Frontiers in Physiology,
Год журнала:
2024,
Номер
15
Опубликована: Апрель 9, 2024
The
effects
of
lithium
(Li)
isotopes
and
their
impact
on
biological
processes
have
recently
gained
increased
attention
due
to
the
significance
Li
as
a
pharmacological
agent
potential
that
isotopic
in
neuroscience
contexts
may
constitute
new
example
quantum
biology.
Previous
studies
shown
two
isotopes,
which
differ
mass
nuclear
spin,
unusual
different
The Journal of Physiology,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 2, 2025
Transient
receptor
potential
ankyrin
1
(TRPA1)
and
melastatin
3
(TRPM3)
are
transduction
channels
of
sensory
neurons
that
play
major
roles
in
peripheral
mechanisms
somatosensation,
including
thermosensation,
chemosensation
nociception.
Recent
studies
suggest
both
also
contribute
to
central
pain
processing
at
the
spinal
cord
level.
TRPA1
TRPM3
highly
permeable
for
Ca2+,
suggesting
they
could
regulate
Ca2+
signalling
synapses.
However,
information
about
TRPA1-
TRPM3-induced
dorsal
horn
(DH)
is
lacking.
Here,
we
describe
a
dual-colour
technique
simultaneously
measuring
concentration
([Ca2+]i)
terminals
DH
by
green
(GCaMP3)
red
(jRGECO1a)
indicators,
using
two-photon
imaging
isolated
mouse
with
attached
roots
(DR).
DR
stimulation
elicited
[Ca2+]i
transients
axonal
boutons
primary
afferents
cell
bodies
neurons.
The
antagonists
AMPA
NMDA
glutamate
receptors,
CNQX
AP5,
inhibited
neurons,
but
not
boutons.
Selective
agonists
TRPM3,
ASP7663
CIM0216,
induced
complex
responses
distinct
partially
overlapping
subsets
Concomitant
elevations
were
observed
which
blocked
AP5.
Patch
clamp
recordings
from
showed
CIM0216
markedly
enhanced
excitatory
synaptic
activity.
In
summary,
our
findings
on
presynaptic
transmission
DH.
KEY
POINTS:
somatosensation
processing.
These
two
receptors
This
study
uses
measure
changes
response
electrical
chemical
an
intact,
ex
vivo
roots.
evoked
synaptically-driven
results
help
us
better
understand
mediated
cord,
potentially
explaining
role
these
Mitochondria-endoplasmic
reticulum
contacts
(MERCs),
also
called
endoplasmic
(ER)-mitochondria
contact
sites
(ERMCS),
are
the
membrane
domains,
where
these
two
organelles
exchange
lipids,
Ca
2+
ions,
and
reactive
oxygen
species.
This
crosstalk
is
a
major
determinant
of
cell
metabolism,
since
it
allows
ER
to
control
mitochondrial
oxidative
phosphorylation
Krebs
cycle,
while
conversely,
mitochondria
provide
sufficient
ATP
proteostasis.
MERC
metabolic
signaling
under
tethers
multitude
regulatory
proteins.
Many
proteins
have
recently
been
discovered
give
rise
rare
diseases
if
their
genes
mutated.
Surprisingly,
share
important
hallmarks
cause
neurological
defects,
sometimes
paired
with,
or
replaced
by
skeletal
muscle
deficiency.
Typical
symptoms
include
developmental
delay,
intellectual
disability,
facial
dysmorphism
ophthalmologic
defects.
Seizures,
epilepsy,
deafness,
ataxia,
peripheral
neuropathy
can
occur
upon
mutation
protein.
Given
that
most
secondary
functions,
some
protein-based
do
not
fit
into
this
categorization.
Typically,
however,
affected
in
those
dominant
functions
unrelated
roles
MERCs
tethering
regulation.
We
discussing
avenues
pharmacologically
target
genetic
leading
based
on
our
novel
insight
defects
lead
common
characteristics
diseases.
These
shared
disorders
raise
hope
they
may
allow
for
similar
treatment
options.
Current Pharmaceutical Design,
Год журнала:
2023,
Номер
29(43), С. 3428 - 3441
Опубликована: Дек. 1, 2023
Aim::
Alzheimer’s
disease
(AD)
has
been
identified
as
a
progressive
brain
disorder
associated
with
memory
dysfunction
and
the
accumulation
of
β-amyloid
plaques
neurofibrillary
tangles
τ
protein.
Mitochondria
is
crucial
in
maintaining
cell
survival,
death,
calcium
regulation,
ATP
synthesis.
Mitochondrial
linked
overload
have
involved
pathogenesis
AD.
CRM2
(Collapsin
response
mediator
protein-2)
endosomal
lysosomal
trafficking
well
autophagy,
their
reduced
level
also
primary
culprit
progression
In
addition,
Cholinergic
neurotransmission
neuroinflammation
are
two
other
mechanisms
implicated
AD
onset
might
be
protective
targets
to
attenuate
progression.
The
microbiota-gut-brain
axis
(MGBA)
another
target
for
treatment.
Crosstalk
between
gut
microbiota
mutually
benefitted
each
other,
dysbiosis
affects
functions
leads
increased
AD-causing
biomarkers.
Despite
complexity
AD,
treatment
only
limited
symptomatic
management.
Therefore,
there
an
urgent
demand
novel
therapeutics
that
pathways
responsible
pathology.
This
review
explores
role
different
possible
therapeutic
protect
against
Background::
Amidst
various
age-related
diseases,
most
deleterious
neurodegenerative
more
than
24
million
people
globally.
Every
year,
approximately
7.7
new
cases
dementia
reported.
However,
date,
no
disease-modifying
therapies
available
treat
Objective::
aim
writing
this
highlight
key
biomarker
proteins
interventions
could
play
mitigating
ongoing
prognosis
disease.
Materials
Methods:
information
about
was
collected
through
multiple
search
engines,
including
PubMed,
Science
Direct,
Clinical
Trials,
Google
Scholar.
Results::
Accumulated
pieces
evidence
reveal
extracellular
aggregation
intracellular
protein
peculiar
features
perpetuated
(AD).
Further,
significant
mitochondria,
calcium,
cholinergic
makes
respiratory
organelle
All
currently
drugs
either
delay
clinical
damage
cells
or
temporarily
some
symptoms
Conclusion::
pathological
deposition
β-amyloid,
acetylcholinesterase
deregulation,
multifactorial
heterogeneity
demands
research
work
field
find
biological
targets.
Frontiers in Physiology,
Год журнала:
2024,
Номер
15
Опубликована: Апрель 9, 2024
The
effects
of
lithium
(Li)
isotopes
and
their
impact
on
biological
processes
have
recently
gained
increased
attention
due
to
the
significance
Li
as
a
pharmacological
agent
potential
that
isotopic
in
neuroscience
contexts
may
constitute
new
example
quantum
biology.
Previous
studies
shown
two
isotopes,
which
differ
mass
nuclear
spin,
unusual
different