OBM Neurobiology,
Journal Year:
2021,
Volume and Issue:
6(1)
Published: Dec. 8, 2021
The
editors
of
OBM
Neurobiology
would
like
to
express
their
sincere
gratitude
the
following
reviewers
for
assessing
manuscripts
in
2021.We
greatly
appreciate
contribution
expert
reviewers,
which
is
crucial
journal's
editorial
process.We
aim
recognize
reviewer
contributions
through
several
mechanisms,
annual
publication
names
one.
Molecular Aspects of Medicine,
Journal Year:
2023,
Volume and Issue:
92, P. 101193 - 101193
Published: June 16, 2023
Glaucoma
is
a
common,
complex,
multifactorial
neurodegenerative
disease
characterized
by
progressive
dysfunction
and
then
loss
of
retinal
ganglion
cells,
the
output
neurons
retina.
most
common
cause
irreversible
blindness
affects
∼80
million
people
worldwide
with
many
more
undiagnosed.
The
major
risk
factors
for
glaucoma
are
genetics,
age,
elevated
intraocular
pressure.
Current
strategies
only
target
pressure
management
do
not
directly
processes
occurring
at
level
cell.
Despite
to
manage
pressure,
as
40%
patients
progress
in
least
one
eye
during
their
lifetime.
As
such,
neuroprotective
that
cell
these
great
therapeutic
need.
This
review
will
cover
recent
advances
from
basic
biology
on-going
clinical
trials
neuroprotection
covering
degenerative
mechanisms,
metabolism,
insulin
signaling,
mTOR,
axon
transport,
apoptosis,
autophagy,
neuroinflammation.
With
an
increased
understanding
both
mechanisms
disease,
we
closer
than
ever
strategy
glaucoma.
Frontiers in Neuroscience,
Journal Year:
2023,
Volume and Issue:
17
Published: March 27, 2023
Identification
of
early
adaptive
and
maladaptive
neuronal
stress
responses
is
an
important
step
in
developing
targeted
neuroprotective
therapies
for
degenerative
disease.
In
glaucoma,
retinal
ganglion
cells
(RGCs)
their
axons
undergo
progressive
degeneration
resulting
from
driven
by
sensitivity
to
intraocular
pressure
(IOP).
Despite
that
can
effectively
manage
IOP
many
patients
progress
vision
loss,
necessitating
development
neuronal-based
therapies.
Evidence
experimental
models
glaucoma
indicates
the
disease
RGCs
experience
altered
excitability
are
challenged
with
dysregulated
potassium
(K+)
homeostasis.
Previously
we
demonstrated
certain
RGC
types
have
distinct
profiles
thresholds
depolarization
block,
which
associated
extracellular
K+.
Here,
used
our
inducible
mouse
model
investigate
how
K+
changes
exposure
elevated
IOP.
controls,
conditions
increased
enhanced
membrane
depolarization,
reduced
action
potential
generation,
widened
potentials.
Consistent
previous
work,
4
weeks
elevation
diminished
light-and
current-evoked
responses.
Compared
found
effects
on
block
threshold,
IOP-exposed
maintaining
greater
excitability.
Finally,
did
not
alter
axon
initial
segment
dimensions,
suggesting
structural
plasticity
alone
cannot
explain
decreased
sensitivity.
Thus,
response
prolonged
process
reduces
while
diminishing
These
experiments
give
insight
into
lay
groundwork
mechanistic
investigation
targets
therapy.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 15, 2025
Resveratrol,
a
polyphenolic
compound
commonly
found
in
natural
plants
and
fruits,
exhibits
potential
preventing
optic
nerve
damage
glaucoma,
as
indicated
by
several
animal
studies.
However,
there
is
presently
dearth
of
relevant
evidence
available
for
comprehensive
summarization.
In
this
study,
we
conducted
an
extensive
search
across
7
electronic
databases,
encompassing
all
pertinent
studies
systematic
review
meta-analysis.
Methodological
quality
was
evaluated
using
SYRCLE's
bias
risk
tool,
with
statistical
analysis
performed
Stata
17.0.
The
primary
outcome
measures
included
the
survival
retinal
ganglion
cells
thickness.
30
revealed
that
resveratrol
can
enhance
expression
Sirtuin
1(SIRT1)
protein
tissue
(SMD:
3.00,
95%
CI:
2.46,
3.53,
P
=
0.095),
boost
rate
4.33,
3.28,
5.38,
<
0.05),
decelerate
thinning
thickness
4.26,
2.77,
5.75,
visual
function.
Its
mechanism
action
may
involve
suppression
pro-inflammatory
cytokine
levels
cell
apoptosis.
Resveratrol
emerges
promising
agent
mitigating
glaucoma-related
damage.
given
research
models
utilized
study
not
fully
reflect
intricate
scenarios
multiple
coexisting
diseases
clinical
settings,
administration
methods
differ
from
those
practice,
future
should
aim
to
provide
higher
facilitate
translation
these
findings.
identifier
[CRD42024535673].
Acta Neuropathologica Communications,
Journal Year:
2024,
Volume and Issue:
12(1)
Published: March 1, 2024
Leber's
hereditary
optic
neuropathy
(LHON)
is
driven
by
mtDNA
mutations
affecting
Complex
I
presenting
as
progressive
retinal
ganglion
cell
dysfunction
usually
in
the
absence
of
extra-ophthalmic
symptoms.
There
are
no
long-term
neuroprotective
agents
for
LHON.
Oral
nicotinamide
provides
a
robust
effect
against
mitochondrial
and
metabolic
other
injuries.
We
explored
potential
to
protect
mitochondria
LHON
modelling
disease
mice
through
intravitreal
injection
inhibitor
rotenone.
Using
MitoV
expressing
mitochondrial-tagged
YFP
cells
we
assessed
morphology
super-resolution
imaging
digital
reconstruction.
Rotenone
induced
inhibition
resulted
wide
loss
fragmentation.
This
was
prevented
oral
treatment.
Mitochondrial
ultrastructure
quantified
transition
electron
microscopy,
demonstrating
cristae
density
following
rotenone
injection,
which
also
These
results
demonstrate
that
protects
during
dysfunction.
Nicotinamide
has
be
useful
treatment
strategy
limit
degeneration.
Molecular Therapy,
Journal Year:
2023,
Volume and Issue:
31(7), P. 2005 - 2013
Published: April 4, 2023
Lenadogene
nolparvovec
(GS010)
was
developed
to
treat
a
point
mutation
in
mitochondrial
ND4
that
causes
Leber
hereditary
optic
neuropathy.
GS010
delivers
human
cDNA
encoding
wild-type
packaged
into
an
rAAV2/2
vector
transduces
retinal
ganglion
cells,
induce
allotopic
expression
of
hybrid
ND4.
clinical
trials
improved
best-corrected
visual
acuity
(BCVA)
up
5
years
after
treatment.
Interestingly,
unilateral
treatment
BCVA
bilaterally.
Subsequent
studies
revealed
DNA
tissues
contralateral
the
injected
eye,
suggesting
migration.
Here
we
tested
whether
intraocular
pressure
(IOP)
elevation
could
influence
transfer
viral
RNA
delivery
IOP-elevated
eye
and
probed
potential
mechanism
mediating
translocation
mice.
We
found
IOP
enhanced
transcripts
tissues,
including
retinas.
Using
conditional
transgenic
mice,
depleted
astrocytic
gap
junction
connexin
43
(Cx43),
required
for
distant
redistribution
metabolic
resources
between
astrocytes
during
stress.
After
injection,
Cx43
knockdown
eradicated
transcript
detection
while
still
detectable
nerves.
Overall,
our
study
indicates
long-range
migration
product
is
by
Cx43-linked
astrocyte
networks.
Molecular Neurodegeneration,
Journal Year:
2023,
Volume and Issue:
18(1)
Published: Sept. 26, 2023
Pro-apoptotic
BAX
is
a
central
mediator
of
retinal
ganglion
cell
(RGC)
death
after
optic
nerve
damage.
activation
occurs
in
two
stages
including
translocation
latent
to
the
mitochondrial
outer
membrane
(MOM)
and
then
permeabilization
MOM
facilitate
release
apoptotic
signaling
molecules.
As
critical
component
RGC
death,
an
attractive
target
for
neuroprotective
therapies
understanding
kinetics
mechanisms
controlling
this
process
RGCs
potentially
valuable
informing
development
strategy.
Frontiers in Ophthalmology,
Journal Year:
2024,
Volume and Issue:
3
Published: Jan. 8, 2024
Glial
cells,
a
type
of
non-neuronal
cell
found
in
the
central
nervous
system
(CNS),
play
critical
role
maintaining
homeostasis
and
regulating
CNS
functions.
Recent
advancements
technology
have
paved
way
for
new
therapeutic
strategies
fight
against
glaucoma.
While
intraocular
pressure
(IOP)
is
most
well-known
modifiable
risk
factor,
significant
number
glaucoma
patients
normal
IOP
levels.
Because
complex,
multifactorial
disease
influenced
by
various
factors
that
contribute
to
its
onset
progression,
it
imperative
we
consider
beyond
effectively
prevent
or
slow
down
disease’s
advancement.
In
realm
neurodegenerative
diseases,
glial
cells
emerged
as
key
players
due
their
pivotal
roles
initiating
hastening
progression.
The
inhibition
dysregulated
function
holds
potential
protect
neurons
restore
brain
function.
Consequently,
represent
an
enticing
candidate
glaucoma,
even
though
majority
research
has
historically
concentrated
solely
on
retinal
ganglion
(RGCs).
addition
neuroprotection
RGCs,
proper
regulation
can
also
facilitate
structural
functional
recovery
retina.
this
review,
offer
overview
recent
understanding
non-cell-autonomous
mechanisms
underlying
pathogenesis
Furthermore,
state-of-the-art
technologies
opened
up
possibilities
regenerating
optic
nerve,
which
was
previously
believed
be
incapable
regeneration.
We
will
delve
into
regeneration
nerve
restoration
visual
International Journal of Molecular Sciences,
Journal Year:
2022,
Volume and Issue:
23(6), P. 2911 - 2911
Published: March 8, 2022
Vision
loss
through
the
degeneration
of
retinal
ganglion
cell
(RGC)
axons
occurs
in
both
chronic
and
acute
conditions
that
target
optic
nerve.
These
include
glaucoma,
which
sensitivity
to
intraocular
pressure
(IOP)
causes
early
RGC
axonal
dysfunction,
nerve
trauma,
rapid
axon
from
site
injury.
In
each
case,
is
irreversible,
necessitating
new
therapeutics
protect,
repair,
regenerate
axons.
Recently,
we
demonstrated
reparative
capacity
using
collagen
mimetic
peptides
(CMPs)
heal
fragmented
neuronal
extracellular
milieu.
This
was
an
important
step
development
neuronal-based
therapies
since
neurodegeneration
involves
matrix
metalloproteinase
(MMP)-mediated
remodeling
collagen-rich
environment
neurons
their
exist.
We
found
delivery
a
CMP
comprising
single-strand
fractions
triple
helix
human
type
I
prevented
dysfunction
inducible
glaucoma
model.
Additionally,
CMPs
also
promoted
neurite
outgrowth
dorsal
root
ganglia,
challenged
vitro
by
partial
digestion
collagen.
Here,
compared
ability
sequence
protect
crush.
A
three-week
+40%
elevation
IOP
caused
67%
degradation
anterograde
transport
superior
colliculus,
primary
projection
rodents.
single
intravitreal
injection
during
period
significantly
reduced
this
degradation.
The
same
delivered
shortly
after
crush
significant
recovery
two-week
following
Together,
these
findings
support
novel
protective
role
for
use
affecting
survival
brain.
Drug Design Development and Therapy,
Journal Year:
2022,
Volume and Issue:
Volume 16, P. 3315 - 3326
Published: Sept. 1, 2022
Puerarin
(PUR)
is
a
major
bioactive
ingredient
extracted
from
the
root
of
Pueraria
lobata
(Willd.)
Ohwi,
which
known
as
Gegen
in
traditional
Chinese
medicine.
Conventional
PUR
ophthalmic
dosage
forms
such
solutions
and
suspensions
have
many
drawbacks,
including-rapid
precorneal
elimination
drug
mainly
due
to
lacrimal
duct
drainage.
The
purpose
this
study
develop
thermal
responsive
situ
gel
system
containing
PUR-loaded
human
albumin
nanoparticles
(PUR-HSA-NPs
ISG).The
has
required
sol-gel
phase
transition
temperature,
therefore
can
be
used
for
local
ocular
administration
treat
glaucoma.
formulation
was
evaluated
its
viscosity
vitro
release.
In
vivo
eye
irritation
rabbits.
study,
animal
model
glaucoma
evaluate
pharmacodynamics
PUR-HSA-NPs
ISG
vivo.Morphologically,
exhibited
normal
spherical
shape
with
no
aggregation
or
degradation.
It
had
mean
size
64.8
nm,
drug-loading
encapsulation
efficiency
were
7.1%±0.3%
80.7%±7.4%,
respectively.
gelation
temperature
prepared
thermogelling
37°C.
Meanwhile,
showed
thixotropic
behavior
downward
curve
exhibiting
lower
shear
stress
values
compared
corresponding
points
on
upward
curve.
pharmacological
results
continuous
reduction
IOP
value
long
time
that
remained
lower-level
range
drop
group.
According
pharmacodynamic
results,
Bcl-2/Bax
ratio
group
closest
1
(0.8798,
24
h),
obvious
tissue
cell
apoptosis.Through
it
found
an
ideal
delivery
system.
hoped
product
could
further
promoted
clinical
applications
future.