Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Sept. 14, 2022
Coronavirus-19
(COVID-19)
disease
is
driven
by
an
unchecked
immune
response
to
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
virus
which
alters
host
mitochondrial-associated
mechanisms.
Compromised
mitochondrial
health
results
in
abnormal
reprogramming
of
glucose
metabolism,
can
disrupt
extracellular
signalling.
We
hypothesized
that
examining
energy-related
signalling
metabolites
implicated
SARS-CoV-2
infection
would
provide
potential
biomarkers
for
predicting
risk
COVID-19
illness.
used
a
semi-targeted
serum
metabolomics
approach
273
patients
with
different
severity
grades
recruited
at
phase
determine
relative
abundance
tricarboxylic
acid
(Krebs)
cycle-related
known
signaling
properties
(pyruvate,
lactate,
succinate
and
α-ketoglutarate).
Abundance
levels
were
evaluated
validation
cohort
(n=398)
using
quantitative
fluorimetric
assays.
Increased
four
a-ketoglutarate
succinate)
found
critically
ill
targeted
approaches
(p<0.05).
The
combined
strategy
proposed
herein
enabled
us
establish
circulating
pyruvate
(p<0.001)
together
body
mass
index
(p=0.025),
C-reactive
protein
(p=0.039),
D-Dimer
creatinine
(p=0.043)
levels,
are
independent
predictors
critical
COVID-19.
Furthermore,
classification
regression
tree
(CART)
analysis
provided
cut-off
value
(24.54
µM;
p<0.001)
as
early
criterion
accurately
classify
outcomes.
Our
findings
support
link
between
pathogenesis
immunometabolic
dysregulation,
show
fluorometric
quantification
cost-effective
clinical
decision
tool
improve
patient
stratification
prognosis
prediction.
Microbiome,
Journal Year:
2022,
Volume and Issue:
10(1)
Published: Aug. 25, 2022
Abstract
Background
Succinate
is
produced
by
both
human
cells
and
gut
bacteria
couples
metabolism
to
inflammation
as
an
extracellular
signaling
transducer.
Circulating
succinate
elevated
in
patients
with
obesity
type
2
diabetes
linked
numerous
complications,
yet
no
studies
have
specifically
addressed
the
contribution
of
microbiota
systemic
or
explored
consequences
reducing
intestinal
levels
this
setting.
Results
Using
germ-free
microbiota-depleted
mouse
models,
we
show
that
a
significant
source
circulating
succinate,
which
obesity.
We
also
vivo
therapeutic
treatments
selected
diminish
obese
mice.
Specifically,
demonstrate
Odoribacter
laneus
promising
probiotic
based
on
its
ability
deplete
improve
glucose
tolerance
inflammatory
profile
two
independent
models
(
db/db
mice
diet-induced
mice).
Mechanistically,
partly
mediated
receptor
1.
Supporting
these
preclinical
findings,
inverse
correlation
between
plasma
fecal
cohort
severe
associated
several
components
metabolic
syndrome
including
waist
circumference,
triglycerides,
uric
acid,
among
others,
primary
determinant
insulin
sensitivity
evaluated
euglycemic-hyperinsulinemic
clamp.
Conclusions
Overall,
our
work
uncovers
O.
next-generation
obesity-related
inflammation.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: June 11, 2024
Succinate,
traditionally
viewed
as
a
mere
intermediate
of
the
tricarboxylic
acid
(TCA)
cycle,
has
emerged
critical
mediator
in
inflammation.
Disruptions
within
TCA
cycle
lead
to
an
accumulation
succinate
mitochondrial
matrix.
This
excess
subsequently
diffuses
into
cytosol
and
is
released
extracellular
space.
Elevated
cytosolic
levels
stabilize
hypoxia-inducible
factor-1α
by
inhibiting
prolyl
hydroxylases,
which
enhances
inflammatory
responses.
Notably,
also
acts
extracellularly
signaling
molecule
engaging
receptor
1
on
immune
cells,
thus
modulating
their
pro-inflammatory
or
anti-inflammatory
activities.
Alterations
have
been
associated
with
various
disorders,
including
rheumatoid
arthritis,
bowel
disease,
obesity,
atherosclerosis.
These
associations
are
primarily
due
exaggerated
cell
Given
its
central
role
inflammation,
targeting
pathways
offers
promising
therapeutic
avenues
for
these
diseases.
paper
provides
extensive
review
succinate's
involvement
processes
highlights
potential
targets
future
research
possibilities
development.
Metabolism,
Journal Year:
2023,
Volume and Issue:
145, P. 155630 - 155630
Published: June 13, 2023
Succinate
and
succinate
receptor
1
(SUCNR1)
are
linked
to
fibrotic
remodeling
in
models
of
non-alcoholic
fatty
liver
disease
(NAFLD),
but
whether
they
have
roles
beyond
the
activation
hepatic
stellate
cells
remains
unexplored.
We
investigated
succinate/SUCNR1
axis
context
NAFLD
specifically
hepatocytes.We
studied
phenotype
wild-type
Sucnr1-/-
mice
fed
a
choline-deficient
high-fat
diet
induce
steatohepatitis
(NASH),
explored
function
SUCNR1
murine
primary
hepatocytes
human
HepG2
treated
with
palmitic
acid.
Lastly,
plasma
expression
were
analyzed
four
independent
cohorts
patients
different
stages.Sucnr1
was
upregulated
response
diet-induced
NASH.
Sucnr1
deficiency
provoked
both
beneficial
(reduced
fibrosis
endoplasmic
reticulum
stress)
detrimental
(exacerbated
steatosis
inflammation
reduced
glycogen
content)
effects
liver,
disrupted
glucose
homeostasis.
Studies
vitro
revealed
that
hepatocyte
injury
increased
expression,
which
when
activated
improved
lipid
homeostasis
damaged
hepatocytes.
In
humans,
good
determinant
progression
advanced
stages.
population
at
risk
NAFLD,
circulating
elevated
index
(FLI)
≥60.
Indeed,
had
predictive
value
for
diagnosed
by
FLI,
prediction
moderate/severe
through
biopsy
added
an
FLI
algorithm.We
identify
as
target
extracellular
during
uncover
hitherto
unknown
regulator
metabolism.
Our
clinical
data
highlight
potential
markers
diagnose
NASH,
respectively.
Pharmacological Research,
Journal Year:
2023,
Volume and Issue:
194, P. 106865 - 106865
Published: July 22, 2023
Succinate
is
a
vital
signaling
metabolite
produced
by
the
host
and
gut
microbiota.
has
been
shown
to
regulate
metabolic
homeostasis
inhibit
obesity-associated
inflammation
in
macrophages
engaging
its
cognate
receptor,
SUCNR1.
However,
contribution
of
succinate-SUCNR1
axis
intestinal
barrier
dysfunction
obesity
remains
unclear.
In
present
study,
we
explored
effects
on
high-fat
diet
(HFD)-induced
dysfunction.
Using
SUCNR1-deficient
mouse
model
under
HFD
feeding
conditions,
identified
impairment.
Our
results
showed
that
administration
decreased
goblet
cell
numbers
mucus
production,
promoted
pro-inflammatory
responses,
induced
microbiota
composition
imbalance,
increased
permeability,
caused
mucosal
Dietary
succinate
supplementation
was
sufficient
activate
type
2
immune
response,
trigger
differentiation
barrier-promoting
cells,
suppress
inflammation,
restore
HFD-induced
impairment
dysbiosis,
eventually
exert
anti-obesity
effects.
SUNNR1-deficient
mice
failed
improve
function
phenotype
mice.
data
indicate
protective
role
Diabetologia,
Journal Year:
2024,
Volume and Issue:
67(3), P. 430 - 442
Published: Jan. 5, 2024
Beyond
their
conventional
roles
in
intracellular
energy
production,
some
traditional
metabolites
also
function
as
extracellular
messengers
that
activate
cell-surface
G-protein-coupled
receptors
(GPCRs)
akin
to
hormones
and
neurotransmitters.
These
signalling
metabolites,
often
derived
from
nutrients,
the
gut
microbiota
or
host's
intermediary
metabolism,
are
now
acknowledged
key
regulators
of
various
metabolic
immune
responses.
This
review
delves
into
multi-dimensional
aspects
succinate,
a
dual
metabolite
with
roots
both
mitochondria
microbiome.
It
connects
dots
between
succinate's
role
Krebs
cycle,
mitochondrial
respiration,
its
double-edge
transmitter
within
outside
cell.
We
aim
provide
an
overview
succinate-succinate
receptor
1
(SUCNR1)
axis
diabetes,
discussing
potential
use
succinate
biomarker
novel
prospect
targeting
SUCNR1
manage
complications
associated
diabetes.
further
propose
strategies
manipulate
succinate-SUCNR1
for
better
diabetes
management;
this
includes
pharmacological
modulation
innovative
approaches
concentrations,
such
administration
indirect
strategies,
like
modulation.
The
nature
terms
origins
roles,
offers
rich
landscape
understanding
intricate
connections
diseases,
indicates
promising
pathways
developing
new
therapeutic
strategies.
Molecular Cell,
Journal Year:
2024,
Volume and Issue:
84(5), P. 955 - 966.e4
Published: Feb. 6, 2024
SUCNR1
is
an
auto-
and
paracrine
sensor
of
the
metabolic
stress
signal
succinate.
Using
unsupervised
molecular
dynamics
(MD)
simulations
(170.400
ns)
mutagenesis
across
human,
mouse,
rat
SUCNR1,
we
characterize
how
a
five-arginine
motif
around
extracellular
pole
TM-VI
determines
initial
capture
succinate
in
vestibule
(ECV)
to
either
stay
or
move
down
orthosteric
site.
Metadynamics
demonstrate
low-energy
binding
both
sites,
with
energy
barrier
corresponding
intermediate
stage
during
which
succinate,
associated
water
cluster,
unlocks
hydrogen-bond-stabilized
conformationally
constrained
loop
(ECL)-2b.
Importantly,
simultaneous
two
molecules
through
"sequential"
"bypassing"
mode
frequent
endpoint.
The
mono-carboxylate
NF-56-EJ40
antagonist
enters
between
TM-I
-II
does
not
unlock
ECL-2b.
It
proposed
that
occupancy
high-affinity
sites
required
for
selective
activation
by
high
local
concentrations.
Journal of Clinical Investigation,
Journal Year:
2024,
Volume and Issue:
134(12)
Published: May 7, 2024
Pancreatic
β-cell
dysfunction
is
a
key
feature
of
type
2
diabetes,
and
novel
regulators
insulin
secretion
are
desirable.
Here
we
report
that
the
succinate
receptor
(SUCNR1)
expressed
in
β-cells
up-regulated
hyperglycemic
states
mice
humans.
We
found
acts
as
hormone-like
metabolite
stimulates
via
SUCNR1-Gq-PKC-dependent
mechanism
human
β-cells.
Mice
with
β-cell-specific
Sucnr1
deficiency
exhibit
impaired
glucose
tolerance
on
high-fat
diet,
indicating
SUCNR1
essential
for
preserving
diet-induced
resistance.
Patients
show
an
enhanced
nutritional-related
response,
which
correlates
potentiation
during
intravenous
administration.
These
data
demonstrate
succinate/SUCNR1
axis
activated
by
high
identify
GPCR-mediated
amplifying
pathway
relevant
to
hyperinsulinemia
prediabetic
states.