iScience,
Год журнала:
2024,
Номер
28(1), С. 111587 - 111587
Опубликована: Дек. 12, 2024
TWIK-1
belongs
to
the
two-pore
domain
K+
(K2P)
channel
family,
which
plays
an
essential
role
in
background
conductance
of
cells.
Despite
development
exon
2-deleted
Twik-1
knockout
(KO)
mice,
physiological
has
remained
largely
unknown.
Here,
we
observed
that
KO
mice
expressed
internally
deleted
(TWIK-1
ΔEx2)
protein,
unexpectedly
acts
as
a
functional
channel.
The
nKO
1
was
targeted
using
CRISPR-Cas9
technique
provides
strong
evidence
mediates
currents
are
responsible
for
passive
astrocytes.
Deficiency
TWIK-1-mediated
astrocytic
increased
susceptibility
kainic
acid-induced
seizures.
This
study
paves
way
studies
on
conductance.
In
addition,
1-targeted
would
help
elucidate
roles
TWIK-1.
Cells,
Год журнала:
2024,
Номер
13(2), С. 150 - 150
Опубликована: Янв. 12, 2024
The
blood-brain
barrier
(BBB)
is
a
fundamental
structure
that
protects
the
composition
of
brain
by
determining
which
ions,
metabolites,
and
nutrients
are
allowed
to
enter
from
blood
or
leave
it
towards
circulation.
BBB
structurally
composed
layer
capillary
endothelial
cells
(BCECs)
bound
each
other
through
tight
junctions
(TJs).
However,
its
development
as
well
maintenance
properties
controlled
contact
BCECs:
pericytes,
glial
cells,
even
neurons
themselves.
Astrocytes
seem,
in
particular,
have
very
important
role
controlling
most
BBB.
Here,
we
will
focus
on
these
latter
since
comprehension
their
roles
physiology
has
been
continuously
expanding,
including
ability
participate
neurotransmission
complex
functions
such
learning
memory.
Accordingly,
pathological
conditions
alter
astrocytic
can
BBB's
integrity,
thus
compromising
many
activities.
In
this
review,
also
refer
different
kinds
vitro
models
used
study
properties,
evidencing
modifications
under
conditions.
Brain Sciences,
Год журнала:
2024,
Номер
14(6), С. 558 - 558
Опубликована: Май 30, 2024
Mood
disorders
and
substance
use
disorder
(SUD)
are
of
immense
medical
social
concern.
Although
significant
progress
on
neuronal
involvement
in
mood
reward
circuitries
has
been
achieved,
it
is
only
relatively
recently
that
the
role
glia
these
attracted
attention.
Detailed
understanding
glial
functions
devastating
diseases
could
offer
novel
interventions.
Here,
following
a
brief
review
involved
regulation
perception,
specific
contributions
neurotrophic
factors,
neuroinflammation,
gut
microbiota
to
highlighted.
In
this
context,
cells
(e.g.,
microglia,
astroglia,
oligodendrocytes,
synantocytes)
phenotypic
manifestation
or
SUD
emphasized.
addition,
knowledge
potential
development
therapeutics
touched
upon.
Antioxidants,
Год журнала:
2024,
Номер
13(6), С. 709 - 709
Опубликована: Июнь 12, 2024
Psychosis,
defined
as
a
set
of
symptoms
that
results
in
distorted
sense
reality,
is
observed
several
psychiatric
disorders
addition
to
schizophrenia.
This
paper
reviews
the
literature
relevant
underlying
neurobiology
psychosis.
The
dopamine
hypothesis
has
been
major
influence
study
neurochemistry
psychosis
and
development
antipsychotic
drugs.
However,
it
became
clear
early
on
other
factors
must
be
involved
dysfunction
In
current
review,
reported
how
these
factors,
namely
dysregulation
neurotransmitters
[dopamine,
serotonin,
glutamate,
γ-aminobutyric
acid
(GABA)],
neuroinflammation,
glia
(microglia,
astrocytes,
oligodendrocytes),
hypothalamic–pituitary–adrenal
axis,
gut
microbiome,
oxidative
stress,
mitochondrial
contribute
interact
with
one
another.
Research
increased
knowledge
complexity
psychotic
disorders.
Potential
new
pharmacotherapies,
including
combinations
drugs
(with
pre-
probiotics
some
cases)
affecting
mentioned
above,
have
suggested.
Similarly,
putative
biomarkers,
particularly
those
related
immune
system,
proposed.
Future
research
both
pharmacotherapy
biomarkers
will
require
better-designed
studies
conducted
an
all
stages
consider
confounders
such
sex
differences
comorbidity.
The
dysfunction
of
mitochondria,
the
primary
source
cellular
energy
and
producer
reactive
oxygen
species
(ROS),
is
associated
with
brain
aging
neurodegenerative
diseases.
Scientific
evidence
indicates
that
light
in
visible
near-infrared
spectrum
can
modulate
mitochondrial
activity,
a
phenomenon
known
medicine
as
photobiomodulation
therapy
(PBM-t).
beneficial
effects
PBM-t
on
dementia
neurodegeneration
have
been
reviewed
literature.
However,
molecular
mechanisms
underlying
these
findings
yet
to
be
fully
elucidated.
This
study
investigates
mechanism
behind
dose-dependent
glutamate
release
nerve
terminals
after
irradiation
810
nm,
1
W
for
60
s
continuous,
cm2,
W/cm2,
J,
J/cm2
(810
nm-1
W)
or
0.1
6
nm-0.1
W),
focusing
activities.
results
show
PBM
modulated
metabolism
cortical
supported
power-dependent
increase
oxidative
phosphorylation
(OxPhos)
activity
when
stimulated
pyruvate
plus
malate
(P/M)
succinate
(succ)
respiratory
substrates.
PBM-induced
OxPhos
was
sensitive
adding
rotenone
(Complex
I
inhibitor)
antimycin
A
III
synaptosomes
were
P/M,
but
only
succ.
allowed
us
observe
efflux,
disrupted
presence
rotenone,
partially
restored
by
due
pathway
led
Complex
II.
suggests
PBM,
acting
could
facilitate
physiological
communication
within
neuron-astrocyte
network
through
vesicular
release,
potentially
regulating
healthy
function
dysfunction.
Life,
Год журнала:
2024,
Номер
14(10), С. 1234 - 1234
Опубликована: Сен. 26, 2024
Microbes
have
inhabited
the
earth
for
hundreds
of
millions
years
longer
than
humans.
The
microbiota-gut-brain
axis
(MGBA)
represents
a
bidirectional
communication
pathway.
These
communications
occur
between
central
nervous
system
(CNS),
enteric
(ENS),
and
emotional
cognitive
centres
brain.
field
research
on
gut-brain
has
grown
significantly
during
past
two
decades.
Signalling
occurs
gut
microbiota
brain
through
neural,
endocrine,
immune,
humoral
pathways.
A
substantial
body
evidence
indicates
that
MGBA
plays
pivotal
role
in
various
neurological
diseases.
include
Alzheimer's
disease
(AD),
autism
spectrum
disorder
(ASD),
Rett
syndrome,
attention
deficit
hyperactivity
(ADHD),
non-Alzheimer's
neurodegeneration
dementias,
fronto-temporal
lobe
dementia
(FTLD),
Wilson-Konovalov
(WD),
multisystem
atrophy
(MSA),
Huntington's
chorea
(HC),
Parkinson's
(PD),
multiple
sclerosis
(MS),
amyotrophic
lateral
(ALS),
temporal
epilepsy
(TLE),
depression,
schizophrenia
(SCZ).
Furthermore,
correlation
therapeutics
will
be
discussed.
Conversely,
mood
delivery,
exercise,
psychotropic
agents,
stress,
neurologic
drugs
can
influence
MGBA.
By
understanding
MGBA,
it
may
possible
to
facilitate
into
microbial-based
interventions
therapeutic
strategies
Neurochemistry International,
Год журнала:
2024,
Номер
178, С. 105790 - 105790
Опубликована: Июнь 7, 2024
Neurodegenerative
diseases
are
characterized
by
the
progressive
loss
of
neuronal
structure
and
function,
posing
a
tremendous
burden
on
health
systems
worldwide.
Although
underlying
pathological
mechanisms
for
various
neurodegenerative
still
unclear,
common
hallmark
is
abundance
neuroinflammatory
processes,
which
affect
both
disease
onset
progression.
In
this
review,
we
explore
pathways
role
neuroinflammation
in
further
assess
potential
use
curcumin,
natural
spice
with
antioxidant
anti-inflammatory
properties
that
has
been
extensively
used
worldwide
as
traditional
medicine
therapeutic
agent.
Following
examination
preclinical
clinical
studies
assessed
curcumin
agent,
highlight
bioavailability
body
discuss
challenges
benefits
using
compound
treating
neurodegeneration.
elucidating
involvement
aging
neurodegeneration
great
developing
future
CNS-related
targets,
research
required
to
elucidate
Curcumin
affects
brain
physiology,
especially
BBB
integrity,
under
physiological
conditions.
Frontiers in Pharmacology,
Год журнала:
2023,
Номер
14
Опубликована: Окт. 24, 2023
This
systematic
review
analyzes
monosodium
glutamate
(MSG)
in
the
Alzheimer’s
disease-like
condition
to
enhance
translational
research.
Our
seeks
understand
how
MSG
affects
brain
and
causes
degenerative
disorders.
Due
significant
preclinical
data
linking
toxicity
disease
lack
of
a
comprehensive
or
meta-analysis,
we
initiated
study
on
MSG’s
potential
link.
We
searched
PubMed,
ScienceDirect,
ProQuest,
DOAJ,
Scopus
for
animal
research
English
language
papers
without
time
constraints.
used
PRISMA-P
framework
PICO
technique
collect
population,
intervention
exposure,
comparison,
result
data.
It
was
registered
PROSPERO
as
CRD42022371502.
affected
mice’s
exploratory
behaviors
short-term
working
memory.
The
brain,
hippocampus,
cerebellar
tissue
demonstrated
neuronal
injury-related
histological
histomorphometric
changes.
A
total
70%
MSG-treated
mice
had
poor
nesting
behavior.
treated
also
more
hyperphosphorylated
tau
protein
their
cortical
hippocampus
neurons.
Glutamate
glutamine
levels
increased
with
MSG,
dose-dependent
mixed
horizontal
locomotor,
grooming,
anxiety
responses
reduced.
treatment
significantly
decreased
phospho-CREB
levels,
supporting
idea
that
neurons
were
harmed,
despite
CREB
mRNA
expression.
High
doses
drastically
lower
serum
serotonin
levels.
In
conclusion,
showed
AD-like
pathology,
atrophy,
memory
impairment.
Further
longer
span
deeper
behavioral
characterization
is
needed.
Systematic
registration
:
https://www.crd.york.ac.uk/prospero/
,
identifier
[CRD42022371502].
Rare
diseases
are
a
diverse
group
of
disorders
that,
despite
each
individual
condition's
rarity,
collectively
affect
significant
portion
the
global
population.
Currently
approximately
10,000
rare
exist
globally,
with
80%
these
being
identified
as
having
genetic
origins.
In
this
Review,
we
examine
data
from
CAS
Content
Collection
to
summarize
scientific
progress
in
area
diseases.
We
publication
landscape
an
effort
provide
insights
into
current
advances
and
developments.
then
discuss
evolution
key
concepts
field,
associations,
well
major
technologies
development
pipelines
disease
treatments.
focus
our
attention
on
three
specific
diseases:
(i)
amyotrophic
lateral
sclerosis,
terminal
neurodegenerative
affecting
central
nervous
system
resulting
progressive
loss
motor
neurons
that
control
voluntary
muscles;
(ii)
Huntington's
disease,
another
causes
degeneration
nerve
cells
brain,
wide
impact
person's
functional
abilities;
(iii)
myasthenia
gravis,
chronic
autoimmune
synaptopathy
leading
skeletal
muscle
weakness.
While
pathogenesis
is
elucidated,
there
neither
cure
nor
preventative
treatment
available,
only
symptomatic
treatment.
The
objective
paper
broad
overview
evolving
knowledge
specifically
biology
genetics
spotlighted
diseases,
outline
challenges
evaluate
growth
opportunities,
aim
further
efforts
solving
remaining
challenges.