Plantaginis Herba attenuates adriamycin-induced nephropathy: Molecular mechanism insights by integrated transcriptomic and experimental validation
Journal of Ethnopharmacology,
Год журнала:
2025,
Номер
341, С. 119331 - 119331
Опубликована: Янв. 6, 2025
Язык: Английский
Proteomics and phosphoproteomics analysis of acute pancreatitis alleviated by forsythoside B
Journal of Proteomics,
Год журнала:
2025,
Номер
315, С. 105414 - 105414
Опубликована: Фев. 25, 2025
Язык: Английский
Artificial intelligence accelerates the identification of nature-derived potent LOXL2 inhibitors
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Март 27, 2025
Abstract
The
role
of
LOXL2
in
cancer
has
been
widely
demonstrated,
but
current
therapies
targeting
are
not
yet
fully
developed.
We
believe
that
selective
nature-derived
inhibition
may
provide
a
better
therapeutic
approach
for
the
treatment
cancer.
Therefore,
we
adopted
comprehensive
combining
deep
learning
and
traditional
computer-aided
drug
design
methods
to
screen
inhibitors.
Bioactivity
affinity
potential
inhibitors
were
determined
by
molecular
docking
virtual
screening.
At
same
time,
experimentally
tested
effect
on
cells.
Validation
showed
it
could
inhibit
proliferation
migration,
promote
apoptosis
CT26
cells,
reduce
expression
level
protein.
As
result,
identified
potent
inhibitor:
natural
product
Forsythoside
A,
demonstrated
A
an
inhibitory
tumors.
Язык: Английский
Polyphyllin VI Ameliorates Pulmonary Fibrosis by Suppressing the MAPK/ERK and PI3K/AKT Signaling Pathways via Upregulating DUSP6
Phytotherapy Research,
Год журнала:
2024,
Номер
38(12), С. 5930 - 5948
Опубликована: Окт. 17, 2024
ABSTRACT
Pulmonary
fibrosis
(PF)
is
a
lethal
disease
caused
by
inordinate
repair
of
damaged
lungs,
for
which
limited
strategies
are
available.
Polyphyllin
VI
(PPVI),
extracted
and
isolated
from
Paris
polyphylla
Smith
var.
chinensis
(Franch.)
Hara,
has
been
regarded
as
an
important
traditional
Chinese
herbal
medicine
the
treatment
respiratory
system
diseases.
This
study
evaluated
effects
PPVI
on
PF
its
underlying
mechanism.
Experimental
procedure
For
evaluating
anti‐PF
effect
PPVI,
we
established
in
vivo
mouse
model
via
intratracheal
infusion
bleomycin
(BLM)
mice
vitro
induced
TGF‐β1
NIH/3T3,
HPF
A549,
respectively.
Subsequently,
mechanism
was
further
explored
using
RNA
sequencing
(RNA‐Seq).
The
results
demonstrated
that
significantly
inhibited
inflammation,
oxidative
damage,
epithelial‐mesenchymal
transition.
Furthermore,
indicated
ameliorated
modulating
inflammation
stress
responses.
dual
specificity
phosphatase
6
(DUSP6),
shared
most
significant
differentially
expressed
gene
associated
with
response
after
treatment.
Mechanistically,
silencing
DUSP6
can
eliminate
suppressive
impact
activation
fibroblast
phosphorylation
ERK
AKT.
Summarily,
our
findings
revealed
potential
mitigating
upregulating
highlighted
regulatory
function
pathogenesis
PF.
Язык: Английский
Hydroxytyrosol Alleviates Acute Liver Injury by Inhibiting the TNF-α/PI3K/AKT Signaling Pathway via Targeting TNF-α Signaling
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(23), С. 12844 - 12844
Опубликована: Ноя. 29, 2024
Acute
liver
injury
(ALI)
is
an
to
tissue
caused
by
viruses,
drugs,
alcohol,
and
oxygen
deprivation,
one
of
the
most
common
serious
clinical
disorders.
Hydroxytyrosol
(HT)
a
naturally
occurring
polyphenolic
compound
isolated
from
forsythia
has
excellent
anti-inflammatory
properties.
However,
effect
mechanisms
HT
in
ALI
remain
unclear.
We
used
LPS/D-GalN
induced
experimental
mouse
model
AML12
cells
reveal
efficacy
potential
ALI,
HE
staining
was
for
evaluation
pathologies.
A
biochemical
assay
detect
changes
function,
RNA-seq
conducted
underlying
WB,
RT-qPCR,
IF
were
assess
effects
action.
Furthermore,
vitro
against
protection
mechanism.
significant
alleviated
LPS/D-GalN-induced
mice
suppressing
inflammatory.
In
terms
RNA-seq,
improved
TNF,
ECM-receptor
interaction,
PI3K/AKT
signaling
pathway,
it
downregulated
mRNA
levels
VCAM-1,
CXCL5,
TNF-α
IL-6
liver.
Mechanically,
targeting
TNF-α,
thereby
inhibiting
TNF-α/PI3K/AKT
pathway.
Язык: Английский