Journal of Agricultural and Food Chemistry,
Journal Year:
2020,
Volume and Issue:
68(39), P. 10697 - 10708
Published: Sept. 5, 2020
Sesamol,
a
liposoluble
lignan
extract,
has
already
been
proved
to
possess
potent
anti-inflammatory
properties,
and
it
could
also
regulate
gut
dysfunction.
The
purpose
of
the
present
research
is
explore
protective
effect
sesamol
on
colitis
mice.
In
current
research,
treatment
(100
mg/kg
bodyweight/day)
for
6
weeks
inhibited
dextran
sulphate
sodium
(DSS)-induced
bodyweight
loss
Transmission
electron
microscopy
hematoxylin
eosin
staining
results
showed
that
DSS-induced
histopathological
changes
mice
were
recovered
by
supplementation.
addition,
inflammatory
responses
supplementation
via
NF-κB
signaling
pathway
in
colon.
Moreover,
prevented
barrier
damages
enhancing
expression
tight
junction
proteins
(occludin,
claudin-1,
ZO-1)
recovering
mucus
layer.
Furthermore,
increased
short-chain
fatty
acid
(SCFAs)
contents
acetate,
propionate,
butyrate.
changed
microbiome
structure
relative
abundance
Coprococcuscus,
Butyricicoccus,
Odoribacter,
AF12
conclusion,
effectively
ameliorate
promoting
microecology.
International Journal of Environmental Research and Public Health,
Journal Year:
2020,
Volume and Issue:
17(20), P. 7618 - 7618
Published: Oct. 19, 2020
The
gut
microbiota
encompasses
a
diverse
community
of
bacteria
that
carry
out
various
functions
influencing
the
overall
health
host.
These
comprise
nutrient
metabolism,
immune
system
regulation
and
natural
defence
against
infection.
presence
certain
is
associated
with
inflammatory
molecules
may
bring
about
inflammation
in
body
tissues.
Inflammation
underlies
many
chronic
multisystem
conditions
including
obesity,
atherosclerosis,
type
2
diabetes
mellitus
bowel
disease.
be
triggered
by
structural
components
which
can
result
cascade
pathways
involving
interleukins
other
cytokines.
Similarly,
by-products
metabolic
processes
bacteria,
some
short-chain
fatty
acids,
play
role
inhibiting
processes.
In
this
review,
we
aimed
to
provide
an
overview
relationship
between
highlight
relevant
knowledge
gaps
field.
Based
on
current
literature,
it
appears
as
composition
differs
individuals
contingent
variety
factors
like
diet
genetics,
possess
pro-inflammatory
effects
whilst
others
harbour
those
anti-inflammatory
effects.
Recent
technological
advancements
have
allowed
for
better
methods
characterising
microbiota.
Further
research
continually
improve
our
understanding
interact
elucidate
reasons
behind
varying
presentations
same
disease
varied
responses
treatment
different
individuals.
Furthermore,
inform
clinical
practice
microbes
employed
probiotic
therapies
or
used
identify
suitable
prebiotic
therapies.
Cells,
Journal Year:
2021,
Volume and Issue:
10(11), P. 3164 - 3164
Published: Nov. 14, 2021
The
gut
microbiota
is
responsible
for
recovering
energy
from
food,
providing
hosts
with
vitamins,
and
a
barrier
function
against
exogenous
pathogens.
In
addition,
it
involved
in
maintaining
the
integrity
of
intestinal
epithelial
barrier,
crucial
functional
maturation
immune
system.
Western
diet
(WD)—an
unhealthy
high
consumption
fats—can
be
broadly
characterized
by
overeating,
frequent
snacking,
prolonged
postprandial
state.
term
WD
commonly
known
intuitively
understood.
However,
strict
digital
expression
nutrient
ratios
not
precisely
defined.
Based
on
US
data
1908–1989,
calory
intake
available
fats
increased
32%
to
45%.
Besides
metabolic
aspects
(hyperinsulinemia,
insulin
resistance,
dyslipidemia,
sympathetic
nervous
system
renin-angiotensin
overstimulation,
oxidative
stress),
consequences
excessive
fat
(high-fat
diet—HFD)
comprise
dysbiosis,
dysfunction,
permeability,
leakage
toxic
bacterial
metabolites
into
circulation.
These
can
strongly
contribute
development
low-grade
systemic
inflammation.
This
narrative
review
highlights
most
important
recent
advances
linking
HFD-driven
dysbiosis
HFD-related
inflammation,
presents
pathomechanisms
these
phenomena,
examines
possible
causative
relationship
between
pro-inflammatory
status
changes.
EBioMedicine,
Journal Year:
2020,
Volume and Issue:
52, P. 102649 - 102649
Published: Feb. 1, 2020
Host-microbiota
interactions
involving
inflammatory
and
metabolic
pathways
have
been
linked
to
the
pathogenesis
of
multiple
immune-mediated
diseases
conditions
like
diabetes
obesity.
Accumulating
evidence
suggests
that
alterations
in
gut
microbiome
could
play
a
role
cardiovascular
disease.
This
review
focuses
on
recent
advances
our
understanding
interplay
between
diet,
microbiota
disease,
with
emphasis
heart
failure
coronary
artery
Whereas
much
literature
has
focused
circulating
levels
diet-
microbiota-dependent
metabolite
trimethylamine-N-oxide
(TMAO),
several
sequencing-based
studies
demonstrated
compositional
functional
microbiomes
both
diseases.
Some
characteristics
are
consistent
across
study
cohorts,
such
as
decreased
abundance
microbes
capacity
for
producing
butyrate.
However,
published
generally
lack
essential
covariates
diet
clinical
data,
too
small
capture
substantial
variation
microbiome,
parallel
plasma
samples,
limiting
ability
translate
actual
function
reflected
by
microbiota-related
metabolites.
attempts
give
directions
future
order
demonstrate
utility
gut-heart
axis.
Nutrients,
Journal Year:
2020,
Volume and Issue:
12(10), P. 2982 - 2982
Published: Sept. 29, 2020
Gut
microbiota
and
its
metabolites
such
as
short
chain
fatty
acids
(SCFA),
lipopolysaccharides
(LPS),
trimethylamine-N-oxide
(TMAO)
impact
cardiovascular
health.
In
this
review,
we
discuss
how
gut
can
affect
hypertension
atherosclerosis.
Hypertensive
patients
were
shown
to
have
lower
alpha
diversity,
abundance
of
SCFA-producing
microbiota,
higher
gram-negative
bacteria,
which
are
a
source
LPS.
Animal
studies
point
towards
direct
role
for
SCFAs
in
blood
pressure
regulation
show
that
LPS
has
pro-inflammatory
effects.
Translocation
into
the
systemic
circulation
is
consequence
increased
permeability.
Atherosclerosis,
multifactorial
disease,
influenced
by
through
multiple
pathways.
Many
focused
on
pro-atherogenic
TMAO,
however,
it
not
clear
if
causal
factor.
addition,
play
key
bile
acid
metabolism
some
interventions
targeting
receptors
tend
decrease
Concluding,
atherosclerosis
many
pathways,
providing
wide
range
potential
therapeutic
targets.
Challenges
ahead
include
translation
findings
mechanisms
humans
development
target
risk
modulation
microbes
metabolites.
FEBS Journal,
Journal Year:
2020,
Volume and Issue:
287(5), P. 833 - 855
Published: Jan. 19, 2020
The
intestinal
milieu
harbours
the
gut
microbiota,
consisting
of
a
complex
community
bacteria,
archaea,
fungi,
viruses
and
protozoans
that
bring
to
host
organism
an
endowment
cells
genes
more
numerous
than
its
own.
In
last
10
years,
mounting
evidence
has
highlighted
prominent
influence
mutualistic
bacterial
communities
on
human
health.
Microbial
colonization
occurs
alongside
with
immune
system
development
plays
role
in
physiology.
microbiota
does
not
undergo
significant
fluctuations
throughout
adult
life.
However,
infections,
antibiotic
treatment,
lifestyle,
surgery
diet
might
profoundly
affect
it.
Gut
dysbiosis,
defined
as
marked
alterations
amount
function
microorganisms,
is
correlated
aetiology
chronic
noncommunicable
diseases,
ranging
from
cardiovascular,
neurologic,
respiratory
metabolic
illnesses
cancer.
this
review,
we
focus
interplay
among
provide
perspective
their
unique
metabolites
pathogenesis
and/or
progression
various
disorders.
We
discuss
interventions
based
microbiome
studies,
faecal
transplantation,
probiotics
prebiotics,
introduce
concept
correcting
dysbiosis
can
ameliorate
disease
symptoms,
thus
offering
new
approach
towards
treatment.
European Heart Journal,
Journal Year:
2021,
Volume and Issue:
43(6), P. 518 - 533
Published: Sept. 8, 2021
Abstract
Aims
Atherosclerotic
cardiovascular
disease
(ACVD)
is
a
major
cause
of
mortality
and
morbidity
worldwide,
increased
low-density
lipoproteins
(LDLs)
play
critical
role
in
development
progression
atherosclerosis.
Here,
we
examined
for
the
first
time
gut
immunomodulatory
effects
microbiota-derived
metabolite
propionic
acid
(PA)
on
intestinal
cholesterol
metabolism.
Methods
results
Using
both
human
animal
model
studies,
demonstrate
that
treatment
with
PA
reduces
blood
total
LDL
levels.
In
apolipoprotein
E−/−
(Apoe
−/−)
mice
fed
high-fat
diet
(HFD),
reduced
absorption
aortic
atherosclerotic
lesion
area.
Further,
regulatory
T-cell
numbers
interleukin
(IL)-10
levels
microenvironment,
which
turn
suppressed
expression
Niemann-Pick
C1-like
1
(Npc1l1),
transporter.
Blockade
IL-10
receptor
signalling
attenuated
PA-related
reduction
augmented
severity
HFD-fed
Apoe
−/−
mice.
To
translate
these
preclinical
findings
to
humans,
conducted
randomized,
double-blinded,
placebo-controlled
study
(clinical
trial
no.
NCT03590496).
Oral
supplementation
500
mg
twice
daily
over
course
8
weeks
significantly
[−15.9
mg/dL
(−8.1%)
vs.
−1.6
(−0.5%),
P
=
0.016],
[−19.6
(−7.3%)
−5.3
(−1.7%),
0.014]
non-high-density
lipoprotein
[PA
placebo:
−18.9
(−9.1%)
−0.6
0.002]
subjects
elevated
baseline
Conclusion
Our
reveal
novel
immune-mediated
pathway
linking
Npc1l1
homeostasis.
The
highlight
immune
system
as
potential
therapeutic
target
control
dyslipidaemia
may
introduce
new
avenue
prevention
ACVDs.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2022,
Volume and Issue:
12
Published: June 20, 2022
In
the
last
two
decades,
considerable
interest
has
been
shown
in
understanding
development
of
gut
microbiota
and
its
internal
external
effects
on
intestine,
as
well
risk
factors
for
cardiovascular
diseases
(CVDs)
such
metabolic
syndrome.
The
intestinal
plays
a
pivotal
role
human
health
disease.
Recent
studies
revealed
that
can
affect
host
body.
CVDs
are
leading
cause
morbidity
mortality,
patients
favor
death
over
chronic
kidney
For
function
host,
molecules
have
to
penetrate
epithelium
or
surface
cells
host.
Gut
utilize
trimethylamine,
N-oxide,
short-chain
fatty
acids,
primary
secondary
bile
acid
pathways.
By
affecting
these
living
cells,
heart
failure,
atherosclerosis,
hypertension,
myocardial
fibrosis,
infarction,
coronary
artery
Previous
relation
stroke
pathogenesis
consequences
provide
new
therapeutic
prospects.
This
review
highlights
interplay
between
metabolites
addresses
related
interventions
treatment
CVDs.
Clinical Science,
Journal Year:
2020,
Volume and Issue:
134(6), P. 657 - 676
Published: March 1, 2020
Abstract
Cardiovascular
diseases
(CVDs)
are
the
leading
cause
of
morbidity
and
mortality
worldwide.
Metabolic
dysfunction
is
a
fundamental
core
mechanism
underlying
CVDs.
Previous
studies
generally
focused
on
roles
long-chain
fatty
acids
(LCFAs)
in
However,
growing
body
study
has
implied
that
short-chain
(SCFAs:
namely
propionate,
malonate,
butyrate,
2-hydroxyisobutyrate
(2-HIBA),
β-hydroxybutyrate,
crotonate,
succinate,
glutarate)
their
cognate
acylations
(propionylation,
malonylation,
butyrylation,
2-hydroxyisobutyrylation,
β-hydroxybutyrylation,
crotonylation,
succinylation,
glutarylation)
participate
Here,
we
attempt
to
provide
an
overview
landscape
metabolic
pattern
SCFAs
Especially,
would
focus
newly
identified
CVDs,
including
atherosclerosis,
hypertension,
heart
failure.