Clinical Toxicology,
Journal Year:
2024,
Volume and Issue:
62(8), P. 477 - 482
Published: Aug. 2, 2024
Recent
decades
have
witnessed
an
extraordinary
global
crisis
of
drug
misuse.
Although
opioid
analgesics
receive
the
most
attention,
numerous
other
drugs
increased
rates
Neuropsychiatric Disease and Treatment,
Journal Year:
2025,
Volume and Issue:
Volume 21, P. 815 - 825
Published: April 1, 2025
Pregnancy
leads
to
vulnerabilities
and
susceptibilities
mental
disorders.
Miscarriage,
as
an
adverse
pregnancy
outcome,
following
curettage
for
treatment,
add
the
risks
of
further
psychiatric
disorders,
including
depression,
anxiety,
insomnia,
etc.,
current
approaches
prevention
are
unsatisfactory.
Ketamine
its
S-enantiomer
esketamine
can
prevent
postpartum
even
treats
depressive
symptoms
after
miscarriage
curettage,
but
their
side
effects
bring
limitations.
Ascorbic
acid
(AA,
Vitamin
C)
modulate
mood
enhance
ketamine's
antidepressant
efficacy
synergistically,
reducing
dosages
potentially.
The
purpose
this
study
is
clarify
beneficial
modification
AA
on
preventing
depression
other
disorders
in
patients
with
painless
well
interaction
between
esketamine.
This
a
2×2
factorial,
double-blinded,
randomized,
controlled
trial
that
will
recruit
women
undergoing
curettage.
A
total
424
participants
be
recruited
randomly
1:1:1:1
allocated
four
groups
(106
each):
Group
A0K0
(normal
saline
normal
saline),
A0K1
esketamine),
A1K0
(AA
A1K1
esketamine).
primary
outcome
incidence
postoperative
day
7,
assessed
Edinburgh
Postnatal
Depression
Scale
(EPDS).
secondary
outcomes
include
EPDS
score,
assessments
sleep,
pain,
events,
perianesthetic
data
patient
satisfaction.
provides
clinical
trial-based
evidence
alone
or
combination/interacting
emerging
rapid-acting
Our
expected
suggest
AA's
potential
application
optimizing
strategies
promoting
post-miscarriage
health,
possible
adjunctive
improvement
(es)ketamine's
usage
antidepressants.
One
major
limitation
single-center
study,
results
might
biased
due
regional
factors.
Journal of Psychopharmacology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 17, 2025
Background:
The
amino
acid
L-alanine,
has
been
shown
to
be
elevated
in
biofluids
during
major
depression
but
its
relevance
remains
unexplored.
Aim:
We
have
investigated
the
effects
of
repeated
L-alanine
administration
on
emotional
behaviours
and
central
gene
expression
mice.
Methods:
Mice
received
a
daily,
2-week
intraperitoneal
injection
either
saline
or
at
100
200
mg/kg
were
exposed
open
field,
light–dark
box
forced
swim
test.
transporters
(asc-1,
ASCT2),
glycine
receptor
subunits
(GlyRs),
NMDA
(GluNs)
mRNAs
measured,
together
with
western
blots
signalling
protein
mammalian
target
rapamycin
(mTOR).
Since
modulates
glucose
homeostasis,
peripheral
metabolomes
evaluated
1
H-NMR.
Results:
mg/kg,
not
both
male
female
mice
increased
latency
float
reduced
floating
time
test,
had
no
effect
anxious
behaviour
field
tests.
There
was
significant
reduction
encoding
asc-1
ASCT2
GluN2B
hippocampus
following
only.
On
blots,
hippocampal
immunoreactivity
reduced,
mTOR
group.
1H-NMR
revealed
gender-specific
changes
forebrain,
plasma
liver
only
L-alanine.
Conclusions:
Our
data
suggest
that
may
antidepressant-like
involve
modulation
glutamate
neurotransmission
independently
metabolism.
In
depression,
therefore,
homeostatic
response
pathophysiological
processes,
though
this
will
require
further
investigation.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 8, 2024
Abstract
Induction
of
neuroplasticity
has
become
the
dominant
explanatory
framework
for
rapid
and
sustained
therapeutic
effects
classic
psychedelics.
Within
this
broad
concept,
examination
morphological
neuronal
plasticity,
such
as
dendritic
arbor
growth,
is
widely
used
to
assess
novel
At
molecular
level,
it
been
reported
that
serotonergic
psychedelic
compounds
mediate
dendritogenesis
via
master
regulator
TrkB,
either
directly
BDNF/TrkB
signaling
potentiation
or
indirectly
through
5-HT2A
receptor.
To
examine
these
hypotheses
in
detail,
we
developed
a
robust
multimodal
screening
platform
unbiased,
semi-automated
quantification
cellular
morphology
multiplex
same
cortical
neurons.
We
found
primary
cultures
psychedelics
do
not
modulate
TrkB
receptor
BDNF-TrkB
signaling.
also
5HT2a
gene
expression
functional
levels
are
low,
induce
contrast
significant
elicited
by
BDNF.
Our
results
challenge
recently
published
field
indicate
need
rigorous
experimental
methods
study
manifestations
induced
clinically
therapeutics.
Current Neuropharmacology,
Journal Year:
2024,
Volume and Issue:
23(1), P. 75 - 84
Published: Aug. 16, 2024
:
Many
features
of
major
depressive
disorder
are
mirrored
in
rodent
models
psychological
stress.
These
have
been
used
to
examine
the
relationship
between
activation
hypothalamic-
pituitary
axis
response
stress,
development
oxidative
stress
and
neuroinflammation,
dominance
cholinergic
neurotransmission
associated
increase
REM
sleep
pressure.
Rodent
also
provided
valuable
insights
into
impairment
glycolysis
brain
glucose
utilization
by
under
resulting
decrease
energy
production
reduction
glutamate/GABA-glutamine
cycling.
The
rapidly
acting
antidepressants,
scopolamine,
ketamine
ECT,
all
raise
extracellular
glutamate
scopolamine
specifically
shown
cycling
men
rodents
with
corresponding
short-term
relief
depression.
nightly
use
gammahydroxybutyrate
(GHB)
may
achieve
more
permanent
results
even
act
prophylactically
prevent
or
recurrence
GHB
is
a
GABAB
agonist
restores
normal
balance
monoaminergic
inhibiting
neurotransmission.
It
relieves
GHB’s
metabolism
generates
NADPH,
key
antioxidant
cofactor.
Its
succinate,
tricarboxylic
acid
cycle
intermediate,
provide
cell
synthesize
glutamate.
In
both
animals
man,
increases
level
European Archives of Psychiatry and Clinical Neuroscience,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 29, 2024
Changes
in
glutamatergic
neuroplasticity
has
been
proposed
as
one
of
the
core
mechanisms
underlying
pathophysiology
depression.
In
consequence
components
synapse
have
explored
potential
targets
for
antidepressant
treatment.
The
rapid
effect
NMDA
receptor
antagonist
ketamine
and
subsequent
approval
its
S-enantiomer
(i.e.
esketamine),
set
precedent
investigation
into
other
acting
antidepressants
(RAADs).
this
review,
we
discuss
different
We
describe
important
clinical
outcomes
several
key
molecules
targeting
their
applicability
RAADs.
Specifically,
here
focus
on
substances
beyond
(es)ketamine,
which
meaningful
data
from
trials
are
available,
including
arketamine,
esmethadone,
nitrous
oxide
glutamate
modulators.
Molecules
only
successful
preclinical
settings
case
reports/series
marginally
discussed.
With
aim
underscore
critical
role
modulation
advancing
therapy,
thereby
possibly
enhancing
but
also
to
reducing
burden
depression
through
faster
therapeutic
effects.
Journal of Chemical Neuroanatomy,
Journal Year:
2024,
Volume and Issue:
141, P. 102468 - 102468
Published: Oct. 9, 2024
Parkinson's
disease
manifests
as
neurological
alterations
within
dendritic
spines
in
the
striatal
and
neocortical
brain
regions,
where
their
functionality
closely
correlates
with
morphology.
However,
impact
of
current
pharmacotherapy
on
spine
neuroplasticity,
crucial
for
novel
drug
development
psychiatric
disorders,
remains
unclear.
This
study
investigated
effects
6-OHDA
intrastriatal
bilateral
lesions
male
adult
rats
behavior
neuroplasticity
cortical
neurons.
Furthermore,
it
evaluated
influence
chronic
co-administration
pramipexole
(PPX),
a
D3
receptor
agonist,
rasagiline
(Ras),
selective
MAO-B
inhibitor,
these
alterations.
Lesioned
animals
exhibited
impaired
balance
behavior,
no
improvement
following
PPX-Ras
treatment.
The
lesion
decreased
density
caudate
putamen
(CPU)
spiny
projection
neurons
(SPNs),
change
unaffected
by
treatment,
though
increased
mushroom
reduced
stubby
In
nucleus
accumbens
(NAcc)
SPNs
prefrontal
cortex
layer
3
(PFC-3)
pyramidal
cells,
remained
unaltered,
but
bifurcated
NAcc,
while
increasing
decreasing
PFC-3
lesioned
rats.
These
findings
emphasize
importance
promising
targets
innovative
pharmacotherapies
disease.