Endocrine Metabolic & Immune Disorders - Drug Targets,
Journal Year:
2023,
Volume and Issue:
24(6), P. 709 - 716
Published: Nov. 30, 2023
Background:
The
increase
in
portal
insulin
levels
has
been
shown
to
upregulate
growth
hormone
receptor
expression
the
liver,
leading
increased
insulin-like
hormone-
1
levels.
Metformin
inhibits
hepatic
gluconeogenesis
and
reduces
fasting
insulin.
Objective:
We
evaluated
effect
of
metformin
treatment
patients
with
acromegaly
on
hormone,
hormone-1,
pituitary
adenoma
size.
Methods:
Patients
who
were
followed
up
diagnosis
Istanbul
University-
Cerrahpaşa,
Cerrahpaşa
Medical
Faculty
evaluated.
divided
into
three
groups
after
adenectomy
as
those
received
somatostatin
ligand
(group
A),
only
B),
C).
Groups
A
B
compared
each
other,
group
C
among
themselves.
Results:
While
median
factor-1
level
decreased
170
ng/ml
Group
treatment,
229
B,
a
statistically
significant
difference
was
found
between
two
(p
=0.020).
There
no
post-treatment
residual
sizes
>0.005).
In
C,
there
values
pre-and
post-metformin
=0.078);
however,
from
205
168
during
be
=0.027).
Conclusion:
Due
acromegaly,
it
can
used
disease
control,
well
diabetes
treatment.
Nutrients,
Journal Year:
2025,
Volume and Issue:
17(1), P. 178 - 178
Published: Jan. 2, 2025
The
connections
between
sarcopenia
and
various
chronic
conditions,
including
type
2
diabetes
(T2DM),
metabolic
syndrome
(MetS),
liver
disease
have
been
highlighted
recently.
There
is
also
a
high
occurrence
of
in
dysfunction-associated
steatotic
(MASLD)
patients,
who
are
often
disregarded.
Both
experimental
clinical
findings
suggest
complex,
bidirectional
relationship
MASLD
sarcopenia.
While
vitamin
D,
testosterone,
specific
drug
therapies
show
promise
mitigating
sarcopenia,
consensus
on
effective
treatments
lacking.
Recent
focus
lifestyle
interventions
emphasizes
dietary
therapy
exercise
for
sarcopenic
obesity
MASLD.
Challenges
arise
as
weight
loss,
primary
treatment,
may
lead
to
muscle
mass
reduction.
therapeutic
approach
morbidly
obese
patients
includes
bariatric
surgery
(BS).
BS
induces
loss
stabilizes
imbalances,
but
its
impact
nuanced,
underscoring
the
need
further
research.
Our
aim
provide
comprehensive
review
interplay
offer
insight
into
most
recent
challenges
discoveries,
overlooked
or
unrecognized
poses
significant
managing
these
patients.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 2, 2025
Abstract
Overconsumption
of
added
sugars
such
as
fructose
has
been
associated
with
a
remarkable
decline
in
metabolic
health.
Fructose
is
primarily
metabolized
by
the
small
intestines
and
liver,
via
phosphorylation
mediated
ketohexokinase
(KHK).
KHK
activity
traditionally
viewed
lacking
negative
feedback
mechanisms,
those
present
to
limit
glucose
metabolism,
leading
excessive
fat
accumulation
characteristic
dysfunction-associated
liver
disease
(MASLD).
In
this
study,
we
observe
downregulation
hepatocytes
diet-induced
genetic
models
MASLD.
Reduced
coincides
decreased
flux
fructose-derived
carbons
into
glycolytic
amino
acid
pathways,
suggesting
presence
mechanisms
that
KHK-mediated
fructolysis
liver.
We
subsequently
focused
on
growth
hormone
(GH)/insulin-like
factor
(IGF)
signaling
pathway
potential
mechanism
antagonizing
expression.
transgenic
mice
enhanced
GH
signaling,
levels
are
reduced,
whereas
reduced
leads
increased
Additionally,
administration
IGF-1
cell
cultures
induces
time-dependent
degradation
KHK,
facilitated
direct
interactions
between
receptor
(IGF-1R).
Single-nuclei
RNA
sequencing
revealed
elevated
IGF-1R
expression
from
MASLD
mice,
supported
human
patient
samples,
which
also
show
Taken
together,
these
findings
describe
novel
GH/IGF-1
regulates
offering
new
insights
how
adapts
stress
fructose-driven
dysfunction.
Biology,
Journal Year:
2025,
Volume and Issue:
14(3), P. 274 - 274
Published: March 7, 2025
Recent
advancements
in
tissue
engineering
and
stem
cell
science
have
positioned
bone
disease
treatment
as
a
promising
frontier
regenerative
medicine.
This
review
explores
the
hormonal
signaling
pathways
critical
to
regeneration,
with
focus
on
their
clinical
relevance.
Key
endocrine
factors,
including
thyroid
hormones
(T3
T4),
insulin-like
growth
factor
1
(IGF-1),
morphogenetic
proteins
(BMPs),
parathyroid
hormone
(PTH),
calcitonin,
fibroblast
23
(FGF23),
play
pivotal
roles
remodeling
by
regulating
osteoblast
activity,
resorption,
mineralization.
These
factors
primarily
act
through
Wnt/β-catenin,
BMP,
FGF
pathways,
which
govern
repair
regeneration.
While
animal
models,
such
axolotls,
zebrafish,
Xenopus
laevis,
provide
valuable
findings
about
these
mechanisms,
translating
into
human
applications
presents
challenges.
underscores
therapeutic
potential
of
modulating
networks
enhance
regeneration
while
cautioning
against
possible
adverse
effects,
uncontrolled
proliferation
or
metabolic
imbalances.
By
integrating
knowledge
from
this
work
provides
foundation
for
optimizing
hormone-based
therapies
treatment.
Current Oncology,
Journal Year:
2023,
Volume and Issue:
30(6), P. 5574 - 5592
Published: June 9, 2023
Liver
transplantation
is
a
treatment
option
for
nonresectable
patients
with
early-stage
HCC,
more
significant
advantages
when
Milan
criteria
are
fulfilled.
An
immunosuppressive
regimen
required
to
reduce
the
risk
of
graft
rejection
after
transplantation,
and
CNIs
represent
drugs
choice
in
this
setting.
However,
their
inhibitory
effect
on
T-cell
activity
accounts
higher
tumour
regrowth.
mTOR
inhibitors
(mTORi)
have
been
introduced
as
an
alternative
approach
conventional
CNI-based
regimens
address
both
immunosuppression
cancer
control.
The
PI3K-AKT-mTOR
signalling
pathway
regulates
protein
translation,
cell
growth,
metabolism,
frequently
deregulated
human
tumours.
Several
studies
suggested
role
mTORi
reducing
HCC
progression
LT,
accounting
lower
recurrence
rate.
Furthermore,
controls
renal
damage
associated
CNI
exposure.
Conversion
stabilizing
recovering
dysfunction,
suggesting
essential
renoprotective
effect.
Limitations
therapeutic
related
negative
impact
lipid
glucose
metabolism
well
proteinuria
development
wound
healing.
This
review
aims
summarize
roles
managing
undergoing
LT.
Strategies
overcome
common
adverse
effects
also
proposed.
Endocrine Journal,
Journal Year:
2023,
Volume and Issue:
70(10), P. 959 - 967
Published: Jan. 1, 2023
An
association
exists
between
nonalcoholic
fatty
liver
disease
(NAFLD)
and
growth
hormone
(GH).
Patients
with
deficiency
(GHD)
may
be
more
susceptible
to
NAFLD.
The
prevalence
of
NAFLD
steatohepatitis
(NASH)
in
GHD
patients
is
currently
unknown.
Multiple
databases
were
searched
for
experiments
related
(or
NASH)
GHD.
Screening,
quality
evaluation
data
extraction
carried
out
independently
by
two
authors.
Analyses
used
random
or
fixed
effects
models,
including
prevalence,
NASH
odds
ratio
(OR)
95%
confidence
interval
(CI).
We
included
10
studies
a
total
782
participants.
results
showed
that
the
was
51%
(95%
CI:
39–63).
risk
significantly
higher
than
controls
(age-,
sex-
body
mass
index-matched,
without
GHD)
(pooled
OR
=
4.27,
1.33–13.68%,
p
0.015).
18%
5–31).
general
population,
especially
NASH.
There
need
develop
targeted
strategies
early
identification,
prevention,
control
NAFLD/NASH
Biology,
Journal Year:
2024,
Volume and Issue:
13(7), P. 494 - 494
Published: July 3, 2024
Large-scale
mortality
events
have
occurred
during
the
winter
in
Atlantic
salmon
sea
cages
Eastern
Canada
and
Iceland.
Thus,
held
at
3
°C
that
were
apparently
healthy
(i.e.,
asymptomatic)
had
'early'
'advanced'
symptoms
of
'winter
syndrome'/'winter
disease'
(WS/WD),
we
measured
hepatic
lipid
classes
fatty
acid
levels,
transcript
expression
34
molecular
markers
liver
disease
(FLD;
a
clinical
sign
WS/WD).
In
addition,
correlated
our
results
with
previously
reported
characteristics
associated
this
disease's
progression
these
same
individuals.
Total
triacylglycerol
(TAG)
levels
increased
by
~50%,
32
genes
was
dysregulated,
fish
FLD.
TAG
positively
inflammation
(
Frontiers in Endocrinology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 2, 2024
Context
Although
the
role
of
insulin-like
growth
factor
I
(IGF-1)
in
nonalcoholic
fatty
liver
disease
(NAFLD)
has
garnered
attention
recent
years,
few
studies
have
examined
both
reduced
and
elevated
levels
IGF-1.
Objective
The
aim
this
study
was
to
examine
potential
relationship
between
IGF-1
risk
new-onset
NAFLD
patients
with
pituitary
neuroendocrine
tumors
(PitNET).
Methods
We
employed
multivariable
Cox
regression
models
two-piecewise
assess
association
NAFLD.
Hazard
ratios
(HRs)
their
corresponding
95%
confidence
intervals
(CIs)
were
calculated
quantify
association.
Furthermore,
a
dose-response
correlation
lgIGF-1
development
plotted.
Additionally,
we
also
performed
subgroup
analysis
series
sensitivity
analysis.
Results
A
total
3,291
PitNET
enrolled
present
study,
median
duration
follow-up
65
months.
Patients
either
or
at
baseline
found
be
higher
compared
normal
IGF-1(log-rank
test,
P
<
0.001).
In
adjusted
model
(model
IV),
participants
IGF-1,
HRs
those
2.33
(95%
CI
1.75,
3.11)
2.2
1.78,
2.7).
non-adjusted
models,
our
revealed
U-shaped
Moreover,
results
from
analyses
consistent
main
results.
Conclusions
There
trend
PitNET.
Further
evaluation
discoveries
is
warranted.