Diabetology,
Год журнала:
2022,
Номер
3(4), С. 583 - 595
Опубликована: Ноя. 7, 2022
Type
2
diabetes
(T2D)
has
increased
worldwide
at
an
alarming
rate.
Metabolic
syndrome
(MetS)
is
a
major
risk
factor
for
T2D
development.
One
of
the
main
reasons
abrupt
rise
in
MetS
incidence,
besides
sedentary
lifestyle,
westernized
diet
consumption,
with
high
content
industrialized
foods,
rich
added
dietary
sugars
(DS),
mainly
sucrose
and
fructose.
It
been
suggested
that
higher
intake
DS
could
impair
metabolic
function,
inducing
MetS,
predisposing
to
T2D.
However,
it
remains
poorly
explored
how
excessive
modulates
mitochondrial
key
player
metabolism.
This
review
explores
relationship
between
consumption
dysfunction
associated
development,
pointing
contribution
diet-induced
accumulation
advanced
glycation
end-products
(AGEs),
brief
insights
on
impact
maternal
high-sugar
AGEs
during
gestation
offspring
developing
later
life,
contributing
perpetuate
propagation.
Journal of Translational Medicine,
Год журнала:
2024,
Номер
22(1)
Опубликована: Сен. 23, 2024
Abstract
During
embryonic
and
neonatal
development,
mitochondria
have
essential
effects
on
metabolic
energetic
regulation,
shaping
cell
fate
decisions
leading
to
significant
short-
long-term
offspring
health.
Therefore,
perturbation
mitochondrial
function
can
a
pathological
effect
pregnancy.
Several
shreds
of
evidence
collected
in
preclinical
models
revealed
that
severe
dysfunction
is
incompatible
with
life
or
leads
critical
developmental
defects,
highlighting
the
importance
correct
during
embryo-fetal
development.
The
mechanism
impairing
development
unknown
may
include
dysfunctional
switch
differentiating
cells
due
decreased
ATP
production
altered
apoptotic
signalling.
Given
central
role
fetal
typical
Mitochondrial
Diseases
(MDs)
should,
principle,
be
detectable
However,
little
known
about
clinical
manifestations
MDs
In
this
manuscript,
we
review
suggesting
affect
highlight
maternal
outcomes
provide
wake-up
call
for
targeted
genetic
diagnosis.
World Journal of Clinical Pediatrics,
Год журнала:
2024,
Номер
14(1)
Опубликована: Дек. 20, 2024
Gestational
diabetes
mellitus
(GDM)
is
a
metabolic
disorder,
recognised
during
24-28
weeks
of
pregnancy.
GDM
linked
with
adverse
newborn
outcomes
such
as
macrosomia,
premature
delivery,
cardiovascular,
and
neurological
disorders.
Recent
investigations
have
focused
on
the
correlation
genetic
factors
β-cell
function
insulin
secretary
genes
(transcription
factor
7
like
2,
potassium
voltage-gated
channel
subfamily
q
member
1,
adiponectin
etc.
)
maternal
metabolism
gestation
leading
to
GDM.
Epigenetic
alterations
DNA
methylation,
histone
modification,
miRNA
expression
can
influence
gene
play
dominant
role
in
feto-maternal
pathways.
Interactions
between
environment,
resulting
differential
patterns
may
lead
Researchers
suggested
that
women
are
more
susceptible
resistance,
which
alters
intrauterine
surroundings,
hyperglycemia
hyperinsulinemia.
modifications
affecting
neuroendocrine
activities,
metabolism,
increase
risk
obesity
type
2
offspring.
There
currently
no
treatment
or
effective
preventive
method
for
GDM,
since
molecular
processes
resistance
not
well
understood.
The
present
review
was
undertaken
understand
pathophysiology
its
effects
neonatal
outcomes.
In
addition,
study
epigenetic
will
provide
researchers
search
predictive
biomarkers.
Biology of Sex Differences,
Год журнала:
2021,
Номер
12(1)
Опубликована: Ноя. 2, 2021
Abstract
Women
with
preeclampsia
(PE)
have
a
greater
risk
of
developing
hypertension,
cardiovascular
disease
(CVD),
and
renal
later
in
life.
Angiotensin
II
type
I
receptor
agonistic
autoantibodies
(AT1-AAs)
are
elevated
women
PE
during
pregnancy
up
to
2-year
postpartum
(PP),
the
reduced
uterine
perfusion
pressure
(RUPP)
rat
model
PE.
Blockade
AT1-AA
specific
7
amino
acid
peptide
binding
sequence
(‘n7AAc’)
improves
pathophysiology
observed
RUPP
rats;
however,
long-term
effects
inhibition
PP
is
unknown.
Pregnant
Sprague
Dawley
rats
were
divided
into
three
groups:
normal
pregnant
(NP)
(
n
=
16),
15),
+
‘n7AAc’
16).
Gestational
day
14,
surgery
was
performed
(144
μg/day)
administered
via
osmotic
minipump.
At
10-week
PP,
mean
arterial
(MAP),
glomerular
filtration
rate
(GFR)
cardiac
functions,
mitochondria
function
assessed.
MAP
vs.
NP
(126
±
4
116
3
mmHg,
p
<
0.05),
but
normalized
(109
mmHg)
0.05).
heart
size
by
’n7AAc’
Complex
IV
protein
abundance
enzymatic
activity,
along
glutamate/malate-driven
respiration
(complexes
I,
III,
IV),
which
prevented
‘n7AAc’.
not
only
blood
pregnancy,
also
changes
pressure,
hypertrophy,
mitochondrial
PP.
Nutrients,
Год журнала:
2023,
Номер
15(5), С. 1281 - 1281
Опубликована: Март 4, 2023
Obesogenic
environments
such
as
Westernized
diets,
overnutrition,
and
exposure
to
glycation
during
gestation
lactation
can
alter
peripheral
neuroendocrine
factors
in
offspring,
predisposing
for
metabolic
diseases
adulthood.
Thus,
we
hypothesized
that
obesogenic
the
perinatal
period
reprograms
offspring
energy
balance
mechanisms.
Four
rat
models
were
studied:
maternal
diet-induced
obesity
(DIO);
early-life
induced
by
postnatal
overfeeding;
glycation;
overfeeding
combined
with
glycation.
Metabolic
parameters,
expenditure,
storage
pathways
visceral
adipose
tissue
(VAT)
liver
analyzed.
Maternal
DIO
increased
VAT
lipogenic
[NPY
receptor-1
(NPY1R),
NPY
receptor-2
(NPY2R),
ghrelin
receptor],
but
also
lipolytic/catabolic
mechanisms
[dopamine-1
receptor
(D1R)
p-AMP-activated
protein
kinase
(AMPK)]
male
while
reducing
NPY1R
females.
Postnatally
overfed
animals
only
exhibited
higher
NPY2R
levels
VAT,
females
presented
downregulation.
reduces
expandability
decreasing
animals.
Regarding
liver,
D1R
was
decreased
all
models,
fat
accumulation
both
sexes
inflammatory
infiltration.
The
response
showed
a
sexual
dysmorphism,
glycotoxins
led
thin-outside-fat-inside
phenotype
conditions
impaired
balance,
increasing
risk
Oecologia,
Год журнала:
2023,
Номер
201(3), С. 637 - 648
Опубликована: Март 1, 2023
Understanding
the
consequences
of
heat
exposure
on
mitochondrial
function
is
crucial
as
mitochondria
lie
at
core
metabolic
processes,
also
affecting
population
dynamics.
In
adults,
metabolism
varies
with
temperature
but
can
depend
thermal
conditions
experienced
during
development.
We
exposed
zebra
finches
to
two
alternative
treatments
early
development:
"constant",
maintained
birds
ambient
35
°C
from
parental
pair
formation
fledglings'
independence,
while
"periodic"
heated
broods
40
°C,
6
h
daily
nestling
stage.
Two
years
later,
we
acclimated
both
experiments
25
for
21
days,
before
exposing
them
artificial
(40
5
10
days).
After
conditions,
measured
red
blood
cells'
using
a
high-resolution
respirometer.
found
significantly
decreased
Routine,
Oxidative
Phosphorylation
(OxPhos)
and
Electron
Transport
System
maximum
capacity
(ETS)
after
treatments.
addition,
"constant"
in
life
showed
lower
oxygen
consumption
Proton
Leak
(Leak)
stage
treatment
adults.
Females
higher
respiration
ETS
independent
treatments,
this
pattern
was
reversed
OxPhos
coupling
efficiency
(OxCE).
Our
results
show
that
short-term
acclimation
involved
reduced
respiration,
reaction
adult
depends
intensity,
duration
early-life
stages.
study
provides
insight
into
complexity
underlying
variation
raises
questions
adaptive
value
long-lasting
physiological
adjustments
triggered
by
environment.
iScience,
Год журнала:
2024,
Номер
27(3), С. 109276 - 109276
Опубликована: Фев. 20, 2024
Chronic
stress
episodes
increase
metabolic
disease
risk
even
after
recovery.
We
propose
that
persistent
detrimentally
impacts
hepatic
reprogramming,
particularly
mitochondrial
function.
In
male
C57BL/6
mice
chronic
variable
(Cvs)
reduced
energy
expenditure
(EE)
and
body
mass
despite
increased
intake
versus
controls.
This
coincided
with
decreased
glucose
metabolism
lipid
β-oxidation,
correlating
EE.
After
Cvs,
function
revealed
thermodynamic
efficiency
(ƞ-opt)
of
complex
CI,
positively
blood
NEFA
inversely
Cvs
recovery,
the
flexibility
hepatocytes
was
lost.
Reduced
CI-driving
NAD+/NADH
ratio,
diminished
methylation-related
one-carbon
cycle
components
hinted
at
epigenetic
regulation.
Although
initial
DNA
methylation
differences
were
minimal
they
diverged
during
recovery
phase.
Here,
altered
enrichment
linked
transcriptional
networks
observed.
conclusion,
rapidly
initiates
reprogramming
metabolism,
supported
by
lasting
modifications.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(10), С. 5431 - 5431
Опубликована: Май 16, 2024
Maternal
type
2
diabetes
mellitus
(T2DM)
has
been
shown
to
result
in
foetal
programming
of
the
hypothalamic-pituitary-adrenal
(HPA)
axis,
leading
adverse
outcomes.
T2DM
is
preceded
by
prediabetes
and
shares
similar
pathophysiological
complications.
However,
no
studies
have
investigated
effects
maternal
on
HPA
axis
function
postnatal
offspring
development.
Hence,
this
study
pregestational
Pre-diabetic
(PD)
non-pre-diabetic
(NPD)
female
Sprague
Dawley
rats
were
mated
with
non-prediabetic
males.
After
gestation,
male
pups
born
from
PD
NPD
groups
collected.
Markers
function,
adrenocorticotropin
hormone
(ACTH)
corticosterone,
measured
all
dams
pups.
Glucose
tolerance,
insulin
gene
expressions
mineralocorticoid
(MR)
glucocorticoid
(GR)
receptors
further
at
birth
their
developmental
milestones.
The
results
demonstrated
increased
basal
concentrations
ACTH
corticosterone
group
comparison
NPD.
Furthermore,
show
an
increase
concentrations,
disturbed
MR
GR
expression,
glucose
intolerance
resistance
assessed
via
Homeostasis
Model
Assessment
(HOMA)
indices
compared
These
observations
reveal
that
associated
dysregulation
impacting
development
along
impaired
handling.
Abstract
Age
is
a
prominent
risk
factor
for
cardiometabolic
disease,
often
leading
to
heart
structural
and
functional
changes.
However,
precise
molecular
mechanisms
underlying
cardiac
remodeling
dysfunction
exclusively
resulting
from
physiological
aging
remain
elusive.
Previous
research
demonstrated
age‐related
alterations
in
baboons,
analogous
humans.
The
goal
of
this
study
identify
early
preceding
adaptations,
shedding
light
on
the
regulation
age‐associated
Unbiased
transcriptomics
left
ventricle
samples
are
performed
female
baboons
aged
7.5–22.1
years
(human
equivalent
≈30–88
years).
Weighted‐gene
correlation
network
pathway
enrichment
analyses
performed,
with
histological
validation.
Modules
transcripts
negatively
correlated
age
implicated
declined
metabolism‐oxidative
phosphorylation,
tricarboxylic
acid
cycle,
glycolysis,
fatty‐acid
β‐oxidation.
Transcripts
positively
suggested
metabolic
shift
toward
glucose‐dependent
anabolic
pathways,
including
hexosamine
biosynthetic
(HBP).
This
associated
increased
glycosaminoglycan
synthesis,
modification,
precursor
synthesis
via
HBP,
extracellular
matrix
accumulation,
verified
histologically.
Upregulated
matrix‐induced
signaling
coincided
followed
by
hypertrophy‐related
pathways.
Overall,
these
findings
revealed
transcriptional
metabolism
favoring
accumulation
through
HBP
before
hypertrophy.
Unveiling
provides
potential
targets
diseases,
offering
novel
insights
into
mechanisms.