Ovarian vascular aging: a hidden driver of mid-age female fertility decline
Ge Wang,
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Ruihua Yang,
No information about this author
Hua Zhang
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et al.
npj Aging,
Journal Year:
2025,
Volume and Issue:
11(1)
Published: March 30, 2025
Although
ovarian
reserve
remains
sufficient,
function
declines
in
mid-age,
leading
to
reduced
fertility
around
age
35,
with
the
causes
remaining
unclear.
Recent
studies
highlight
vascular
aging
as
a
key
factor
this
decline,
age-related
reductions
remodeling
disrupting
oocyte
development.
Salidroside,
natural
compound
that
reverses
and
promotes
angiogenesis,
presents
promising
strategy
rejuvenate
health
enhance
fertility,
offering
potential
for
preserving
reproductive
aged
women.
Language: Английский
Single-oocyte proteome-transcriptome co-profiling reveals a role of dysregulated lactate metabolism in oocyte aging
Xudong Fu,
No information about this author
Cao Lanrui,
No information about this author
Yirong Jiang
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et al.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 9, 2025
Abstract
The
declined
oocyte
quality
with
age
is
a
major
risk
factor
for
female
infertility.
Although
transcriptomic
changes
have
been
examined
in
aged
oocytes,
the
proteomic
landscape,
which
reflects
primary
functional
executors
of
genes,
and
factors
shaping
remains
largely
unexplored.
This
gap
limits
our
understanding
molecular
features
driving
aging.
To
address
this,
we
performed
single-cell
proteome/transcriptome
co-profiling
GV
MII-aged
oocytes
from
mice
humans,
revealing
species-
stage-specific
proteomic/transcriptomic
during
Strikingly,
observed
uncoupled
alterations,
indicating
that
are
not
primarily
driven
by
RNA
alterations.
Leveraging
profiling,
captured
heterogeneity
revealed
MCT4
as
conserved
aging
biomarker.
Functional
studies
suggested
mediated
via
lactate
export,
its
inhibition
improved
quality.
These
findings
indicated
altered
metabolism
driver
intervention
target
underscored
value
profiling
dissecting
Language: Английский
Research Progress on the Interaction Between SIRT1 and Mitochondrial Biochemistry in the Aging of the Reproductive System
Yang Li,
No information about this author
Kai Kang,
No information about this author
Huimingda Bao
No information about this author
et al.
Biology,
Journal Year:
2025,
Volume and Issue:
14(6), P. 643 - 643
Published: June 2, 2025
The
protein
associated
with
the
silencing
information
regulator
2-associated
enzyme1
(SIRT1)
is
a
highly
conserved
nicotinamide
adenine
dinucleotide
(NAD+)-dependent
deacetylase
and
key
member
of
sirtuin
family.
SIRT1
plays
an
essential
role
in
various
cellular
physiological
processes,
primarily
localized
nucleus
but
also
active
cytoplasm
mitochondria.
Recent
studies
have
demonstrated
its
capacity
to
delay
aging
multiple
organs
tissues,
although
underlying
mechanisms
remain
incompletely
understood.
Additionally,
exerts
significant
influence
on
metabolic
regulation
genetic
processes.
As
primary
source
energy,
mitochondria
are
central
numerous
biological
functions.
Mitochondrial
dysfunction
has
been
implicated
onset
progression
diseases
increasingly
recognized
for
aging-related
This
article
investigates
interaction
between
regulating
reproductive
system
elucidates
their
potential
action,
providing
insights
clinical
research
into
aging.
Language: Английский