Nicotinic Acetylcholine Receptors in Glial Cells as Molecular Target for Parkinson’s Disease
Cells,
Год журнала:
2024,
Номер
13(6), С. 474 - 474
Опубликована: Март 7, 2024
Parkinson’s
disease
(PD)
is
a
progressive
neurodegenerative
characterized
by
resting
tremor,
bradykinesia,
rigidity,
and
postural
instability
that
also
includes
non-motor
symptoms
such
as
mood
dysregulation.
Dopamine
(DA)
the
primary
neurotransmitter
involved
in
this
disease,
but
cholinergic
imbalance
has
been
implicated.
Current
intervention
PD
focused
on
replenishing
central
DA,
which
provides
remarkable
temporary
symptomatic
relief
does
not
address
neuronal
loss
progression
of
disease.
It
well
established
nicotinic
receptors
(nAChRs)
can
regulate
DA
release
nicotine
itself
may
have
neuroprotective
effects.
Recent
studies
identified
nAChRs
nonneuronal
cell
types,
including
glial
cells,
where
they
inflammatory
responses.
Given
crucial
role
neuroinflammation
dopaminergic
degeneration
involvement
microglia
astrocytes
response,
provide
novel
therapeutic
target
prevention
and/or
treatment
PD.
In
review,
following
brief
discussion
PD,
we
focus
cells
and,
specifically,
their
pathology
treatment.
Язык: Английский
Heavy Metal Interactions with Neuroglia and Gut Microbiota: Implications for Huntington’s Disease
Cells,
Год журнала:
2024,
Номер
13(13), С. 1144 - 1144
Опубликована: Июль 3, 2024
Huntington’s
disease
(HD)
is
a
rare
but
progressive
and
devastating
neurodegenerative
characterized
by
involuntary
movements,
cognitive
decline,
executive
dysfunction,
neuropsychiatric
conditions
such
as
anxiety
depression.
It
follows
an
autosomal
dominant
inheritance
pattern.
Thus,
child
who
has
parent
with
the
mutated
huntingtin
(mHTT)
gene
50%
chance
of
developing
disease.
Since
HTT
protein
involved
in
many
critical
cellular
processes,
including
neurogenesis,
brain
development,
energy
metabolism,
transcriptional
regulation,
synaptic
activity,
vesicle
trafficking,
cell
signaling,
autophagy,
its
aberrant
aggregates
lead
to
disruption
numerous
pathways
neurodegeneration.
Essential
heavy
metals
are
vital
at
low
concentrations;
however,
higher
concentrations,
they
can
exacerbate
HD
disrupting
glial–neuronal
communication
and/or
causing
dysbiosis
(disturbance
gut
microbiota,
GM),
both
which
neuroinflammation
further
Here,
we
discuss
detail
interactions
iron,
manganese,
copper
glial–neuron
GM
indicate
how
this
knowledge
may
pave
way
for
development
new
generation
disease-modifying
therapies
HD.
Язык: Английский
Ferroptosis as an emerging target in sickle cell disease
Current Research in Toxicology,
Год журнала:
2024,
Номер
7, С. 100181 - 100181
Опубликована: Янв. 1, 2024
Sickle
cell
disease
(SCD)
is
an
inherited
hemoglobin
disorder
marked
by
red
blood
sickling,
resulting
in
severe
anemia,
painful
episodes,
extensive
organ
damage,
and
shortened
life
expectancy.
In
SCD,
increased
iron
levels
can
trigger
ferroptosis,
a
specific
type
of
death
characterized
reactive
oxygen
species
(ROS)
lipid
peroxide
accumulation,
leading
to
damage
impairments.
The
intricate
interplay
between
iron,
inflammation,
oxidative
stress
SCD
underscores
the
necessity
thoroughly
understanding
these
processes
for
development
innovative
therapeutic
strategies.
This
review
highlights
importance
balancing
complex
interactions
among
various
factors
exploitation
knowledge
developing
novel
therapeutics
this
devastating
disease.
Язык: Английский
Status epilepticus alters hippocampal ultrastructure in kainic acid rat model
Tissue and Cell,
Год журнала:
2025,
Номер
94, С. 102789 - 102789
Опубликована: Фев. 10, 2025
Язык: Английский
Structural analysis and bioavailability study of low-molecular-weight chondroitin sulfate‑iron complexes prepared by photocatalysis-Fenton reaction
Carbohydrate Polymers,
Год журнала:
2024,
Номер
342, С. 122435 - 122435
Опубликована: Июнь 25, 2024
Язык: Английский
Intercellular Adhesion Molecule 1 (ICAM-1): An Inflammatory Regulator with Potential Implications in Ferroptosis and Parkinson’s Disease
Cells,
Год журнала:
2024,
Номер
13(18), С. 1554 - 1554
Опубликована: Сен. 15, 2024
Intercellular
adhesion
molecule
1
(ICAM-1/CD54),
a
transmembrane
glycoprotein,
has
been
considered
as
one
of
the
most
important
molecules
during
leukocyte
recruitment.
It
is
encoded
by
ICAM1
gene
and
plays
central
role
in
inflammation.
Its
crucial
many
inflammatory
diseases
such
ulcerative
colitis
rheumatoid
arthritis
are
well
established.
Given
that
neuroinflammation,
underscored
microglial
activation,
key
element
neurodegenerative
Parkinson’s
disease
(PD),
we
investigated
whether
ICAM-1
this
progressive
neurological
condition
and,
if
so,
to
elucidate
underpinning
mechanisms.
Specifically,
were
interested
potential
interaction
between
ICAM-1,
glial
cells,
ferroptosis,
an
iron-dependent
form
cell
death
recently
implicated
PD.
We
conclude
there
exist
direct
indirect
(via
cells
T
cells)
influences
on
ferroptosis
further
elucidation
these
interactions
can
suggest
novel
intervention
for
devastating
disease.
Язык: Английский
Nicotinic Acetylcholine Receptors in Glial Cells as Molecular Target for Parkinson’s Disease
Опубликована: Март 4, 2024
Parkinson’s
disease
(PD)
is
a
progressive
neurodegenerative
characterized
by
resting
tremor,
bradykinesia,
rigidity,
postural
instability,
that
also
includes
non-motor
symptoms
such
as
mood
dysregulation.
Dopamine
(DA)
the
primary
neurotransmitter
involved
in
this
disease,
but
cholinergic
imbalance
has
been
implicated.
Current
intervention
PD
focused
on
replenishing
central
DA,
which
provides
remarkable
temporary
symptomatic
relief
does
not
address
neuronal
loss
and
progression
of
disease.
It
well
established
nicotinic
receptors
(nAChRs)
can
regulate
DA
release
nicotine
itself
may
have
neuroprotective
effects.
Recent
studies
identified
nAChRs
nonneuronal
cell
types
including
glial
cells,
where
they
inflammatory
responses.
Given
crucial
role
neuroinflammation
dopaminergic
degeneration,
involvement
microglia
astrocytes
response,
provide
novel
therapeutic
target
prevention
and/or
treatment
PD.
In
review,
following
brief
discussion
PD,
we
focus
cells
specifically
their
pathology
treatment.
Язык: Английский
Heavy Metals Interactions with Neuroglia and Gut Microbiota: Implications for Huntington’s Disease
Опубликована: Июнь 12, 2024
Huntington’s
disease
(HD)
is
a
rare
but
progressive
and
devastating
neurodegenerative
characterized
by
involuntary
movements,
cognitive
decline,
executive
dysfunction,
neuropsychiatric
conditions
such
as
anxiety
depression.
It
follows
an
autosomal
dominant
inheritance
pattern.
Thus,
child
who
has
parent
with
the
mutated
huntingtin
(mHTT)
gene
50%
chance
of
developing
disease.
Since
HTT
protein
involved
in
many
critical
cellular
processes
including
neurogenesis,
brain
development,
energy
metabolism,
transcriptional
regulation,
synaptic
activity,
vesicle
trafficking,
cell
signaling,
autophagy,
its
aberrant
aggregates
lead
to
disruption
numerous
pathways
neurodegeneration.
Essential
heavy
metals
are
vital
at
low
concentrations,
however,
higher
can
exacerbate
HD
disrupting
glial-neuronal
communication,
and/or
causing
dysbiosis
(disturbance
gut
microbiota,
GM),
both
which
neuroinflammation
further
Here,
we
discuss
detail
interactions
iron,
manganese
copper
glial-neuron
communication
GM
indicate
how
this
knowledge
may
pave
way
for
development
new
generation
disease-modifying
therapies
HD.
Язык: Английский
Intercellular Adhesion Molecule 1 (ICAM-1): An Inflammatory Regulator with Potential Implications in Ferroptosis and Parkinson’s Disease
Опубликована: Авг. 14, 2024
Intercellular
adhesion
molecule
1
(ICAM-1/CD54),
a
transmembrane
glycoprotein,
has
been
considered
as
one
of
the
most
important
molecules
during
leukocyte
recruitment.
It
is
encoded
by
ICAM1
gene
and
plays
central
role
in
inflammation.
It’s
crucial
many
inflammatory
diseases
such
ulcerative
colitis
rheumatoid
arthritis
are
well
established.
Given
that
neuroinflammation,
underscored
microglial
activation,
key
element
neurodegenerative
Parkinson’s
disease
(PD),
we
investigated
whether
ICAM-1
this
progressive
neurological
condition
if
so,
elucidate
underpinning
mechanisms.
Specifically,
were
interested
potential
interaction
between
ICAM-1,
glial
cells
ferroptosis,
an
iron-dependent
form
cell
death
recently
implicated
PD.
We
conclude
there
exist
direct
indirect
(via
T
cells)
influences
on
ferroptosis
further
elucidation
these
interactions
can
suggest
novel
intervention
for
devastating
disease.
Язык: Английский