Polysaccharide from Panax japonicus C.A. Mey prevents non-alcoholic fatty liver disease development based on regulating liver metabolism and gut microbiota in mice
Yi Wu,
No information about this author
Wen Yin,
No information about this author
Ping Hao
No information about this author
et al.
International Journal of Biological Macromolecules,
Journal Year:
2024,
Volume and Issue:
260, P. 129430 - 129430
Published: Jan. 18, 2024
Language: Английский
Effect of Tetrastigma hemsleyanum leaves and Extract supplementation on liver metabolomics and the gut microbiota in alcohol-induced liver injury
Kexin Tao,
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Han Peng,
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Xin Bi
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et al.
Food Bioscience,
Journal Year:
2024,
Volume and Issue:
58, P. 103617 - 103617
Published: Jan. 20, 2024
Language: Английский
Exploring the mechanism of SLXG for treating nonalcoholic fatty liver disease based on network pharmacology and molecular docking
Medicine,
Journal Year:
2025,
Volume and Issue:
104(6), P. e40255 - e40255
Published: Feb. 7, 2025
Background:
The
Shugan
Lidan
Decoction
and
Chaihu
formula
are
traditional
Chinese
medicine
formulas
for
treating
liver
diseases,
with
a
history
of
over
1000
years.
By
comprehensively
improving
2
medicinal
formulas,
Xiaoshi
Granules
(SLXG)
has
been
developed
the
treatment
nonalcoholic
fatty
disease
(NAFLD)
other
liver-related
metabolic
diseases.
Methods:
First,
effective
active
ingredients
targets
SLXG
were
determined
using
Traditional
Medicine
Systems
Pharmacology
Database
Analysis
Platform
database.
NAFLD
identified
GeneCards,
OMIM,
CTD
databases,
intersection
decoction
was
obtained.
then
subjected
to
protein–protein
interaction
network
analysis,
Kyoto
encyclopedia
genes
genomes
(KEGG)
enrichment
gene
ontology
analysis.
KEGG
analysis
revealed
pathway.
Molecular
docking
performed
validate
binding
between
crucial
enriched
in
this
pathway
corresponding
SLXG.
Results:
A
total
219
related
from
239
non-duplicated
drug
obtained
24
target
both
drug-
disease-related
6
results
showed
that
13
gene–active
ingredient
bindings
had
energy
less
than
−6.5.
Conclusion:
use
pharmacology
molecular
technology
mechanism
action
treatment,
thus
laying
theoretical
foundation
clinical
application
therapy.
Language: Английский
SUSTAINABLE AND CONTEMPORARY APPROACHES TO EXPLORE THE NUTRITIONAL AND PROCESSING PERSPECTIVES OF BUCKWHEAT: CURRENT EVIDENCE AND PROSPECTS
Zunaira Basharat,
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Tabussam Tufail,
No information about this author
Feng Shao
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et al.
Food Bioscience,
Journal Year:
2025,
Volume and Issue:
unknown, P. 106312 - 106312
Published: March 1, 2025
Language: Английский
Effect and mechanism of polysaccharide from Crataegus pinnatifida on nonalcoholic fatty liver disease
Haiyan Fan,
No information about this author
Meng Yan,
No information about this author
Yongshuai Jing
No information about this author
et al.
Journal of Functional Foods,
Journal Year:
2025,
Volume and Issue:
129, P. 106876 - 106876
Published: May 10, 2025
Language: Английский
Structure characterization and cryoprotective activity of an exopolysaccharide from Pseudoalteromonas sp. LP6-12-2
Food Bioscience,
Journal Year:
2024,
Volume and Issue:
57, P. 103557 - 103557
Published: Jan. 1, 2024
Language: Английский
New insights into the hepato-protective effects of ferulic acid based on transcriptomic and metabolomic profiling
Journal of Functional Foods,
Journal Year:
2024,
Volume and Issue:
122, P. 106554 - 106554
Published: Nov. 1, 2024
Language: Английский
Foxa2 attenuates steatosis and inhibits the NF-κB/IKK signaling pathway in nonalcoholic fatty liver disease
Li Yang,
No information about this author
Qiang Ma,
No information about this author
Jiayu Chen
No information about this author
et al.
PeerJ,
Journal Year:
2023,
Volume and Issue:
11, P. e16466 - e16466
Published: Dec. 7, 2023
Objective
Forkhead
box
a2
(Foxa2)
is
proven
to
be
an
insulin-sensitive
transcriptional
regulator
and
affects
hepatic
steatosis.
This
study
aims
investigate
the
mechanism
by
which
Foxa2
nonalcoholic
fatty
liver
disease
(NAFLD).
Methods
Animal
cellular
models
of
NAFLD
were
constructed
using
high-fat
diet
(HFD)
feeding
oleic
acid
(OA)
stimulation,
respectively.
mice
received
tail
vein
injections
either
overexpressing
negative
control
(oe-NC)
or
(oe-Foxa2)
for
four
weeks.
HepG2
cells
transfected
with
oe-NC
oe-Foxa2
48
h
before
OA
stimulation.
Histological
changes
lipid
accumulation
assessed
hematoxylin-eosin
staining
oil
red
O
staining,
Expression
Foxa2,
NF-κB/IKK
pathway
proteins,
synthesis
β-oxidation
protein
in
HFD
OA-induced
was
detected
western
blot.
Results
expression
downregulated
cells.
overexpression
attenuated
injury,
reduced
levels
aspartate
aminotransferase,
alanine
total
cholesterol,
triglyceride
Moreover,
decreased
proteins
increased
tissues.
Furthermore,
p-NF-κB/NF-κB
p-IKK/IKK
Additionally,
lipopolysaccharide
(NF-κB/IKK
activator)
administration
reversed
downregulation
upregulation
protein.
Conclusion
NAFLD.
ameliorated
steatosis
inhibited
activation
signaling
pathway.
Language: Английский