Frontiers in Pharmacology,
Год журнала:
2023,
Номер
14
Опубликована: Ноя. 15, 2023
Lipid-lowering
therapy
is
an
important
tool
for
the
treatment
of
lipid
metabolic
diseases,
which
are
increasing
in
prevalence.
However,
failure
conventional
lipid-lowering
drugs
to
achieve
desired
efficacy
some
patients,
and
side-effects
these
drug
regimens,
highlight
urgent
need
novel
drugs.
The
liver
intestine
production
removal
endogenous
exogenous
lipids,
respectively,
have
impact
on
circulating
levels.
Elevated
lipids
predisposes
individual
deposition
vascular
wall,
affecting
function.
Berberine
(BBR)
modulates
clearance
by
regulating
cellular
targets
such
as
cluster
differentiation
36
(CD36),
acetyl-CoA
carboxylase
(ACC),
microsomal
triglyceride
transfer
protein
(MTTP),
scavenger
receptor
class
B
type
1
(SR-BI),
low-density
lipoprotein
(LDLR),
ATP-binding
cassette
transporter
A1
(ABCA1).
It
influences
intestinal
synthesis
metabolism
modulating
gut
microbiota
composition
metabolism.
Finally,
BBR
maintains
function
targeting
proteins
endothelial
nitric
oxide
synthase
(eNOS)
lectin-like
oxidized
receptor-1
(LOX-1).
This
paper
elucidates
summarizes
pharmacological
mechanisms
berberine
diseases
from
a
multi-organ
(liver,
intestine,
system)
multi-target
perspective.
Current Opinion in Clinical Nutrition & Metabolic Care,
Год журнала:
2022,
Номер
25(4), С. 248 - 255
Опубликована: Июнь 28, 2022
Nonalcoholic
fatty
liver
disease
(NAFLD)
is
now
the
most
prevalent
form
of
globally,
affecting
about
25%
world's
adult
population.
It
more
common
in
those
living
with
obesity,
where
it
may
affect
as
many
80%
individuals.
The
aim
this
article
to
describe
recent
human
studies
evaluating
influence
omega-3
acids
on
de
novo
lipogenesis
(DNL)
and
hepatic
acid
partitioning
between
incorporation
into
triacylglycerols
(TAGs)
β-oxidation,
discuss
relevance
these
effects
context
NAFLD,
provide
an
overview
mechanisms
that
might
be
involved.The
eicosapentaenoic
(EPA)
docosahexaenoic
(DHA)
decrease
DNL
partition
away
from
TAG
synthesis
toward
β-oxidation.
EPA
DHA
multiple
transcription
factors
resulting
down-regulation
pathway
upregulation
net
result
decreased
accumulation
lowering
circulating
concentrations.
Human
trials
demonstrate
can
fat
patients
NAFLD.Increased
intake
reduce
likelihood
could
used
NAFLD.
Biomolecules & Therapeutics,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 20, 2024
AMP-activated
protein
kinase
(AMPK)
activators
have
garnered
significant
attention
for
their
potential
to
prevent
the
progression
of
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
into
fibrosis
and
fundamentally
improve
function.
The
broad
spectrum
pathways
regulated
by
AMPK
makes
them
promising
alternatives
conventional
replacement
therapies
limited
pharmacological
treatments
currently
available.
In
this
study,
we
aim
illustrate
newly
detailed
multiple
mechanisms
MASLD
based
on
multiple-hit
hypothesis.
This
model
posits
that
impaired
lipid
metabolism,
combined
with
insulin
resistance
imbalance,
initiates
inflammatory
cascades,
gut
dysbiosis,
accumulation
toxic
metabolites,
ultimately
promoting
accelerating
irreversible
hepatocellular
carcinoma
(HCC).
plays
a
multifaceted
protective
role
against
these
pathological
conditions
regulating
several
key
downstream
signaling
pathways.
It
regulates
biological
effectors
critical
responses,
such
as
SIRT1,
Nrf2,
mTOR,
TGF-β,
through
complex
interrelated
mechanisms.
Due
intricate
connections,
AMPK's
is
pivotal
in
managing
disorders.
review,
demonstrate
specific
roles
its
related
Several
agents
directly
activate
binding
agonists,
while
some
others
indirectly
modulating
upstream
molecules,
including
adiponectin,
LKB1,
AMP:
ATP
ratio.
As
can
target
each
stage
progression,
development
offers
immense
expand
therapeutic
strategies
diseases
MASH,
MASLD,
fibrosis.
Frontiers in Pharmacology,
Год журнала:
2023,
Номер
14
Опубликована: Ноя. 15, 2023
Lipid-lowering
therapy
is
an
important
tool
for
the
treatment
of
lipid
metabolic
diseases,
which
are
increasing
in
prevalence.
However,
failure
conventional
lipid-lowering
drugs
to
achieve
desired
efficacy
some
patients,
and
side-effects
these
drug
regimens,
highlight
urgent
need
novel
drugs.
The
liver
intestine
production
removal
endogenous
exogenous
lipids,
respectively,
have
impact
on
circulating
levels.
Elevated
lipids
predisposes
individual
deposition
vascular
wall,
affecting
function.
Berberine
(BBR)
modulates
clearance
by
regulating
cellular
targets
such
as
cluster
differentiation
36
(CD36),
acetyl-CoA
carboxylase
(ACC),
microsomal
triglyceride
transfer
protein
(MTTP),
scavenger
receptor
class
B
type
1
(SR-BI),
low-density
lipoprotein
(LDLR),
ATP-binding
cassette
transporter
A1
(ABCA1).
It
influences
intestinal
synthesis
metabolism
modulating
gut
microbiota
composition
metabolism.
Finally,
BBR
maintains
function
targeting
proteins
endothelial
nitric
oxide
synthase
(eNOS)
lectin-like
oxidized
receptor-1
(LOX-1).
This
paper
elucidates
summarizes
pharmacological
mechanisms
berberine
diseases
from
a
multi-organ
(liver,
intestine,
system)
multi-target
perspective.