Expert Review of Neurotherapeutics,
Journal Year:
2022,
Volume and Issue:
22(11-12), P. 1009 - 1018
Published: Nov. 2, 2022
Background
The
current
paucity
of
clinical
evidence
limits
the
use
cannabis-based
medicinal
products
(CBMPs)
in
post-traumatic
stress
disorder
(PTSD).
This
study
investigates
health-related
quality
life
(HRQoL)
changes
and
adverse
events
patients
prescribed
CBMPs
for
PTSD.Methods
A
case-series
from
UK
Medical
Cannabis
Registry
was
analyzed.
HRQoL
assessed
at
1-,
3-,
6-months
using
validated
patient
reported
outcome
measures
(PROMs).
Adverse
were
analyzed
according
to
Common
Terminology
Criteria
Events
version
4.0.
Statistical
significance
defined
as
p
<
0.050.Results
Of
162
included
patients,
88.89%
(n
=
144)
current/previous
cannabis
users.
Median
daily
CBMP
dosages
5.00
(IQR:
0.00–70.00)
mg
cannabidiol
145.00
100.00–200.00)
Δ9-tetrahydrocannabinol.
Significant
improvements
observed
PTSD
symptoms,
sleep,
anxiety
across
all
follow-up
periods
(p
0.050).
There
220
(135.8%)
by
33
(20.37%),
with
majority
graded
mild
or
moderate
severity
190,
117.28%).
Insomnia
fatigue
had
greatest
incidence
20,
12.35%).Conclusions
Associated
who
initiated
therapy.
analysis
suggests
acceptability
safety
up
6
months.
may
inform
randomized
placebo-controlled
trials,
required
confirm
causality
determine
optimal
dosing.
Applied Biosciences,
Journal Year:
2025,
Volume and Issue:
4(1), P. 4 - 4
Published: Jan. 21, 2025
Cannabidiol
(CBD),
a
non-psychoactive
compound
derived
from
Cannabis
sativa,
is
believed
to
have
anxiety-reducing
and
antidepressant
effects.
However,
existing
data
are
inconsistent,
likely
due
variations
in
experimental
designs,
dosages,
stress
models.
This
study
sought
assess
the
impact
of
CBD
on
anxiety
depression-like
behaviors
Wistar
rats
exposed
acute
cold
stress,
as
well
its
pro-
anti-inflammatory
cytokines.
Male
were
treated
with
(2.5,
5,
or
10
mg/kg)
vehicle
for
14
days
subjected
behavioral
tests,
including
elevated
plus
maze,
social
interaction,
forced
swim
tests.
Serum
levels
cytokines
(IL-6,
TNF-α,
IL-1β,
IL-10)
analyzed
post-experiment
using
ELISA.
Results
demonstrated
dose-dependent
anxiolytic
effect
CBD,
significant
improvements
interaction
reductions
anxiety-like
at
5
mg/kg.
All
doses
decreased
immobility
test,
suggesting
Furthermore,
selectively
lowered
IL-6
levels,
key
cytokine
depression
pathogenesis.
These
findings
indicate
that
has
properties,
partially
mediated
by
modulation
inflammatory
processes,
particularly
IL-6.
Trends in Psychiatry and Psychotherapy,
Journal Year:
2022,
Volume and Issue:
unknown
Published: May 26, 2022
Autism
spectrum
disorder
(ASD)
is
characterized
by
persistent
deficits
in
social
communication
and
interaction
restricted
repetitive
patterns
of
behavior.
Some
studies
have
shown
that
substances
derived
from
Cannabis
sativa
improve
the
quality
life
children
with
ASD
without
causing
serious
adverse
effects,
thus
providing
an
alternative
therapeutic
option.
The
objective
this
study
was
to
evaluate
efficacy
safety
a
cannabis
extract
rich
cannabidiol
(CBD)
ASD.
Neuropharmacology,
Journal Year:
2023,
Volume and Issue:
226, P. 109418 - 109418
Published: Jan. 6, 2023
Psychiatric
disorders
associated
with
psychological
trauma,
stress
and
anxiety
are
a
highly
prevalent
increasing
cause
of
morbidity
worldwide.
Current
therapeutic
approaches,
including
medication,
effective
in
alleviating
symptoms
posttraumatic
disorder
(PTSD),
at
least
some
individuals,
but
have
unwanted
side-effects
do
not
resolve
underlying
pathophysiology.
After
period
stagnation,
there
is
renewed
enthusiasm
from
public,
academic
commercial
parties
designing
developing
drug
treatments
for
these
disorders.
Here,
we
aim
to
provide
snapshot
the
current
state
this
field
that
written
neuropharmacologists,
also
practicing
clinicians
interested
lay-reader.
introducing
currently
available
treatments,
summarize
recent/ongoing
clinical
assessment
novel
medicines
PTSD,
grouped
according
primary
neurochemical
targets
their
potential
produce
acute
and/or
enduring
effects.
The
evaluation
putative
targeting
monoamine
(including
psychedelics),
GABA,
glutamate,
cannabinoid,
cholinergic
neuropeptide
systems,
amongst
others,
discussed.
We
emphasize
importance
clinically
assessing
new
medications
based
on
firm
understanding
neurobiology
stemming
rapid
advances
being
made
neuroscience.
This
includes
harnessing
neuroplasticity
bring
about
lasting
beneficial
changes
brain
rather
than
–
as
many
transient
attenuation
symptoms,
exemplified
by
combining
psychotropic/cognitive
enhancing
drugs
psychotherapeutic
approaches.
conclude
noting
other
emerging
trends
promising
phase
development.
Behavioural Neurology,
Journal Year:
2023,
Volume and Issue:
2023, P. 1 - 17
Published: Oct. 12, 2023
Cannabidiol
(CBD),
derived
from
Cannabis
sativa,
has
gained
remarkable
attention
for
its
potential
therapeutic
applications.
This
thorough
analysis
explores
the
increasing
significance
of
CBD
in
treating
neurological
conditions
including
epilepsy,
multiple
sclerosis,
Parkinson's
disease,
and
Alzheimer's
which
present
major
healthcare
concerns
on
a
worldwide
scale.
Despite
lack
available
therapies,
been
shown
to
possess
variety
pharmacological
effects
preclinical
clinical
studies,
making
it
an
intriguing
competitor.
review
brings
together
most
recent
findings
endocannabinoid
neurotransmitter
systems,
as
well
anti-inflammatory
pathways,
that
underlie
CBD's
modes
action.
Synthesized
efficacy
safety
assessments
range
illnesses
are
included,
covering
human
trials,
vitro
animal
models.
The
investigation
includes
how
could
protect
neurons,
control
neuroinflammation,
fend
off
oxidative
stress,
manage
neuronal
excitability.
study
emphasizes
existing
studies
future
possibilities
research,
addressing
research
issues
such
regulatory
complications
contradicting
results,
advocates
further
ideal
dose
methodologies.
By
emphasizing
improve
patient
well-being,
this
presents
revised
viewpoint
suitability
intervention
illnesses.
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
201, P. 107085 - 107085
Published: Feb. 2, 2024
There
is
an
urgent
need
for
novel
fast-acting
antidepressants
adolescent
treatment-resistant
depression
and/or
suicidal
risk,
since
the
selective
serotonin
reuptake
inhibitors
that
are
clinically
approved
age
(i.e.,
fluoxetine
or
escitalopram)
take
weeks
to
work.
In
this
context,
one
of
main
research
lines
our
group
characterize
at
preclinical
level
approaches
rapid-acting
adolescence.
The
present
review
summarizes
potential
use
in
adolescence
non-pharmacological
options,
such
as
neuromodulators
(electroconvulsive
therapy
and
other
innovative
types
brain
stimulation),
well
pharmacological
including
consciousness-altering
drugs
(mainly
ketamine
but
also
classical
psychedelics)
cannabinoids
cannabidiol),
with
promising
responses.
Following
a
brief
analytical
explanation
depression,
we
general
introduction
each
therapeutical
approach
together
clinical
evidence
supporting
its
beneficial
extrapolated
from
prior
successful
examples
adults),
then
report
recent
ongoing
studies
will
aid
improving
inclusion
these
therapies
clinic,
by
considering
sex-,
age-,
dose-related
differences,
factors
might
affect
efficacy
long-term
safety.
Finally,
conclude
providing
future
avenues
maximize
treatment
response,
more
importance
designing
testing
options
safe
depression.
Communications Medicine,
Journal Year:
2022,
Volume and Issue:
2(1)
Published: Nov. 2, 2022
Abstract
Background
Evidence
suggests
cannabidiol
(CBD)
has
anxiolytic
properties,
indicating
potential
for
novel
treatment
strategies.
However,
few
clinical
trials
of
CBD-based
products
have
been
conducted,
and
none
thus
far
examined
the
impact
these
on
cognition.
Methods
For
open-label
stage
trial
NCT02548559,
autoregressive
linear
modeling
assessed
efficacy
tolerability
four-weeks
1
mL
t.i.d.
with
a
full-spectrum,
high-CBD
sublingual
solution
(9.97
mg/mL
CBD,
0.23
Δ−9-tetrahydrocannabinol)
in
14
outpatients
moderate-to-severe
anxiety,
defined
as
≥16
Beck
Anxiety
Inventory
(BAI)
or
≥11
Overall
Severity
Impairment
Scale
(OASIS).
Results
Findings
suggest
significant
improvement
primary
outcomes
measuring
anxiety
secondary
assessing
mood,
sleep,
quality
life,
cognition
(specifically
executive
function)
following
treatment.
is
significantly
reduced
at
week
4
relative
to
baseline
(BAI:
95%
CI
=
[−21.03,
−11.40],
p
<
0.001,
OASIS:
[−9.79,
−6.07],
0.001).
Clinically
response
(≥15%
symptom
reduction)
achieved
maintained
early
most
patients
(BAI
78.6%,
OASIS
92.7%);
cumulative
frequency
responders
reached
100%
by
3.
The
study
drug
well-tolerated,
high
adherence/patient
retention
no
reported
intoxication
serious
adverse
events.
Minor
side
effects,
including
sleepiness/fatigue,
increased
energy,
dry
mouth
are
infrequently
endorsed.
Conclusions
provide
preliminary
evidence
supporting
product
anxiety.
Patients
quickly
achieve
maintain
reduction
effects.
A
definitive
assessment
this
symptoms
will
be
ascertained
ongoing
double-blind,
placebo-controlled
stage.