-induced
EMTs
inhibiting
EMT-associated
migration
cells.
After
treatment
cells
Z6
48
h,
RT-qPCR
Western
blot
results
showed
inhibited
epithelial
supressing
morphological
changes
cells,
up-regulating
E-cadherin
(p
<
0.01,
p
0.001),
down-regulating
Vimentin
0.001).
This
significantly
reduced
mobility
transforming
growth
factor
β1
(TGF-β1)-stimulated
0.001)
assessed
wound
closure,
while
increasing
adhesion
rate
conclusion,
suggest
derivatives,
especially
compound
are
potential
lead
compounds
treating
therefore
deserve
further
investigation.
Archives of Internal Medicine Research,
Год журнала:
2024,
Номер
07(01)
Опубликована: Янв. 1, 2024
Idiopathic
pulmonary
fibrosis
(IPF)
constitutes
a
long-term
disease
with
complex
pathophysiology
composed
of
multiple
molecular
actors
that
lead
to
the
deposition
extracellular
matrix,
loss
function
and
ultimately
patient's
death.
Despite
approval
pirfenidone
nintedanib
for
treatment
disease,
lung
transplant
is
only
solution
fully
recover
respiratory
capacity
gain
quality
life.
One
risk
factors
development
IPF
pre-existing
condition
diabetes
mellitus.
Both,
mellitus,
share
similar
pathological
damage
mechanisms,
including
inflammation,
endoplasmic
reticulum
stress,
mitochondrial
failure,
oxidative
senescence
signaling
from
glycated
proteins
through
receptors.
In
this
critical
review
article,
we
provide
information
about
interrelationship,
examining
mediators
play
an
essential
role
in
both
diseases
identify
targets
interest
potential
drugs.
We
findings
clinical
trials
progression
how
novel
molecules
may
be
used
stop
process.
The
results
highlight
importance
early
detection
addressing
therapeutic
simultaneously
achieve
better
efficacy
potentially
reverse
fibrosis.