Natural bioactive compounds form herbal medicine in Alzheimer’s disease: from the perspective of GSK-3β
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 7, 2025
Alzheimer's
disease
(AD)
is
a
progressive
neurodegenerative
disorder
characterized
by
cognitive
decline
and
memory
loss.
Glycogen
synthase
kinase
3β
(GSK-3β)
plays
pivotal
role
in
AD
pathogenesis,
particularly
tau
protein
hyperphosphorylation.
Natural
bioactive
compounds
have
wide
range
of
sources,
medicinally
valuable
active
compound
can
be
extracted
from
plants,
animals,
microorganisms.
Currently,
studies
found
that
various
natural
plants
the
potential
to
improve
symptoms,
such
as
resveratrol
berberine.
Therefore,
this
review
examines
modulate
GSK-3β
activity
inhibit
hyperphosphorylation
tau,
offering
promising
therapeutic
strategy
for
AD.
We
summarize
current
understanding
alkaloids,
phenols,
flavonoids,
terpenoids
other
compounds,
highlighting
their
mechanisms
action
preclinical
efficacy.
Language: Английский
Dietary Triterpenoids in Functional Food and Drug Ingredients: a review of structure-activity relationships, biosynthesis, applications, and AI-driven strategies
Trends in Food Science & Technology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 104961 - 104961
Published: March 1, 2025
Language: Английский
Ginsenosides Rg1, Rb1 and rare ginsenosides: promising candidate agents for Parkinson's disease and Alzheimer's disease and network pharmacology analysis
Mingchun Jiang,
No information about this author
Jiaxin Chi,
No information about this author
Yifan Qiao
No information about this author
et al.
Pharmacological Research,
Journal Year:
2025,
Volume and Issue:
212, P. 107578 - 107578
Published: Jan. 5, 2025
Ginseng
has
been
commonly
used
as
a
traditional
Chinese
medicine
in
Asian
countries
for
thousands
of
years.
Ginsenosides
are
the
main
pharmacologically
active
ingredients
isolated
from
ginseng
and
have
neuroprotective
effects
treatment
neurodegenerative
disorders,
such
Parkinson's
disease
(PD)
Alzheimer's
(AD).
To
summarise
investigate
protective
roles
ginsenosides
their
underlying
mechanisms
PD
AD,
we
''Ginsenoside",
''Parkinson's
disease",
''Alzheimer's
''anti-inflammatory",
''antioxidant",
''apoptosis"
keywords
to
search
extract
relevant
literature
information
scientific
databases
Elsevier,
PubMed,
Google
Scholar
databases.
In
particular,
network
pharmacology
identify
potential
targets
Rg1
Rb1
AD.
By
analysing
existing
research
advances
results,
found
that
ginsenosides,
primarily
mediated
through
anti-inflammation,
anti-apoptosis
anti-oxidative
stress,
etc,
may
be
associated
with
PI3K/Akt,
BDNF/TrkB,
MAPKs,
NF-κB,
Nrf2
Wnt/β-catenin
signalling
pathways.
This
review
systematically
summarises
different
Rg1,
Rb1,
rare
AD
provides
new
strategies
disorders.
Network
paradigm
using
Rb1.
Language: Английский
Ginsenoside Rg1 in Parkinson’s disease: from basic research to clinical applications
Qianyan Wang,
No information about this author
Wei Lei,
No information about this author
Guang‐Hui Chen
No information about this author
et al.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 16, 2025
This
review
provides
an
in-depth
exploration
of
the
potential
Ginsenoside
Rg1
in
treatment
Parkinson's
disease
(PD).
The
emphasis
this
article
was
therapeutic
mechanisms
Rg1,
which
involved
reduction
inflammation,
antioxidant
properties,
support
for
neuronal
survival
and
regeneration,
regulation
cellular
energy
processes,
enhancement
autophagic
pathways.
may
protect
neurons
improve
both
motor
cognitive
impairments
associated
with
PD
through
multiple
mechanisms.
However,
challenges
exist
clinical
application
such
as
low
bioavailability
well
a
lack
comprehensive
long-term
safety
efficacy
data.
also
reviewed
network
pharmacology
analyses
published
previously
to
identify
explore
molecular
targets
treatment,
while
evaluating
strategies
drug
delivery
technologies,
optimizing
administration
routes,
combination
therapies.
Ultimately,
highlights
necessity
large-scale
trials
validate
discusses
its
clinically.
Language: Английский
Ginsenoside RH4 inhibits Ang II-induced myocardial remodeling by interfering with NFIL3
Yitong Wang,
No information about this author
Xiangbo An,
No information about this author
Feng Wang
No information about this author
et al.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
172, P. 116253 - 116253
Published: Feb. 15, 2024
Ventricular
remodeling
refers
to
the
structural
and
functional
changes
of
heart
under
various
stimuli
or
disease
influences
may
also
be
accompanied
by
myocardial
fibrosis,
where
an
excessive
amount
fibrous
tissue
appears
in
tissue,
affecting
heart's
normal
contraction
relaxation.
Hypertension
is
posing
potential
risk
causing
injury
remodeling.
The
significance
renin-angiotensin-aldosterone
system
(RAAS)
cannot
overlooked.
Drug
targeting
RAAS
can
effectively
lower
blood
pressure
reduce
left
ventricular
mass.
Studies
have
shown
that
ginsenoside
Rh4
inhibit
oxidative
stress
inflammatory
responses.
In
this
study,
a
model
was
established
using
angiotensin
(Ang)
II,
inhibitory
effect
RH4
on
hypertrophy
induced
Ang
II
investigated
pathological
staining
quantitative
polymerase
chain
reaction
(qPCR).
Immunofluorescence
qPCR
demonstrated
causes
generation
reactive
oxygen
species
(ROS)
vitro.
target
identified
transcriptomics.
findings
indicated
could
hypertrophy,
suggesting
cardiovascular
protection
effects.
vitro
experiments
inhibits
hypertrophy.
Transcriptomics
revealed
nuclear
factor
interleukin-3
(NFIL3)
downstream
regulator
Rh4.
By
constructing
AAV9-NFIL3
injecting
it
into
mice,
found
NFIL3
overexpression
interfered
with
anti-Ang
II-induced
These
results
indicate
demonstrates
therapeutic
effects
fibrosis.
Language: Английский
Neuroprotective effects of traditional Chinese medicine Naofucong on diabetic cognitive impairment: Mechanisms involving insulin-degrading enzyme-mediated degradation of Amyloid-β and inhibition of ERK/JNK/p38 MAPK signaling pathway
Yue Tian,
No information about this author
Guangchan Jing,
No information about this author
Ruiying Yin
No information about this author
et al.
Brain Research,
Journal Year:
2024,
Volume and Issue:
unknown, P. 149365 - 149365
Published: Nov. 1, 2024
Language: Английский
Ginsenoside Rk3 Treats Corneal Injury Through the HMGB1/TLR4/NF-κB Pathway
Journal of Agricultural and Food Chemistry,
Journal Year:
2024,
Volume and Issue:
72(44), P. 24387 - 24399
Published: Oct. 22, 2024
The
cornea
serves
as
a
vital
protective
shield
for
the
eye,
safeguarding
its
intricate
internal
structures
from
external
threats.
Damage
to
compromises
this
function,
triggering
inflammation
and
potentially
causing
long-term
harm.
While
ginsenoside
Rk3
has
demonstrated
potential
repairing
corneal
barrier
reducing
inflammation,
effectiveness
in
treating
damage
remains
relatively
unexplored.
This
comprehensive
study
uses
both
vivo
vitro
models
investigate
therapeutic
capabilities
of
Rk3.
Using
two
damage,
benzalkonium
chloride-induced
mouse
model
high
osmolarity-induced
human
epithelial
cell
model,
we
scrutinized
effects
treatment.
Our
results
showed
that
Rk3-treated
mice
manifested
reduced
compared
with
their
untreated
counterparts.
Furthermore,
treated
exhibited
an
organized
arrangement
cells
diminished
stromal
layer
thickness,
indicating
reparative
properties
Additionally,
increased
expression
tight
junction
proteins,
suppressed
inflammatory
factors,
decreased
HMGB1
protein
expression,
thereby
modulating
downstream
signaling
pathways.
Collectively,
our
findings
present
compelling
evidence
is
promising
option
injury.
By
barrier,
mitigating
specific
levels,
opens
new
avenues
managing
damage.
Language: Английский