Iturin A Potentiates Differentiation of Intestinal Epithelial Defense Cells by Modulating Keap1/Nrf2 Signaling to Mitigate Oxidative Damage Induced by Heat-Stable Enterotoxin B
Geng-xiu Zan,
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Hong Qu,
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Xinyang Li
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et al.
Antioxidants,
Journal Year:
2025,
Volume and Issue:
14(4), P. 478 - 478
Published: April 16, 2025
Intestinal
stem
cells
(ISCs)
maintain
epithelial
renewal
through
their
proliferation
and
differentiation
capabilities,
responding
to
various
intestinal
insults.
However,
the
impact
of
iturin
A,
a
natural
antimicrobial
peptide,
on
ISC
viability
its
potential
mitigate
heat-stable
enterotoxin
b
(STb)-induced
damage
remains
unclear.
Our
recent
study
demonstrated
that
oral
administration
A
enhances
tight
junction
protein
expression,
accelerates
crypt-villus
regeneration,
restores
barrier
integrity
in
STb-exposed
mice.
Furthermore,
promotes
differentiation,
significantly
increasing
numbers
goblet
Paneth
jejunum
following
STb
exposure.
Notably,
regulates
homeostasis
by
scavenging
reactive
oxygen
species
(ROS),
while
elevating
total
antioxidant
capacity
(T-AOC),
superoxide
dismutase
(SOD),
glutathione
peroxidase
(GSH-PX)
levels
both
serum
jejunal
mucosa.
Mechanistically,
facilitates
nuclear
factor-erythroid
2-
related
factor
2
(Nrf2)
release
disrupting
Kelch-like
ECH-associated
1
(Keap1),
leading
upregulation
enzyme
4
(GPX4).
In
conclusion,
our
findings
indicate
alleviates
oxidative
stress
induced
modulation
Keap1/Nrf2
pathway
into
cells,
thereby
enhancing
resistance
STb-induced
damage.
Language: Английский
Collagen Peptides and Saccharomyces boulardiiCNCM I‐745 Attenuate Acetic Acid‐Induced Colitis in Rats by Modulating Inflammation and Barrier Permeability
Food Science & Nutrition,
Journal Year:
2025,
Volume and Issue:
13(4)
Published: April 1, 2025
ABSTRACT
Ulcerative
colitis
(UC)
is
an
inflammatory
bowel
disease
characterized
by
recurrent
episodes
of
inflammation
and
tissue
damage,
with
limited
treatment
options.
This
study
aimed
to
investigate
the
effects
collagen
peptides
Saccharomyces
boulardii
on
acetic
acid
(AA)‐induced
colitis.
Thirty‐six
male
Sprague–Dawley
rats
were
randomly
divided
into
following
four
groups:
normal
control
(NC),
(CC),
peptide
(CP;
0.6
g/kg/day),
S.
(SB;
250
mg/day).
Colitis
was
induced
intrarectal
administration
AA
in
all
groups
except
NC,
treatments
administered
daily
for
7
days.
The
therapeutic
evaluated
assessing
activity
index
(DAI),
colon
mass
index,
macroscopic
microscopic
histopathological
changes,
zonula
occludens
(ZO)‐1
protein
expression,
myeloperoxidase
(MPO)
activity.
results
showed
that
CP
SB
substantially
alleviated
DAI
scores
(
p
<
0.05)
reduced
index.
Colon
damages
improved
compared
CC
group
0.01).
Histologically,
both
cell
infiltration,
crypt
ulceration,
showing
a
slightly
more
pronounced
effect.
Immunohistochemical
analysis
revealed
significant
restoration
ZO‐1
expression
treated
groups,
indicating
improvement
intestinal
barrier
integrity
Furthermore,
MPO
significantly
These
findings
are
consistent
previous
studies
highlight
anti‐inflammatory
barrier‐enhancing
probiotics
UC
models.
Language: Английский