Recent advances in nanotechnology for Parkinson’s disease: diagnosis, treatment, and future perspectives
Frontiers in Medicine,
Journal Year:
2025,
Volume and Issue:
12
Published: Jan. 22, 2025
Parkinson’s
disease
is
a
progressive
neurodegenerative
that
destroys
substantia
nigra
dopaminergic
neurons,
causing
tremors,
bradykinesia,
rigidity,
and
postural
instability.
Current
treatment
approaches
primarily
focus
on
symptom
management,
employing
pharmacological,
non-pharmacological,
surgical
methods.
However,
these
treatments
often
result
in
fluctuating
symptoms,
side
effects,
progression.
Here,
the
authors
have
reviewed
emerging
field
of
nanomedicine
as
promising
path
for
treatment,
emphasizing
its
potential
to
overcome
limitations
traditional
therapies.
Nanomedicine
utilizes
nanoparticles
targeted
drug
delivery,
leveraging
their
small
size
high
surface
area
volume
ratio
cross
blood-brain
barrier
deliver
therapeutic
agents
directly
affected
brain
regions.
Various
nanoparticles,
including
lipid-based,
polymeric,
metallic,
carbon-based,
shown
treatment.
Additionally,
nanocarrier
systems
like
liposomes,
nanogels,
dendrimers,
solid
lipid
offer
controlled
sustained
release
agents,
enhancing
bioavailability
reducing
effects.
This
review
provides
insights
into
pathophysiology
disease,
highlighting
mechanisms
neurodegeneration,
role
alpha-synuclein,
disruption
pathways.
It
further
discusses
application
gene
therapy
conjunction
with
interventions.
Language: Английский
Nanodiamond-mediated delivery of microRNA-7 for the neuroprotection of dopaminergic neurons
Frontiers in Bioengineering and Biotechnology,
Journal Year:
2025,
Volume and Issue:
12
Published: Jan. 8, 2025
Parkinson's
disease
(PD)
is
a
neurodegenerative
disorder
characterized
by
the
gradual
loss
of
dopaminergic
neurons
in
substantia
nigra
and
accumulation
α-synuclein
aggregates
known
as
Lewy
bodies.
MicroRNA-7
(miR-7)
targets
gene
SNCA,
which
encodes
α-synuclein,
reducing
its
expression
alleviating
neuronal
damage
PD.
Regulating
post-transcriptional
levels
through
miR-7
effectively
inhibits
production.
Herein,
we
use
nanodiamonds
carriers
to
deliver
(N-7),
can
protect
neurons.
Dopaminergic
efficiently
take
up
N-7
express
miR-7.
reduces
oxidative
stress
restores
dopamine
effectively.
These
findings
suggest
that
nanocomposites
have
significant
potential
treating
Language: Английский
Oxidative Stress and Mitochondrial Impairment: Key Drivers in Neurodegenerative Disorders
Pei Wen,
No information about this author
Zhixin Sun,
No information about this author
Fengting Gou
No information about this author
et al.
Ageing Research Reviews,
Journal Year:
2025,
Volume and Issue:
unknown, P. 102667 - 102667
Published: Jan. 1, 2025
Language: Английский
Regulator of oxidative balance: Research progress of nanozymes in ROS-related diseases
Materials Today Chemistry,
Journal Year:
2025,
Volume and Issue:
44, P. 102540 - 102540
Published: Jan. 22, 2025
Language: Английский
Nanozymes in biomedicine: Unraveling trends, research foci, and future trajectories via bibliometric insights (from 2007 to 2024)
Siyang Cao,
No information about this author
Yingchen Pang,
No information about this author
Yihao Wei
No information about this author
et al.
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown, P. 142798 - 142798
Published: April 1, 2025
Language: Английский
Effects and mechanisms of long-acting glucagon-like peptide-1 receptor agonist semaglutide on microglia phenotypic transformation and neuroinflammation after cerebral ischemia/reperfusion in rats
Rulin Mi,
No information about this author
Hui-Feng Cheng,
No information about this author
Rui Chen
No information about this author
et al.
Brain Circulation,
Journal Year:
2024,
Volume and Issue:
10(4), P. 354 - 365
Published: Oct. 1, 2024
The
optimal
method
for
addressing
cerebral
ischemic
stroke
involves
promptly
restoring
blood
supply.
However,
ischemia-reperfusion
injury
(CIRI)
is
an
unavoidable
consequence
of
this
event.
Neuroinflammation
deemed
the
primary
mechanism
CIRI,
with
various
activation
phenotypes
microglia
playing
a
pivotal
role.
Research
has
demonstrated
that
long-lasting
agonists
glucagon-like
peptide-1
receptor
can
suppress
neuroinflammation
and
microglial
activation.
A
transient
middle
artery
occlusion
(tMCAO)
rat
model
was
established
to
investigate
effects
semaglutide.
Neurological
impairments
were
evaluated
utilizing
modified
neurological
severity
score
on
days
1,
3,
7
postinterventions.
Brains
stained
2,3,5-Triphenyltetrazolium
Chloride
determine
infarct
volume.
To
assess
expression
neuroinflammatory
biomarkers,
we
utilized
immunohistochemistry
immunoblotting.
study
semaglutide
in
tMCAO
could
decrease
deficit
scores
reduce
size
infarcts.
In
addition,
observed
low
levels
cluster
differentiation
68
(CD68,
indicator
M1
activation)
tumor
necrosis
factor
alpha
(a
pro-inflammatory
mediator).
Moreover,
results
indicated
rise
CD206
(an
M2
transforming
growth
beta
anti-inflammatory
mediator),
while
simultaneously
reducing
P65
nuclear
kappa-light-chain-enhancer
activated
B
cells
(NF-κB)
signaling
cascade.
CIRI
model,
exhibits
notable
neuroprotective
rats,
through
regulation
phenotype
transformation
inhibition
NF-κB
Language: Английский
HDAC6 inhibitor-loaded brain-targeted nanocarrier-mediated neuroprotection in methamphetamine-driven Parkinson’s disease
Khang‐Yen Pham,
No information about this author
Shristi Khanal,
No information about this author
Ganesh Bohara
No information about this author
et al.
Redox Biology,
Journal Year:
2024,
Volume and Issue:
79, P. 103457 - 103457
Published: Dec. 5, 2024
The
dynamic
equilibrium
between
acetylation
and
deacetylation
is
vital
for
cellular
homeostasis.
Parkinson's
disease
(PD),
a
neurodegenerative
disorder
marked
by
α-synuclein
(α-syn)
accumulation
dopaminergic
neuron
loss
in
the
substantia
nigra,
associated
with
disruption
of
this
balance.
Therefore,
correcting
imbalance
histone
deacetylase
(HDAC)
inhibitors
represents
promising
treatment
strategy
PD.
CAY10603
(CAY)
potent
selective
HDAC6
inhibitor.
However,
because
its
poor
water
solubility
short
biological
half-life,
it
faces
clinical
limitations.
Herein,
we
engineered
lactoferrin-decorated
CAY-loaded
poly(lactic-co-glycolic
acid)
nanoparticles
(denoted
as
PLGA@CAY@Lf
NPs)
to
effectively
counter
methamphetamine
(Meth)-induced
NPs
showed
enhanced
blood-brain
barrier
crossing
significant
brain
accumulation.
Notably,
CAY
released
from
restored
disrupted
balance
PD,
resulting
neuroprotection
reversing
mitochondrial
dysfunction,
suppressing
reactive
oxygen
species,
inhibiting
α-syn
Additionally,
normalized
dopamine
tyrosine
hydroxylase
levels,
reduced
neuroinflammation,
improved
behavioral
impairments.
These
findings
underscore
potential
treating
Meth-induced
PD
suggest
that
an
innovative
HDAC6-inhibitor-based
can
be
used
treat
Language: Английский
Intragland Expression of the Shh Gene Alleviates Irradiation-Induced Salivary Gland Injury through Microvessel Protection and the Regulation of Oxidative Stress
Meijun Hu,
No information about this author
Hu L,
No information about this author
Tao Yang
No information about this author
et al.
Antioxidants,
Journal Year:
2024,
Volume and Issue:
13(8), P. 904 - 904
Published: July 26, 2024
Radiation-induced
salivary
gland
injury
(RISGI)
is
a
common
complication
of
radiotherapy
in
patients
with
head
and
neck
cancer.
Intragland
expression
the
Sonic
Hedgehog
(Shh)
gene
may
partially
rescue
irradiation
(IR)-induced
hyposalivation
by
preserving
stem/progenitor
cells
parasympathetic
innervation,
maintaining
resident
macrophages,
microvascular
density.
Previous
studies
have
revealed
that
Ad-Rat
Shh
transduction
through
glands
miniature
pigs
can
ameliorate
oxidative
stress-induced
dysfunction
after
radiotherapy.
Changes
parotid
flow
rate
were
analyzed,
tissue
was
collected
at
5
20
weeks
IR.
pathway
vascular
function-related
markers
(vascular
endothelial
growth
factor
(VEGF)
CD31)
stress-related
detected
via
immunohistochemistry,
immunofluorescence,
Western
blotting.
A
stable
Shh-overexpressing
cell
line
generated
from
human
umbilical
vein
(HUVECs)
exposed
to
10
Gy
X-ray
irradiation,
which
proliferation,
senescence,
apoptosis,
function
evaluated.
We
found
intragland
efficiently
alleviated
IR-induced
pig
model.
Our
results
indicate
antioxidative
stress
microvascular-protective
effects
Hh
are
regulated
nuclear
factor-erythroid
2-related
2
(Nrf2).
Language: Английский
Rimota-Gd: Paramagnetic Probe for In Vivo MRI Studies of the Cannabinoid 1 Receptor Distribution in the Mouse Brain
Ouyang Qi,
No information about this author
Fei Zhao,
No information about this author
Jingjing Ye
No information about this author
et al.
ACS Chemical Neuroscience,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 14, 2024
The
cannabinoid
1
receptor
(CB1)
is
highly
expressed
in
the
central
nervous
system,
where
its
physiological
functions
include
regulation
of
energy
balance,
pain,
and
addiction.
Herein,
we
develop
validate
a
technique
to
use
magnetic
resonance
imaging
(MRI)
investigate
distribution
CB1
across
mouse
brains
with
high
spatial
resolution,
expanding
previously
described
vitro
studies
vivo
positron
emission
tomography
(PET).
To
support
MRI
investigations,
developed
ligand
that
specific
for
neuroimaging
CB1.
By
chemically
conjugating
antagonist
rimonabant
acid
gadolinium
chelator,
obtained
paramagnetic
probe
Rimota-Gd.
specificity
binding
relaxation
enhancement
by
permit
MRI-based
localization
We
used
Rimota-Gd
brain
compared
results
an
investigation
using
PET
radioligand
[
Language: Английский