Journal of Hunan University Natural Sciences,
Год журнала:
2023,
Номер
50(12)
Опубликована: Янв. 1, 2023
Schizophrenia
(SCZ)
is
a
chronic
mental
disorder
with
lifetime
risk
of
approximately
1%.
It
characterized
by
profound
disruption
in
cognition,
behavior,
and
sensation
heritability
estimated
at
up
to
80%.
complex
etiology
that
involves
multiple
heterogeneous
genetic
factors.
The
polygenic
model
susceptibility
psychiatric
diseases
explains
variants
genes
determine
the
overall
disease
because
their
multiplicative
effect.
Two
subunits
voltage-gated
calcium
channels,
cacna1c
cacnb2
genes,
play
important
roles
balancing
brain
cells,
single-nucleotide
polymorphisms
(SNPs)
have
been
associated
differently
schizophrenia
different
ethnicities.
SNPs
(rs1006737
&
4765913)
gene
SNP
(rs12257556)
schizophrenia.
In
this
study,
confirmed
diagnosed
patients
age-matched
healthy
control
subjects
were
analyzed
for
association
(rs1006737,
4765913
rs12257556)
Pakistani
patients.
Both
rs4765913)
showed
significant
population.
Moreover,
two
haplotypes
(AT
GA)
out
four
further
verified
For
,
no
was
observed.
results
study
offer
compelling
evidence
strong
link
between
(individual
variant
haplotypes)
Keywords:
polymorphisms,
rs1006737,
rs4765913,
rs12257556.
https://doi.org/10.55463/issn.1674-2974.50.12.10
Journal of Biomedical Science,
Год журнала:
2025,
Номер
32(1)
Опубликована: Март 6, 2025
Neurons
rely
on
the
bloodstream
for
essential
nutrients
and
oxygen,
which
is
facilitated
by
an
intricate
coupling
of
neuronal
vascular
systems.
Central
to
this
neurovascular
interaction
endothelial
growth
factor
(VEGF)
family,
a
group
secreted
factors
traditionally
known
their
roles
in
promoting
cell
proliferation,
migration,
survival
cardiovascular
lymphatic
However,
emerging
evidence
shows
that
VEGFs
also
play
indispensable
nervous
system,
extending
beyond
canonical
angiogenic
lymphangiogenic
functions.
Over
past
two
decades,
have
been
found
exert
direct
effects
neurons,
influencing
key
aspects
function
independently
actions
cells.
In
particular,
it
has
become
increasingly
evident
crucial
functions
development,
regulation,
maintenance
morphology.
Understanding
development
high
scientific
clinical
interest
because
significance
precise
morphology
neural
connectivity
network
function,
as
well
association
morphological
abnormalities
with
neurological
neurodegenerative
disorders.
This
review
begins
overview
VEGF
family
members,
structural
characteristics,
receptors,
established
vasculature.
then
highlights
focuses
exciting
variety
VEGFs,
especially
role
Deleted Journal,
Год журнала:
2025,
Номер
2(1), С. 11 - 15
Опубликована: Янв. 13, 2025
The
significant
decrease
in
dopamine
(DA)
neurotransmitter
levels
the
brain
due
to
degeneration
and
loss
of
dopaminergic
neurons
is
one
main
reasons
for
causes
motor
symptoms
Parkinson
disease.
Vascular
endothelial
growth
factor
has
been
proven
have
a
protective
effect
on
DA
neurons.
Its
synergistic
interaction
with
nerve
can
accelerate
repair
damaged
nerves
improve
central
nervous
system.
However,
presence
blood-brain
barrier
hinders
most
drugs
from
entering
brain.
Exosomes
are
class
nanoscale
extracellular
vesicles
advantages
such
as
higher
safety,
low
immunogenicity,
unique
targeted
homing
ability,
efficient
penetration
barrier,
which
open
new
perspective
drug
delivery
system
provide
possibilities
treatment
neurodegenerative
diseases.
This
article
reviews
research
progress
exosomes
above
2
factors
repair,
ideas
Journal of Anatomy and Histopathology,
Год журнала:
2025,
Номер
14(1), С. 36 - 44
Опубликована: Апрель 7, 2025
The
aim
was
to
study
the
morphological
changes
in
visual
cortex
of
brain
young
and
old
rats
treated
with
a
fructose-fat
diet
(FFD).
Material
methods
.
carried
out
on
male
Wistar
rats,
divided
into
following
groups:
1st
(n=14)
–
intact
6-month-old
received
standard
diet;
2nd
(FFD)
for
90
days
(from
3
months
age);
3rd
(n
=
14)
18-month-old
4th
FFD
15
age).
Histological
sections
were
Nissl
stained.
Immunohistochemical
reaction
performed
detect
expression
vascular
endothelial
growth
factor
(VEGF).
In
layers
II,
IV
V
primary
cortex,
percentage
normochromic
altered
neurons
number
gliocytes
1
mm2
section
calculated.
Differences
between
groups
determined
using
Kruskal–Wallis
multiple
comparison
test.
Results
Morphological
most
pronounced
and,
addition
reversible
neuronal
disorders,
characterized
by
total
chromatolysis
vacuolization
cytoplasm.
FFD,
increase
hyperchromic
shrinkage
observed
layer
IV.
animals,
pathological
neurocytes
found
all
studied
signs
neuronophagia
gliosis
noted.
6-
congestion
perivascular
edema
VEGF
detected.
Conclusion
enhances
age-related
manifested
degenerative
glial
hyperreactivity.
Experimental Neurology,
Год журнала:
2023,
Номер
370, С. 114550 - 114550
Опубликована: Сен. 27, 2023
Preterm
birth
is
a
public
health
priority
worldwide,
with
approximately
15
million
premature
babies
born
each
year.
Oxygen
supplementation
one
of
the
most
common
interventions
for
preterm
infants.
However,
prolonged
oxygen
inhalation
at
supraphysiological
concentrations
can
lead
to
development
bronchopulmonary
dysplasia
(BPD).
In
addition
lifelong
pulmonary
sequelae,
clinical
evidence
suggests
that
BPD
associated
adverse
neurodevelopmental
outcomes,
such
as
motor
impairment,
cognitive
and
behavioral
deficits,
severely
affecting
quality
life
mechanisms
underlying
combination
impairment
remain
unclear.
Therefore,
in
recent
years,
attention
has
also
been
focused
on
effects
hyperoxia
brain
this
review,
we
outline
pathophysiological
injury
caused
by
developmental
exposure
current
animal
models
briefly
describe
pharmacological
therapies
may
be
applicable
injury.
Overall,
more
studies
are
needed
assess
immature
brain,
particularly
combined
analyses
lungs
same
experimental
setting,
elucidate
potential
causes
BPD.
Biomedicines,
Год журнала:
2024,
Номер
12(8), С. 1906 - 1906
Опубликована: Авг. 20, 2024
Hereditary
neurodegenerative
diseases
(hNDDs)
such
as
Alzheimer's,
Parkinson's,
Huntington's
disease,
and
others
are
primarily
characterized
by
their
progressive
nature,
severely
compromising
both
the
cognitive
motor
abilities
of
patients.
The
underlying
genetic
component
in
hNDDs
contributes
to
disease
risk,
creating
a
complex
landscape.
Considering
fact
that
growth
factors
play
crucial
roles
regulating
cellular
processes,
proliferation,
differentiation,
survival,
they
could
have
therapeutic
potential
for
hNDDs,
provided
appropriate
dosing
safe
delivery
approaches
ensured.
This
article
presents
detailed
overview
factors,
explores
treating
emphasizing
neuronal
growth,
synaptic
plasticity.
However,
challenges
proper
dosing,
methods,
patient
variability
can
hinder
clinical
application.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(22), С. 12369 - 12369
Опубликована: Ноя. 18, 2024
Parkinson's
disease
(PD)
is
the
second
most
prevalent
neurodegenerative
disorder.
It
characterized
by
progressive
loss
of
dopaminergic
(DAnergic)
neurons
in
substantia
nigra
and
decreased
dopamine
(DA)
levels,
which
lead
to
both
motor
non-motor
symptoms.
Conventional
PD
treatments
aim
alleviate
symptoms,
but
do
not
delay
progression.
gene
therapy
offers
a
promising
approach
improving
current
treatments,
with
potential
significant
symptoms
cause
fewer
adverse
effects
than
conventional
therapies.
DA
replacement
approaches
enzyme
expression
slow
However,
therapies,
such
as
adeno-associated
virus
(AAV)-glutamic
acid
decarboxylase
(GAD)
L-amino
(AADC)
increase
transmitter
have
been
demonstrated
be
safe
efficient
early-phase
clinical
trials.
Disease-modifying
strategies,
progression,
appear
potent.
These
include
therapies
targeting
downstream
pathways,
neurotrophic
factors,
midbrain
DAnergic
neuronal
all
shown
preclinical
focus
on
maintaining
integrity
neurons,
just
level
itself.
In
particular,
critical
developmental
maintenance
Nurr1
Foxa2,
can
interact
synergistically
neighboring
glia,
paracrine
mode
action,
protect
against
various
toxic
factors.
Similar
outcomes
could
achieved
glial
cells
other
candidate
in-depth
research
needed.
Neurotrophic
neurturin,
glial-cell-line-derived
factor
(GDNF),
brain-derived
(BDNF),
vascular
endothelial
growth
(VEGF),
are
also
being
investigated
for
their
support
neuron
survival.
Additionally,
key
autophagy-lysosome
pathway,
mitochondrial
function,
endoplasmic
reticulum
(ER)
stress,
offer
avenues.
Gene
editing
delivery
techniques
continue
evolve,
presenting
new
opportunities
develop
effective
PD.
The
potassium-chloride
cotransporter
KCC2
is
the
main
extruder
of
Cl-
in
neurons.
It
plays
a
fundamental
role
activity
inhibitory
neurotransmitters
(GABA
and
glycine)
since
low
levels
promote
intracellular
accumulation
leading
to
depolarizing
GABA
glycine.
Downregulation
this
occurs
neurological
disorders
characterized
by
hyperexcitability,
such
as
epilepsy,
neuropathic
pain
spasticity.
also
downregulated
after
axotomy.
If
muscle
reinnervation
allowed,
recover
motoneurons.
Therefore,
we
argued
that
target-derived
neurotrophic
factors
might
be
involved
regulation
expression.
For
purpose,
performed
axotomy
extraocular
motoneurons
monocular
enucleation
adult
rats,
pellet
containing
either
VEGF
or
BDNF
was
chronically
implanted
orbit.
Double
confocal
immunofluorescence
ChAT
carried
out
brainstem
sections.
Axotomy
led
decrease
neuropil
soma
motoneurons,
peaking
at
15
days
post-lesion,
with
exception
abducens
motoneuron
somata.
administration
prevented
axotomy-induced
downregulation.
By
contrast,
maintained
reduced
following
suggesting
downregulation
finding
prevents
opens
new
possibilities
for
treatment
coursing
neuronal
hyperactivity
due