Nanomaterials,
Journal Year:
2024,
Volume and Issue:
14(24), P. 2017 - 2017
Published: Dec. 15, 2024
Our
group
has
synthesized
a
pleiotropic
synthetic
nanozyme
redox
mediator
we
term
“pleozyme”
that
displays
multiple
enzymatic
characteristics,
including
acting
as
superoxide
dismutase
mimetic,
oxidizing
NADH
to
NAD+,
and
H2S
polysulfides
thiosulfate.
Benefits
have
been
seen
in
acute
chronic
neurological
disease
models.
The
molecule
is
sourced
from
coconut-derived
activated
charcoal
undergone
harsh
oxidization
with
fuming
nitric
acid,
which
alters
the
structure
chemical
yielding
3–8
nm
discs
broad
potential.
Prior
work
showed
pleozymes
localize
mitochondria
increase
oxidative
phosphorylation
glycolysis.
Here,
measured
cellular
NAD+
levels
after
pleozyme
treatment
observed
increased
total
but
not
levels.
A
13C-glucose
metabolic
flux
analysis
suggested
stimulate
generation
of
pyruvate
lactate
glycolytically
tricarboxylic
acid
(TCA)
cycle,
pointing
malate
decarboxylation.
Analysis
intracellular
fatty
abundances
suggests
β-oxidation,
concomitant
succinyl-
acetyl-CoA.
Pleozymes
ATP,
potentially
via
flexible
enhancement
NAD+-dependent
catabolic
pathways
such
glycolysis,
through
TCA
cycle.
These
effects
may
be
favorable
for
pathologies
compromise
metabolism
brain
injury.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer,
Journal Year:
2025,
Volume and Issue:
unknown, P. 189259 - 189259
Published: Jan. 1, 2025
As
immunosuppressive
cells,
Regulatory
T
cells
(Tregs)
exert
their
influence
on
tumor
immune
escape
within
the
microenvironment
(TME)
by
effectively
suppressing
activity
of
other
thereby
significantly
impeding
anti-tumor
response.
In
recent
years,
metabolic
characteristics
Tregs
have
become
a
focus
research,
especially
important
role
lipid
metabolism
in
maintaining
function
Tregs.
Consequently,
targeted
interventions
aimed
at
modulating
been
recognized
as
an
innovative
and
promising
approach
to
enhance
effectiveness
immunotherapy.
This
review
presents
comprehensive
overview
pivotal
regulating
Tregs,
with
specific
targeting
augment
responses.
Furthermore,
we
discuss
potential
opportunities
challenges
associated
this
strategy,
aiming
provide
novel
insights
for
enhancing
efficacy
cancer
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 9, 2025
Carbohydrates,
lipids,
bile
acids,
various
inorganic
salt
ions
and
organic
acids
are
the
main
nutrients
or
indispensable
components
of
human
body.
Dysregulation
in
processes
absorption,
transport,
metabolism,
excretion
these
metabolites
can
lead
to
onset
severe
metabolic
disorders,
such
as
type
2
diabetes,
non-alcoholic
fatty
liver
disease,
gout
hyperbilirubinemia.
As
second
largest
membrane
receptor
supergroup,
several
major
families
solute
carrier
(SLC)
supergroup
have
been
found
play
key
roles
transport
substances
carbohydrates,
urate,
monocarboxylates
zinc
ions.
Based
on
common
dysregulation
related
substances,
we
explored
relationship
between
SLC
diseases,
providing
examples
drugs
targeting
proteins
that
approved
currently
clinical/preclinical
research
well
SLC-related
diagnostic
techniques
clinical
use
under
investigation.
By
highlighting
connections,
aim
provide
insights
may
contribute
development
improved
treatment
strategies
targeted
therapies
for
disorders.
Experimental Physiology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 24, 2025
Abstract
In
health,
the
liver
is
a
metabolically
flexible
organ
that
plays
key
role
in
regulating
systemic
lipid
and
glucose
concentrations.
There
constant
flux
of
fatty
acids
(FAs)
to
from
multiple
sources,
including
adipose
tissue,
dietary,
endogenously
synthesized
non‐lipid
precursors,
intrahepatic
droplets
recycling
triglyceride‐rich
remnants.
Within
liver,
FAs
are
used
for
triglyceride
synthesis,
which
can
be
oxidized,
stored
or
secreted
very
low‐density
lipoproteins
into
circulation.
The
processes
FA
uptake,
synthesis
intracellular
partitioning
storage,
oxidation
secretory
pathways
tightly
regulated.
An
imbalance
these
causes
accumulate
associated
with
development
metabolic
dysfunction‐associated
steatotic
disease.
It
well
appreciated
many
factors
influence
partitioning,
although
there
good
evidence
both
phenotype
(e.g.,
sex,
ethnicity
adiposity)
dietary
macronutrient
composition
play
accumulation,
their
interaction
remains
poorly
understood.
aim
this
review
explore
how
respective
delivery,
disposal
altered
by
understand
might
vivo,
humans.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 3, 2025
Diabetes
mellitus
(DM)
ranks
among
the
most
prevalent
chronic
metabolic
diseases,
characterized
primarily
by
a
persistent
elevation
in
blood
glucose
levels.
This
condition
typically
stems
from
either
insufficient
insulin
secretion
or
functional
defect
itself.
Clinically,
diabetes
is
classified
into
type
1
(T1DM)
and
2
(T2DM),
with
T2DM
comprising
nearly
90%
of
all
diagnosed
cases.
Notably,
global
incidence
has
surged
dramatically
over
recent
decades.
The
adenylate-activated
protein
kinase
(AMPK)
signaling
pathway
crucial
regulating
cellular
energy
metabolism,
marking
it
as
significant
therapeutic
target
for
related
complications.
Natural
products,
their
diverse
origins,
multifaceted
bioactivities,
relative
safety,
hold
considerable
promise
modulating
AMPK
pathway.
review
article
explores
advances
research
on
natural
products
that
pathway,
aiming
to
inform
development
innovative
antidiabetic
therapies.
Metabolism,
Journal Year:
2025,
Volume and Issue:
unknown, P. 156157 - 156157
Published: Feb. 1, 2025
Highlights•MSDC-0602K
differentially
affects
BM-MSCs
and
AT-MSCs.•Bioorthogonal
click
chemistry
allowed
measurement
of
pyruvate
pools.•Subcellular
metabolic
flux
analysis
revealed
rewiring
pathways.•Metabolic
TG
synthesis
showed
distinct
adipogenic
strategies.AbstractObjectiveInsulin-sensitizing
drugs,
despite
their
broad
use
against
type
2
diabetes,
can
adversely
affect
bone
health,
the
mechanisms
underlying
these
side
effects
remain
largely
unclear.
Here,
we
investigated
different
a
series
thiazolidinediones,
including
rosiglitazone,
pioglitazone,
second-generation
compound
MSDC-0602
K,
on
human
mesenchymal
stem
cells
(MSCs).MethodsWe
developed
13C
subcellular
metabolomic
tracer
measuring
separate
mitochondrial
cytosolic
metabolite
pools,
lipidomic
network-based
isotopologue
models,
bioorthogonal
chemistry,
to
demonstrate
that
K
affected
marrow-derived
MSCs
(BM-MSCs)
adipose
tissue-derived
(AT-MSCs).
In
BM-MSCs,
promoted
osteoblastic
differentiation
suppressed
adipogenesis.
This
effect
was
clearly
from
earlier
drugs
AT-MSCs.ResultsFluxomic
data
reveal
unexpected
differences
between
this
drug's
provide
mechanistic
insight
into
pharmacologic
inhibition
carrier
1
(MPC).
Our
study
demonstrates
retains
capacity
inhibit
MPC,
akin
rosiglitazone
but
unlike
enabling
utilization
alternative
pathways.
Notably,
exhibits
limited
lipogenic
potential
compared
both
each
which
employs
strategy.ConclusionsThese
findings
indicate
new-generation
do
not
compromise
structure,
offering
safer
for
treating
insulin
resistance.
Moreover,
results
highlight
ability
cell
compartment-specific
labeling
by
reactions
metabolomics
complex
lipids
discover
molecular
within
intersection
carbohydrate
lipid
metabolism.Graphical
abstract
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: March 28, 2025
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
is
a
heterogeneous
cancer
with
significant
global
incidence.
This
study
investigates
glycolysis-
lactate
metabolism-related
genes
(GALMRGs)
in
HNSCC,
focusing
on
their
impact
prognosis,
the
tumor
immune
microenvironment,
potential
as
therapeutic
biomarkers.
Analysis
of
data
from
Cancer
Genome
Atlas
Gene
Expression
Omnibus
identified
16
GALMRGs
that
were
differentially
expressed
HNSCC
compared
to
normal
tissues.
Functional
analysis
revealed
involvement
pyruvate
metabolism
HIF-1
signaling
pathways.
Weighted
gene
co-expression
network
two
module
genes,
CDKN3
SLC2A1.
Five
key
(CAV1,
CDKN3,
LDHA,
MB,
PER2)
through
univariate,
multivariate,
LASSO
regression
analyses
used
construct
prognostic
model.
model
demonstrated
strong
predictive
accuracy
for
overall
survival,
stratifying
patients
into
high-
low-risk
groups.
Immune
infiltration
showed
negative
correlation
between
resting
activated
mast
cells,
had
higher
mutational
burden,
suggesting
better
response
immunotherapy.
Consensus
clustering
classified
distinct
molecular
subtypes
differing
expression
genes.
GALMRG-based
promising
biomarker
predicting
outcomes
immunotherapy
responses,
providing
valuable
insights
personalized
treatment
strategies.