Journal of Nutrition and Metabolism,
Journal Year:
2025,
Volume and Issue:
2025(1)
Published: Jan. 1, 2025
Genistein[5,7‐dihydroxy‐3‐(4‐hydroxyphenyl)chromen‐4‐one]
is
a
phytoestrogens
known
to
positively
impact
various
cardiovascular
disease
(CVD)
risk
factors.
However,
not
all
studies
have
yielded
consistent
results,
and
existing
meta‐analyses
comprehensively
addressed
CVD
We
conducted
systematic
search
of
the
PubMed,
ISI
Web
Science,
Embase,
Cochrane
Library
databases
up
June
2024,
following
PRISMA
2020
guidelines.
included
adult
randomized
controlled
trials
(RCTs)
that
examined
pure
genistein
supplementation
without
other
combined
interventions
reported
on
at
least
one
factor.
Data
extraction
quality
assessment
were
performed
independently
by
two
authors
using
standardized
form
Collaboration
Scale.
A
total
21
RCTs
included,
with
941
participants
in
group
918
control
group.
Statistical
analyses
R
software
meta
package.
The
meta‐analysis
revealed
that,
compared
placebo
group,
significantly
improved
levels
TC
([MD
95%
CI:
−9.38
[−14.64,
−4.12];
p
<
0.001]),
LDL‐C
−11.14
[−19.42,
−2.86];
Lp(a)
−0.69
[−0.98,
−0.41];
0.01),
SBP
−8.32
[−12.44,
−4.20];
DBP
−3.57
[−5.25,
−1.89];
P
=
0.04]),
fasting
blood
glucose
−3.98
[−6.79,
−1.17];
insulin
−1.79
[−2.05,
−1.54];
HOMA‐IR
−0.56
[−0.64,
−0.49];
homocysteine
−0.74
[−1.05,
−0.42];
0.01).
there
no
significant
improvements
TG,
HDL‐C,
CRP
levels.
observed
align
clinically
meaningful
thresholds
for
reduction.
Substantial
heterogeneity
most
outcomes
was
explored
via
subgroup
analysis.
Subgroup
based
treatment
duration,
geographic
region,
or
participant
health
status,
assessed
I
2
statistic.
analysis
did
reveal
any
differences,
indicating
influenced
factors
such
as
status.
Overall,
this
provides
evidence
intake
reduces
several
important
factors,
including
TC,
LDL‐C,
Lp(a),
SBP,
DBP,
glucose,
insulin,
HOMA‐IR,
Redox Biology,
Journal Year:
2023,
Volume and Issue:
63, P. 102760 - 102760
Published: May 23, 2023
Cancer
cells
and
ischemic
diseases
exhibit
unique
metabolic
responses
adaptations
to
energy
stress.
Forkhead
box
O
3a
(FoxO3a)
is
a
transcription
factor
that
plays
an
important
role
in
cell
metabolism,
mitochondrial
dysfunction
oxidative
stress
response.
Although
the
AMP-activated
protein
kinase
(AMPK)/FoxO3a
signaling
pathway
pivotal
maintaining
homeostasis
under
conditions
of
stress,
AMPK/FoxO3a
mitochondria-associated
ferroptosis
has
not
yet
been
fully
elucidated.
We
show
glucose
starvation
induced
activation
inhibited
by
erastin.
Inhibition
AMPK
or
loss
FoxO3a
cancer
condition
can
sensitize
these
ferroptosis.
Glucose
deprivation
mitochondria-related
gene
expression,
reduced
DNA(mtDNA)
copy
number,
decreased
expression
proteins
lowered
levels
respiratory
complexes
inducing
FoxO3a.
Loss
promoted
membrane
potential
hyperpolarization,
oxygen
consumption,
lipid
peroxide
accumulation
abolished
protective
effects
on
vitro.
In
addition,
we
identified
FDA-approved
antipsychotic
agent,
potent
agonist
trifluoperazine,
which
largely
ferroptosis-associated
cerebral
ischemia-reperfusion
(CIR)
injuries
rats
through
AMPK/FoxO3a/HIF-1α
mitochondria-dependent
mechanisms.
found
binds
promoters
SLC7A11
reduces
CIR-mediated
glutamate
excitotoxicity
inhibiting
SLC7A11.
Collectively,
results
suggest
modulation
regulates
activity
alters
The
regulation
may
play
crucial
controls
balance
confers
resistance
CIR
injuries.
Journal of Neuroinflammation,
Journal Year:
2024,
Volume and Issue:
21(1)
Published: April 2, 2024
Abstract
Background
Senescent
astrocytes
play
crucial
roles
in
age-associated
neurodegenerative
diseases,
including
Parkinson’s
disease
(PD).
Metformin,
a
drug
widely
used
for
treating
diabetes,
exerts
longevity
effects
and
neuroprotective
activities.
However,
its
effect
on
astrocyte
senescence
PD
remains
to
be
defined.
Methods
Long
culture-induced
replicative
model
1-methyl-4-phenylpyridinium/α-synuclein
aggregate-induced
premature
model,
mouse
of
were
investigate
the
metformin
vivo
vitro.
Immunofluorescence
staining
flow
cytometric
analyses
performed
evaluate
mitochondrial
function.
We
stereotactically
injected
AAV
carrying
GFAP-promoter-cGAS-shRNA
substantia
nigra
pars
compacta
regions
specifically
reduce
astrocytic
cGAS
expression
clarify
potential
molecular
mechanism
by
which
inhibited
PD.
Results
showed
that
vitro
mice.
Mechanistically,
normalized
function
DNA
release
through
mitofusin
2
(Mfn2),
leading
inactivation
cGAS-STING,
delayed
prevented
neurodegeneration.
Mfn2
overexpression
reversed
inhibitory
role
cGAS-STING
activation
senescence.
More
importantly,
ameliorated
dopamine
neuron
injury
behavioral
deficits
mice
reducing
accumulation
senescent
via
inhibition
activation.
Deletion
abolished
suppressive
Conclusions
This
work
reveals
delays
inhibiting
Mfn2-cGAS
suggest
is
promising
therapeutic
agent
diseases.
Current Medicine,
Journal Year:
2024,
Volume and Issue:
3(1)
Published: April 15, 2024
Abstract
Mitochondria
serve
as
the
primary
site
for
metabolizing
three
major
nutrients,
underscoring
their
pivotal
role
in
cellular
energy
metabolism
and
regulation
of
signaling
pathways.
Mitochondrial
homeostatic
imbalance
is
a
key
pathological
cause
development
many
diseases.
Hence,
preserving
mitochondrial
homeostasis
vital
normal
growth
cells
organisms.
Living
organisms
have
evolved
intricate
regulatory
mechanisms
to
ensure
homeostasis.
This
review
focuses
on
recent
advancements
comprehending
responsible
maintaining
addresses
current
challenges
this
field.
We
also
provide
an
overview
functions
mitochondria
both
physiological
conditions.
Emphasizing
potential
therapeutic
implications,
we
discuss
strategies
homeostasis,
recognizing
its
significance
mitigating
various
health
Graphical
Phytotherapy Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 8, 2025
Osteoporosis
is
divided
into
primary
and
secondary
types.
Primary
osteoporosis
may
result
from
estrogen
deficiency
in
postmenopausal
women,
imbalanced
bone
remodeling
the
elderly,
or
adolescent-type
development.
Secondary
can
be
caused
by
factors
like
long-term
glucocorticoid
treatment,
chronic
kidney
disease
(CKD),
deprivation,
oxidative
stress,
diabetes,
obesity.
This
review
focuses
on
therapeutic
potential
of
soy
isoflavones
for
osteoporosis.
At
cellular
level,
isoflavones,
as
natural
plant
extracts
phytoestrogens,
are
crucial
osteoblastogenesis
differentiation,
osteoclastogenesis,
osteoclast
mineralization,
marrow
mesenchymal
stromal
cell
differentiation.
They
also
maintain
calcium
homeostasis
regulating
extracellular
vitamin
D
levels.
In
terms
mitigate
it
endoplasmic
reticulum
mitochondria,
thus
senescence,
autophagy,
processes.
Moreover,
relieve
symptoms
related
to
CKD
inhibit
secretion,
which
directly
indirectly
benefits
treatment
Overall,
have
treat
enhancing
health,
metabolism,
alleviating
stress.
Future
research
should
explore
phytoestrogens
treating
exploration
focus
clarifying
safety,
identifying
side
effects,
determining
optimal
dosage
regimen,
developing
strategies
any
adverse
reactions.
addition,
further
large-scale,
multicenter
human
clinical
trials
necessary
accurately
evaluate
actual
effect
Journal of Orthopaedic Translation,
Journal Year:
2024,
Volume and Issue:
46, P. 53 - 64
Published: May 1, 2024
Osteoporosis
is
one
of
the
most
common
bone
diseases
in
middle-aged
and
elderly
populations
worldwide.
The
development
new
drugs
to
treat
disease
a
key
focus
research.
Current
treatments
for
osteoporosis
are
mainly
directed
at
promoting
osteoblasts
inhibiting
osteoclasts.
However,
there
currently
no
ideal
approach
treatment.
l-arginine
semi-essential
amino
acid
involved
number
cellular
processes,
including
nitric
production,
protein
biosynthesis,
immune
responses.
We
previously
reported
that
l-arginine-derived
compounds
can
play
regulatory
role
homeostasis.
To
investigate
specific
effect
on
Mildly
aged
ovariectomized
mouse
models
were
used
study
effects
osteogenesis
angiogenesis,
assessed
by
micro-computed
tomography
immunostaining
tissue.
osteogenesis,
adipogenesis
was
further
studied
vitro
using
obtained
from
cranial
cap
bone,
endothelial
cells,
an
adipogenic
cell
line.
Specific
methods
assess
these
processes
included
lipid
staining,
migration,
tube-forming,
wound-healing
assays.
Protein
mRNA
expression
determined
select
biomarkers.
found
attenuated
loss
promoted
angiogenesis.
increased
activity
vascular
whereas
it
inhibited
vitro.
In
addition,
we
altered
PINK1/Parkin
Bnip3
mitochondria
osteoblast-lineage
thereby
mitophagy
protecting
cells
ROS.
Similarly,
treatment
effectively
ameliorated
model.
promotes
angio-osteogenesis,
inhibits
adipogenesis,
mediated
PINK1/Parkin-
Bnip3-mediated
mitophagy.
L-arginine
supplementation
may
be
effective
adjunct
therapy
osteoporosis.
Advanced Healthcare Materials,
Journal Year:
2023,
Volume and Issue:
13(1)
Published: Aug. 26, 2023
Abstract
With
the
discovery
of
intrinsic
enzyme‐like
activity
metal
oxides,
nanozymes
garner
significant
attention
due
to
their
superior
characteristics,
such
as
low
cost,
high
stability,
multi‐enzyme
activity,
and
facile
preparation.
Notably,
in
field
biomedicine,
primarily
focus
on
disease
detection,
antibacterial
properties,
antitumor
effects,
treatment
inflammatory
conditions.
However,
potential
for
application
regenerative
medicine,
which
addresses
wound
healing,
nerve
defect
repair,
bone
regeneration,
cardiovascular
treatment,
is
garnering
interest
well.
This
review
introduces
an
innovative
strategy
within
realm
medicine.
The
primary
this
approach
lies
facilitation
osteochondral
regeneration
through
modulation
pathological
microenvironment.
catalytic
mechanisms
four
types
representative
are
first
discussed.
microenvironment
inhibiting
followed
by
summarizing
therapy
mechanism
barriers
introduced.
Further,
therapeutic
diseases
included.
To
improve
efficiency
facilitate
clinical
translation,
future
applications
also
discussed
some
challenges
addressed.