Rambam Maimonides Medical Journal,
Journal Year:
2022,
Volume and Issue:
13(4), P. e0026 - e0026
Published: Oct. 27, 2022
Medical
cannabis
is
becoming
an
acceptable
treatment
modality
in
medicine,
especially
for
pain
relief.
Concurrently,
use
more
prevalent
worldwide,
a
public
demand-driven
trend
despite
the
lack
of
established
scientific
basis.
This
observational
open-label
study
sought
to
investigate
effectiveness
therapy
alleviating
low
back
symptoms.Two
types
modalities
were
sequentially
administered
chronic
patients.
After
initial
1-month
washout
period
(WO1),
first
was
cannabidiol
(CBD)-rich
sublingual
extract
10
months.
Following
another
period,
second
modality,
Δ9-tetrahydrocannabinol
(THC)-rich
smoked
inflorescence
(whole
dried
flowers)
12
months.Enrolled
24
patients
whose
advanced
imaging
studies
(i.e.
computerized
tomography
or
magnetic
resonance
lumbar
spine)
revealed
disc
herniation
spinal
stenosis.
Three
dropped
out
but
resumed
participation
receive
THC-rich
smoking
therapy.
minimum
2
years,
had
reduced
lower
symptoms,
as
assessed
by
Oswestry
Disability
Index,
SF-12
patient-reported
outcome
questionnaire,
and
visual
analogue
scale.
Pain
reduction
not
significant
during
part
study;
however,
inhaled
study.Our
findings
indicate
that
effective
than
CBD-rich
treating
safe
pain.
JAMA Network Open,
Journal Year:
2023,
Volume and Issue:
6(12), P. e2347373 - e2347373
Published: Dec. 13, 2023
This
survey
study
characterizes
past-year
use
prevalence
and
factors
associated
with
of
cannabidiol,
cannabigerol,
cannabinol,
Δ8-tetrahydrocannabinol
among
US
adults.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(10), P. 2397 - 2397
Published: May 20, 2024
The
resurgence
of
cannabis
(Cannabis
sativa
L.)
has
been
propelled
by
changes
in
the
legal
framework
governing
its
cultivation
and
use,
increased
demand
for
hemp-derived
products,
studies
recognizing
industrial
health
benefits
hemp.
This
led
to
creation
novel
high-cannabidiol,
low-Δ9-tetrahydrocannabinol
varieties,
enabling
hemp
crop
expansion
worldwide.
review
elucidates
recent
implications
Europe,
with
a
focus
on
legislative
impacts
practices,
prospective
breeding
efforts,
dynamic
scientific
landscape
surrounding
this
crop.
We
also
current
cultivars’
cannabinoid
composition
European
market
major
differences
that
United
States.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: July 13, 2024
Abstract
Cannabigerol
(CBG)
is
a
phytocannabinoid
increasing
in
popularity,
with
preclinical
research
indicating
it
has
anxiolytic
and
antidepressant
effects.
However,
there
are
no
published
clinical
trials
to
corroborate
these
findings
humans.
The
primary
objective
of
this
study
was
examine
acute
effects
CBG
on
anxiety,
stress,
mood.
Secondary
objectives
were
whether
produces
subjective
drug
or
motor
cognitive
impairments.
A
double-blind,
placebo-controlled
cross-over
field
trial
conducted
34
healthy
adult
participants.
Participants
completed
two
sessions
(with
one-week
washout
period)
via
Zoom.
In
each,
they
provided
ratings
mood,
prior
double-blind
administration
20
mg
hemp-derived
placebo
tincture
(T0).
These
collected
again
after
participants
ingested
the
product
an
online
survey
(T1),
Trier
Social
Stress
Test
(T2),
verbal
memory
test
DRUID
impairment
app
(T3).
Relative
placebo,
significant
main
effect
overall
reductions
anxiety
as
well
stress
at
T1.
also
enhanced
relative
placebo.
There
evidence
impairment.
may
represent
novel
option
reduce
adults.
Pharmaceuticals,
Journal Year:
2023,
Volume and Issue:
16(10), P. 1442 - 1442
Published: Oct. 11, 2023
Cannabigerol
(CBG),
derived
from
the
cannabis
plant,
acts
as
an
acute
analgesic
in
a
model
of
cisplatin-induced
peripheral
neuropathy
(CIPN)
mice.
There
are
no
curative,
long-lasting
treatments
for
CIPN
available
to
humans.
We
investigated
ability
chronic
CBG
alleviate
mechanical
hypersensitivity
due
mice
by
measuring
responses
7
and
14
days
daily
CBG.
found
that
treatment
(i.p.)
consecutive
significantly
reduced
male
female
with
pain
sensitivity
up
60–70%
baseline
levels
(p
<
0.001
all),
24
h
after
last
injection.
Additionally,
we
did
not
evoke
tolerance
incur
significant
weight
change
or
adverse
events.
The
efficacy
was
independent
estrous
cycle
phase.
Therefore,
administration
can
provide
at
least
antinociceptive
effect
These
findings
support
study
neuropathic
therapy,
which
without
both
males
females.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(6), P. 1145 - 1145
Published: May 22, 2024
Chemotherapy-induced
peripheral
neuropathy
(CIPN)
is
one
of
the
most
prevalent
and
dose-limiting
complications
in
chemotherapy
patients,
with
estimates
at
least
30%
patients
experiencing
persistent
for
months
or
years
after
treatment
cessation.
An
emerging
potential
intervention
CIPN
cannabinoid-based
pharmacotherapies.
We
have
previously
demonstrated
that
psychoactive
CB1/CB2
cannabinoid
receptor
agonist
Δ9-tetrahydrocannabinol
(Δ9-THC)
non-psychoactive,
minor
phytocannabinoid
cannabidiol
(CBD)
can
attenuate
paclitaxel-induced
mechanical
sensitivity
a
mouse
model
CIPN.
then
showed
two
compounds
acted
synergically
when
co-administered
model,
giving
credence
to
so-called
entourage
effect.
others
also
CBD
several
opioid-associated
behaviors.
Most
recently,
it
was
reported
another
cannabinoid,
cannabigerol
(CBG),
attenuated
cisplatin-associated
mice.
Therefore,
goals
present
set
experiments
were
determine
single
combined
effects
(CBG)
oxaliplatin-associated
sensitivity,
naloxone-precipitated
morphine
withdrawal,
acute
antinociception
male
C57BL/6
Results
CBG
reversed
only
under
select
dosing
conditions,
interactive
sub-additive
synergistic
depending
upon
conditions
too.
Pretreatment
selective
α2-adrenergic,
CB1,
CB2
antagonist
significantly
effect
CBG.
decreased
jumping
behavior
alone
synergistically
combination,
while
antinociceptive
CBD.
Taken
together,
may
therapeutic
like
as
rodent
models,
its
opioids
other
phytocannabinoids
should
continue
be
characterized.
Scientific Reports,
Journal Year:
2022,
Volume and Issue:
12(1)
Published: Aug. 19, 2022
Saliva
serves
multiple
important
functions
within
the
body
that
we
typically
take
for
granted,
such
as
helping
prepare
food
swallowing
and
defense
against
oral
pathogens.
Dry
mouth
is
a
primary
symptom
of
Sjӧgren's
syndrome
side
effect
many
drug
treatments.
Cannabis
users
frequently
report
dry
mouth,
but
basis
this
still
unknown.
If
effects
occur
via
endogenous
cannabinoid
signaling
system,
then
may
represent
novel
mechanism
regulation
salivation.
We
examined
expression
CB1
receptors
in
submandibular
salivary
gland
using
immunohistochemistry
tested
salivation
by
THC
cannabinoid-related
ligands.
now
are
expressed
axons
cholinergic
neurons
innervating
gland.
No
staining
seen
epithelial
cells
(acinar
ductal),
or
myoepithelial
(MECs).
Treatment
with
(4
mg/kg,
IP)
receptor
agonist
CP55940
(0.5
mg/kg)
reduced
both
male
female
mice
1
h
after
treatment.
CBD
had
no
on
its
own
reversed
concentration-dependent
manner.
Neither
antagonist
SR141716
nor
CB2-selective
JWH133
an
also
found
fatty
acid
amide
hydrolase
(FAAH),
enzyme
metabolizes
endocannabinoid
anandamide
related
lipids,
regulates
Salivation
was
FAAH
knockout
well
treated
blocker
URB597
mg/kg).
mice.
protein
detected
intracellularly
acinar
not
ductal
cells.
In
lipidomics
experiments,
chiefly
elevated
levels
acylethanolamines,
including
anandamide,
acyglycines.
Our
results
consistent
model
wherein
endocannabinoids
activate
likely
acts
plugging
into
activating
to
reduce
salivation,
thus
offering
underlying
reported
cannabis
users.
Pain and Therapy,
Journal Year:
2024,
Volume and Issue:
13(5), P. 1063 - 1094
Published: Aug. 3, 2024
Interest
in
medical
cannabis
and
cannabis-based
medicinal
products
(CBMPs)
has
increased
greatly
recent
years.
Two
cannabinoids
are
of
principal
importance;
delta-9-tetrahydrocannabinol
(∆9-THC),
the
primary
psychoactive
component,
also
cannabidiol
(CBD),
considered
non-intoxicating.
Each
distinct
mechanisms
action
different
therapeutic
potentials.
CBMPs
differ
their
∆9-THC
CBD
components;
predominantly
∆9-THC,
balanced
formulations
with
equivalent
elements,
CBD-predominant
products.
In
this
narrative
review,
we
evaluate
published
evidence
for
clinical
benefits
overall
well-being.
We
review
safety
profile
discuss
potential
dependence
CBMPs.
Evidence
can
be
drawn
from
a
wide
range
randomized
other
controlled
studies
observational
real-world
studies.
Most
data
registry
supportive
∆9-THC-based
(∆9-THC-predominant
or
CBMPs)
management
chronic
neuropathic
pain.
Balanced
effective
reducing
spasticity
multiple
sclerosis.
show
benefit
providing
symptomatic
anxiety,
nausea,
improving
sleep,
but
place
specific
is
more
subtle,
choice
guided
by
circumstances.
Symptomatic
improvements
accompanied
improved
quality
life
Safety
indicate
that
generally
well
tolerated
most
patients
without
contraindications.
The
majority
adverse
effects
non-serious,
transient;
principally
associated
dose-dependent.
contrast
to
recreational
use,
there
little
have
any
dependence.
Muscle & Nerve,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 12, 2025
ABSTRACT
A
unifying
mechanistic
cause
for
amyotrophic
lateral
sclerosis
(ALS)
remains
uncertain.
Multiple
pathophysiological
processes
appear
to
occur
simultaneously.
Cannabinoids,
including
delta‐9‐tetrahydrocannabinol
(THC),
cannabidiol
(CBD),
cannabigerol
(CBG),
and
others
found
in
cannabis,
cannabis
extracts
(CEs),
have
activity
these
pathogenic
pathways,
which
led
increasing
interest
cannabinoids
as
therapeutic
agents
ALS.
The
use
of
a
treatment
strategy
is
substantiated
by
preclinical
evidence
suggesting
role
the
endocannabinoid
system
(ECS)
ALS
other
neurodegenerative
disorders.
Preclinical
data
indicate
that
CEs
powerful
antioxidative,
anti‐inflammatory,
neuroprotective
effects
SOD1
G93A
mouse
model
murine
models
has
been
shown
prolong
neuronal
cell
survival,
leads
delayed
onset
disease
state,
slows
progression
disease.
Although
research
humans
limited,
few
studies
suggest
CBD,
humans,
provide
benefits
both
motor
symptoms,
rigidity,
cramps,
fasciculations,
non‐motor
symptoms
sleep
quality,
pain,
emotional
quality
life,
depression.
There
need
further,
well‐designed
clinical
trials
validate
further
an
individual
cannabinoid,
or
combination
cannabinoids,
disease‐modifying
therapy