Autism Research,
Journal Year:
2024,
Volume and Issue:
17(7), P. 1300 - 1321
Published: March 18, 2024
This
review
highlights
a
key
role
of
the
serotonergic
system
in
brain
development
and
distortions
normal
early
stages
fetal
life
resulting
cascades
abnormalities,
including
defects
neurogenesis,
neuronal
migration,
growth,
differentiation,
arborization,
as
well
defective
circuit
formation
cortex,
subcortical
structures,
brainstem,
cerebellum
autistic
subjects.
In
autism,
regulation
growth
are
most
frequent
ubiquitous
developmental
changes
associated
with
impaired
neuron
smaller
size,
distorted
shape,
loss
spatial
orientation,
distortion
cortex
organization.
Common
autism
include
multiregional
focal
dysplastic
contributing
to
local
distortion,
epileptogenic
activity,
epilepsy.
There
is
discrepancy
between
more
than
500
reports
demonstrating
contribution
autism's
behavioral
anomalies,
highlighted
by
lack
studies
subjects'
brainstem
raphe
nuclei,
center
innervation,
diagnostic
features
spectrum
disorder
(ASD).
Discovery
severe
auditory
deficits
other
anomalies
leading
hearing
cascade
alterations,
social
verbal
communication
individuals
another
argument
intensify
postmortem
type
topography
of,
severity
nuclei
their
abnormal
broad
functional
comorbid
conditions
ASD.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(17)
Published: April 24, 2024
MDMA
(3,4-methylenedioxymethamphetamine)
is
a
psychoactive
drug
with
powerful
prosocial
effects.
While
sometimes
termed
an
"empathogen,"
empirical
studies
have
struggled
to
clearly
demonstrate
these
effects
or
pinpoint
underlying
mechanisms.
Here,
we
paired
the
social
transfer
of
pain
and
analgesia-behavioral
tests
modeling
empathy
in
mice-with
region-specific
neuropharmacology,
optogenetics,
transgenic
manipulations
explore
MDMA's
action
as
empathogen.
We
report
that
MDMA,
given
intraperitoneally
infused
directly
into
nucleus
accumbens
(NAc),
robustly
enhances
analgesia.
Optogenetic
stimulation
5-HT
release
NAc
recapitulates
implicating
signaling
core
mechanism.
Last,
systemic
optogenetic
inputs
restores
deficits
empathy-like
behaviors
Metabolites,
Journal Year:
2025,
Volume and Issue:
15(3), P. 210 - 210
Published: March 20, 2025
Tryptophan
is
an
essential
amino
acid
critical
for
human
health.
It
plays
a
pivotal
role
in
numerous
physiological
and
biochemical
processes
through
its
metabolism.
The
kynurenine
(KYN)
pathway
serves
as
the
principal
metabolic
route
tryptophan,
producing
bioactive
metabolites,
including
KYN,
quinolinic
acid,
3-hydroxykynurenine.
Numerous
studies
are
actively
investigating
relationship
between
tryptophan
metabolism
functions.
These
highlighting
interactions
among
metabolites
that
may
exert
synergistic
or
antagonistic
effects,
such
neuroprotective
neurotoxic,
pro-oxidative
antioxidant
activities.
Minor
disruptions
homeostasis
of
these
can
result
immune
dysregulation,
contributing
to
spectrum
diseases.
diseases
include
neurological
disorders,
mental
illnesses,
cardiovascular
conditions,
autoimmune
diseases,
chronic
kidney
disease.
Therefore,
understanding
roles
KYN
elucidating
contribution
health
regulation.
present
review
emphasizes
their
mechanisms
disease
development,
aiming
establish
theoretical
basis
leveraging
dietary
nutrients
enhance
British Journal of Pharmacology,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Aug. 14, 2023
Abstract
Autism
spectrum
disorders
(ASDs)
are
diagnosed
in
1/100
children
worldwide,
based
on
two
core
symptoms:
deficits
social
interaction
and
communication,
stereotyped
behaviours.
G
protein‐coupled
receptors
(GPCRs)
the
largest
family
of
cell‐surface
that
transduce
extracellular
signals
to
convergent
intracellular
signalling
downstream
cellular
responses
commonly
dysregulated
ASD.
Despite
hundreds
GPCRs
being
expressed
brain,
only
23
genetically
associated
with
ASD
according
Simons
Foundation
Research
Initiative
(SFARI)
gene
database:
oxytocin
OTR;
vasopressin
V
1A
1B
;
metabotropic
glutamate
mGlu
5
7
GABA
B2
dopamine
D
1
,
2
3
serotoninergic
5‐HT
β
‐adrenoceptor;
cholinergic
M
adenosine
A
2A
angiotensin
AT
cannabinoid
CB
chemokine
CX
CR1;
orphan
GPR37
GPR85;
olfactory
OR1C1,
OR2M4,
OR2T10
OR52M1.
Here,
we
review
therapeutic
potential
these
GPCRs,
as
well
for
For
each
GPCR,
discuss
its
genetic
association,
pharmacological
manipulation
animal
models,
pharmacopoeia
symptoms
rank
them
factors.
Among
highlight
OTR
more
promising
targets
We
dysregulation
their
is
a
pathological
mechanism
Their
has
begun
multiple
could
mitigate
International Journal of Molecular Sciences,
Journal Year:
2022,
Volume and Issue:
23(16), P. 9259 - 9259
Published: Aug. 17, 2022
Autism
Spectrum
Disorders
(ASDs)
are
a
group
of
neurodevelopmental
pathologies
whose
current
treatment
is
neither
curative
nor
effective.
Anthocyanins
naturally
occurring
compounds
abundant
in
blueberries
and
other
red
fruits
which
have
been
shown
to
be
successful
the
several
neurological
diseases,
at
least
vitro
vivo
disease
models.
The
aim
present
work
was
study
ability
an
anthocyanin-rich
extract
(ARE)
obtained
from
Portuguese
alleviate
autism-like
symptoms
valproic
acid
(VPA)
mouse
model
ASD
get
insights
into
underlying
molecular
mechanisms
such
benefits.
Therefore,
pregnant
BALB/c
females
were
treated
subcutaneously
with
single
dose
VPA
(500
mg/kg)
or
saline
on
gestational
day
12.5.
Male
offspring
mice
orally
ARE
(30
mg/kg/day)
vehicle
for
three
weeks,
further
subjected
behavioral
tests
biochemical
analysis.
Our
data
suggested
that
alleviated
behaviors
utero
VPA-exposed
and,
same
time,
decreased
both
neuroinflammation
gut
inflammation,
modulated
microbiota
composition,
increased
serotonin
levels
cerebral
prefrontal
cortex
gut,
reduced
synaptic
dysfunction
verified
autistic
mice.
Overall,
our
suggests
anthocyanins
extracted
could
constitute
effective
strategy
ameliorate
typical
through
modulation
microbiota-gut-brain
axis.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: June 14, 2024
Neurodevelopmental
disorders
(NDDs)
include
a
broad
spectrum
of
pathological
conditions
that
affect
>4%
children
worldwide,
share
common
features
and
present
variegated
genetic
origin.
They
clinically
defined
diseases,
such
as
autism
(ASD),
attention-deficit/hyperactivity
disorder
(ADHD),
motor
Tics
Tourette’s
syndromes,
but
also
much
more
heterogeneous
like
intellectual
disability
(ID)
epilepsy.
Schizophrenia
(SCZ)
has
recently
been
proposed
to
belong
NDDs.
Relatively
causes
NDDs
are
copy
number
variations
(CNVs),
characterised
by
the
gain
or
loss
portion
chromosome.
In
this
review,
we
focus
on
deletions
duplications
at
16p11.2
chromosomal
region,
associated
with
NDDs,
ID,
ASD
epilepsy
SCZ.
Some
core
phenotypes
presented
human
carriers
could
be
recapitulated
in
animal
cellular
models,
which
highlighted
prominent
neurophysiological
signalling
alterations
underpinning
CNVs-associated
phenotypes.
provide
an
overview
genes
within
locus,
including
those
partially
known
unknown
function
well
non-coding
RNAs.
A
particularly
interesting
interplay
was
observed
between
MVP
MAPK3
modulating
some
deletion.
Elucidating
their
role
intracellular
functional
links
will
key
step
devise
novel
therapeutic
strategies
for
CNVs-related
syndromes.