World Journal of Diabetes,
Journal Year:
2024,
Volume and Issue:
15(9), P. 1916 - 1931
Published: Aug. 27, 2024
Diabetic
nephropathy
(DN)
is
the
most
frequent
chronic
microvascular
consequence
of
diabetes,
and
podocyte
injury
malfunction
are
closely
related
to
development
DN.
Studies
have
shown
that
corilagin
(Cor)
has
hepatoprotective,
anti-inflammatory,
antibacterial,
antioxidant,
anti-hypertensive,
anti-diabetic,
anti-tumor
activities.
The FASEB Journal,
Journal Year:
2024,
Volume and Issue:
38(13)
Published: July 3, 2024
Abstract
Renal
ischemia–reperfusion
injury
(IRI)
is
an
integral
process
in
renal
transplantation,
which
results
compromised
graft
survival.
Macrophages
play
important
role
both
the
early
inflammatory
period
and
late
fibrotic
response
to
IRI.
In
this
study,
we
investigated
whether
scutellarin
(SCU)
could
protect
against
IRI
by
regulating
macrophage
polarization.
Mice
were
given
SCU
(5–50
mg/kg)
gavage
1
h
earlier,
followed
a
unilateral
function
pathological
assessed
24
after
reperfusion.
The
showed
that
administration
of
50
mg/kg
significantly
improved
pathology
mice.
addition,
alleviated
IRI‐induced
apoptosis.
Meanwhile,
it
reduced
infiltration
inhibited
pro‐inflammatory
Moreover,
RAW
264.7
cells
primary
bone
marrow‐derived
macrophages
(BMDMs)
exposed
SCU,
found
150
μM
these
polarize
phenotype
induced
lipopolysaccharide
(LPS)
interferon‐γ
(IFN‐γ).
However,
has
no
influence
on
anti‐inflammatory
polarization
vivo
vitro
interleukin‐4
(IL‐4).
Finally,
explored
effect
activation
mitogen‐activated
protein
kinase
(MAPK)
pathway
vitro.
We
suppressed
MAPK
pathway,
including
extracellular
signal‐regulated
(ERK),
Jun
N‐terminal
(JNK),
p38.
Our
demonstrated
protects
kidney
inhibiting
toward
via
suggesting
may
be
therapeutically
treatment
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(24)
Published: June 22, 2023
Gene
therapy
that
employs
therapeutic
nucleic
acids
to
modulate
gene
expression
has
shown
great
promise
for
diseases
therapy,
and
its
clinical
application
relies
on
the
development
of
effective
vector.
Herein
a
novel
delivery
strategy
by
just
using
natural
polyphenol
(-)-epigallocatechin-3-O-gallate
(EGCG)
as
raw
material
is
reported.
EGCG
first
intercalates
into
yield
complex,
which
then
oxidizes
self-polymerizes
form
tea
polyphenols
nanoparticles
(TPNs)
encapsulation.
This
general
method
load
any
types
with
single
or
double
strands
short
long
sequences.
Such
TPNs-based
vector
achieves
comparable
loading
capacity
commonly
used
cationic
materials,
but
showing
lower
cytotoxicity.
TPNs
can
effectively
penetrate
inside
cells,
escape
from
endo/lysosomes,
release
in
response
intracellular
glutathione
exert
biological
functions.
To
demonstrate
vivo
application,
an
anti-caspase-3
small
interfering
ribonucleic
acid
loaded
treat
concanavalin
A-induced
acute
hepatitis,
excellent
efficacy
obtained
combination
intrinsic
activities
work
provides
simple,
versatile,
cost-effective
strategy.
Given
biocompatibility
biofunctions,
this
holds
potential
various
diseases.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(13), P. 6874 - 6874
Published: June 22, 2024
The
interferon
regulatory
factors
(IRFs)
family
comprises
11
members
that
are
involved
in
various
biological
processes
such
as
antiviral
defense,
cell
proliferation
regulation,
differentiation,
and
apoptosis.
Recent
studies
have
highlighted
the
roles
of
IRF1-9
a
range
liver
diseases,
including
hepatic
ischemia-reperfusion
injury
(IRI),
alcohol-induced
injury,
Con
A-induced
nonalcoholic
fatty
disease
(NAFLD),
cirrhosis,
hepatocellular
carcinoma
(HCC).
IRF1
is
progression
IRI
through
signaling
pathways
PIAS1/NFATc1/HDAC1/IRF1/p38
MAPK
IRF1/JNK.
regulation
downstream
IL-12,
IL-15,
p21,
p38,
HMGB1,
JNK,
Beclin1,
β-catenin,
caspase
3,
8,
IFN-γ,
IFN-β
other
genes
IRI,
development
HCC
PD-L1,
IL-6,
IL-8,
CXCL1,
CXCL10,
CXCR3.
In
addition,
IRF3-PPP2R1B
IRF4-FSTL1-DIP2A/CD14
NAFLD.
Other
IRF
also
play
moderately
important
functions
different
diseases.
Therefore,
given
significance
IRFs
diseases
lack
comprehensive
compilation
their
molecular
mechanisms
this
review
dedicated
to
exploring
Phytomedicine,
Journal Year:
2023,
Volume and Issue:
120, P. 155077 - 155077
Published: Sept. 10, 2023
Autoimmune
hepatitis
(AIH)
poses
an
important
public
health
concern
worldwide,
with
few
therapeutic
options
available.
Cornuside,
a
primary
cornel
iridoid
glycoside
present
in
Cornus
officinalis
Sieb.
et
Zucc.,
is
well-known
traditional
Chinese
medicine
that
possesses
anti-inflammatory,
antioxidant
and
anti-apoptotic
properties.
However,
the
effects
of
cornuside
on
autoimmune
diseases
including
AIH
still
not
defined,
neither
clear
mechanisms
suppression
inflammatory
responses.The
study
was
aimed
to
investigate
using
murine
models.A
model
induced
by
concanavalin
A
(Con
A)
used
examine
pharmacological
activity
suppressing
responses
vivo.C57BL/6J
mice
were
intravenously
different
doses
challenged
18
mg/kg
Con
3
h
later.
Network
analysis
performed
identify
potential
target
genes
signaling
pathways
AIH.
Next
serum
liver
tissues
collected
12
after
injection
analyze
levels
markers
for
hepatic
injury,
apoptosis,
oxidative
stress,
immune
responses,
inflammation.Network
revealed
may
modulate
stress
apoptosis
Compared
group,
pretreatment
significantly
reduced
alanine
aminotransferase
aspartate
aminotransferase,
improving
histopathological
damage
livers.
In
addition,
decreased
malondialdehyde,
myeloperoxidase,
but
increased
superoxide
dismutase
levels,
suggesting
relieving
stress.
Furthermore,
suppressed
activation
T
natural
killer
cells,
whereas
proportion
myeloid-derived
suppressor
cells
increased.
The
production
proinflammatory
cytokines,
interleukin
(IL)-6,
IL-12,
IL-1β,
tumor
necrosis
factor-alpha
(TNF-α),
also
clearly
decreased.
Finally,
western
blot
displayed
inhibited
phosphorylation
extracellular
receptor
kinase
(ERK)
c-Jun
N-terminal
(JNK).We
demonstrated
has
protective
A-induced
immune-mediated
through
ERK
JNK
pathways,
as
well
modulating
recruitment
cells.
The FASEB Journal,
Journal Year:
2024,
Volume and Issue:
38(2)
Published: Jan. 24, 2024
Abstract
Immune‐mediated
acute
hepatic
injury
is
characterized
by
the
destruction
of
a
large
number
hepatocytes
and
severe
liver
function
damage.
Interleukin‐28A
(IL‐28A),
member
IL‐10
family,
notable
for
its
antiviral
properties.
However,
despite
advances
in
our
understanding
IL‐28A,
role
immune‐mediated
remains
unclear.
The
present
study
investigated
IL‐28A
concanavalin
A
(Con
A)‐induced
immune
injury.
After
Con
injection
mice,
level
significantly
increased.
deficiency
was
found
to
protect
mice
from
injury,
prolong
survival
time,
reduce
serum
aspartate
aminotransferase
alanine
levels.
In
contrast,
recombinant
aggravated
mice.
proportion
activated
M1
macrophages
lower
IL‐28A‐deficiency
group
than
wild‐type
mouse
group.
adoptive
transfer
experiments,
WT
could
exacerbate
symptoms
Furthermore,
expression
proinflammatory
cytokines,
including
tumor
necrosis
factor‐α
(TNF‐α),
IL‐12,
IL‐6,
IL‐1β,
decreased
Western
blotting
demonstrated
that
limit
macrophage
polarization
modulating
nuclear
factor
(NF)‐κB,
mitogen‐activated
protein
kinase
(MAPK),
interferon
regulatory
(IRF)
signaling
pathways.
summary,
deletion
plays
an
important
protective
A‐induced
model
inhibits
activation
inhibiting
NF‐κB,
MAPK,
IRF
These
results
provide
potential
new
target
treatment
immune‐related
Inflammation,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 26, 2024
Sappanone
A
(SAP),
a
high-isoflavone
compound
derived
from
the
traditional
Chinese
medicine
Sumu,
exhibits
various
pharmacological
activities,
including
anti-inflammatory
and
anti-oxidant
effects.
However,
its
protective
effects
on
liver
have
rarely
been
reported.
The
aim
of
this
study
was
to
investigate
SAP
immune-mediated
injury
induced
by
concanavalin
(Con
A)
in
mice
explore
underlying
molecular
mechanisms.
Mice
were
administered
intraperitoneally
(50
mg/kg
body
weight).
Three
hours
later,
Con
(18
mg/kg)
injected
via
tail
vein
induce
damage.
Livers
blood
collected
12
h
after
challenge.
Liver
cell
apoptosis,
oxidative
stress,
M1
macrophage
activation
vivo
investigated.
Bone
marrow-derived
macrophages
used
confirm
polarization
vitro.
results
indicated
that
decreased
transaminase
levels,
inhibited
improved
stress
mouse
livers.
Furthermore,
significantly
reduced
proportion
macrophages,
expression
CD86,
downregulated
macrophage-related
inflammatory
cytokines.
Moreover,
SAP-treated
alleviated
damage
caused
compared
non-SAP-treated
macrophages.
Mechanistically,
phosphorylation
key
molecules
MAPK
NF-κB
signaling
pathways
resulting
an
inhibitory
effect
activation.
Taken
together,
alleviates
suppressing
polarization,
which
is
partially
associated
with
pathways.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 696 - 696
Published: Jan. 15, 2025
Hepatic
fibrosis
(HF)
is
an
important
pathological
state
in
the
progression
of
chronic
liver
disease
to
end-stage
and
usually
triggered
by
alcohol,
nonalcoholic
fatty
liver,
hepatitis
viruses,
autoimmune
(AIH),
or
cholestatic
disease.
Research
on
novel
therapies
has
become
a
hot
topic
due
reversibility
HF.
into
molecular
mechanisms
pathology
HF
potential
drug
screening
relies
reliable
rational
biological
models,
mainly
including
animals
cells.
Hence,
number
modeling
approaches
have
been
attempted
based
human
dietary,
pathological,
physiological
factors
development
In
this
review,
classical
methods
last
10
years
were
collected
from
electronic
databases,
Web
Science,
PubMed,
ScienceDirect,
ResearchGate,
Baidu
Scholar,
CNKI.
Animal
models
are
induced
chemical
toxicants,
special
diets,
pathogenic
microorganisms,
surgical
operations,
gene
editing.
The
advantages
limitations
hepatic
stellate
cells
(HSCs),
organoids,
3D
coculture-based
established
vitro
also
proposed
summarized.
This
information
provides
scientific
basis
for
discovery
mechanism
treatment