BMC Musculoskeletal Disorders,
Journal Year:
2025,
Volume and Issue:
26(1)
Published: March 22, 2025
Adipogenesis
is
intricately
linked
to
the
onset
and
progression
of
muscle
aging;
however,
relevant
biomarkers
remain
unclear.
This
study
sought
identify
key
genes
associated
with
adipogenesis
in
context
aging.
Firstly,
gene
expression
profiles
from
biopsies
vastus
lateralis
both
young
elderly
population
were
retrieved
GEO
database.
After
intersecting
results
differential
analysis,
weighted
co-expression
network
sets
adipogenesis-related
genes,
29
expressed
(ARDEGs)
selected.
Connectivity
Map
(cMAP)
analysis
identified
tamsulosin,
fraxidin,
alaproclate
as
target
compounds.
In
further,
using
three
machine
learning
algorithms
friends
four
hub
ARDEGs,
ESRRA,
RXRG,
GADD45A,
CEBPB
verified
vivo
aged
mice
muscles.
Immune
infiltration
showed
a
strong
link
between
several
immune
cells
ARDEGs.
all,
these
findings
suggested
that
could
serve
related
Redox Biology,
Journal Year:
2023,
Volume and Issue:
61, P. 102649 - 102649
Published: Feb. 27, 2023
Senescence
of
bone
marrow
mesenchymal
stem
cells
(BMMSCs)
induced
by
chronic
oxidative
stress
is
an
important
factor
contributes
to
the
postmenopausal
osteoporosis
(PMOP).
Mitochondrial
quality
control
takes
a
pivotal
role
in
regulating
and
cell
senescence.
Genistein
major
isoflavone
soy
products,
which
best
known
for
its
ability
inhibit
loss
both
women
ovariectomized
(OVX)
rodents.
Here
we
show
that
OVX-BMMSCs
displayed
premature
senescence,
elevated
reactive
oxygen
species
(ROS)
level
mitochondria
dysfunction,
while
genistein
rescued
these
phenotypes.
Using
network
pharmacology
molecular
docking,
identified
estrogen-related
receptor
α
(ERRα)
as
potential
target
genistein.
Knockdown
ERRα
greatly
abolished
anti-senescence
effect
on
OVX-BMMSCs.
Further,
mitochondrial
biogenesis
mitophagy
were
inhibited
knockdown
In
vivo,
trabecular
p16INK4a
expression,
upregulated
sirtuin
3
(SIRT3)
peroxisome
proliferator-activated
gamma
coactivator
one
alpha
(PGC1α)
expression
area
proximal
tibia
OVX
rats.
Together,
this
study
revealed
ameliorates
senescence
through
ERRα-mediated
mitophagy,
provided
basis
advancement
development
therapeutic
strategies
against
PMOP.
Communications Biology,
Journal Year:
2024,
Volume and Issue:
7(1)
Published: June 11, 2024
Abstract
Organismal
adaptations
to
spaceflight
have
been
characterized
at
the
molecular
level
in
model
organisms,
including
Drosophila
and
C.
elegans
.
Here,
we
extend
work
energy
metabolism
sex
hormone
signaling
mice
humans.
We
found
induced
changes
insulin
estrogen
rodents
Murine
were
most
prominent
liver,
where
observed
inhibition
of
receptor
with
concomitant
hepatic
resistance
steatosis.
Based
on
metabolic
demand,
pathways
mediated
by
vary
among
muscles,
specifically
between
soleus
extensor
digitorum
longus.
In
humans,
related
genes
pathways.
Pathway
analysis
demonstrated
resistance,
signaling,
stress
response,
viral
infection.
These
data
strongly
suggest
need
for
further
research
reproductive
endocrinologic
effects
space
travel,
if
are
become
a
successful
interplanetary
species.
Journal of Clinical Investigation,
Journal Year:
2024,
Volume and Issue:
134(18)
Published: Sept. 16, 2024
Autoimmune
diseases
are
a
leading
cause
of
disability
worldwide.
Most
autoimmune
occur
more
often
in
women
than
men,
with
rheumatic
being
among
those
most
highly
expressed
women.
Several
key
factors,
identified
mainly
animal
models
and
cell
culture
experiments,
important
increasing
disease
females.
These
include
sex
hormones,
immune
genes
including
found
on
the
X
chromosome,
sex-specific
epigenetic
effects
by
estrogen
environment,
regulation
messenger
RNA
microRNAs
extracellular
vesicles.
Evidence
is
also
emerging
that
viruses
as
well
drugs
or
toxins
damage
mitochondria
may
contribute
to
increased
levels
autoantibodies
against
nuclear
mitochondrial
antigens,
which
common
many
diseases.
The
purpose
this
Review
summarize
our
current
understanding
mechanisms
determine
differences
disease.
Pharmacological Reviews,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100053 - 100053
Published: March 1, 2025
Neurodegenerative
diseases
(NDs),
such
as
Alzheimer
disease,
Parkinson
Huntington
amyotrophic
lateral
sclerosis,
and
frontotemporal
dementia,
are
well
known
to
pose
formidable
challenges
for
their
treatment
due
intricate
pathogenesis
substantial
variability
among
patients,
including
differences
in
environmental
exposures
genetic
predispositions.
One
of
the
defining
characteristics
NDs
is
widely
reported
be
buildup
misfolded
proteins.
For
example,
disease
marked
by
amyloid
beta
hyperphosphorylated
Tau
aggregates,
whereas
exhibits
α-synuclein
aggregates.
Amyotrophic
sclerosis
dementia
exhibit
TAR
DNA-binding
protein
43,
superoxide
dismutase
1,
fused-in
sarcoma
involves
mutant
huntingtin
polyglutamine
These
proteins
key
biomarkers
also
serve
potential
therapeutic
targets,
they
can
addressed
through
autophagy,
a
process
that
removes
excess
cellular
inclusions
maintain
homeostasis.
Various
forms
macroautophagy,
chaperone-mediated
microautophagy,
hold
promise
eliminating
toxic
implicated
NDs.
In
this
review,
we
focus
on
elucidating
regulatory
connections
between
autophagy
NDs,
summarizing
cause
exploring
impact
mechanisms,
discussing
how
regulate
aggregation.
Moreover,
underscore
activation
strategy
across
different
small
molecules
capable
activating
pathways,
rapamycin
targeting
mTOR
pathway
clear
Sertraline
AMPK/mTOR/RPS6KB1
Tau,
further
illustrate
NDs'
intervention.
Together,
these
findings
would
provide
new
insights
into
current
research
trends
propose
small-molecule
drugs
promising
strategies
future
ND
therapies.
SIGNIFICANCE
STATEMENT:
This
review
provides
an
in-depth
overview
eliminate
aggregates
neurodegenerative
diseases.
It
elucidates
fascinating
interrelationships
"chasing
escaping"
phenomenon.
discusses
progress
utilizing
activate
improve
efficacy
therapies
removing
Frontiers in Science,
Journal Year:
2025,
Volume and Issue:
3
Published: March 25, 2025
Age-related
neurodegenerative
disorders,
including
dementia,
are
a
major
global
health
concern.
This
article
describes
the
first
comprehensive,
data-driven
molecular
model
of
neuro-glia-vascular
system
to
explore
complex
relationships
between
aging
brain,
energy
metabolism,
blood
flow,
and
neuronal
activity.
Comprising
16,800
interaction
pathways,
includes
all
key
enzymes,
transporters,
metabolites,
circulatory
factors
vital
for
electrical
We
found
significant
alterations
in
metabolite
concentrations
differential
effects
on
adenosine
triphosphate
(ATP)
supply
neurons
astrocytes
within
subcellular
compartments
aged
brains
identified
reduced
sodium/potassium
triphosphatase
(Na
+
/K
-ATPase)
activity
as
leading
cause
impaired
action
potentials.
The
predicts
that
metabolic
pathways
cluster
more
closely
suggesting
loss
robustness
adaptability.
Additionally,
displays
flexibility,
undermining
its
capacity
efficiently
respond
stimuli
recover
from
damage.
Through
transcription
factor
analysis,
estrogen-related
receptor
alpha
(ESRRA)
emerged
central
target
connected
these
aging-related
changes.
An
unguided
optimization
search
pinpointed
potential
interventions
capable
restoring
brain’s
flexibility
generation.
These
strategies
include
increasing
nicotinamide
adenine
dinucleotide
(NADH)
cytosol-mitochondria
shuttle,
NAD
pool,
ketone
β-hydroxybutyrate,
lactate,
Na
-ATPase,
while
reducing
glucose
levels.
is
open
sourced
help
guide
further
research
into
brain
metabolism.
Biomedicine & Pharmacotherapy,
Journal Year:
2019,
Volume and Issue:
117, P. 109047 - 109047
Published: June 5, 2019
NAFLD
is
a
vital
health
problem
worldwide;
however,
no
effective
treatment
currently
available
for
NAFLD.
Intensive
studies
have
indicated
the
efficacy
of
genistein
(GE),
bioactive
isoflavone
extracted
from
soy,
in
treating
In
addition
to
its
oestrogen-like
effects,
GE
known
multiple
molecular
instance,
lipid
and
glucose
metabolism-promoting
effects
activities
against
peroxidation,
inflammation,
fibrosis,
NAFLD-related
tumours.
Here,
this
review
summarizes
potential
role
prevention
some
targets
signalling
pathways
Oxidative Medicine and Cellular Longevity,
Journal Year:
2020,
Volume and Issue:
2020, P. 1 - 34
Published: Sept. 16, 2020
Human
SARS-CoV-2
infection
is
characterized
by
a
high
mortality
rate
due
to
some
patients
developing
large
innate
immune
response
associated
with
cytokine
storm
and
acute
respiratory
distress
syndrome
(ARDS).
This
at
the
molecular
level
decreased
energy
metabolism,
altered
redox
state,
oxidative
damage,
cell
death.
Therapies
that
increase
levels
of
(R)-beta-hydroxybutyrate
(R-BHB),
such
as
ketogenic
diet
or
consuming
exogenous
ketones,
should
restore
metabolism
state.
R-BHB
activates
anti-inflammatory
GPR109A
signaling
inhibits
NLRP3
inflammasome
histone
deacetylases,
while
has
been
shown
protect
mice
from
influenza
virus
through
protective
γδ
T
increasing
electron
transport
chain
gene
expression
metabolism.
During
virus-induced
storm,
metabolic
flexibility
compromised
increased
reactive
oxygen
species
(ROS)
nitrogen
(RNS)
downregulate,
inactivate
many
enzymes
central
including
pyruvate
dehydrogenase
complex
(PDC).
leads
an
crisis
decreases
B
proliferation
results
in
production
It
hypothesized
moderately
high-fat
together
ketone
supplementation
first
signs
will
mitochondrial
bypassing
block
PDC.
R-BHB-mediated
restoration
nucleotide
coenzyme
ratios
state
decrease
ROS
RNS
blunt
allowing
cells
responsible
for
adaptive
immunity.
Limitations
proposed
therapy
include
following:
it
unknown
if
human
lung
functions
are
enhanced
ketosis,
risk
ketoacidosis
must
be
assessed
prior
initiating
treatment,
permissive
dietary
fat
carbohydrate
ketones
boost
function
not
yet
established.
The
third
limitation
could
addressed
studies
influenza-infected
mice.
A
clinical
study
warranted
where
COVID-19
consume
combined
ester
raise
blood
1
2
mM
measured
outcomes
symptom
severity,
length
infection,
case
fatality
rate.
Frontiers in Endocrinology,
Journal Year:
2021,
Volume and Issue:
12
Published: Nov. 25, 2021
Adult
and
childhood
obesity
have
reached
pandemic
level
proportions.
The
idea
that
caloric
excess
insufficient
levels
of
physical
activity
leads
to
is
a
commonly
accepted
answer
for
unwanted
weight
gain.
This
paradigm
offers
an
inconclusive
explanation
as
the
world
continually
moves
towards
unhealthier
heavier
existence
irrespective
energy
balance.
Endocrine
disrupting
chemicals
(EDCs)
are
resemble
natural
hormones
disrupt
endocrine
function
by
interfering
with
body’s
endogenous
hormones.
A
subset
EDCs
called
obesogens
been
found
cause
metabolic
disruptions
such
increased
fat
storage,
in
vivo
.
Obesogens
act
on
system
through
multiple
avenues
affect
homeostasis
variety
systems
gut
microbiome
adipose
tissue
functioning.
Obesogenic
compounds
shown
disturbances
later
life
can
even
pass
into
future
generations,
post
exposure.
rising
rates
related
disease
demanding
increasing
attention
chemical
screening
efforts
worldwide
preventative
strategies
keep
public
generations
safe.
review
addresses
most
current
findings
known
their
effects
system,
mechanisms
action
which
they
upon,
were
identified
with.
interplay
between
obesogens,
brown
tissue,
major
topics
will
be
covered.