bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: Dec. 7, 2022
Abstract
The
gut-brain
axis
is
increasingly
recognized
as
an
important
pathway
involved
in
cocaine
use
disorder.
Microbial
products
of
the
murine
gut
have
been
shown
to
affect
striatal
gene
expression,
and
depletion
microbiome
by
antibiotic
treatment
alters
cocaine-induced
behavioral
sensitization
C57BL/6J
male
mice.
Some
reports
suggest
that
correlated
with
drug
self-administration
behavior
Here
we
profile
composition
naïve
its
response
two
Collaborative
Cross
(CC)
strains.
These
strains
display
extremely
divergent
responses
sensitization.
A
high-responding
strain,
CC004/TauUncJ
(CC04),
has
a
contains
greater
amount
Lactobacillus
than
cocaine-nonresponsive
strain
CC041/TauUncJ
(CC41).
CC41
characterized
abundance
Eisenbergella,
Robinsonella
Ruminococcus
.
In
cocaine,
CC04
increased
Barnsiella
population,
while
displays
no
significant
changes.
PICRUSt
functional
analysis
potential
shows
number
modules
altered
after
exposure
specifically
those
encoding
for
tryptophan
synthesis,
glutamine
metabolism,
menaquinone
synthesis
(vitamin
K2).
Depletion
revealed
cocaine-sensitization
following
antibiotics
female
Depleting
males
infusions
during
intravenous
dose-response
curve.
Together
these
data
genetic
differences
cocaine-related
behaviors
may
involve
microbiome.
FUNDING
U01DA043809
JAB,
GMW
P50DA039841
EJC
Brain Sciences,
Journal Year:
2024,
Volume and Issue:
14(6), P. 558 - 558
Published: May 30, 2024
Mood
disorders
and
substance
use
disorder
(SUD)
are
of
immense
medical
social
concern.
Although
significant
progress
on
neuronal
involvement
in
mood
reward
circuitries
has
been
achieved,
it
is
only
relatively
recently
that
the
role
glia
these
attracted
attention.
Detailed
understanding
glial
functions
devastating
diseases
could
offer
novel
interventions.
Here,
following
a
brief
review
involved
regulation
perception,
specific
contributions
neurotrophic
factors,
neuroinflammation,
gut
microbiota
to
highlighted.
In
this
context,
cells
(e.g.,
microglia,
astroglia,
oligodendrocytes,
synantocytes)
phenotypic
manifestation
or
SUD
emphasized.
addition,
knowledge
potential
development
therapeutics
touched
upon.
Brain Sciences,
Journal Year:
2024,
Volume and Issue:
14(8), P. 769 - 769
Published: July 30, 2024
Substance
use
disorders
(SUDs)
are
complex
biopsychosocial
diseases
that
cause
neurocognitive
deficits
and
neurological
impairments
by
altering
the
gene
expression
in
reward-related
brain
areas.
Repeated
drug
gives
rise
to
alterations
DNA
methylation,
histone
modifications,
of
microRNAs
several
areas
may
be
associated
with
development
psychotic
symptoms.
The
first
section
this
review
discusses
how
substance
contributes
symptoms
via
epigenetic
alterations.
Then,
we
present
more
evidence
about
link
between
SUDs
next
presents
associations
paternal
maternal
exposure
substances
brains
offspring
role
diet
preventing
substance-induced
impairments.
introduce
potential
therapeutic
agents/approaches
such
as
methyl-rich
diets
modify
for
alleviating
or
depression
SUDs.
Next,
discuss
use–gut
microbiome
interactions
contribute
through
gut
microbiome-derived
metabolites
become
new
therapeutics
normalizing
aberrations.
Finally,
address
possible
challenges
future
perspectives
patients
modulating
diets,
epigenome,
microbiome.
BMC Medicine,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: Jan. 21, 2025
Abstract
Background
The
co-occurrence
of
diabetes
and
mental
disorders
is
an
exceedingly
common
comorbidity
with
poor
prognosis.
We
aim
to
investigate
the
impact
green
space,
garden
natural
environment
on
risk
among
population
living
diabetes.
Methods
performed
a
longitudinal
analysis
based
39,397
participants
from
UK
Biobank.
Residential
space
modeled
land
use
data
Land
Cover
Map
were
assigned
residential
address
for
each
participant.
Cox
proportional
hazards
model
was
used
analyze
associations
between
nature
exposures
Casual
mediation
quantify
indirect
effect
air
pollution.
Results
During
mean
follow-up
7.55
years,
4513
incident
cases
identified,
including
2952
depressive
1209
anxiety
disorders.
Participants
at
300
m
buffer
in
second
third
tertiles
had
7%
(HR
=
0.93,
95%CI:
0.86–0.99)
12%
0.88,
0.82–0.94)
lower
risks
compared
those
first
tertile,
respectively.
incidence
patients
will
decrease
by
13%
when
exposed
tertile
buffer.
individually
prevented
6.65%
10.18%
incidents
patients.
statistically
decreased
1000
0.84,
95%
CI:
0.78–0.90).
Protective
effects
three
against
also
observed.
Air
pollution,
particularly
nitrogen
dioxide,
oxides,
fine
particulate
matter,
significantly
contributed
disorders,
mediating
48.3%,
29.2%,
62.4%
associations,
Conclusions
could
mitigate
patients,
pollution
playing
vital
mediator.
This
highlights
potential
local
governments
enhance
sustainability
such
interventions,
grounded
public
health
urban
planning,
through
strategic
planning
initiatives.
Graphical
Abstract
The
gut‐brain
axis
is
increasingly
recognized
as
an
important
pathway
involved
in
cocaine
use
disorder.
Microbial
products
of
the
murine
gut
have
been
shown
to
affect
striatal
gene
expression,
and
depletion
microbiome
by
antibiotic
treatment
alters
cocaine‐induced
behavioral
sensitization
C57BL/6J
male
mice.
Some
reports
suggest
that
correlated
with
drug
self‐administration
behavior
Here,
we
profile
composition
naïve
its
response
two
collaborative
cross
(CC)
strains.
These
strains
display
extremely
divergent
responses
sensitization.
A
high‐responding
strain,
CC004/TauUncJ
(CC04),
has
a
contains
greater
amount
Lactobacillus
than
cocaine‐nonresponsive
strain
CC041/TauUncJ
(CC41).
CC41
characterized
abundance
Eisenbergella
,
Robinsonella
Ruminococcus.
In
cocaine,
CC04
increased
Barnsiella
population,
while
displays
no
significant
changes.
PICRUSt
functional
analysis
potential
shows
number
modules
altered
after
exposure
specifically
those
encoding
for
tryptophan
synthesis,
glutamine
metabolism,
menaquinone
synthesis
(vitamin
K2).
Depletion
revealed
cocaine‐sensitization
following
antibiotics
female
Depleting
males
infusions
during
intravenous
dose–response
curve.
Together
these
data
genetic
differences
cocaine‐related
behaviors
may
involve
microbiome.
World Journal of Clinical Cases,
Journal Year:
2024,
Volume and Issue:
12(14), P. 2359 - 2369
Published: April 29, 2024
BACKGROUND
Non-alcoholic
fatty
liver
disease
(NAFLD)
and
alcohol-related
(ArLD)
constitute
the
primary
forms
of
chronic
disease,
their
incidence
is
progressively
increasing
with
changes
in
lifestyle
habits.
Earlier
studies
have
documented
a
correlation
between
occurrence
development
prevalent
mental
disorders
liver.
AIM
To
investigate
disorders,
thus
necessitating
implementation
mendelian
randomization
(MR)
study
to
elucidate
this
association.
METHODS
Data
on
NAFLD
ArLD
were
retrieved
from
genome-wide
association
catalog,
while
information
including
Alzheimer's
schizophrenia,
anxiety
disorder,
attention
deficit
hyperactivity
disorder
(ADHD),
bipolar
major
depressive
multiple
personality
obsessive-compulsive
(OCD),
post-traumatic
stress
(PTSD),
schizophrenia
was
acquired
psychiatric
genomics
consortium.
A
two-sample
MR
method
applied
mediators
significant
associations.
RESULTS
After
excluding
weak
instrumental
variables,
causal
relationship
identified
some
disorders.
Specifically,
findings
indicated
that
associated
significantly
elevated
risk
developing
ADHD
(OR:
5.81,
95%CI:
5.59-6.03,
P
<
0.01),
5.73,
5.42-6.05,
=
0.03),
OCD
6.42,
5.60-7.36,
PTSD
5.66,
5.33-6.01,
0.01).
Meanwhile,
increased
55.08,
3.59-845.51,
61.50,
6.69-565.45,
52.09,
4.24-639.32,
CONCLUSION
Associations
found
genetic
predisposition
an
broad
range
namely
OCD,
PTSD,
highlighting
significance
preventive
measures
against
patients
disease.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(6), P. e0302195 - e0302195
Published: June 12, 2024
Individuals
with
Alcohol
Use
Disorder
(AUD)
typically
have
comorbid
chronic
health
conditions,
including
anxiety
and
depression
disorders,
increased
sleep
disruption,
poor
nutrition
status,
along
gut
microbial
dysbiosis.
To
better
understand
the
effects
of
dysbiosis
previously
shown
in
individuals
AUD,
microbiome
metabolome
were
investigated
between
three
cohorts.
Two
groups
AUD
included
treatment-seeking
newly
abstinent
for
at
least
six
weeks
(AB:
N
=
10)
non-treatment-seeking
currently
drinking
(CD:
9)
individuals.
The
third
group
was
age,
gender,
BMI-matched
healthy
controls
(HC:
12).
Deep
phenotyping
during
two
outpatient
National
Institutes
Health
Clinical
Center
visits
performed,
clinical,
psychological,
medical,
metabolic,
dietary,
experimental
assessments.
Alpha
beta
diversity
differential
taxa
metabolite
abundance
examined
across
groups.
Metabolites
derived
from
lipid
super-pathway
identified
to
be
more
abundant
AB
compared
CD
HC
appeared
most
clinically
different
respect
their
metabolome.
These
findings
highlight
potential
long-term
alcohol
use
even
short-term
abstinence.
Major
depressive
disorder
(MDD)
and
substance
use
(SUD)
are
of
immense
medical
social
concerns.
Although
significant
progress
on
neuronal
involvement
in
mood
reward
circuitries
has
been
achieved,
only
relatively
recently
the
role
glia
these
disorders
have
attracted
attention.
Detail
understanding
glial
function
devastating
diseases
could
offer
novel
interventions.
Here,
following
a
brief
review
involved
regulation
perception,
specific
contribution
neurotrophic
factors,
neuroinflammation
gut
microbiota
to
highlighted.
In
this
context,
cells
(e.g.,
microglia,
astroglia,
oligodendrocytes
synantocytes)
phenotypic
manifestation
MDD
or
SUD
emphasized.
addition,
potential
knowledge
developing
therapeutics
is
touched
upon.