Macromolecular Bioscience,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 24, 2025
Abstract
Inflammation
is
an
essential
physiological
defense
mechanism
against
harmful
stimuli,
yet
dysregulated
inflammatory
responses
are
closely
associated
with
the
pathogenesis
of
numerous
acute
and
chronic
diseases.
Recent
advances
highlight
remarkable
anti‐inflammatory
potential
bioactive
macromolecules,
particularly
cyclodextrins
(CDs)
their
engineered
derivatives,
which
emerging
as
promising
therapeutic
agents.
This
review
systematically
introduces
different
CDs
CD‐derived
macromolecules
that
demonstrate
properties,
emphasis
on
molecular
mechanisms
action.
Native
exhibit
direct
effects
through
host‐guest
interactions,
enabling
selective
sequestration
pathogenic
components
such
cholesterol
crystals
proteins
drive
cascades.
Moreover,
chemically
modified
CD
derivatives
incorporating
functional
groups
enhanced
capabilities
in
neutralizing
mediators
modulating
immune
cell
responses.
work
further
discusses
expanding
applications
these
across
diverse
conditions,
ranging
from
tissue
injuries
to
autoimmune
disorders.
Finally,
this
critically
analyzes
crucial
challenges
opportunities
translating
CD‐based
macromolecular
therapies
into
clinical
practice,
addressing
key
considerations
biocompatibility,
targeted
delivery,
efficacy
optimization.
Receptors,
Journal Year:
2025,
Volume and Issue:
4(1), P. 2 - 2
Published: Jan. 26, 2025
Glucagon-like
peptide-1
receptor
agonists
(GLP-1RAs),
including
dulaglutide,
liraglutide,
semaglutide,
and
exenatide,
are
effective
treatments
for
type
2
diabetes
mellitus
(T2DM)
obesity.
These
agents
mimic
the
action
of
endogenous
incretin
glucagon-like
(GLP-1)
by
enhancing
insulin
secretion,
inhibiting
glucagon
release,
promoting
weight
loss
through
appetite
suppression.
GLP-1RAs
have
recently
been
suggested
to
neuroprotective
effects,
suggesting
their
potential
as
treatment
neurodegenerative
disorders,
such
Alzheimer’s
disease
(AD).
AD
T2DM
share
several
common
pathophysiological
mechanisms,
resistance,
chronic
inflammation,
oxidative
stress,
mitochondrial
dysfunction.
shared
mechanisms
suggest
that
therapeutic
targeting
metabolic
dysfunction
may
also
be
beneficial
conditions.
Preclinical
studies
on
in
models,
both
vitro
vivo,
demonstrated
promising
reductions
amyloid-beta
accumulation,
decreased
tau
hyperphosphorylation,
improved
synaptic
plasticity,
enhanced
neuronal
survival.
Despite
encouraging
results
from
preclinical
challenges
need
addressed
before
can
widely
used
treatment.
Ongoing
clinical
trials
investigating
cognitive
benefits
patients,
aiming
establish
role
a
option
AD.
This
review
aimed
examine
current
literature
GLP-1
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(3), P. 1062 - 1062
Published: Jan. 26, 2025
Alzheimer’s
disease
(AD)
is
a
complex
and
progressive
neurodegenerative
condition
with
significant
societal
impact.
Understanding
the
temporal
dynamics
of
its
pathology
essential
for
advancing
therapeutic
interventions.
Empirical
anatomical
evidence
indicates
that
network
decoupling
occurs
as
result
gray
matter
atrophy.
However,
scarcity
longitudinal
clinical
data
presents
challenges
computer-based
simulations.
To
address
this,
first-principles-based,
physics-constrained
Bayesian
framework
proposed
to
model
time-dependent
connectome
during
neurodegeneration.
This
diffusion
segments
pathological
progression
into
discrete
time
windows
optimizes
distributions
biomarker
regression,
conceptualized
learning
problem.
The
employs
variational
autoencoder-like
architecture
computational
enhancements
stabilize
improve
training
efficiency.
Experimental
evaluations
demonstrate
meta-models
outperform
traditional
static
models.
models
were
evaluated
using
both
synthetic
real-world
MRI
PET
datasets
measure
amyloid
beta,
tau,
glucose
metabolism.
successfully
distinguishes
normative
aging
from
AD
pathology.
Findings
provide
novel
support
“decoupling”
hypothesis
reveal
eigenvalue-based
destabilization
in
AD.
Future
optimization
model,
integrated
data,
expected
applications
personalized
medicine
other
diseases.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(5), P. 1935 - 1935
Published: Feb. 24, 2025
The
role
of
amyloid
beta
peptide
(Aβ)
in
memory
regulation
has
been
a
subject
substantial
interest
and
debate
neuroscience,
because
both
physiological
clinical
issues.
Understanding
the
dual
nature
Aβ
is
crucial
for
developing
effective
treatments
Alzheimer's
disease
(AD).
Moreover,
accurate
detection
quantification
methods
isoforms
have
tested
diagnostic
purposes
therapeutic
interventions.
This
review
provides
insight
into
current
knowledge
about
vivo
vitro
by
fluid
tests
brain
imaging
(PET),
which
allow
preclinical
recognition
disease.
Currently,
priority
development
new
therapies
given
to
potential
changes
progression
In
light
increasing
amounts
data,
this
was
focused
on
employment
Rejuvenation Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
Emerging
evidence
suggests
that
bioactive
peptides
from
various
foods
have
therapeutic
potentials
in
improving
cognitive
function
Alzheimer's
disease
(AD)
and
mild
impairment
(MCI).
We
aimed
to
explore
the
characteristics
of
these
their
mechanisms
on
AD/MCI
using
a
network
pharmacology
approach.
compiled
dataset
cognition-enhancing
literatures
identified
shared
targets
between
Swiss
Target
Predication,
PharmMapper,
OMIM,
GeneCards,
TTD,
Drugbank
databases.
then
performed
functional
enrichment
analysis
constructed
gene–gene
interaction
identify
key
hub
targets.
Additionally,
we
investigated
transcription
factors
(TFs)
microRNAs
(miRNAs)
regulating
genes.
Molecular
docking
dynamic
simulations
were
AutoDock
Vina
GROMACS.
59
oligopeptides,
typically
short
rich
arginine.
These
predicted
interact
with
222
potential
relevant
AD/MCI,
pathways
mainly
involving
neuroactive
ligand-receptor
interactions
inflammation.
15
targets,
regulated
by
144
TFs
95
miRNAs.
Notably,
containing
"Trp-Tyr"
sequence
demonstrated
strong
binding
affinities
many
especially
matrix
metalloproteinase-9.
The
findings
provided
valuable
insights
into
molecular
through
which
may
act
against
highlight
for
future
exploration
natural
foods.
Cell Proliferation,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 24, 2025
ABSTRACT
Ageing
is
often
accompanied
by
cognitive
decline
and
an
increased
risk
of
dementia.
Exercise
a
powerful
tool
for
slowing
brain
ageing
enhancing
function,
as
well
alleviating
depression,
improving
sleep,
promoting
overall
well‐being.
The
connection
between
exercise
healthy
particularly
intriguing,
with
exercise‐induced
pathways
playing
key
roles.
This
review
explores
the
link
health,
focusing
on
how
skeletal
muscle
influences
through
muscle–brain
crosstalk.
We
examine
interaction
well‐known
myokines,
including
brain‐derived
neurotrophic
factor,
macrophage
colony‐stimulating
vascular
endothelial
growth
factor
cathepsin
B.
Neuroinflammation
accumulates
in
leads
to
decline,
impaired
motor
skills
susceptibility
neurodegenerative
diseases.
Finally,
we
evidence
effects
neuronal
myelination
central
nervous
system,
crucial
maintaining
health
throughout
lifespan.