Endocrinology,
Journal Year:
2022,
Volume and Issue:
163(10)
Published: Aug. 8, 2022
Abstract
The
period
of
brain
sexual
differentiation
is
characterized
by
the
development
hormone-sensitive
neural
circuits
that
govern
subsequent
presentation
sexually
dimorphic
behavior
in
adulthood.
Perturbations
hormones
endocrine-disrupting
chemicals
(EDCs)
during
this
developmental
interfere
with
an
organism’s
endocrine
function
and
can
disrupt
normative
organization
male-
or
female-typical
circuitry.
This
well
for
reproductive
social
behaviors
their
underlying
circuitry
hypothalamus
other
limbic
regions
brain;
however,
cognitive
are
also
dimorphic,
potentially
vulnerable
to
EDC
exposure
critical
periods
development.
review
provides
recent
evidence
sex-specific
changes
brain’s
monoaminergic
systems
(dopamine,
serotonin,
norepinephrine)
after
relates
these
outcomes
sex
differences
cognition
such
as
affective,
attentional,
learning/memory
behaviors.
Environment International,
Journal Year:
2023,
Volume and Issue:
180, P. 108228 - 108228
Published: Sept. 27, 2023
Early-life
exposure
to
environmental
endocrine
disruptors
(EDCs)
is
a
potential
risk
factor
for
autism
spectrum
disorder
(ASD).
Exposure
nonylphenol
(NP),
typical
EDC,
known
cause
some
long-term
behavioural
abnormalities.
Moreover,
these
abnormal
behaviours
are
the
most
frequent
psychiatric
co-morbidities
in
ASD.
However,
direct
evidence
link
between
NP
early
life
and
ASD-like
phenotypes
still
missing.
In
present
study,
induced
by
valproic
acid
treatment
were
considered
as
positive
control.
We
investigated
impacts
on
social
following
early-life
NP,
explored
effects
of
this
neuronal
dendritic
spines,
mitochondria
function,
oxidative
stress,
endoplasmic
reticulum
(ER)
stress.
Furthermore,
primary
cultured
rat
neurons
employed
vitro
model
evaluate
changes
spine
caused
stress
ER
specifically
modulated
further
explore
their
roles
changes.
Our
results
indicated
rats
exposed
showed
mild
behaviours.
we
also
found
activation
triggered
may
contribute
decrease
synaptic
dysfunction,
which
underlie
neurobehavioural
abnormalities
NP.
Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(36), P. 15984 - 15996
Published: Aug. 28, 2024
Exposure
to
bisphenol
A
(BPA)
during
gestation
and
lactation
is
considered
be
a
potential
risk
factor
for
autism
spectrum
disorder
(ASD)
in
both
humans
animals.
As
novel
alternative
BPA,
4-hydroxy-4′-isopropoxydiphenylsulfone
(BPSIP)
frequently
detected
breast
milk
placental
barrier
systems,
suggesting
transmission
from
the
mother
offspring
increased
of
exposure.
Gestation
are
critical
periods
central
nervous
system
development,
which
vulnerable
certain
environmental
pollutants.
Herein,
we
investigated
behavioral
impacts
neurobiological
effects
early-life
exposure
BPSIP
(0.02,
0.1,
0.5
mg/kg
body
weight/day)
mice
offspring.
Behavioral
studies
indicated
that
induced
ASD-like
behaviors,
including
elevated
anxiety-related
behavior
decreased
spatial
memory,
male
female
pups.
distinct
pattern
reduced
social
novelty
was
observed
only
offspring,
accompanied
by
significant
alterations
antioxidant
levels.
Transcriptome
analysis
demonstrated
differentially
expressed
genes
(DEGs)
were
mainly
enriched
pathways
related
behaviors
neurodevelopment,
consistent
with
phenotype.
Besides,
decrease
protein
levels
complex
IV
(COX
IV)
across
all
tested
populations
suggests
profound
impact
on
mitochondrial
function,
potentially
leading
abnormal
energy
metabolism
individuals
autism.
Additionally,
changes
synaptic
proteins,
evidenced
synapsin
1
(SYN1)
postsynaptic
density
protein-95
(PSD95)
cerebellum
hippocampus,
support
notion
involvement.
These
findings
suggest
may
induce
sex-specific
neurotoxic
involve
oxidative
stress,
generation,
plasticity.
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(24), P. 13201 - 13201
Published: Dec. 8, 2021
Bisphenol
A
(BPA)
is
an
environmental
risk
factor
for
autism
spectrum
disorder
(ASD).
BPA
exposure
dysregulates
ASD-related
genes
in
the
hippocampus
and
neurological
functions
of
offspring.
However,
whether
prenatal
has
impact
on
prefrontal
cortex,
another
brain
region
highly
implicated
ASD,
through
what
mechanisms
have
not
been
investigated.
Here,
we
demonstrated
that
disrupts
transcriptome–interactome
profiles
cortex
neonatal
rats.
Interestingly,
list
BPA-responsive
was
significantly
enriched
with
known
ASD
candidate
genes,
as
well
were
dysregulated
postmortem
tissues
cases
from
multiple
independent
studies.
Moreover,
several
differentially
expressed
offspring’s
targets
transcription
factors,
including
AR,
ESR1,
RORA.
The
hypergeometric
distribution
analysis
revealed
may
regulate
expression
such
these
factors
a
sex-dependent
manner.
molecular
docking
novel
potential
BPA,
RORA,
SOX5,
TCF4,
YY1.
Our
findings
indicated
increase
mechanisms,
which
should
be
investigated
further.
Endocrinology,
Journal Year:
2022,
Volume and Issue:
163(10)
Published: Aug. 8, 2022
Abstract
The
period
of
brain
sexual
differentiation
is
characterized
by
the
development
hormone-sensitive
neural
circuits
that
govern
subsequent
presentation
sexually
dimorphic
behavior
in
adulthood.
Perturbations
hormones
endocrine-disrupting
chemicals
(EDCs)
during
this
developmental
interfere
with
an
organism’s
endocrine
function
and
can
disrupt
normative
organization
male-
or
female-typical
circuitry.
This
well
for
reproductive
social
behaviors
their
underlying
circuitry
hypothalamus
other
limbic
regions
brain;
however,
cognitive
are
also
dimorphic,
potentially
vulnerable
to
EDC
exposure
critical
periods
development.
review
provides
recent
evidence
sex-specific
changes
brain’s
monoaminergic
systems
(dopamine,
serotonin,
norepinephrine)
after
relates
these
outcomes
sex
differences
cognition
such
as
affective,
attentional,
learning/memory
behaviors.