European Journal of Clinical Investigation,
Journal Year:
2023,
Volume and Issue:
53(7)
Published: March 1, 2023
Nephrotic
syndrome
is
common
in
children
and
adults
worldwide,
steroid-sensitive
nephrotic
(SSNS)
accounts
for
80%.
Aberrant
metabolism
involvement
early
SSNS
sparsely
studied,
its
pathogenesis
remains
unclear.
Therefore,
the
goal
of
this
study
was
to
investigate
changes
initiated
patients-related
metabolites
through
serum
urine
metabolomics
discover
novel
potential
metabolic
pathways.Serum
samples
(27
56
controls)
(17
24
were
collected.
Meanwhile,
non-targeted
analyses
performed
by
ultra-high-performance
liquid
chromatography-quadrupole
time
flight-mass
spectrometry
(UHPLC-QTOF-MS)
determine
SSNS.
We
applied
causal
inference
model,
DoWhy
assess
effects
several
selected
metabolites.
An
ultraperformance
chromatography-tandem
mass
(UPLC-MS/MS)
used
validate
hits
(D-mannitol,
dulcitol,
D-sorbitol,
XMP,
NADPH,
NAD,
bilirubin,
α-KG-like)
41
43
controls.
In
addition,
pathways
explored.Compared
urine,
analysis
more
clearly
discriminated
at
194
differential
five
obtained
group.
Eight
identified
establishing
diagnostic
model
SSNS,
four
variables
had
a
positive
effect.
After
validation
targeted
MS,
except
others
have
similar
trends
like
untargeted
analysis.With
further
quantitative
analysis,
we
found
seven
may
be
new
biomarkers
risk
prediction
diagnosis
Aging and Disease,
Journal Year:
2023,
Volume and Issue:
14(5), P. 1633 - 1633
Published: Jan. 1, 2023
Fibrosis
is
the
abnormal
accumulation
of
extracellular
matrix
proteins
such
as
collagen
and
fibronectin.
Aging,
injury,
infections,
inflammation
can
cause
different
types
tissue
fibrosis.
Numerous
clinical
investigations
have
shown
a
correlation
between
degree
liver
pulmonary
fibrosis
in
patients
telomere
length
mitochondrial
DNA
content,
both
which
are
signs
aging.
Aging
involves
gradual
loss
function
over
time,
results
homeostasis
and,
ultimately,
an
organism's
fitness.
A
major
feature
aging
senescent
cells.
Senescent
cells
abnormally
continuously
accumulate
late
stages
life,
contributing
to
age-related
deterioration,
among
other
characteristics.
Furthermore,
generates
chronic
inflammation,
decreases
organ
function.
This
finding
suggests
that
closely
related.
The
transforming
growth
factor-beta
(TGF-β)
superfamily
plays
crucial
role
physiological
pathological
processes
aging,
immune
regulation,
atherosclerosis,
In
this
review,
functions
TGF-β
normal
organs,
fibrotic
tissues
discussed:
signalling
altered
with
age
indicator
pathology
associated
addition,
review
discusses
potential
targeting
noncoding.
British Journal of Pharmacology,
Journal Year:
2023,
Volume and Issue:
181(1), P. 162 - 179
Published: Aug. 19, 2023
Abstract
Background
and
Purpose
Membranous
nephropathy
(MN)
is
an
immune‐mediated
glomerular
disease
in
adults.
Antibody‐
antigen‐bonding
mechanisms
have
been
largely
clarified,
but
the
subepithelium
immune
complex
deposition‐mediated
downstream
molecular
are
currently
unresolved.
Increasing
evidence
has
suggested
that
gut
microbiota
contribute
to
MN
pathogenesis.
Experimental
Approach
In
this
study,
we
identified
alterations
faecal
serum
metabolites
mediate
aryl
hydrocarbon
receptor
(AhR)
mechanism
cationic
bovine
albumin
(CBSA)‐induced
rats
patients
with
idiopathic
(IMN).
Key
Results
Impaired
renal
function
correlated
relative
abundance
of
reduced
probiotics,
Lactobacillus
Bifidobacterium
,
altered
levels
tryptophan‐produced
indole
derivatives
(TPIDs)
rats.
Further
results
showed
five
namely
johnsonii
murinus
vaginalis
reuteri
animalis
positively
decreased
indole‐3‐pyruvic
acid,
indole‐3‐aldehyde
tryptamine
negatively
increased
indole‐3‐lactic
acid
indole‐3‐acetic
Altered
probiotics
TPIDs
also
were
observed
IMN.
studies
exhibited
a
significant
increase
intrarenal
mRNA
expression
AhR
its
target
genes
CYP1A1
CYP1A2
CYP1B1
which
accompanied
by
protein
down‐regulated
cytoplasmic
AhR,
up‐regulated
nuclear
IMN
patients.
Conclusion
Implications
Activation
signalling
pathway
may
involve
TPIDs.
These
data
suggest
could
influence
through
engage
host
receptors.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
14
Published: Jan. 16, 2024
Renal
fibrosis
is
increasingly
recognized
as
a
global
public
health
problem.
Acute
kidney
injury
(AKI)
and
chronic
disease
(CKD)
both
result
in
renal
fibrosis.
Oxidative
stress
inflammation
play
central
roles
progressive
are
closely
linked
form
vicious
cycle
which
oxidative
induces
through
various
molecular
mechanisms.
Ample
evidence
has
indicated
that
hyperactive
nuclear
factor
kappa
B
(NF-ƙB)
signaling
pathway
plays
pivotal
role
Hyperactive
NF-ƙB
causes
the
activation
recruitment
of
immune
cells.
Inflammation,
turn,
triggers
production
reactive
oxygen
species
nitrogen
by
activating
leukocytes
resident
These
events
mediate
organ
apoptosis,
necrosis,
Therefore,
developing
strategy
to
target
important
for
effective
treatment
This
Review
summarizes
effect
on
context
AKI
CKD
(immunoglobulin
A
nephropathy,
membranous
diabetic
hypertensive
transplantation).
Therapies
targeting
pathway,
including
natural
products,
also
discussed.
In
addition,
NF-ƙB-dependent
non-coding
RNAs
involved
crucial
targets
development
treatments
disease.
provides
clear
pathophysiological
rationale
specific
concept-driven
therapeutic
pathway.
Abstract
Background
Late‐onset
depression
(LOD)
is
defined
as
primary
that
first
manifests
after
the
age
of
65.
Luteolin
(LUT)
a
natural
flavonoid
has
shown
promising
antidepressant
effects
and
improvement
in
neurological
function
previous
studies.
Aims
In
this
study,
we
utilized
UPLC–MS/MS
non‐targeted
metabolomics
techniques,
along
with
molecular
docking
technology
experimental
validation,
to
explore
mechanism
LUT
treating
LOD
from
perspective.
Results
The
behavioral
results
our
study
demonstrate
significantly
ameliorated
anxiety
depression‐like
behaviors
while
enhancing
cognitive
rats.
Metabolomic
analysis
revealed
on
rats
were
primarily
mediated
through
glycerophospholipid
metabolic
pathway
hippocampus
prefrontal
cortex.
levels
key
lipid
metabolites,
phosphatidylserine
(PS),
phosphatidylcholine
(PC),
phosphatidylethanolamine
(PE),
altered
by
treatment,
PC
PE
showing
significant
correlations
indices.
Molecular
indicated
had
strong
binding
activity
synthase
1
(PTDSS1),
2
(PTDSS2),
decarboxylase
(PISD),
which
are
involved
transformation
synthesis
PC,
PE,
PS.
Lastly,
explored
reasons
for
opposing
trends
PS
cortex
perspective
autophagy,
may
be
attributable
bidirectional
regulation
autophagy
distinct
brain
regions.
Conclusions
Our
alterations
metabolism
pathways
both
Moreover,
appears
regulate
disorders
specifically
modulating
different
regions
rats,
consequently
alleviating
behavior
these
animals.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: March 8, 2024
Arachidonic
acid
(AA)
is
a
main
component
of
cell
membrane
lipids.
AA
mainly
metabolized
by
three
enzymes:
cyclooxygenase
(COX),
lipoxygenase
(LOX)
and
cytochrome
P450
(CYP450).
Esterified
hydrolysed
phospholipase
A
2
into
free
form
that
further
COX,
LOX
CYP450
to
wide
range
bioactive
mediators,
including
prostaglandins,
lipoxins,
thromboxanes,
leukotrienes,
hydroxyeicosatetraenoic
acids
epoxyeicosatrienoic
acids.
Increased
mitochondrial
oxidative
stress
considered
be
central
mechanism
in
the
pathophysiology
kidney.
Along
with
increased
stress,
apoptosis,
inflammation
tissue
fibrosis
drive
progressive
loss
kidney
function,
affecting
glomerular
filtration
barrier
tubulointerstitium.
Recent
studies
have
shown
its
active
derivative
eicosanoids
play
important
roles
regulation
physiological
function
pathogenesis
disease.
These
factors
are
potentially
novel
biomarkers,
especially
context
their
involvement
inflammatory
processes
stress.
In
this
review,
we
introduce
metabolic
pathways
discuss
molecular
mechanisms
which
these
affect
progression
acute
injury
(AKI),
diabetic
nephropathy
(DN)
renal
carcinoma
(RCC).
This
review
may
provide
new
therapeutic
targets
for
identification
AKI
CKD
continuum.
Pharmaceutical Biology,
Journal Year:
2024,
Volume and Issue:
62(1), P. 423 - 435
Published: May 17, 2024
Context
Diabetic
kidney
disease
(DKD)
affects
nearly
40%
of
diabetic
patients,
often
leading
to
end-stage
renal
that
requires
replacement
therapies,
such
as
dialysis
and
transplantation.
The
gut
microbiota,
an
integral
aspect
human
evolution,
plays
a
crucial
role
in
this
condition.
Traditional
Chinese
medicine
(TCM)
has
shown
promising
outcomes
ameliorating
DKD
by
addressing
the
microbiota.