Hepatology Communications,
Год журнала:
2024,
Номер
8(4)
Опубликована: Март 29, 2024
Background:
Alcohol-associated
liver
disease
(ALD)
is
a
major
health
care
challenge
worldwide
with
limited
therapeutic
options.
Although
mesenchymal
stem/stromal
cells
(MSCs)
represent
newly
emerging
approach
to
treat
ALD,
thus
far,
there
have
been
extensive
efforts
try
and
enhance
their
efficacy,
including
genetically
engineering
MSCs.
FGF21,
an
endocrine
stress-responsive
hormone,
has
shown
regulate
energy
balance,
glucose,
lipid
metabolism
the
homing
of
MSCs
toward
injured
sites.
Therefore,
purpose
this
study
was
investigate
whether
that
overexpress
FGF21
(FGF21-MSCs)
improve
effect
in
treating
ALD.
Methods:
Human
umbilical
cord-derived
served
as
gene
delivery
vehicle
for
gene.
were
transduced
using
lentiviral
vectors
mediate
overexpression.
We
utilized
both
chronic
Lieber-DeCarli
Gao-binge
models
ethanol-induced
injury
observe
FGF21-MSCs.
Liver
phenotypically
evaluated
by
performing
biochemical
methods,
histology,
inflammatory
cytokine
levels.
Results:
Compared
alone,
administration
overexpressing
FGF21(FGF21-MSCs)
treatment
significantly
enhanced
ALD
mice,
indicated
alleviation
reduced
steatosis,
infiltration,
oxidative
stress,
hepatic
apoptosis,
promotion
regeneration.
Mechanistically,
could
facilitate
immunomodulatory
function
on
macrophages
setting
metabolic
commitment
phosphorylation,
which
enables
exhibit
anti-inflammatory
inclination.
Conclusions:
Our
data
elucidate
MSC
modification
may
help
exploration
effective
MSCs-based
cell
therapies
Medicine & Science in Sports & Exercise,
Год журнала:
2023,
Номер
55(5), С. 873 - 883
Опубликована: Янв. 5, 2023
Alcoholics
develop
muscle
atrophy
and
weakness
from
excessive
ethanol
(EtOH)
intake.
To
date,
most
research
has
examined
outcomes
of
alcohol-induced
under
basal
or
unstressed
conditions
despite
physical
stress
being
a
normal
occurrence
in
physiological
setting.
Therefore,
this
study
set
out
to
determine
if
recovery
torque
is
impaired
after
repetitive
bouts
skeletal
during
short-term
(experiment
1)
long-term
2)
EtOH
consumption.Twenty
male
female
mice
were
assigned
receive
either
20%
their
drinking
water
100%
water.
Short-
consumption
was
predetermined
be
intake
starting
at
4
26
wk,
respectively.
Anterior
crural
muscles
performed
repeated
using
vivo
eccentric
contractions,
with
tetanic
isometric
measured
immediately
pre-
postinjury.
A
total
10
completed
14
d
between
each
bout
within
1-5
6-10
2),
12
wk
5
6.Mice
consuming
had
blood
alcohol
concentrations
up
270
mg·dL
-1
.
In
experiment
1,
five
contractions
did
not
reduce
torque,
regardless
sex
treatment
(
P
≥
0.173).
Similarly,
2,
preinjury
torques
differ
day
values
0.322).
However,
there
group
effect
for
6
weaker
than
controls
≤
0.002).Excessive
short-
misuse
mouse
model
affect
the
muscle's
ability
regain
strength
suggesting
that
may
as
detrimental
once
predicted.
Life Sciences,
Год журнала:
2023,
Номер
327, С. 121818 - 121818
Опубликована: Июнь 1, 2023
Chronic
alcohol
consumption
in
rodents
induces
mesenteric
collecting
lymphatic
vessel
hyperpermeability,
lymph
leakage,
and
consequent
immunometabolic
dysregulation
of
the
perilymphatic
adipose
tissue
(PLAT).
The
specific
components
mediating
PLAT
remain
to
be
identified.
Specifically,
whether
impacts
composition
is
unknown.
This
study
aimed
determine
associated
changes
plasma
proteome.
Adult
male
rats
were
fed
a
Lieber–DeCarli
liquid
diet
containing
36
%
calories
from
for
10
weeks.
Time-matched
control
animals
pair-fed.
At
sacrifice
was
collected
2
h
using
lymph-fistula
technique
prior
sacrifice.
Quantitative
discovery-based
proteomics
identified
total
703
proteins.
An
integrative
approach
combining
Ingenuity
Pathway
Analysis
(IPA)
an
unbiased
network
analysis
WGCNA
(Weighted
Gene
Co-expression
Network
Analysis)
used
analyze
data.
IPA
results
significant
upregulation
cluster
apolipoproteins
alcohol-fed
compared
with
pair-fed
controls
downregulation
34
proteins
animals.
several
candidate
hub
that
also
significantly
differentially
expressed
controls.
module
without
enrichment
Of
59
contained
within
this
module,
only
Future
studies
will
investigate
further
functionality
affected
by
feeding
both
plasma.
Neurobiology of Stress,
Год журнала:
2023,
Номер
29, С. 100603 - 100603
Опубликована: Дек. 25, 2023
Chronic
stress
and
alcohol
(ethanol)
use
are
highly
interrelated
can
change
an
individual's
behavior
through
molecular
adaptations
that
do
not
the
DNA
sequence,
but
instead
gene
expression.
A
recent
wealth
of
research
has
found
these
nongenomic
changes
be
transmitted
across
generations,
which
could
partially
account
for
"missing
heritability"
observed
in
genome-wide
association
studies
disorder
other
stress-related
neuropsychiatric
disorders.
In
this
review,
we
summarize
behavioral
outcomes
inheritance
chronic
ethanol
exposure
germline
mechanisms
give
rise
to
heritability.
doing
so,
outline
need
further
to:
(1)
Investigate
individual
paternal,
maternal,
biparental
stress-
ethanol-related
inheritance;
(2)
Synthesize
dissect
cross-generational
exposure;
(3)
Determine
preconception
contribute
alcohol-related
disease
risk,
using
cancer
as
example.
detailed
understanding
effects
and/or
will
yield
novel
insight
into
impact
ancestral
perturbations
on
risk
generations
uncover
actionable
targets
improve
human
health.
Brazilian Journal of Health Review,
Год журнала:
2024,
Номер
7(1), С. 7660 - 7684
Опубликована: Фев. 29, 2024
Introdução:
O
álcool
tem
sido
consumido
desde
os
primórdios
da
civilização
e
se
tornou
parte
integrante
de
diferentes
culturas
ao
longo
do
tempo,
sendo
seu
consumo
excessivo
reconhecido
como
uma
doença
na
era
contemporânea.
Apesar
disso,
o
número
usuários
crescido
cada
vez
mais.
alcoolismo
representa
um
desafio
significativo
saúde
pública,
que
está
associado
a
série
desequilíbrios
nos
sistemas
orgânicos.
Metodologia:
estudo
trata-se
revisão
integrativa
literatura
acerca
dos
mecanismos
fisiopatológicos
envolvem
formação
danos
celulares
induzidos
pela
toxicidade
álcool.
A
estratégia
usada
para
levantamento
artigos
foi
busca
ativa
por
estudos
base
dados
PubMed.
Resultados
Discussões:
Os
pelo
podem
ser
divididos
em
três
principais,
são
direta,
modulação
processos
injúrias
via
radicais
livres,
todos
podendo
causados
etanol,
bem
seus
resíduos
metabólicos
com
destaque
acetaldeído.
Praticamente
orgânicos
humanos
sofrem
relacionados
bebidas
alcoólicas,
variando
acordo
dose,
padrão
ingestão
metabolismo
inato
indivíduo.
Conclusão:
efeitos
adversos
todo
corpo,
afetando
principalmente
sistema
cardiovascular,
digestório,
endócrino,
nervoso,
musculoesquelético,
imunológico
respiratório,
tornando
necessária
abordagem
multidisciplinar
entender
mitigar
esses
efeitos,
promovendo
pública.
Hepatology Communications,
Год журнала:
2024,
Номер
8(4)
Опубликована: Март 29, 2024
Background:
Alcohol-associated
liver
disease
(ALD)
is
a
major
health
care
challenge
worldwide
with
limited
therapeutic
options.
Although
mesenchymal
stem/stromal
cells
(MSCs)
represent
newly
emerging
approach
to
treat
ALD,
thus
far,
there
have
been
extensive
efforts
try
and
enhance
their
efficacy,
including
genetically
engineering
MSCs.
FGF21,
an
endocrine
stress-responsive
hormone,
has
shown
regulate
energy
balance,
glucose,
lipid
metabolism
the
homing
of
MSCs
toward
injured
sites.
Therefore,
purpose
this
study
was
investigate
whether
that
overexpress
FGF21
(FGF21-MSCs)
improve
effect
in
treating
ALD.
Methods:
Human
umbilical
cord-derived
served
as
gene
delivery
vehicle
for
gene.
were
transduced
using
lentiviral
vectors
mediate
overexpression.
We
utilized
both
chronic
Lieber-DeCarli
Gao-binge
models
ethanol-induced
injury
observe
FGF21-MSCs.
Liver
phenotypically
evaluated
by
performing
biochemical
methods,
histology,
inflammatory
cytokine
levels.
Results:
Compared
alone,
administration
overexpressing
FGF21(FGF21-MSCs)
treatment
significantly
enhanced
ALD
mice,
indicated
alleviation
reduced
steatosis,
infiltration,
oxidative
stress,
hepatic
apoptosis,
promotion
regeneration.
Mechanistically,
could
facilitate
immunomodulatory
function
on
macrophages
setting
metabolic
commitment
phosphorylation,
which
enables
exhibit
anti-inflammatory
inclination.
Conclusions:
Our
data
elucidate
MSC
modification
may
help
exploration
effective
MSCs-based
cell
therapies