Cureus,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 19, 2025
N,
N-dimethyltryptamine
(DMT)
is
a
potent
hallucinogenic
compound
with
increasing
recreational
use
despite
limited
safety
data.
While
DMT
has
been
linked
to
psychosis,
delusional
parasitosis
as
specific
manifestation
remains
unreported.
We
present
novel
case
of
60-year-old
female
veteran
chronic
post-traumatic
stress
disorder
(PTSD),
history
major
depressive
disorder,
past
marijuana
use,
and
no
prior
psychiatric
hospitalizations,
who
developed
persistent
delusions
parasitic
infestation
following
prolonged
intravenous
(IV)
DMT.
She
was
referred
acute
inpatient
psychiatry
by
the
residential
PTSD
program
in
same
hospital
system,
where
she
expressed
upon
intake
there
strong
conviction
that
worms
were
coming
out
her
skin.
Upon
admission
psychiatry,
patient
presented
severe
anxiety
about
minor
appearing
skin
excoriations.
These
likely
result
consequent
precipitator
delusion
parasite-infected
eight
months
ago
during
plumbing
leak
home.
A
review
records
revealed
endorsement
these
symptoms
multiple
providers
over
months.
also
reported
using
IV
at
home
1-2
times
per
month
for
18
As
timing
hallucinogen
development
psychotic
not
fully
consistent,
concern
primary
exacerbated
substance
use.
Her
persisted
initial
haloperidol
treatment
initiated
hospitalization
but
improved
after
15
days
hospitalization,
clearance
psychoeducation.
This
suggests
potential
link
between
parasitosis,
published
studies
have
specifically
explored
this
association,
highlighting
need
further
research,
particularly
repeated
administration.
Biological Psychiatry Cognitive Neuroscience and Neuroimaging,
Journal Year:
2024,
Volume and Issue:
9(5), P. 472 - 489
Published: Feb. 1, 2024
Psychedelic
compounds,
including
psilocybin,
LSD,
DMT,
and
5-MeO-DMT
all
of
which
are
serotonin
(5-HT)
2A
receptor
agonists
being
investigated
as
potential
treatments.
This
review
aims
to
summarize
the
current
clinical
research
on
these
four
compounds
mescaline
guide
future
research.
Their
mechanism/s
action,
pharmacokinetics,
pharmacodynamics,
efficacy,
safety
were
reviewed.
While
evidence
for
therapeutic
indications,
with
exception
psilocybin
depression,
is
still
relatively
scarce,
we
noted
no
differences
in
psychedelic
effects
beyond
effect
duration.
It
remains
therefore
unclear
whether
different
profiles
contribute
compounds.
More
needed
differentiate
order
inform
might
be
best
uses.
Frontiers in Psychiatry,
Journal Year:
2024,
Volume and Issue:
14
Published: Jan. 8, 2024
There
is
growing
scientific
evidence
for
the
therapeutic
benefits
of
Amazonian
plant-based
psychedelic
"ayahuasca"
neuropsychiatric
disorders
such
as
depression
and
anxiety.
However,
there
are
certain
challenges
when
incorporating
botanical
ayahuasca
into
biomedical
research
clinical
therapy
environments.
Formulations
inspired
by
ayahuasca,
which
contain
specific
standardized
active
components,
a
potential
remedy.
American Journal of Psychiatry,
Journal Year:
2025,
Volume and Issue:
182(1), P. 33 - 46
Published: Jan. 1, 2025
Unlike
classical
antidepressants,
psychedelics
such
as
psilocybin
have
been
shown
to
induce
a
rapid
antidepressant
response.
In
the
wake
of
this
development,
interest
has
emerged
in
ultra-fast,
short-acting
5-methoxy-N,N-dimethyltryptamine
(5-MeO-DMT)
and
N,N-dimethyltryptamine
(DMT)
with
expectation
that
these
can
produce
effects
following
an
intense
but
brief
psychedelic
intervention.
The
current
paper
reviews
clinical
pharmacology
5-MeO-DMT
DMT
their
potential
benefits
challenges
treatment
depression.
Both
compounds
display
affinities
for
variety
monoamine
receptors
transporters,
mostly
so
serotonergic
(5HT)
receptors,
including
5HT
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Feb. 7, 2024
Abstract
Psilocybin,
a
serotonergic
psychedelic,
is
being
increasingly
researched
in
clinical
studies
for
the
treatment
of
psychiatric
disorders.
The
relatively
lengthy
duration
oral
psilocybin’s
acute
effects
(4–6
h)
may
have
pragmatic
and
cost-effectiveness
limitations.
Here,
we
explored
intravenous
(IV)
N,N-Dimethyltryptamine
(DMT),
closely
related,
but
faster-acting
psychedelic
intervention,
on
mental
health
outcomes
healthy
volunteers.
Data
reported
from
two
separate
analyses:
(1)
A
comparison
health-related
variables
1
week
after
7,
14,
18,
20
mg
IV
DMT
versus
saline
placebo
(n
=
13)
and,
(2)
prospective
dataset
assessing
before
2
weeks
17).
Mental
included
measures
depression
severity
(QIDS-SR16),
trait
anxiety
(STAI-T),
Neuroticism
(NEO-FFI),
wellbeing
(WHO-5),
meaning
life
(MLQ),
optimism
(LOT-R),
gratitude
(GQ-6).
In
both
placebo-controlled
datasets,
significant
improvements
scores
were
found
1–2
administration.
Significant
reductions
only
sample.
Finally,
changes
correlated
with
peak
experiences
(assessed
via
‘Oceanic
Boundlessness’).
While
use
cohorts
pooled
analysis
limits
generalizability
these
correlational
findings,
results
suggest
that
reduce
depressive
symptomatology
by
inducing
experiences.
short
half-life
its
potential
flexible
dosing
controlled
infusions
makes
it
an
appealing
candidate
medicine.
Further
research
samples
needed
to
corroborate
therapeutic
DMT.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 29, 2024
In
vivo
,
psilocybin
is
rapidly
dephosphorylated
to
psilocin
which
induces
psychedelic
effects
by
interacting
with
the
5-HT
2A
receptor.
Psilocin
primarily
undergoes
glucuronidation
or
conversion
4-hydroxyindole-3-acetic
acid
(4-HIAA).
Herein,
we
investigated
psilocybin’s
metabolic
pathways
in
vitro
and
conducting
a
thorough
analysis
of
enzymes
involved.
Metabolism
studies
were
performed
using
human
liver
microsomes
(HLM),
cytochrome
P450
(CYP)
enzymes,
monoamine
oxidase
(MAO),
UDP-glucuronosyltransferase
(UGT).
metabolism
was
examined
male
C57BL/6J
mice
plasma
samples.
Approximately
29%
metabolized
HLM,
while
recombinant
CYP2D6
CYP3A4
nearly
100%
40%
psilocin,
respectively.
Notably,
4-HIAA
4-hydroxytryptophol
(4-HTP)
detected
HLM
but
not
CYPs.
MAO-A
transformed
into
minimal
amounts
4-HTP.
4-HTP
only
present
.
Neither
nor
showed
relevant
interactions
at
assessed
receptors.
contrast
data,
UGT1A10
did
extensively
metabolize
Furthermore,
two
putative
metabolites
observed.
N
-methyl-4-hydroxytryptamine
(norpsilocin)
identified
(CYP2D6)
mice,
an
oxidized
metabolite
humans.
However,
genotype
influence
concentrations
study
population.
conclusion,
MAO-A,
CYP2D6,
are
involved
psilocin’s
metabolism.
The
discovery
norpsilocin
humans
further
unravels
Despite
limitations
replicating
phase
II
these
findings
hold
significance
for
studying
drug-drug
advancing
research
on
as
therapeutic
agent.
Journal of Psychopharmacology,
Journal Year:
2024,
Volume and Issue:
38(5), P. 425 - 431
Published: Feb. 22, 2024
Background:
Recent
interest
in
the
potential
therapeutic
effects
of
psychedelics
has
led
to
investigations
into
their
influence
on
molecular
signaling
pathways
within
brain.
Aims:
Integrated
review
and
analysis
different
studies
this
field.
Methods:
A
systematic
search
was
conducted
across
international
databases
including
Embase,
Scopus,
Web
Science,
PubMed
from
inception
9
July
2023.
Eligibility
criteria
encompassed
published
peer-reviewed
evaluating
changes
brain-derived
neurotrophic
factor
(BDNF)
levels
after
psychedelic
consumption.
Outcomes:
total
nine
were
included
our
study.
The
meta-analysis
demonstrated
significantly
higher
BDNF
consumers
compared
healthy
controls,
with
a
pooled
standardized
mean
difference
0.26
(95%
CI:
0.10–0.42,
I
2
=
38.51%,
p
<
0.001).
Leave-one-out
indicated
robustness
results
upon
removal
individual
psychedelics.
No
significant
publication
bias
observed.
highlight
neuroplasticity
by
altering
levels.
Conclusions:
More
precisely,
documented
rise
indicates
neurobiological
mechanism
which
could
enhance
synaptic
plasticity
foster
growth
neurons.
Given
limited
data
available
topic,
conclusions
remain
uncertain.
Consequently,
we
highly
recommend
additional
research
more
extensive
sample
sizes
yield
reliable
evidence
Clinical Pharmacokinetics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 21, 2025
N,N-Dimethyltryptamine
(DMT)
is
currently
being
studied
for
its
therapeutic
potential
in
various
psychiatric
disorders.
An
understanding
of
pharmacokinetics
(PK)
essential
to
determine
appropriate
dose
ranges
future
clinical
studies.
We
conducted
a
systematic
literature
review
on
the
PK
DMT.
Clinical
studies
that
administered
known
amounts
DMT
and
reported
data
and/or
parameters
humans
were
included.
Additionally,
raw
requested
from
authors
extracted
publications.
In
total,
219
references
retrieved,
which
13
publications
included,
covering
eight
distinct
datasets.
All
intravenously
infusion
schemes,
except
one
intramuscular
administration.
High
variability
dose-normalized
exposure
differences
bolus
versus
administration
observed.
extensively
redistributed
other
tissues,
based
biphasic
elimination
profile
high
volume
distribution
terminal
phase
(range
123–1084
L).
It
eliminated
rapidly,
with
half-life
4.8–19.0
min
clearance
8.1–46.8
L/min.
This
result
rapid
metabolization
indole-3-acetic
acid
(IAA),
also
reflected
fact
time
maximum
concentration
IAA
similar
demonstrates
have
been
characterized
limited
extent,
lack
details
regards
demographics,
absolute
doses,
parameters.
Additional
are
necessary
investigate
intersubject
following
or
prolonged
infusion.
Addressing
these
issues
development
as
pharmacotherapeutic
neuropsychiatry.
Pharmacological Reports,
Journal Year:
2023,
Volume and Issue:
75(6), P. 1362 - 1380
Published: Oct. 24, 2023
Abstract
Psychedelics
are
powerful
psychoactive
substances
that
alter
perception
and
mood
processes.
Their
effectiveness
in
the
treatment
of
psychiatric
diseases
was
known
before
their
prohibition.
An
increasing
number
recent
studies,
due
to
indisputable
resurgence
serotonergic
hallucinogens,
have
shown
efficacy
alleviating
depression,
anxiety,
substance
abuse
therapies,
existential
distress
patients
facing
life-threatening
illness.
generally
considered
be
physiologically
safe
with
low
toxicity
addictive
potential.
However,
agonism
at
receptors
should
context
possible
serotonin-related
cardiotoxicity
(5-HT2A/2B
5-HT4
receptors),
influence
on
platelet
aggregation
(5-HT2A
receptor),
proarrhythmic
The
use
psychedelics
has
also
been
associated
significant
sympathomimetic
effects
both
experimental
clinical
studies.
Therefore,
present
review
aims
provide
a
critical
discussion
cardiovascular
safety
psilocybin,
d-lysergic
acid
diethylamide
(LSD),
N,N-dimethyltryptamine,
ayahuasca,
mescaline,
based
results
research
trials
humans.
Experimental
studies
inconsistent
information
potential
psychedelics.
Data
from
point
relative
psychedelic-assisted
therapies
population
“healthy”
volunteers.
there
is
insufficient
evidence
carried
out
microdoses
psychedelics,
still
lack
data
disease.
exact
determination
psychedelic
(especially
long-term
therapies)
requires
further
research.