4,4-Dimethylsterols Reduces Fat Accumulation via Inhibiting Fatty Acid Amide Hydrolase In Vitro and In Vivo
Research,
Год журнала:
2024,
Номер
7
Опубликована: Янв. 1, 2024
4,4-Dimethylsterols
constitute
a
unique
class
of
phytosterols
responsible
for
regulating
endogenous
cannabinoid
system
(ECS)
functions.
However,
precise
mechanism
through
which
4,4-dimethylsterols
affect
fat
metabolism
and
the
linkage
to
ECS
remain
unresolved.
In
this
study,
we
identified
that
4,4-dimethylsterols,
distinct
from
4-demethseterols,
act
as
inhibitors
fatty
acid
amide
hydrolases
(FAAHs)
both
in
vivo
vitro.
Genetic
ablation
FAAHs
(
faah-1
)
abolishes
effects
on
accumulation
locomotion
behavior
Caenorhabditis
elegans
model.
We
confirmed
dietary
intervention
with
high-fat
diet
(HFD)
mouse
model
leads
significant
reduction
body
weight
(>11.28%)
improved
lipid
profiles
liver
adipose
tissues
increased
fecal
triacylglycerol
excretion.
Untargeted
targeted
metabolomics
further
verified
influence
unsaturated
biosynthesis
elevate
oleoyl
ethanolamine
levels
intestine.
propose
potential
molecular
engage
binding
interactions
catalytic
pocket
(Ser241)
FAAH-1
protein
due
shielded
polarity,
arising
presence
2
additional
methyl
groups
(CH
3
).
Consequently,
represent
an
unexplored
beneficial
coordinate
activity
reduce
accumulation,
offers
new
insight
into
strategies
treating
diet-induced
obesity.
Язык: Английский
Erratum to “Sleep Promotion by 3-Hydroxy-4-iminobutyric Acid in Walnut Diaphragma Juglandis Fructus ”
Research,
Год журнала:
2025,
Номер
8
Опубликована: Янв. 1, 2025
[This
corrects
the
article
DOI:
10.34133/research.0216.].
Язык: Английский
Foods for Sleep Improvement: A Review of the Potential and Mechanisms Involved
Foods,
Год журнала:
2025,
Номер
14(7), С. 1080 - 1080
Опубликована: Март 21, 2025
Insomnia
affects
one-third
of
the
world’s
population;
negative
effects
insomnia
are
significant,
and
traditional
medications
have
numerous
side
cause
considerable
suffering.
This
has
aroused
interest
in
obtaining
sleep-improving
substances
from
foods.
study
conducted
a
comprehensive
literature
review
using
Web
Science
PubMed
with
keywords
like
“sleep”,
“insomnia”,
“food”.
A
subsequent
summary
revealed
that
certain
foods,
including
milk,
Ziziphus
jujuba,
Lactuca
sativa,
ginseng,
Schisandra
chinensis,
Juglans
regia,
etc.,
purported
to
enhance
sleep
quality
by
prolonging
duration,
reducing
latency,
alleviating
anxiety.
The
mechanisms
these
foods’
mainly
occur
via
central
nervous
system,
particularly
gamma-aminobutyric
acid
(GABA)ergic
5-hydroxytryptamine
(5-HT)ergic
systems.
Although
this
supports
fact
they
potential,
further
research
is
needed.
There
also
issues
such
as
more
limited
fewer
mechanisms,
pharmacokinetic
studies,
models
being
involved.
These
need
be
addressed
future
adequately
address
problem
insomnia.
It
hoped
will
contribute
into
foods
properties
and,
future,
provide
an
effective
natural
alternative
for
those
seeking
medication.
Язык: Английский
Brain Short-Chain Fatty Acids Induce ACSS2 to Ameliorate Depressive-Like Behavior via PPARγ–TPH2 Axis
Research,
Год журнала:
2024,
Номер
7
Опубликована: Янв. 1, 2024
Short-chain
fatty
acids
(SCFAs)
have
been
increasingly
evidenced
to
be
important
bioactive
metabolites
of
the
gut
microbiota
and
transducers
in
controlling
diverse
psychiatric
or
neurological
disorders
via
microbiota–gut–brain
axis.
However,
precise
mechanism
by
which
brain
SCFAs
extert
multiple
beneficial
effects
is
not
completely
understood.
Our
previous
research
has
demonstrated
that
acetyl-coenzyme
A
synthetase
short-chain
family
member
2
(ACSS2)
a
novel
target
rapid
long-lasting
antidepressant
responses.
Here,
we
show
micromolar
significantly
augment
both
total
cellular
nuclear
ACSS2
trigger
tryptophan
hydroxylase
(TPH2)
promoter
histone
acetylation
its
transcription
SH-SY5Y
cells.
In
chronic-restraint-stress-induced
depression
mice,
neuronal
knockdown
stereotaxic
injection
adeno-associated
virus
hippocampus
abolished
SCFA-mediated
improvements
depressive-like
behaviors
supporting
required
for
Mechanistically,
peroxisome-proliferator-activated
receptor
gamma
(PPARγ)
identified
as
partner
activate
TPH2
transcription.
Importantly,
PPARγ
also
responsible
antidepressant-like
ACSS2–TPH2
To
further
support
therapeutic
effects,
d
-mannose,
naturally
present
hexose,
can
reverse
dysbiosis
chronic-restraint-stress-exposure
mice
protect
against
ACSS2–PPARγ–TPH2
summary,
axis
play
antidepressive-like
-mannose
suggested
an
inducer
resisting
depression.
Язык: Английский