Effects of Acrylamide on Mouse Implantation and Decidualization
Yang Hong-yuan,
No information about this author
Huina Luo,
No information about this author
Z.Q. Wang
No information about this author
et al.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(9), P. 4129 - 4129
Published: April 26, 2025
Acrylamide
is
a
class
2A
carcinogen
with
neurotoxicity
and
genotoxicity.
In
addition
to
industrial
production,
it
ubiquitous
in
high-temperature
heated
high-carbohydrate
foods.
Numerous
studies
have
confirmed
the
toxicity
of
ACR
on
reproduction.
Implantation
decidualization
are
crucial
processes
during
establishment
pregnancy
rodents
humans.
However,
its
effect
uterine
implantation
remains
poorly
understood.
The
objective
this
study
elucidate
mechanism
by
which
affects
mice.
exposed
daily
drinking
water
female
mice,
dose
calculated
according
body
weight
After
3
months
administration
at
concentrations
0,
20,
30
mg
ACR/kg/d,
mice
mated
male
induce
pregnancy.
Compared
control
group,
treatment
significantly
reduces
number
embryo
implantations
litter
size.
leads
abnormal
expression
endometrial
receptivity-related
molecules
luminal
epithelium
day
4
pregnancy,
including
decrease
p-STAT3
level
an
increase
MUC1
MSX1
levels.
decidualization-related
obviously
downregulated
ACR.
Furthermore,
results
abnormality
oxidative
stress-
ferroptosis-related
protein
levels
site
5.
conclusion,
acrylamide
can
impair
mouse
disrupting
stress
ferroptosis.
Language: Английский
Expression and purification of recombinant glutaredoxin 1 and protection against oxidative stress injury during cerebral ischemia-reperfusion injury
Z Li,
No information about this author
Tong Lin,
No information about this author
Yu Sun
No information about this author
et al.
Protein Expression and Purification,
Journal Year:
2025,
Volume and Issue:
unknown, P. 106689 - 106689
Published: Feb. 1, 2025
Language: Английский
Tomatidine Alleviates Intervertebral Disc Degeneration by Activating the Nrf2/HO-1/GPX4 Signaling Pathway
Ze Li,
No information about this author
Pu Cheng,
No information about this author
Huifeng Xi
No information about this author
et al.
Drug Design Development and Therapy,
Journal Year:
2024,
Volume and Issue:
Volume 18, P. 6313 - 6329
Published: Dec. 1, 2024
Intervertebral
disc
degeneration
(IDD)
is
a
leading
cause
of
low
back
pain,
and
developing
new
molecular
drugs
targets
for
IDD
direction
future
treatment
strategies.
The
aim
this
study
to
investigate
the
effects
mechanisms
tomatidine
in
ameliorating
lumbar
IDD.
Nucleus
pulposus
cells
(NPCs)
exposed
lipopolysaccharides
were
used
as
an
vitro
model
changes
expression
extracellular
matrix
components
associated
signaling
pathway
molecules.
A
instability
was
simulate
Tomatidine
(Td)
then
administered
intraperitoneally,
its
evaluated
through
histopathological
analysis.
In
vitro,
Td
significantly
promoted
ECM
anabolism,
inhibited
catabolism,
reduced
oxidative
stress
ferroptosis
LPS-stimulated
NPCs.
When
Nrf2
inhibited,
exacerbated,
protective
on
NPCs
lost,
suggesting
Nrf2/HO-1/GPX4
axis
critical
therapeutic
Td.
vivo,
analysis
demonstrated
that
ameliorated
murine
model.
alleviates
vivo
by
activating
inhibit
This
mechanism
suggests
promising
candidate
treatment.
Language: Английский