The Journal of Immunology,
Journal Year:
2017,
Volume and Issue:
198(2), P. 572 - 580
Published: Jan. 1, 2017
Abstract
The
mammalian
gastrointestinal
tract
and
associated
mucosal
immune
system
harbor
a
large
repertoire
of
metabolites
prokaryotic
eukaryotic
origin
that
play
important
roles
in
development
physiology.
These
often
bioactive
small
molecules
originate
from
nutrition-
environmental-related
sources,
or
are
endogenously
produced
modulated
by
the
host
its
microbiota.
A
complex
network
interactions
exists
between
intestinal
This
intimate
cross-talk
may
be
driven
metabolite
secretion
signaling,
features
profound
influences
on
immunity
physiology,
including
endocrine,
metabolic,
nervous
function
health
disease.
Alterations
microbiome-associated
levels
activity
implicated
pathogenesis
growing
number
illnesses.
In
this
review
we
discuss
influence
microbiome-modulated
metabolites,
with
an
emphasis
cell
function.
We
further
highlight
emerging
data
potentially
implicating
misbalance
host-microbiome–associated
Circulation Research,
Journal Year:
2017,
Volume and Issue:
120(7), P. 1183 - 1196
Published: March 30, 2017
Significant
interest
in
recent
years
has
focused
on
gut
microbiota-host
interaction
because
accumulating
evidence
revealed
that
intestinal
microbiota
play
an
important
role
human
health
and
disease,
including
cardiovascular
diseases.
Changes
the
composition
of
associated
with
referred
to
as
dysbiosis,
have
been
linked
pathologies
such
atherosclerosis,
hypertension,
heart
failure,
chronic
kidney
obesity,
type
2
diabetes
mellitus.
In
addition
alterations
composition,
metabolic
potential
identified
a
contributing
factor
development
Recent
studies
can
elicit
variety
effects
host.
Indeed,
microbiome
functions
like
endocrine
organ,
generating
bioactive
metabolites,
impact
host
physiology.
Microbiota
interact
through
many
pathways,
trimethylamine/trimethylamine
Frontiers in Immunology,
Journal Year:
2018,
Volume and Issue:
9
Published: April 9, 2018
Cytokine
dysregulation
is
believed
to
play
a
key
role
in
the
remodeling
of
immune
system
at
older
age,
with
evidence
pointing
an
inability
fine-control
systemic
inflammation,
which
seems
be
marker
unsuccessful
aging.
This
reshaping
cytokine
expression
pattern,
progressive
tendency
toward
pro-inflammatory
phenotype
has
been
called
'inflamm-aging'.
Despite
research
there
no
clear
understanding
about
causes
'inflamm-aging'
that
underpin
most
major
age-related
diseases
including
atherosclerosis,
diabetes,
Alzheimer's
disease,
rheumatoid
arthritis,
cancer
and
aging
itself.
While
inflammation
part
normal
repair
response
for
healing,
essential
keeping
us
safe
from
bacterial
viral
infections
noxious
environmental
agents,
not
all
good.
When
becomes
prolonged
persists,
it
can
become
damaging
destructive.
Several
common
molecular
pathways
have
identified
are
associated
both
low-grade
inflammation.
The
change
redox
balance,
increase
senescent
cells
SASP
decline
effective
autophagy
trigger
inflammasome,
suggest
may
possible
delay
itself
by
suppressing
mechanisms
or
improving
timely
resolution
Conversely
learning
genetic
long-lived
cohorts
who
exemplify
good
quality
Here
we
will
discuss
some
current
ideas
highlight
appear
contribute
imbalance
dysregulation,
'inflammageing'
parainflammation.
Evidence
these
findings
drawn
cardiovascular
disease
two
Circulation Research,
Journal Year:
2014,
Volume and Issue:
116(3), P. 448 - 455
Published: Nov. 7, 2014
Trimethylamine-N-oxide
(TMAO),
a
gut
microbial-dependent
metabolite
of
dietary
choline,
phosphatidylcholine
(lecithin),
and
l-carnitine,
is
elevated
in
chronic
kidney
diseases
(CKD)
associated
with
coronary
artery
disease
pathogenesis.To
both
investigate
the
clinical
prognostic
value
TMAO
subjects
versus
without
CKD,
test
hypothesis
that
plays
direct
contributory
role
development
progression
renal
dysfunction.We
first
examined
relationship
between
fasting
plasma
all-cause
mortality
over
5-year
follow-up
521
stable
CKD
(estimated
glomerular
filtration
rate,
<60
mL/min
per
1.73
m(2)).
Median
level
among
was
7.9
μmol/L
(interquartile
range,
5.2-12.4
μmol/L),
which
markedly
higher
(P<0.001)
than
non-CKD
(n=3166).
Within
subjects,
(fourth
quartile)
2.8-fold
increased
risk.
After
adjustments
for
traditional
risk
factors,
high-sensitivity
C-reactive
protein,
estimated
levels
remained
predictive
(hazard
ratio,
1.93;
95%
confidence
interval,
1.13-3.29;
P<0.05).
provided
significant
incremental
(net
reclassification
index,
17.26%;
P<0.001
differences
area
under
receiver
operator
characteristic
curve,
63.26%
65.95%;
P=0.036).
Among
portend
poorer
prognosis
within
cohorts
high
low
cystatin
C.
In
animal
models,
choline
or
directly
led
to
progressive
tubulointerstitial
fibrosis
dysfunction.Plasma
are
patients
long-term
survival.
Chronic
exposures
increase
contributes
dysfunction
models.
BioMed Research International,
Journal Year:
2018,
Volume and Issue:
2018, P. 1 - 8
Published: Jan. 1, 2018
Probiotics
are
microbial
strains
that
beneficial
to
health,
and
their
potential
has
recently
led
a
significant
increase
in
research
interest
use
modulate
the
gut
microbiota.
The
animal
is
complex
ecosystem
of
host
cells,
microbiota,
available
nutrients,
microbiota
prevents
several
degenerative
diseases
humans
animals
via
immunomodulation.
its
influence
on
human
nutrition,
metabolism,
physiology,
immunity
addressed,
probiotic
species
discussed
improve
understanding
modulation
This
paper
provides
broad
review
Lactobacillus
spp.,
Bifidobacterium
other
coliform
bacteria
as
most
promising
role
prevention
diseases,
such
obesity,
diabetes,
cancer,
cardiovascular
malignancy,
liver
disease,
inflammatory
bowel
disease.
also
discusses
recent
study
Saccharomyces
spp.
which
inflammation
was
prevented
by
promotion
proinflammatory
immune
function
production
short-chain
fatty
acids.
A
summary
alteration
with
future
perspectives
provided.
Circulation,
Journal Year:
2019,
Volume and Issue:
139(11), P. 1407 - 1421
Published: Jan. 17, 2019
Arterial
hypertension
and
its
organ
sequelae
show
characteristics
of
T
cell-mediated
inflammatory
diseases.
Experimental
anti-inflammatory
therapies
have
been
shown
to
ameliorate
hypertensive
end-organ
damage.
Recently,
the
CANTOS
study
(Canakinumab
Antiinflammatory
Thrombosis
Outcome
Study)
targeting
interleukin-1β
demonstrated
that
therapy
reduces
cardiovascular
risk.
The
gut
microbiome
plays
a
pivotal
role
in
immune
homeostasis
health.
Short-chain
fatty
acids
(SCFAs)
are
produced
from
dietary
fiber
by
bacteria
affect
host
homeostasis.
Here,
we
investigated
effects
SCFA
propionate
2
different
mouse
models
damage.To
investigate
effect
SCFAs
on
cardiac
damage
atherosclerosis,
wild-type
NMRI
or
apolipoprotein
E
knockout-deficient
mice
received
(200
mmol/L)
control
drinking
water.
To
induce
hypertension,
were
infused
with
angiotensin
II
(1.44
mg·kg-1·d-1
subcutaneous)
for
14
days.
accelerate
development
knockout
(0.72
28
Cardiac
atherosclerosis
assessed
using
histology,
echocardiography,
vivo
electrophysiology,
immunofluorescence,
flow
cytometry.
Blood
pressure
was
measured
radiotelemetry.
Regulatory
cell
depletion
PC61
antibody
used
examine
mode
action
propionate.Propionate
significantly
attenuated
hypertrophy,
fibrosis,
vascular
dysfunction,
both
models.
Susceptibility
ventricular
arrhythmias
reduced
propionate-treated
II-infused
mice.
Aortic
atherosclerotic
lesion
area
decreased
Systemic
inflammation
mitigated
treatment,
quantified
as
reduction
splenic
effector
memory
frequencies
helper
17
cells
models,
decrease
local
infiltration
Cardioprotective
abrogated
regulatory
cell-depleted
mice,
suggesting
is
cell-dependent.Our
data
emphasize
an
immune-modulatory
their
importance
suggest
lifestyle
modifications
leading
augmented
production
could
be
beneficial
nonpharmacological
preventive
strategy
patients
disease.
Scientific Reports,
Journal Year:
2015,
Volume and Issue:
5(1)
Published: Sept. 23, 2015
Accumulating
evidence
suggests
that
the
gut
microbiota
is
an
important
factor
in
mediating
development
of
obesity-related
metabolic
disorders,
including
type
2
diabetes.
Metformin
and
berberine,
two
clinically
effective
drugs
for
treating
diabetes,
have
recently
been
shown
to
exert
their
actions
through
modulating
microbiota.
In
this
study,
we
demonstrated
metformin
berberine
similarly
shifted
overall
structure
rats.
Both
showed
reverting
effects
on
high-fat
diet-induced
structural
changes
The
diversity
was
significantly
reduced
by
both
berberine-
metformin-treatments.
Nearest
shrunken
centroids
analysis
identified
134
operational
taxonomic
units
(OTUs)
responding
treatments,
which
close
associations
with
obese
phenotypes.
Sixty
out
OTUs
were
decreased
drugs,
while
those
belonging
putative
short-chain
fatty
acids
(SCFA)-producing
bacteria,
Allobaculum,
Bacteriodes,
Blautia,
Butyricoccus,
Phascolarctobacterium,
markedly
increased
and,
a
lesser
extent,
metformin.
Taken
together,
our
findings
suggest
similarity
microbiota,
enrichment
SCFA-producing
bacteria
reduction
microbial
diversity,
may
contribute
beneficial
host.