Food Frontiers,
Journal Year:
2023,
Volume and Issue:
4(1), P. 394 - 406
Published: Jan. 13, 2023
Abstract
The
study
aimed
to
examine
the
effect
of
ginseng
polysaccharide
(GP)
on
acute
alcoholic
liver
injury
(AALI)
and
determine
its
underlying
molecular
mechanism.
GP's
in
vitro
vivo
hepatoprotective
effects
were
evaluated
using
LO2
cells
alcohol‐induced
C57BL/6
male
mice.
Cell
Counting
Kit‐8,
immunofluorescence,
hematoxylin‐eosin,
immunohistochemistry,
Western
blot
(WB)
used
detect
lipid
metabolism
autophagy
levels
liver.
It
was
mainly
composed
glucose,
galactose,
arabinose
a
molar
ratio
12.9:1.6:1.0.
Experiments
demonstrated
that
administration
GP
significantly
increased
increase
cell
viability.
In
addition,
it
can
inhibit
lipogenesis,
enhance
lipolysis,
stimulate
autophagy.
mice,
also
inhibited
hepatic
histological
lesions,
prevented
alanine
aminotransferase
aspartate
elevation,
improved
abnormal
metabolism,
boosted
hepatocyte
analysis
mechanisms
revealed
promotes
expression
proteins
AALI
thereby
alleviating
it.
Journal of Agricultural and Food Chemistry,
Journal Year:
2024,
Volume and Issue:
72(4), P. 2165 - 2177
Published: Jan. 17, 2024
Purple
sweet
potato
polysaccharide
(PSPP-1)
is
a
novel
glucan;
this
study
aimed
to
examine
the
anti-inflammatory
effect
of
PSPP-1
and
elucidate
its
potential
mechanisms.
Lipopolysaccharide
(LPS)-induced
RAW264.7
was
used
as
model
inflammation,
cell
viability,
levels
nitric
oxide
(NO),
reactive
oxygen
species
(ROS),
calcium
ion
(Ca2+)
were
analyzed.
ELISA
qPCR
assess
productions
mRNA
expression
cytokines,
Western
blotting
protein
expressions
in
TLR-mediated
pathway,
macrophage
polarization,
inflammasome
activation.
The
results
demonstrated
inhibited
proliferation
markedly
decreased
NO,
ROS,
Ca2+
levels.
Moreover,
suppressed
secretions
pro-inflammatory
cytokines
increased
those
cytokines.
Furthermore,
could
exert
effects
through
different
pathways
mediated
by
both
TLR2
TLR4,
which
modulated
essential
proteins
myeloid
differentiation
factor
88
(MyD88)-dependent
toll/IL-1
receptor
domain-containing
adaptor-inducing
interferon-β
(TRIF)-dependent
signaling
pathways.
even
regulated
polarization
M1/M2
macrophages
nucleotide
oligomerization
domain-like
3
(NLRP3)
These
findings
indicate
that
can
suppress
LPS-induced
inflammation
via
multiple
may
be
agent
for
therapeutic
inflammation-related
pathophysiological
processes
disorders.
Metabolites,
Journal Year:
2023,
Volume and Issue:
13(2), P. 243 - 243
Published: Feb. 7, 2023
Inflammatory
bowel
diseases
(IBDs)
are
related
to
nuclear
factor
erythroid
2-related
2
(Nrf2)
dysregulation.
In
vitro
and
in
vivo
studies
using
phytocompounds
as
modulators
of
the
Nrf2
signaling
IBD
have
already
been
published.
However,
no
existing
review
emphasizes
whole
scenario
for
potential
plants
regulators
models
colitis-associated
colorectal
carcinogenesis.
For
these
reasons,
this
study
aimed
build
a
that
could
fill
void.
The
PubMed,
EMBASE,
COCHRANE,
Google
Scholar
databases
were
searched.
literature
showed
medicinal
phytochemicals
regulated
on
IBD-associated
cancer
by
amplifying
expression
Nrf2-mediated
phase
II
detoxifying
enzymes
diminishing
NF-κB-related
inflammation.
These
effects
improve
environment,
mucosal
barrier,
colon,
crypt
disruption,
reduce
ulceration
microbial
translocation,
consequently,
disease
activity
index
(DAI).
Moreover,
modulation
can
regulate
various
genes
involved
cellular
redox,
protein
degradation,
DNA
repair,
xenobiotic
metabolism,
apoptosis,
contributing
prevention
cancer.
Journal of Functional Foods,
Journal Year:
2023,
Volume and Issue:
108, P. 105771 - 105771
Published: Sept. 1, 2023
The
current
study
was
designed
to
determine
the
curative
potential
of
astragalin
(AST)
against
polystyrene
microplastics
(PS-MPs)
induced
hepatic
toxicity
in
rats.
PS-MPs
exposure
decreased
expression
Nrf-2
and
anti-oxidant
enzymes,
while
increasing
Keap-1
expression.
activities
glutathione-S-transferase,
catalase,
glutathione,
glutathione
peroxidase,
superoxide
dismutase,
reductase
heme
oxygenase-1
were
decreased,
besides
levels
malondialdehyde
reactive
oxygen
species
also
increased
following
PS-MPs.
intoxication
elevated
aspartate
aminotransferase,
alanine
transaminase,
alkaline
phosphatase
levels,
as
well
cyclooxygenase-2
activity,
interleukin-6,
interleukin-1
beta,
nuclear
factor-kappa
B
tumor
necrosis
factor-alpha
escalated.
Furthermore,
Bcl-2
down-regulated,
Bax
Caspase-3
expressions
upregulated
exposure.
Histopathological
assessment
revealed
substantial
liver
damages
treated
However,
AST
supplementation
substantially
recovered
PS-MPs-induced
histological
anomalies.
Therefore,
can
be
used
a
agent
treat
PS-MPs-prompted
hepatotoxicity
due
its
anti-apoptotic,
anti-inflammatory
potentials.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(10), P. e30983 - e30983
Published: May 1, 2024
Recent
clinical
studies
have
confirmed
the
effectiveness
of
Qianhua
Gout
Capsules
(QGC)
in
treatment
gouty
arthritis
(GA).
However,
specific
regulatory
targets
and
mechanisms
action
QGC
are
still
unclear.
To
address
this
gap,
we
utilized
network
pharmacology,
molecular
docking,
pharmacodynamic
approaches
to
investigate
bioactive
components
associated
GA.
By
employing
UPLC-Q
Exactive-MS,
identified
compounds
present
QGC,
with
active
ingredients
defined
as
those
oral
bioavailability
≥30
%
drug
similarity
≥0.18.
Subsequently,
these
were
determined
using
TCMSP
database,
while
GA-related
from
DisGeNET,
GeneCards,
TTD,
OMIM,
DrugBank
databases.
Further
analysis
including
PPI
analysis,
GO
KEGG
pathway
enrichment
was
conducted
on
targets.
Validation
predicted
results
performed
a
GA
rat
model,
evaluating
pathological
changes,
inflammatory
markers,
protein
expression.
Our
revealed
total
130
components,
44
16
potential
shared
targets,
GO-enriched
terms,
47
signaling
pathways
related
disease
Key
included
quercetin,
kaempferol,
β-sitosterol,
luteolin,
wogonin.
The
highlighted
five
(PPARG,
IL-6,
MMP-9,
IL-1β,
CXCL-8)
highest
connectivity,
predominantly
enriched
IL-17
pathway.
Molecular
docking
experiments
demonstrated
strong
binding
CXCL8,
MMP9,
PPARG
top
compounds.
Furthermore,
animal
efficacy
treating
rats,
showing
reductions
TNF-α,
MDA
levels,
increases
SOD
levels
serum.
In
synovial
tissues,
upregulated
CXCL8
expression,
downregulating
IL-6
conclusion,
study
applied
pharmacology
approach
uncover
composition
predict
its
pharmacological
interactions,
demonstrate
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
176, P. 116891 - 116891
Published: June 12, 2024
Ulcerative
colitis
(UC)
is
a
chronic
inflammatory
bowel
disease
primarily
affecting
the
mucosa
of
colon
and
rectum.
UC
characterized
by
recurrent
episodes,
often
necessitating
lifelong
medication
use,
imposing
significant
burden
on
patients.
Current
conventional
advanced
treatments
for
have
disadvantages
insufficient
efficiency,
susceptibility
to
drug
resistance,
notable
adverse
effects.
Therefore,
developing
effective
safe
drugs
has
become
an
urgent
need.
Autophagy
intracellular
degradation
process
that
plays
important
role
in
intestinal
homeostasis.
Emerging
evidence
suggests
aberrant
autophagy
involved
development
UC,
modulating
can
effectively
alleviate
experimental
colitis.
A
growing
number
studies
established
interplay
with
endoplasmic
reticulum
stress,
gut
microbiota,
apoptosis,
NLRP3
inflammasome,
all
which
contribute
pathogenesis
UC.
In
addition,
variety
epithelial
cells,
including
absorptive
goblet
Paneth
as
well
other
cell
types
like
neutrophils,
antigen-presenting
stem
cells
gut,
mediate
through
autophagy.
To
date,
many
found
natural
products
hold
potential
exert
therapeutic
effects
regulating
This
review
focuses
possible
pharmacological
mechanisms
target
recent
years,
aiming
provide
basis
new
development.