Cutting-edge biotherapeutics and advanced delivery strategies for the treatment of metabolic dysfunction-associated steatotic liver disease spectrum
Journal of Controlled Release,
Journal Year:
2025,
Volume and Issue:
380, P. 433 - 456
Published: Feb. 11, 2025
Language: Английский
Non-Alcoholic Fatty Liver Disease in Everyday Clinical Practice: From Diagnosis to Therapy
Life,
Journal Year:
2025,
Volume and Issue:
15(3), P. 363 - 363
Published: Feb. 25, 2025
Non-alcoholic
fatty
liver
disease
(NAFLD)
is
currently
one
of
the
most
common
hepatic
disorders
observed
in
daily
medical
practice
[...]
Language: Английский
Hepatokines and MASLD: The GLP1-Ras-FGF21-Fetuin-A Crosstalk as a Therapeutic Target
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(19), P. 10795 - 10795
Published: Oct. 8, 2024
The
introduction
of
the
term
“Metabolic
Steatotic
Liver
Disease”
(MASLD)
underscores
critical
role
metabolic
dysfunction
in
development
and
progression
chronic
liver
disease
emphasizes
need
for
strategies
that
address
both
its
comorbidities.
In
recent
years,
a
liver-focused
perspective
has
revealed
altered
endocrine
function
fatty
is
key
contributor
to
dysregulation
observed
MASLD.
Due
secretory
capacity,
liver’s
increased
production
proteins
known
as
“hepatokines”
been
linked
insulin
resistance,
explaining
why
MASLD
often
precedes
other
organs
ultimately
contributes
systemic
disease.
Among
these
hepatokines,
fibroblast
growth
factor
21
(FGF21)
fetuin-A
play
central
roles
regulating
abnormalities
associated
with
MASLD,
their
dysregulated
secretion
response
stress
implicated
This
review
postulates
modulation
by
GLP1-Ras
may
mediate
beneficial
effects
drugs,
which
have
attention
emerging
pharmacotherapy
By
discussing
crosstalk
between
GLP1-Ras-FGF21-fetuin-A,
this
hypothesizes
possible
novel
GLP1-FGF21
dual
agonist
contribute
management
diseases.
Although
research
needed
go
into
details
crosstalk,
topic
help
researchers
explore
mechanisms
type
manage
Language: Английский
Lactobacillus delbrueckii subsp. lactis CKDB001 Ameliorates Metabolic Complications in High-Fat Diet-Induced Obese Mice
Hyunsoo Jang,
No information about this author
Hyunchae Joung,
No information about this author
Jaeryang Chu
No information about this author
et al.
Nutrients,
Journal Year:
2024,
Volume and Issue:
16(24), P. 4260 - 4260
Published: Dec. 10, 2024
Background/Objectives:
Functional
probiotics,
particularly
Lactobacillus
delbrueckii
subsp.
lactis
CKDB001,
have
shown
potential
as
a
therapeutic
option
for
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD).
However,
their
effects
not
been
confirmed
in
vivo
systems.
Here,
we
investigated
the
of
L.
CKDB001
on
insulin
resistance,
dyslipidemia,
MASLD,
and
lipid
metabolism
murine
model
high-fat
diet
(HFD)-induced
obesity.
Methods:
The
mice
were
divided
into
four
groups
(n
=
12
per
group)—normal
chow
(NCD),
high
fat
(HFD),
HFD
with
(LL),
resmetirom
(positive
control
(PC),
thyroid
receptor
β
agonist).
experimental
animals
fed
NCD
or
weeks,
followed
by
an
additional
12-week
oral
treatment
LL
resmetirom.
Results:
supplementation
reduced
body
weight,
levels,
HOMA-IR
compared
those
group,
indicating
improved
sensitivity.
Additionally,
serum
triglyceride
(TG)
levels
without
affecting
total
cholesterol
(TC)
levels.
consumption
increased
weight
hepatic
TG
TC
ectopic
accumulation;
however,
reversed
these
changes,
liver-specific
effect
metabolism.
Furthermore,
administration
attenuated
NAFLD
activity
scores,
fibrosis,
function
markers
(aspartate
aminotransferase),
enhanced
Adenosine
monophosphate-activated
protein
kinase
(AMPK)
phosphorylation.
did
considerably
affect
expression
genes
related
to
In
epididymal
adipose
tissue,
leptin
but
had
no
adiponectin;
additionally,
histological
analysis
showed
increase
adipocyte
size,
potentially
linked
energy
Conclusions:
Collectively,
findings
suggest
that
could
be
promising
candidate
improving
sensitivity,
reducing
accumulation,
mitigating
MASLD.
Language: Английский
Knock-Out of IKKepsilon Ameliorates Atherosclerosis and Fatty Liver Disease by Alterations of Lipid Metabolism in the PCSK9 Model in Mice
U. Weiß,
No information about this author
Eleonora Mungo,
No information about this author
Michelle Haß
No information about this author
et al.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(19), P. 10721 - 10721
Published: Oct. 5, 2024
The
inhibitor-kappaB
kinase
epsilon
(IKKε)
represents
a
non-canonical
IκB
that
modulates
NF-κB
activity
and
interferon
I
responses.
Inhibition
of
this
pathway
has
been
linked
with
atherosclerosis
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD),
yet
the
results
are
contradictory.
In
study,
we
employed
combined
model
hepatic
PCSK9D377Y
overexpression
high-fat
diet
for
16
weeks
to
induce
steatosis.
development
atherosclerotic
plaques,
serum
lipid
concentrations,
metabolism
in
adipose
tissue
were
compared
between
wild-type
IKKε
knock-out
mice.
formation
progression
plaques
markedly
reduced
knockout
mice,
accompanied
by
cholesterol
levels,
fat
deposition,
macrophage
infiltration
within
plaque.
Additionally,
fatty
was
diminished
these
which
may
be
attributed
decreased
levels
multiple
species,
particularly
monounsaturated
acids,
triglycerides,
ceramides
serum.
modulation
several
proteins
suggests
de
novo
lipogenesis
inflammatory
response
suppressed
as
consequence
inhibition.
conclusion,
our
data
suggest
is
involved
mechanisms
both
MASLD.
therefore
represent
novel
approach
treatment
cardiovascular
diseases.
Language: Английский
Editorial: Enhancing targeted screening of people living with HIV for liver fibrosis
Alimentary Pharmacology & Therapeutics,
Journal Year:
2024,
Volume and Issue:
60(10), P. 1453 - 1454
Published: Oct. 17, 2024
LINKED
CONTENT
This
article
is
linked
to
Allende
et
al
paper.
To
view
this
article,
visit
https://doi.org/10.1111/apt.18236
.
Language: Английский