Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(23), P. 10275 - 10286
Published: June 3, 2024
The
pronounced
lethality
of
N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine
quinone
(6PPD-quinone
or
6PPDQ)
toward
specific
salmonids,
while
sparing
other
fish
species,
has
received
considerable
attention.
However,
the
underlying
cause
this
species-specific
toxicity
remains
unresolved.
This
study
explored
6PPDQ
toxicokinetics
and
intestinal
microbiota
composition
in
adult
zebrafish
during
a
14-day
exposure
to
environmentally
realistic
concentrations,
followed
by
7-day
recovery
phase.
Predominant
accumulation
occurred
brain,
intestine,
eyes,
with
lowest
levels
liver.
Six
metabolites
were
found
undergo
hydroxylation,
two
additionally
undergoing
O-sulfonation.
Semiquantitative
analyses
revealed
that
predominant
metabolite
featured
hydroxy
group
situated
on
phenyl
ring
adjacent
quinone.
was
further
validated
assessing
enzyme
activity
determining
silico
binding
interactions.
Notably,
affinity
between
phase
I
II
enzymes
exceeded
corresponding
coho
salmon
1.04–1.53
times,
suggesting
higher
potential
for
detoxification
tolerant
species.
Whole-genome
sequencing
significant
increases
genera
Nocardioides
Rhodococcus
after
6PPDQ.
Functional
annotation
pathway
enrichment
predicted
these
would
be
responsible
biodegradation
metabolism
xenobiotics.
These
findings
offer
crucial
data
comprehending
6PPDQ-induced
toxicity.
Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(21), P. 9113 - 9124
Published: May 14, 2024
The
antioxidant
N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenediamine
(6PPD)
and
its
oxidized
quinone
product
6PPD-quinone
(6PPD-Q)
in
rubber
have
attracted
attention
due
to
the
ecological
risk
that
they
pose.
Both
6PPD
6PPD-Q
been
detected
various
environments
humans
cohabit.
However,
date,
a
clear
understanding
of
biotransformation
potential
biomarker
for
exposure
are
lacking.
To
address
this
issue,
study
presents
comprehensive
analysis
extensive
across
species,
encompassing
both
vitro
vivo
models.
We
tentatively
identified
17
metabolites
vitro,
15
mice
vivo,
confirmed
presence
two
human
urine
samples.
Interestingly,
different
patterns
were
observed
species.
Through
semiquantitative
based
on
peak
areas,
we
found
almost
all
underwent
within
24
h
mice,
primarily
via
hydroxylation
subsequent
glucuronidation.
This
suggests
rapid
metabolic
processing
mammals,
underscoring
importance
identifying
effective
biomarkers
exposure.
Notably,
monohydroxy
6PPD-Q-O-glucuronide
consistently
most
predominant
our
studies,
highlighting
as
key
epidemiological
research.
These
findings
represent
first
data
set
mammalian
systems,
offering
insights
into
pathways
involved
possible
biomarkers.
Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(23), P. 10275 - 10286
Published: June 3, 2024
The
pronounced
lethality
of
N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine
quinone
(6PPD-quinone
or
6PPDQ)
toward
specific
salmonids,
while
sparing
other
fish
species,
has
received
considerable
attention.
However,
the
underlying
cause
this
species-specific
toxicity
remains
unresolved.
This
study
explored
6PPDQ
toxicokinetics
and
intestinal
microbiota
composition
in
adult
zebrafish
during
a
14-day
exposure
to
environmentally
realistic
concentrations,
followed
by
7-day
recovery
phase.
Predominant
accumulation
occurred
brain,
intestine,
eyes,
with
lowest
levels
liver.
Six
metabolites
were
found
undergo
hydroxylation,
two
additionally
undergoing
O-sulfonation.
Semiquantitative
analyses
revealed
that
predominant
metabolite
featured
hydroxy
group
situated
on
phenyl
ring
adjacent
quinone.
was
further
validated
assessing
enzyme
activity
determining
silico
binding
interactions.
Notably,
affinity
between
phase
I
II
enzymes
exceeded
corresponding
coho
salmon
1.04–1.53
times,
suggesting
higher
potential
for
detoxification
tolerant
species.
Whole-genome
sequencing
significant
increases
genera
Nocardioides
Rhodococcus
after
6PPDQ.
Functional
annotation
pathway
enrichment
predicted
these
would
be
responsible
biodegradation
metabolism
xenobiotics.
These
findings
offer
crucial
data
comprehending
6PPDQ-induced
toxicity.