Archives of Neuroscience,
Journal Year:
2024,
Volume and Issue:
11(4)
Published: Oct. 27, 2024
Context:
Spinal
cord
injury
(SCI)
is
a
devastating
condition
that
results
in
severe
disability
and
significant
comorbidities.
The
complex
pathophysiology
of
SCI
repair
difficulties
understanding
neural
regeneration
are
treatment
challenges.
Objectives:
aim
this
study
to
systematically
review
the
diverse
applications
various
fish
species
as
models
for
research.
Evidence
Acquisition:
PRISMA
guidelines
were
used
observational
interventional
studies
utilized
models,
published
from
inception
July
2023.
Two
independent
reviewers
screened
performed
data
extraction.
One
reviewer
assessed
risk
bias
included
studies.
Results:
Five
thousand
six
hundred
thirty-three
records
reviewed,
144
met
inclusion
criteria
categorized
by
species.
majority
employed
complete
transection
injuries,
with
remainder
being
crush
laser
electro-ablations,
demyelination
substances.
Zebrafish
(Danio
rerio)
most
commonly
102/144
(71%),
primarily
larval
models.
Other
Lamprey
(Petromyzon
marinus
Lethenteron
reissneri);
Goldfish
(Carassius
auratus);
European
eel
(Anguilla
Anguilla);
Knifefish
(Apteronotus
leptorhynchus
Apteronotus
albifrons);
Sailfin
Molly
(Poecilia
latipinna);
African
turquoise
killifish
(Nothobranchius
furzeri).
Conclusions:
This
systematic
highlights
particularly
zebrafish,
goldfish,
eels,
important
further
defining
regenerative
processes.
These
provide
less
model
gain
insights
into
apoptosis
glial
networks.
Stem Cell Research & Therapy,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Dec. 18, 2024
Neural
stem
cells
(NSCs)
have
increasingly
been
recognized
as
the
most
promising
candidates
for
cell-based
therapies
central
nervous
system
(CNS)
injuries,
primarily
due
to
their
pluripotent
differentiation
capabilities,
well
remarkable
secretory
and
homing
properties.
In
recent
years,
extensive
research
efforts
initiated
explore
therapeutic
potential
of
NSC
transplantation
CNS
yielding
significant
advancements.
Nevertheless,
owing
formation
adverse
microenvironment
at
post-injury
leading
suboptimal
survival,
differentiation,
integration
within
host
neural
network
transplanted
NSCs,
NSC-based
often
fall
short
achieving
optimal
outcomes.
To
address
this
challenge,
genetic
modification
has
developed
an
attractive
strategy
improve
outcomes
therapies.
This
is
mainly
attributed
its
not
only
enhance
capacity
NSCs
but
also
boost
a
range
biological
activities,
such
secretion
bioactive
factors,
anti-inflammatory
effects,
anti-apoptotic
properties,
immunomodulation,
antioxidative
functions,
angiogenesis.
Furthermore,
empowers
play
more
robust
neuroprotective
role
in
context
nerve
injury.
review,
we
will
provide
overview
advances
roles
mechanisms
genetically
modified
with
various
genes
treatment
injuries
disorders.
Also,
update
on
current
technical
parameters
suitable
functional
recovery
clinical
studies
are
summarized.
Stem Cell Research & Therapy,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 28, 2025
Transplantation
of
nasal
mucosa-derived
mesenchymal
stem
cells
(EMSCs)
overexpressing
neuropeptide
S
(NPS)
is
a
promising
approach
for
treating
spinal
cord
injury
(SCI).
Despite
the
potential
cell
therapy,
challenges
remain
regarding
survival
and
differentiation
control.
We
aimed
to
conduct
orthotopic
transplantation
transected
treat
rats
with
complete
SCI.
In
this
study,
we
loaded
NPS-overexpressing
EMSCs
onto
hydrogels
enhance
in
vivo
promote
neuronal
both
vitro
vivo.
However,
co-culture
promoted
greater
neural
(P
<
0.01).
When
transplanted
vivo,
showed
area
compared
without
gene
modification
within
4
weeks
after
implantation
Compared
those
other
groups,
stable
overexpression
NPS-EMSCs
rat
model
SCI
significantly
improved
treatment
effect,
reduced
glial
scar
formation,
regeneration
endogenous
proliferation
into
neurons,
motor
function.
These
results
indicate
that
effect
may
be
achieved
by
through
activation
PI3K/Akt/GSK3β
signaling
pathway.
Overall,
therapeutic
rats,
strongly
supporting
clinical
applications.
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(7), P. 2203 - 2203
Published: March 24, 2025
Recovery
from
traumatic
spinal
cord
injury
(tSCI)
is
challenging
due
to
the
limited
regenerative
capacity
of
central
nervous
system
restore
cells,
myelin,
and
neural
connections.
At
clinical
level,
fundamental
pillars
treatment
are
reduction
in
secondary
damage
(neuroprotection)
rehabilitation;
these
tools
we
have
mitigate
disability
caused
by
(SCI).
To
date,
treatments
on
which
neuroprotection
has
been
based
prevention
acute
respiratory
failure
avoid
hypoxia,
early
hemodynamic
control,
neuroprotective
drugs
surgical
management.
Optimizing
control
ensure
adequate
perfusion
may
be
key
management
SCI.
While
agents
like
methylprednisolone
fallen
into
disuse,
several
promising
therapies
currently
being
tested
trials.
In
terms
treatment,
although
their
impact
neurological
recovery
remains
debated,
appropriate
bone
decompression
followed
duroplasty
selected
cases
increasingly
recommended.
Advances
cell
hold
significant
potential
for
enhancing
both
functional
outcomes
SCI
patients.
Moreover,
emerging
neuromodulation
techniques,
such
as
transcutaneous
epidural
stimulation,
along
with
innovations
rehabilitation
technologies-such
robotic
systems
exoskeletons-are
becoming
indispensable
improving
locomotion
overall
mobility
individuals
This
article
provides
an
update
advances
against
tSCI,
cellular
therapies,
new
therapies.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 10, 2025
Following
spinal
cord
injury
(SCI),
blood-borne
monocytes
infiltrate
the
cord,
differentiate
into
macrophages,
and
dominate
lesion
site.
Inflammatory
responses
mediated
by
macrophages
determine
nerve
regeneration
functional
recovery
after
SCI.
Tauroursodeoxycholic
acid
(TUDCA)
shows
a
neuroprotective
effect
in
different
SCI
animal
models.
However,
underlying
mechanism
of
TUDCA
regulating
monocytes/macrophages
to
impact
has
not
been
elucidated
clearly.
This
study
aims
investigate
on
monocyte/macrophage
distribution
subacute
stage
Transwell
analysis,
Bromodeoxyuridine
(BrdU)
staining,
TUNEL
staining
were
performed
evaluate
inflammatory
response
neural
stem
cells
(NSCs)
proliferation
migration,
neuron
survival,
axon
degeneration
vitro.
H&E
RNA
sequencing,
series
immunofluorescent
pathological
progress,
gene
expression
changes,
distribution,
treatment
mice.
We
found
restored
NSCs
migration
reduced
neurons
apoptosis
promoted
wound
healing,
down-regulated
genes
related
response,
up-regulated
development
Our
provided
evidence
that
regulated
improved
microenvironment
promote
Medicina,
Journal Year:
2024,
Volume and Issue:
60(9), P. 1384 - 1384
Published: Aug. 24, 2024
Nanomedicine
is
a
newer,
promising
approach
to
promote
neuroprotection,
neuroregeneration,
and
modulation
of
the
blood–brain
barrier.
This
review
includes
integration
various
nanomaterials
in
neurological
disorders.
In
addition,
gelatin-based
hydrogels,
which
have
huge
potential
due
biocompatibility,
maintenance
porosity,
enhanced
neural
process
outgrowth,
are
reviewed.
Chemical
modification
these
especially
with
guanidine
moieties,
has
shown
improved
neuron
viability
underscores
tailored
biomaterial
design
applications.
further
discusses
strategies
modulate
barrier—a
factor
critically
associated
effective
delivery
drugs
central
nervous
system.
These
advances
bring
supportive
solutions
solving
conditions
innovative
therapies
for
their
treatment.
Nanomedicine,
as
applied
neuroscience,
presents
significant
leap
forward
new
therapeutic
that
might
help
raise
treatment
management
disorders
much
better
levels.
Our
aim
was
summarize
current
state-of-knowledge
this
field.
Journal of dementia and Alzheimer's disease,
Journal Year:
2024,
Volume and Issue:
1(2), P. 109 - 125
Published: Nov. 6, 2024
Alzheimer’s
disease
(AD)
is
a
brain
disorder
that
more
prevalent
in
developed
nations
and
remains
one
of
most
intractable
conditions
so
far.
It
characterized
by
gradual
onset,
prolonged
progression,
an
unclear
pathophysiology.
At
the
present
time,
there
are
no
effective
treatments
available
for
disease.
However,
human
neural
stem
cells
(hNSCs)
have
capacity
to
substitute
lost
neurons
functional
manner,
strengthen
synaptic
networks
been
compromised,
repair
damaged
brain.
Due
unavailability
restorative
therapeutics,
significant
global
burden
on
economy.
When
it
comes
treatment
neurodegenerative
diseases,
NSCs
provide
potentially
game-changing
approach
treating
Through
delivery
trophic
factors
promote
viability
regeneration
experimental
animals
suffering
from
disorders,
these
potential
facilitate
beneficial
recuperation.
Positive
outcomes
may
be
achieved
variety
ways,
including
replacement
cells,
combining
secretion
neurotrophic
factors,
formation
endogenous
transdifferentiation.
Conversely,
obstacles
need
overcome
before
NSC-based
can
used
clinical
settings.
This
review
article
discusses
current
developments
use
(NSCs)
(AD).
In
addition,
we
highlight
difficulties
opportunities
involved
with
cell
transplant