Ecotoxicology and Environmental Safety,
Год журнала:
2025,
Номер
290, С. 117763 - 117763
Опубликована: Янв. 1, 2025
Oxytetracycline
(OTC),
a
crop-absorbable
antibiotic,
poses
health
risk
to
humans
through
the
food
chain.
Conversely,
24-epibrassinolide
(EBL),
plant
growth
hormone,
mitigates
toxic
effects
of
various
pollutants
on
plants.
However,
mechanism
by
which
exogenous
EBL
affects
rape
seedlings
exposed
OTC
remains
largely
unknown.
In
this
study,
we
found
that
environmental
concentrations
significantly
inhibited
and
metabolism,
whereas
could
restore
characteristics.
Exogenous
decreased
reactive
oxygen
species
(ROS)
accumulation,
alleviating
OTC-induced
cell
membrane
lipid
peroxidation.
This
was
achieved
increasing
antioxidant
capacity
secondary
metabolism
levels.
Notably,
our
findings
suggested
stimulated
glutathione
S-transferase
(GST)
reductase
(GR)
activities,
enhancing
reduced
synthesis
participating
in
detoxification.
residues
+
OTC-treated
at
21
d
were
29
%
compared
with
alone.
Further
transcriptomic
metabolomic
analyses
revealed
differentially
expressed
genes
metabolites
alone
or
combined
treatment
groups
primarily
involved
regulation
phenylpropanoid
biosynthesis,
lant
hormone
signal
transduction
pathways
response
phytotoxic
detoxification
mechanisms,
as
control
group.
Nature Metabolism,
Год журнала:
2021,
Номер
3(12), С. 1706 - 1726
Опубликована: Дек. 6, 2021
Abstract
Ageing-associated
functional
decline
of
organs
and
increased
risk
for
age-related
chronic
pathologies
is
driven
in
part
by
the
accumulation
senescent
cells,
which
develop
senescence-associated
secretory
phenotype
(SASP).
Here
we
show
that
procyanidin
C1
(PCC1),
a
polyphenolic
component
grape
seed
extract
(GSE),
increases
healthspan
lifespan
mice
through
its
action
on
cells.
By
screening
library
natural
products,
find
GSE,
PCC1
as
one
active
components,
have
specific
effects
At
low
concentrations,
appears
to
inhibit
SASP
formation,
whereas
it
selectively
kills
cells
at
higher
possibly
promoting
production
reactive
oxygen
species
mitochondrial
dysfunction.
In
rodent
models,
depletes
treatment-damaged
tumour
microenvironment
enhances
therapeutic
efficacy
when
co-administered
with
chemotherapy.
Intermittent
administration
either
irradiated,
cell-implanted
or
naturally
aged
old
alleviates
physical
dysfunction
prolongs
survival.
We
identify
senotherapeutic
agent
vivo
activity
high
potential
further
development
clinical
intervention
delay,
alleviate
prevent
pathologies.
Frontiers in Pharmacology,
Год журнала:
2021,
Номер
11
Опубликована: Янв. 14, 2021
The
ovarian
system
comprises
vital
organs
in
females
and
is
of
great
significance
for
the
maintenance
reproductive
potential
endocrine
stability.
Although
complex
pathogenesis
undoubtedly
contributes
to
aging,
increasing
attention
being
paid
extensive
influence
oxidative
stress.
However,
role
stress
aging
yet
be
fully
elucidated.
Exploring
stress-related
processes
might
a
promising
strategy
against
aging.
In
this
review,
compelling
evidence
shown
that
plays
etiology
promotes
development
other
aging-related
etiologies,
including
telomere
shortening,
mitochondrial
dysfunction,
apoptosis,
inflammation.
addition,
some
natural
antioxidants
such
as
quercetin,
resveratrol,
curcumin
have
protective
ovaries
through
multiple
mechanisms.
These
findings
raise
prospect
modulator-natural
therapeutic
interventions
delaying
Antioxidants,
Год журнала:
2022,
Номер
11(8), С. 1618 - 1618
Опубликована: Авг. 20, 2022
The
antioxidant,
anti-inflammatory
and
antibacterial
activities
of
hesperetin,
hesperidin
glucoside
with
different
solubility
were
compared
in
vitro.
Hesperetin
was
prepared
by
enzymatic
hydrolysis
from
hesperidin,
composed
mono-glucoside
through
transglycosylation.
Solubility
the
compounds
different:
partition
coefficient
(log
P)
2.85
±
0.02
for
2.01
-3.04
0.03
glucoside.
showed
a
higher
effect
than
on
radical
scavenging
activity
antioxidant
assays,
while
similar
activity.
Cytotoxicity
low
order
glucoside,
hesperetin
murine
macrophage
RAW264.7
cells.
Treatment
cells
each
compound
reduced
levels
inflammatory
mediators,
nitric
oxide
(NO),
prostaglandin
E2
(PGE2),
tumor
necrosis
factor
alpha
(TNF-α)
interleukin-6
(IL-6).
most
effective
at
relatively
concentrations,
however,
also
concentration.
both
Gram-positive
-negative
bacteria,
similarly
depending
bacterial
strain.
In
conclusion,
form
aglycone
more
potent
biological
However,
highly
soluble
form,
has
been
shown
to
increase
poorly
hesperidin.
Foods,
Год журнала:
2022,
Номер
11(6), С. 882 - 882
Опубликована: Март 20, 2022
Flavonoids
are
well
known
for
their
extensive
health
benefits.
However,
few
studies
compared
the
differences
between
flavonoid
O-glycoside
and
C-glycoside.
In
this
work,
(isoquercitrin),
C-glycoside
(orientin),
aglycones
(quercetin
luteolin)
were
chosen
to
compare
on
antioxidant
activities
metabolism
during
in
vitro
digestion
vivo.
digestion,
initial
activity
of
two
was
very
high;
however,
they
both
decreased
more
sharply
than
glycosides
intestinal
phase.
The
glycosidic
bond
broken
gastric
stage,
while
remained
unchanged.
vivo,
plasma
elevated
activity;
urine
higher
O-glycoside.
These
results
indicate
that
closely
related
structural
characteristics
different
samples.
Aglycones
possessed
but
unstable
structures.
On
contrary,
sugar
substituents
reduced
flavonoids
improving
stability
helping
maintain
after
digestion.
Especially
stable
because
C-C
is
C-O
bond,
which
contributes
difference
absorption
This
study
provided
a
new
perspective
comparing
O-glycoside,
C-glycoside,
structure-activity
relationship
metabolism.
Nature Metabolism,
Год журнала:
2023,
Номер
5(11), С. 1887 - 1910
Опубликована: Окт. 30, 2023
Abstract
Senescent
cells
remain
metabolically
active,
but
their
metabolic
landscape
and
resulting
implications
underexplored.
Here,
we
report
upregulation
of
pyruvate
dehydrogenase
kinase
4
(PDK4)
upon
senescence,
particularly
in
some
stromal
cell
lines.
display
a
PDK4-dependent
increase
aerobic
glycolysis
enhanced
lactate
production
maintain
mitochondrial
respiration
redox
activity,
thus
adopting
special
form
reprogramming.
Medium
from
PDK4
+
promotes
the
malignancy
recipient
cancer
vitro,
whereas
inhibition
causes
tumor
regression
vivo.
We
find
that
reactive
oxygen
species
via
NOX1
to
drive
senescence-associated
secretory
phenotype,
suppression
reduces
DNA
damage
severity
restrains
phenotype.
In
preclinical
trials,
alleviates
physical
dysfunction
prevents
age-associated
frailty.
Together,
our
study
confirms
hypercatabolic
nature
senescent
reveals
link
between
cellular
production,
possibly,
age-related
pathologies,
including
not
limited
cancer.
Frontiers in Pharmacology,
Год журнала:
2023,
Номер
14
Опубликована: Май 12, 2023
Taxifolin
is
a
flavonoid
compound,
originally
isolated
from
the
bark
of
Douglas
fir
trees,
which
often
found
in
foods
such
as
onions
and
olive
oil,
also
used
commercial
preparations,
has
attracted
interest
nutritionists
medicinal
chemists
due
to
its
broad
range
health-promoting
effects.
It
powerful
antioxidant
with
excellent
antioxidant,
anti-inflammatory,
anti-microbial
other
pharmacological
activities.
This
review
focuses
on
breakthroughs
taxifolin
for
treatment
diseases
2019
2022
according
various
systems
human
body,
nervous
system,
immune
digestive
basis
this
review,
we
summarize
problems
current
research
try
suggest
solutions
future
directions.
Antioxidants,
Год журнала:
2021,
Номер
10(11), С. 1696 - 1696
Опубликована: Окт. 27, 2021
The
effects
of
rutin
and
glycoside
with
different
solubility
were
compared
on
antioxidant
activity
anti-inflammatory
in
vitro
the
platelet
aggregation
blood
coagulation
vivo.
Rutin
(consisting
mono-glucoside
di-glucoside)
was
prepared
via
enzymatic
transglycosylation
from
rutin.
showed
a
higher
effect
than
radical
scavenging
assays.
toxicity
murine
macrophage
RAW264.7
cells.
They
had
similar
levels
nitric
oxide
(NO),
prostaglandin
E
(PGE)
2
pro-inflammatory
cytokines
(such
as
tumor
necrosis
factor
(TNF)-α,
interleukin
(IL)-6)
Both
glycosides
similarly
reduced
rate
to
controls
vitro.
also
delayed
prothrombin
time
(PT)
activated
partial
thromboplastin
(APTT)
an
test.
repeated
administration
evaluated
vivo
using
SD
rats.
administered
group
significantly
decreased
that
control
group.
On
other
hand,
PT
APTT
not
In
conclusion,
differences
activities
vitro,
while
they
reduction
NO,
PGE2,
TNF-α
IL-6
rates,
both
condition.
Comparing
vivo,
effective
but
only
coagulation.
Saudi Pharmaceutical Journal,
Год журнала:
2022,
Номер
30(7), С. 918 - 926
Опубликована: Апрель 30, 2022
Hyperuricemia
becomes
a
public
health
problem
worldwide.
It
is
not
only
major
risk
factor
for
gout
but
also
associated
with
the
development
of
life-threatening
diseases
such
as
chronic
kidney
disease
and
cardiovascular
diseases.
Although
there
are
several
available
therapeutic
drugs,
some
serious
adverse
effects
contraindications
concerned.
These
drive
search
an
alternative
therapy
that
effective
safe.
Quercetin
particular
interesting
since
it
has
been
reported
numerous
pharmacological
activities,
especially
anti-hyperuricemia,
antioxidant,
anti-inflammation
amelioration
metabolic
syndromes
which
comorbidities
hyperuricemia
gout.
In
addition,
quercetin
widely
used
supplement
many
however,
use
indicated.
Therefore,
this
review
aims
to
gather
summarize
published
data
regarding
efficacy
in
preclinical
clinical
studies
along
possible
mechanism
action,
safety
aspect
order
support
dietary
prevention
management
gouty
arthritis
and/or
or
combination
minimize
side
conventional
drugs.