Risk Element Interaction with an Emerging Contaminant in Mammals: The Case of Arsenic and Carbamazepine Orally Taken up by Microtus arvalis L. as a Model Organism
Frank Boahen,
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Jiřina Száková,
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Zuzana Čadková
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et al.
Applied Sciences,
Journal Year:
2025,
Volume and Issue:
15(3), P. 1662 - 1662
Published: Feb. 6, 2025
Arsenic
(As),
a
well-known
‘traditional’
environmental
contaminant,
and
carbamazepine
(CBZ),
an
emerging
contaminant
of
pharmaceutical
category,
are
both
frequently
detected
in
the
environment
have
been
shown
to
exhibit
toxicity
at
exposure
concentrations
present
environment.
This
study
aimed
assess
single
combined
effects
these
pollutants
on
adult
common
vole
(Microtus
arvalis
L.),
model
mammalian
organism.
assessed
As
CBZ
accumulation,
their
biotransformation
processes,
antioxidant
enzyme
defence
responses
after
sole
exposure.
The
animals
were
fed
diet
containing
either
low
(1.25
mg/kg)
or
high
level
(166
As.
Moreover,
half
exposed
via
drinking
water
infused
with
10
ng/L
CBZ,
second
had
use
devoid
CBZ.
results
showed
enhanced
total
species
contents
organs
+
group
compared
group.
High
did
not
cause
uptake
liver
There
was
potential
accumulation
groups
(CBZ
CBZ),
raising
concerns
about
toxic
mammals
from
long-term
Glutathione
peroxidase
(GPx)
activity,
reflecting
against
co-exposure
two
pollutants,
that
exhibited
comparable
activity
control
group,
while
down-regulation
up-regulation.
These
findings
suggest
experienced
minimal
oxidative
stress
conditions,
similar
rapid
adaptation
response
curtail
offset
tissue
damage
slow
adaptation/response
this
experiment
indicate
possible
interactions
various
could
alter
individual
necessity
investigating
for
better
understanding
risk
real
conditions.
Language: Английский
Chronic Exposure to Arsenic and Fluoride Starting at Gestation Alters Liver Mitochondrial Protein Expression and Induces Early Onset of Liver Fibrosis in Male Mouse Offspring
Biological Trace Element Research,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 27, 2024
Abstract
The
presence
of
arsenic
(As)
and
fluoride
(F
−
)
in
drinking
water
is
concern
due
to
the
enormous
number
individuals
exposed
this
condition
worldwide.
Studies
cultured
cells
animal
models
have
shown
that
As-
or
F-induced
hepatotoxicity
primarily
associated
with
redox
disturbance
altered
mitochondrial
homeostasis.
To
explore
hepatotoxic
effects
chronic
combined
exposure
As
F
water,
pregnant
CD-1
mice
were
2
mg/L
(sodium
arsenite)
and/or
25
fluoride).
male
offspring
continued
treatment
up
30
(P30)
90
(P90)
postnatal
days.
GSH
levels,
cysteine
synthesis
enzyme
activities,
transporter
levels
investigated
liver
homogenates,
as
well
expression
biomarkers
ferroptosis
biogenesis-related
proteins.
Serum
transaminase
Hematoxylin–Eosin
Masson
trichrome-stained
tissue
slices
examined.
Combined
at
P30
significantly
reduced
transcription
factor
A
(TFAM)
while
increasing
lipid
peroxidation,
free
Fe
2+
,
p53
expression,
serum
ALT
activity.
At
P90,
upregulation
uptake
was
a
recovery
levels.
Nevertheless,
downregulation
TFAM
now
downstream
inhibition
MT-CO2
mtDNA
fibrotic
damage.
Our
experimental
approach
using
human-relevant
doses
gives
evidence
increased
risk
for
early
damage
elevated
diet
during
intrauterine
period.
Language: Английский