Addiction,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 30, 2025
Abstract
Background
and
aims
This
is
the
first
systematic
review
of
extant
literature
on
all
major
psychedelic‐assisted
treatment
for
alcohol
use
disorder
(AUD),
tobacco
(TUD)
other
substance
disorders
(SUD).
We
aimed
to
summarise
evidence
efficacy
AUD,
TUD,
SUD;
evaluate
its
quality;
offer
recommendations
research.
Methods
was
a
prospectively
registered
narrative
open‐label,
randomised
controlled
trials
(RCT),
observational
studies
d‐lysergic
acid
diethylamide
(LSD),
mescaline,
psilocybin,
ayahuasca,
ketamine,
ibogaine
3,4‐methylenedioxymethamphetamine
(MDMA).
Eligible
had
SUD
outcome
measures
including
craving,
use,
relapse,
remission.
Study
quality
evaluated
using
Cochrane
Collaboration
Risk
Bias
(RoB),
RoB
in
Non‐randomised
Studies
Interventions
tool.
Certainty
RCTs
judged
Grading
Recommendations,
Assessment,
Development,
Evaluations
(GRADE)
Findings
37
(2035
participants)
were
reviewed:
LSD
(14;
n
=
1047);
mescaline
(1;
7);
psilocybin
(4;
135);
ayahuasca
(3;
101);
ketamine
(10;
579);
(5;
166);
MDMA
14).
There
no
serious
adverse
events
reported
any
study.
A
two‐centre,
placebo‐controlled,
phase
2
superiority
RCT
double‐blind,
four‐arm,
placebo‐controlled
AUD
yielded
best
efficacy.
Progression
support
3
secured
from
an
open‐label
study
TUD
nine
cannabis
disorder,
cocaine
opioid
(all
with
high‐RoB
low‐GRADE
certainty).
Conclusions
Psilocybin‐assisted
appears
have
among
treatments
alcohol,
tobacco,
disorders.
Future
research
should
report
safety
events;
screen
person‐level
characteristics
indicating
that
contraindicated;
strive
mitigate
blinding
participants
interventions;
factorial
designs
drug
psychotherapy
trials;
build
consensus
field‐specific
Core
Outcome
Set.
Military Psychology,
Journal Year:
2023,
Volume and Issue:
36(2), P. 184 - 191
Published: Feb. 1, 2023
This
study
evaluated
prospective
associations
of
ibogaine
and
5-MeO-DMT
treatment
for
risky
alcohol
use
post-traumatic
stress
disorder
(PTSD)
symptoms
among
United
States
(US)
Special
Operations
Forces
Veterans
(SOFV).
Data
were
collected
during
standard
clinical
operations
at
pre-treatment
1-month
(1
m),
3-months
(3
6-months
(6
m)
post-treatment
in
an
program
Mexico.
Of
the
86
SOFV
that
completed
treatment,
45
met
criteria
(mean
age
=
44;
male
100%;
White
91%).
There
was
a
significant
reduction
from
(M
7.2,
SD
2.3)
to
1
m
3.6;
3.5)
post-treatment,
which
remained
reduced
through
6
4.0;
2.9;
p
<
.001,
partial
eta
squared
.617).
At
m,
24%
abstinent,
33%
non-risky
drinking,
42%
drinkers.
16%
31%
53%
no
differences
between
responders
(abstinent/non-risky
drinkers)
non-responders
(risky
demographics/clinical
characteristics.
However,
there
very
large
PTSD
symptom
(p
.01,
d
−3.26)
cognitive
functioning
change
−0.99).
Given
these
findings,
future
trials
should
determine
whether
psychedelic-assisted
therapy
holds
promise
individuals
with
complex
trauma
misuse
who
have
not
been
successfully
treated
traditional
interventions.
Frontiers in Pharmacology,
Journal Year:
2021,
Volume and Issue:
12
Published: Nov. 3, 2021
Background
and
Purpose:
Mitragyna
speciosa
extract
kratom
alkaloids
decrease
alcohol
consumption
in
mice
at
least
part
through
actions
the
δ-opioid
receptor
(δOR).
However,
most
potent
opioidergic
alkaloid,
7-hydroxymitragynine,
exhibits
rewarding
properties
hyperlocomotion
presumably
due
to
preferred
affinity
for
mu
opioid
(µOR).
We
hypothesized
that
like
paynantheine
speciogynine
with
reduced
µOR
potency
could
provide
a
starting
point
developing
opioids
an
improved
therapeutic
window
treat
use
disorder.
Experimental
Approach:
characterized
paynantheine,
speciociliatine,
four
novel
kratom-derived
analogs
their
ability
bind
activate
δOR,
µOR,
κOR.
Select
were
assessed
behavioral
assays
male
C57BL/6N
WT
δOR
knockout
mice.
Key
Results:
Paynantheine
(10
mg∙kg
−1
,
i.p.)
produced
aversion
limited
conditioned
place
preference
(CPP)
paradigm
but
did
not
produce
CPP
additional
conditioning
sessions.
robust
antinociception
block
morphine-induced
hyperlocomotion.
Yet,
10
30
doses
(i.p.),
counteract
morphine
CPP.
7-hydroxypaynantheine
7-hydroxyspeciogynine
displayed
relative
7-hydroxymitragynine
vitro
dose-dependently
decreased
voluntary
KO
has
maximally
tolerated
dose
of
(s.c.)
which
it
significant
neither
alter
general
locomotion
nor
induce
noticeable
seizures.
Conclusion
Implications:
Derivatizing
goal
enhancing
reducing
off-target
effects
pathway
develop
lead
compounds
disorder
window.
Journal of Psychedelic Studies,
Journal Year:
2021,
Volume and Issue:
5(2), P. 69 - 82
Published: July 15, 2021
Abstract
Background
Few
studies
have
assessed
the
epidemiology
of
hallucinogenic
substance
use
among
racial
and
ethnic
groups
varying
age
cohorts.
Use
psychedelic
substances
may
differ
people
color
(POC),
due
to
factors
such
as
stigma
discriminatory
drug
enforcement
practices
against
POC.
The
lack
inclusion
POC
in
research
further
underscores
importance
identifying
differences
racial/ethnic
Methods
Data
from
2018
National
Survey
on
Drug
Health
(NSDUH)
was
used
for
this
analysis
(
N
=
56,313,
unweighted),
representative
non-institutionalized
U.S.
population.
Proportions
lifetime
hallucinogen
by
race/ethnicity
were
compared.
past
year
rates
compared
examine
cohort.
Results
Approximately
15.9%
population
over
12
had
a
at
some
point
their
2.0%
year.
Lifetime
most
prevalent
non-Hispanic
White
multi-racial
individuals,
while
Black/African
Americans
reported
lowest
use.
also
highest
proportions
12–34
olds,
individuals
35–49
olds.
Hispanic
higher
12–17
cohort,
but
lower
26–49
old
12–25
50+
older
cohorts
Limitations
is
cross-sectional
self-reported.
“Race”
social
construction
subject
change
time,
NSDUH
ethnoracial
categories
are
limited.
Institutionalized
populations
not
included
study.
Conclusions
Significant
observed.
Findings
work
inform
education,
interventions,
therapeutic
research.
Addiction,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 30, 2025
Abstract
Background
and
aims
This
is
the
first
systematic
review
of
extant
literature
on
all
major
psychedelic‐assisted
treatment
for
alcohol
use
disorder
(AUD),
tobacco
(TUD)
other
substance
disorders
(SUD).
We
aimed
to
summarise
evidence
efficacy
AUD,
TUD,
SUD;
evaluate
its
quality;
offer
recommendations
research.
Methods
was
a
prospectively
registered
narrative
open‐label,
randomised
controlled
trials
(RCT),
observational
studies
d‐lysergic
acid
diethylamide
(LSD),
mescaline,
psilocybin,
ayahuasca,
ketamine,
ibogaine
3,4‐methylenedioxymethamphetamine
(MDMA).
Eligible
had
SUD
outcome
measures
including
craving,
use,
relapse,
remission.
Study
quality
evaluated
using
Cochrane
Collaboration
Risk
Bias
(RoB),
RoB
in
Non‐randomised
Studies
Interventions
tool.
Certainty
RCTs
judged
Grading
Recommendations,
Assessment,
Development,
Evaluations
(GRADE)
Findings
37
(2035
participants)
were
reviewed:
LSD
(14;
n
=
1047);
mescaline
(1;
7);
psilocybin
(4;
135);
ayahuasca
(3;
101);
ketamine
(10;
579);
(5;
166);
MDMA
14).
There
no
serious
adverse
events
reported
any
study.
A
two‐centre,
placebo‐controlled,
phase
2
superiority
RCT
double‐blind,
four‐arm,
placebo‐controlled
AUD
yielded
best
efficacy.
Progression
support
3
secured
from
an
open‐label
study
TUD
nine
cannabis
disorder,
cocaine
opioid
(all
with
high‐RoB
low‐GRADE
certainty).
Conclusions
Psilocybin‐assisted
appears
have
among
treatments
alcohol,
tobacco,
disorders.
Future
research
should
report
safety
events;
screen
person‐level
characteristics
indicating
that
contraindicated;
strive
mitigate
blinding
participants
interventions;
factorial
designs
drug
psychotherapy
trials;
build
consensus
field‐specific
Core
Outcome
Set.