Frontiers in Pharmacology,
Journal Year:
2020,
Volume and Issue:
11
Published: April 30, 2020
Cannabidiol
(CBD),
the
major
non-psychoactive
constituent
of
Cannabis
Sativa
L.,
has
gained
traction
as
a
potential
treatment
for
intractable
chronic
pain
in
many
conditions.
Clinical
evidence
suggests
that
CBD
provides
therapeutic
benefit
certain
forms
epilepsy
and
imparts
analgesia
conditions,
improves
quality
life.
continues
to
be
Schedule
I
or
V
on
list
controlled
substances
Drug
Enforcement
Agency
United
States.
However,
preparations
labeled
are
available
publicly
stores
streets.
use
does
not
always
resolve
pain.
purchased
freely
entails
risk
adulteration
by
potentially
hazardous
chemicals.
As
well,
pregnant
women
is
rising
poses
health-hazard
future
generations.
In
this
mini-review,
we
present
balanced
unbiased
pre-clinical
clinical
findings
beneficial
effects
its
deleterious
prenatal
development.
BMC Psychiatry,
Journal Year:
2020,
Volume and Issue:
20(1)
Published: Jan. 16, 2020
Medicinal
cannabis
has
received
increased
research
attention
over
recent
years
due
to
loosening
global
regulatory
changes.
been
reported
have
potential
efficacy
in
reducing
pain,
muscle
spasticity,
chemotherapy-induced
nausea
and
vomiting,
intractable
childhood
epilepsy.
Yet
its
application
the
field
of
psychiatry
is
lesser
known.The
first
clinically-focused
systematic
review
on
emerging
medical
across
all
major
psychiatric
disorders
was
conducted.
Current
evidence
regarding
whole
plant
formulations
plant-derived
cannabinoid
isolates
mood,
anxiety,
sleep,
psychotic
deficit/hyperactivity
disorder
(ADHD)
discussed;
while
also
detailing
clinical
prescription
considerations
(including
pharmacogenomics),
occupational
public
health
elements,
future
recommendations.
The
literature
conducted
during
2019,
assessing
data
from
case
studies
trials
involving
medicinal
or
for
(neurological
conditions
pain
were
omitted).The
present
therapeutics
nascent,
thereby
it
currently
premature
recommend
cannabinoid-based
interventions.
Isolated
positive
have,
however,
revealed
tentative
support
cannabinoids
(namely
cannabidiol;
CBD)
social
anxiety;
with
mixed
(mainly
positive)
adjunctive
use
schizophrenia.
Case
suggest
that
may
be
beneficial
improving
sleep
post-traumatic
stress
disorder,
however
weak.
Preliminary
findings
indicate
no
benefit
depression
high
delta-9
tetrahydrocannabinol
(THC)
therapeutics,
CBD
mania.
One
isolated
study
indicates
some
an
oral
cannabinoid/terpene
combination
ADHD.
Clinical
prescriptive
consideration
involves
caution
high-THC
(avoidance
youth,
people
anxiety
disorders),
gradual
titration,
regular
assessment,
cardiovascular
respiratory
disorders,
pregnancy
breast-feeding.There
encouraging,
albeit
embryonic,
treatment
a
range
disorders.
Supportive
are
key
isolates,
clinicians
need
mindful
safety
considerations,
especially
if
initiating
higher
dose
THC
formulas.
British Journal of Clinical Pharmacology,
Journal Year:
2019,
Volume and Issue:
85(9), P. 1888 - 1900
Published: June 21, 2019
Aims
Cannabidiol
(CBD)
is
a
cannabis‐derived
medicinal
product
with
potential
application
in
wide‐variety
of
contexts;
however,
its
effective
dose
different
disease
states
remains
unclear.
This
review
aimed
to
investigate
what
doses
have
been
applied
clinical
populations,
order
understand
the
active
range
CBD
variety
medical
contexts.
Methods
Publications
involving
administration
alone
were
collected
by
searching
PubMed,
EMBASE
and
ClinicalTrials.gov
.
Results
A
total
1038
articles
retrieved,
which
35
studies
met
inclusion
criteria
covering
13
Twenty‐three
reported
significant
improvement
primary
outcomes
(e.g.
psychotic
symptoms,
anxiety,
seizures),
ranging
between
<1
50
mg/kg/d.
Plasma
concentrations
not
provided
any
publication.
was
as
well
tolerated
epilepsy
most
frequently
studied
condition,
all
11
demonstrating
positive
effects
on
reducing
seizure
frequency
or
severity
(average
15
mg/kg/d
within
randomised
controlled
trials).
There
no
signal
activity
small
trials
(range
n
=
6–62)
assessing
diabetes,
Crohn's
disease,
ocular
hypertension,
fatty
liver
chronic
pain.
However,
low
2.4
mg/kg/d)
used
these
studies.
Conclusion
highlights
that
has
wide
several
pathologies.
Pharmacokinetic
conclusive
phase
III
elucidate
plasma
contexts
are
severely
lacking
highly
encouraged.
Pharmaceuticals,
Journal Year:
2020,
Volume and Issue:
13(9), P. 219 - 219
Published: Aug. 28, 2020
Cannabidiol
(CBD)
has
substantial
therapeutic
potential,
but
its
development
as
an
effective
drug
by
the
pharmaceutical
industry
is
hindered
intrinsic
characteristics
such
low
bioavailability,
water
solubility,
and
variable
pharmacokinetic
profiles.
Importantly,
lack
of
patentability
substance
also
limits
likelihood
expensive,
full
programme
in
anything
other
than
orphan
indications.
Potential
avenues
to
overcome
these
issues
with
CBD
include
self-emulsifying
delivery
systems,
improved
crystal
formulations
solid-state
formulations,
which
are
mostly
pre-clinical
or
early
clinical
stages
development.
This
review
identifies
compromising
current
CBD,
how
advanced
strategies
can
enable
realise
potential
a
successful
agent.
Journal of Clinical Medicine Research,
Journal Year:
2020,
Volume and Issue:
12(3), P. 129 - 141
Published: Jan. 1, 2020
Considering
data
from
in
vitro
and
vivo
studies,
cannabidiol
(CBD)
seems
to
be
a
promising
candidate
for
the
treatment
of
both
somatic
psychiatric
disorders.
The
aim
this
review
was
collect
dose(s),
dosage
schemes,
efficacy
safety
reports
CBD
use
adults
clinical
studies.
A
systematic
search
performed
PubMed,
Embase
Cochrane
library
articles
published
English
between
January
1,
2000
October
25,
2019.
terms
used
were
related
cannabis
adults.
We
identified
25
studies
(927
patients;
538
men
389
women),
which
22
controlled
trials
(833
patients)
three
observational
designs
(94
five
countries.
Formulations,
dose
schemes
varied
significantly
Varying
effects
randomized
(RCTs),
more
apparent
non-RCTs
minor
issues
general.
From
trials,
we
anxiolytic
with
acute
administration,
therapeutic
social
anxiety
disorder,
psychotic
disorder
substance
In
general,
heterogeneous
showed
substantial
risks
bias.
Although
results
have
been
identified,
considerable
variation
route
administration
employed
across
There
evidence
support
single
positive
effect
on
short
medium-term
symptomatic
improvement
schizophrenia
lack
cognitive
functioning
Overall,
well
tolerated
mild
side
effects.
J
Clin
Med
Res.
2020;12(3):129-141
doi:
https://doi.org/10.14740/jocmr4090
Journal of Cannabis Research,
Journal Year:
2021,
Volume and Issue:
3(1)
Published: Feb. 18, 2021
Abstract
Background
Public
and
medical
interest
in
cannabidiol
(CBD)
has
been
rising,
CBD
is
now
available
from
various
sources.
Research
into
the
effects
of
low-dose
on
outcomes
like
stress,
anxiety,
sleep
problems
have
scarce,
so
we
conducted
an
online
survey
users
to
better
understand
patterns
use,
dose,
self-perceived
CBD.
Methods
The
sample
consisted
387
current
or
past-CBD
who
answered
a
20-question
survey.
was
sent
out
through
email
databases
social
media.
Participants
reported
basic
demographics,
use
patterns,
reasons
for
sleep,
stress.
Results
(
N
=
387)
61.2%
females,
mostly
between
25
54
years
old
(72.2%)
primarily
based
UK
(77.4%).
top
4
using
were
anxiety
(42.6%),
(42.5%),
stress
(37%),
general
health
wellbeing
(37%).
Fifty-four
per
cent
less
than
50
mg
daily,
72.6%
used
sublingually.
Adjusted
logistic
models
show
females
had
lower
odds
males
[OR
0.45,
95%
CI
0.30–0.72]
post-workout
muscle-soreness
0.46,
95%CI
0.24–0.91]
but
higher
1.60,
0.02–2.49]
insomnia
1.87,
1.13–3.11].
Older
individuals
wellbeing,
sore
muscles,
skin
conditions,
focusing,
pain.
Respondents
that
effective
problems,
those
drug
conditions.
Conclusion
This
indicated
take
manage
other
symptoms,
often
low
doses,
these
vary
by
demographic
characteristics.
Further
research
required
how
representative
user,
might
impact
mental
symptoms
problems.
British Journal of Pharmacology,
Journal Year:
2020,
Volume and Issue:
177(21), P. 4967 - 4970
Published: June 10, 2020
Identifying
drugs
effective
in
the
new
coronavirus
disease
2019
(COVID‐19)
is
crucial,
pending
a
vaccine
against
SARS‐CoV2.
We
suggest
hypothesis
that
cannabidiol
(CBD),
non‐psychotropic
phytocannabinoid,
has
potential
to
limit
severity
and
progression
of
for
several
reasons:‐
(a)
High‐cannabidiol
Cannabis
sativa
extracts
are
able
down‐regulate
expression
two
key
receptors
SARS‐CoV2
models
human
epithelia,
(b)
exerts
wide
range
immunomodulatory
anti‐inflammatory
effects
it
can
mitigate
uncontrolled
cytokine
production
responsible
acute
lung
injury,
(c)
being
PPARγ
agonist,
display
direct
antiviral
activity
(d)
agonists
regulators
fibroblast/myofibroblast
activation
inhibit
development
pulmonary
fibrosis,
thus
ameliorating
function
recovered
patients.
hope
our
hypothesis,
corroborated
by
preclinical
evidence,
will
inspire
further
targeted
studies
test
as
support
drug
COVID‐19
pandemic.
Linked
Articles
This
article
part
themed
issue
on
The
Pharmacology
COVID‐19.
To
view
other
articles
this
section
visit
http://onlinelibrary.wiley.com/doi/10.1111/bph.v177.21/issuetoc
Cell Death and Disease,
Journal Year:
2020,
Volume and Issue:
11(8)
Published: Sept. 1, 2020
Abstract
Cannabidiol
(CBD)
is
a
non-intoxicating
phytocannabinoid
from
cannabis
sativa
that
has
demonstrated
anti-inflammatory
effects
in
several
inflammatory
conditions
including
arthritis.
However,
CBD
binds
to
receptors
and
enzymes
and,
therefore,
its
mode
of
action
remains
elusive.
In
this
study,
we
show
increases
intracellular
calcium
levels,
reduces
cell
viability
IL-6/IL-8/MMP-3
production
rheumatoid
arthritis
synovial
fibroblasts
(RASF).
These
were
pronounced
under
by
activating
transient
receptor
potential
ankyrin
(TRPA1),
opening
the
mitochondrial
permeability
transition
pore.
Changes
determined
using
fluorescent
dyes
Cal-520/PoPo3
together
with
titer
blue
luminescent
dye
RealTime-glo.
Cell-based
impedance
measurements
conducted
XCELLigence
system
TRPA1
protein
was
detected
flow
cytometry.
Cytokine
evaluated
ELISA.
reduced
viability,
proliferation,
IL-6/IL-8
RASF.
Moreover,
increased
uptake
cationic
PoPo3
RASF,
which
enhanced
pre-treatment
TNF.
Concomitant
incubation
antagonist
A967079
but
not
TRPV1
capsazepine
on
uptake.
addition,
an
inhibitor
pore,
cyclosporin
A,
also
blocked
IL-8
production.
inhibited
voltage-dependent
anion-selective
channel
DIDS
Decynium-22,
for
all
organic
cation
transporter
isoforms.
RASF
targets.
This
effect
TNF
suggesting
preferentially
targets
activated,
pro-inflammatory
Thus,
possesses
anti-arthritic
activity
might
ameliorate
via
targeting
conditions.