Gut Microbes,
Journal Year:
2024,
Volume and Issue:
16(1)
Published: Nov. 27, 2024
Gut
microbiota
exert
functions
of
high
importance
in
the
intestine.
Furthermore,
there
is
increasing
evidence
for
its
role
immune
regulation
and
maintenance
homeostasis
many
physiological
processes
taking
place
distant
tissues.
In
particular,
this
review,
we
explore
impact
metabolites
produced
by
gut
on
development
atopic
dermatitis
(AD).
Probiotics
prebiotics
balance
promote
generation
bacterial
metabolites,
such
as
short-chain
fatty
acids
tryptophan
derivates,
which
exacerbated
AD
response
through
regulatory
T
cells
IL-10
TGF-β
cytokines.
Metabolites
also
have
a
direct
action
keratinocytes
once
they
reach
bloodstream.
Besides,
probiotics
decrease
levels
associated
with
onset,
phenols.
Understanding
all
these
crosstalk
between
skin
reveals
number
possibilities,
mainly
manipulation
microbiome,
may
represent
therapeutic
strategies
that
can
contribute
to
standard
treatments
patients
improve
their
quality
life.
Metabolites,
Journal Year:
2023,
Volume and Issue:
13(11), P. 1166 - 1166
Published: Nov. 20, 2023
Tryptophan
metabolism
and
gut
microbiota
form
an
integrated
regulatory
axis
that
impacts
immunity,
metabolism,
cancer.
This
review
consolidated
current
knowledge
on
the
bidirectional
interactions
between
microbial
tryptophan
processing
host.
We
focused
how
microbiome
controls
breakdown
via
indole,
kynurenine,
serotonin
pathways.
Dysbiosis
of
induces
disruptions
in
catabolism
which
contribute
to
disorders
like
inflammatory
conditions,
neuropsychiatric
diseases,
metabolic
syndromes,
These
affect
immune
homeostasis,
neurotransmission,
gut-brain
communication.
Elucidating
mechanisms
modulation
could
enable
novel
therapeutic
approaches
psychobiotics
microbiome-targeted
dietary
interventions.
Overall,
further
research
microbiota-tryptophan
has
potential
revolutionize
personalized
diagnostics
treatments
for
improving
human
health.
Journal of Cellular and Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
29(2)
Published: Jan. 1, 2025
ABSTRACT
The
clinical
application
of
doxorubicin
(DOX)
is
limited
due
to
its
cardiotoxicity,
which
primarily
attributed
interaction
with
iron
in
mitochondria,
leading
lipid
peroxidation
and
myocardial
ferroptosis.
This
study
aimed
investigate
the
role
gut
microbiota‐derived
metabolite,
indole‐3‐lactic
acid
(ILA),
mitigating
DOX‐induced
cardiotoxicity
(DIC).
Cardiac
function,
pathological
changes,
ferroptosis
were
assessed
vivo.
cardioprotective
effects
mechanisms
ILA
explored
using
multi‐omics
approaches,
including
single‐nucleus
RNA
sequencing
(snRNA‐seq)
bulk
RNA‐seq,
further
validated
Nrf2
knockout
mice.
findings
revealed
that
DOX
treatment
disrupted
microbiota,
significantly
reducing
levels
tryptophan
metabolite
ILA.
In
DIC
models,
supplementation
markedly
improved
cardiac
reduced
collagen
deposition,
mitigated
atrophy.
snRNA‐seq
analyses
indicated
played
a
crucial
Experimental
data
demonstrated
decreased
both
mice
DOX‐treated
H9C2
cells,
evidenced
by
restoration
GPX4
SLC7A11
reduction
ACSL4.
Mechanistically,
functions
as
ligand
for
aryl
hydrocarbon
receptor
(AhR),
upregulation
expression.
protective
against
abolished
silencing
AhR.
Moreover,
beneficial
on
eliminated
Nrf2‐deficient
conclusion,
exerts
therapeutic
inhibiting
through
activation
AhR/Nrf2
signalling
pathway.
Identifying
microbial
could
offer
viable
strategies
DIC.
International Immunology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 13, 2024
Abstract
The
intricate
and
dynamic
tryptophan
(Trp)
metabolic
pathway
in
both
the
microbiome
host
cells
highlights
its
profound
implications
for
health
disease.
This
involves
complex
interactions
between
cellular
bacteria
processes,
producing
bioactive
compounds
such
as
5-hydroxytryptamine
(5-HT)
kynurenine
derivatives.
Immune
responses
to
Trp
metabolites
through
specific
receptors
have
been
explored,
highlighting
role
of
aryl
hydrocarbon
receptor
inflammation
modulation.
Dysregulation
this
is
implicated
various
diseases,
Alzheimer’s
Parkinson’s
mood
disorders,
neuronal
autoimmune
diseases
multiple
sclerosis
(MS),
cancer.
In
article,
we
describe
impact
5-HT,
Trp,
indole,
on
Furthermore,
review
microbiome-derived
that
affect
immune
contribute
maintaining
homeostasis,
especially
an
experimental
encephalitis
model
MS.
Gut Microbes,
Journal Year:
2024,
Volume and Issue:
16(1)
Published: Oct. 3, 2024
Despite
achieving
endoscopic
remission,
over
20%
of
inflammatory
bowel
disease
(IBD)
patients
experience
chronic
abdominal
pain.
Visceral
pain
and
the
microbiome
exhibit
sex-dependent
interactions,
while
visceral
in
IBD
shows
a
sex
bias.
Our
aim
was
to
evaluate
whether
post-inflammatory
microbial
perturbations
contribute
hypersensitivity
manner.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 6, 2025
Xueshuantong
injection
(Lyophilized)
(XSTI)
is
widely
used
to
treat
cardiovascular
and
cerebrovascular
diseases.
However,
anaphylactoid
reactions
(ARs)
are
frequently
reported
as
one
of
its
side
effects,
the
mechanisms
ARs
their
relationship
with
different
immune
status
still
not
well
understood.
This
article
aims
examine
sensitizing
effect
XSTI,
explore
impact
normal
immunocompromised
states
on
ARs,
analyze
AR-related
metabolic
pathways
by
metabolomics.
An
mouse
model
was
established
through
intraperitoneal
cyclophosphamide
(CTX).
Normal
mice
were
then
treated
saline
(NS),
histamine
(HIS),
respectively.
Behavioral
responses,
auricle
blue
staining,
Evans
(EB)
exudation
indices
evaluate
sensitization
XSTI
both
mice.
Subsequently,
models
statuses
established,
validated
measuring
four
serum
indicators
using
enzyme-linked
immunosorbent
assay
(ELISA).
Finally,
LC-MS
metabolomics
analysis
performed
pathways.
The
intensity
induced
in
found
increase
administered
dose,
exhibiting
higher
AR
intensities
compared
Metabolomic
revealed
significant
changes
XSTI-treated
predicted
from
these
metabolites
include
biotin
metabolism,
histidine
glycerolipid
bile
secretion,
arachidonic
acid
sphingolipid
niacin
nicotinamide
tryptophan
steroid
biosynthesis,
arginine
proline
metabolism.
Research
indicated
that
dose-dependent,
weakened
functions
exhibit
lower
sensitivity.
Through
research,
differential
analyzed,
inducing
predicted.
study
offers
guidance
safe
medication
perspective
organism
susceptibility
lays
a
foundation
for
research
potential
ARs.
IntroductionHepatic
injury
(HI),
characterized
by
the
impairment
of
liver
tissue,
can
be
precipitated
a
multitude
factors
including
trauma,
pharmacological
agents,
and
pathologies,
leading
to
spectrum
functional
anomalies
associated
clinical
sequelae.
Despite
longstanding
application
Dianthus
Superbus
L.
(DS)
in
management
hepatic
disorders,
precise
pathways
through
which
it
modulates
gut
microbiota
their
byproducts
alleviate
damage
remain
largely
elusive.ObjectivesIts
purpose
is
identify
underlying
mechanisms
DS's
therapeutic
effects
on
CCL4-induced
HI
rats.MethodsDS
components
were
analyzed
using
Ultra
Performance
Liquid
Chromatography-Mass
Spectrometer
(UPLC-MS/MS).A
40%
model
SD
rats
was
used
evaluate
efficacy
DS
biochemical
marker
assessment.
Liver
tissue
examined
immunohistochemically
determine
expression
collagen-I
-SMA,
as
well
ZO-1
Occludin
colon
tissues.
Non-targeted
metabolomics
analysis
performed
serum
samples,
while
16S
rDNA
targeted
tryptophan
conducted
fecal
samples.
Further
experiments
investigating
role
included
antibiotic
treatment
transplantation
(FMT).ResultsThis
study
identified
30
chemical
constituents
DS,
correlated
with
disease.
Our
findings
indicate
that
induced
CCL4
show
an
inhibition
DS.A
significant
reduction
mRNA
levels
α-SMA
(p<0.05)
Collagen
I(p<0.05)
detected
immunohistochemistry,
indicating
decrease
severity
HI,and
increase
ZO-1(p<0.05)
Occludin(p<0.05)
colonic
suggesting
improvement
intestinal
barrier
function.
Similar
trends
observed
α-SMA(p<0.05)
I
recipient
underwent
FMT
DS.
metabolomic
indicated
may
exert
hepatoprotective
influencing
biosynthesis
steroid
hormones,
purine
metabolism,
metabolism.
Analysis
gene
sequences
demonstrated
abundance
beneficial
bacterial
groups
such
HT002,
Lactobacillaceae,
Lactobacillus,
Romboutsia.
Transplantation
from
DS-treated
led
enrichment
Lactobacillus
probiotics
relative
pseudo-sterile
controls.
Targeted
feces
restored
multiple
metabolites
normal,
improve
modulating
immune
responses,
reducing
oxidative
stress,
enhancing
function.ConclusionIn
microbiota-dependent
manner,
ameliorates
metabolism
.
It
appears
have
potential
use
modulator
prevention
HI.