bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 23, 2024
Abstract
Sudden
unexpected
death
in
epilepsy
(SUDEP)
is
the
leading
cause
of
refractory
patients.
Despite
previous
accumulating
evidence
has
shown
that
seizure-induced
respiratory
arrest
(S-IRA)
may
play
main
contributor
to
SUDEP
as
an
initiating
event
preeminent
mortality,
specific
underlying
mechanism
action
remains
unclear.
Based
on
our
work,
serotonin
(5-HT)
signaling
dorsal
raphe
nucleus
(DRN)
strongly
implicated
S-IRA
animal
models,
including
DBA/1
mice,
meanwhile,
norepinephrine
(NE)
neurons
locus
coeruleus
(LC)
also
plays
a
vital
role
regulating
function
its
own.
Superficially,
monoaminergic
neuron,
important
neurotransmitters
central
nervous
system,
have
similar
modes
maintenance
system
balance,
and
each
them
regulatory
effect
SUDEP.
However,
it
be
investigated
whether
neuron
family
(NE
5-HT)
are
related
SUDEP,
what
even
more
curious
two
intrinsically
linked.
Thus,
we
hypothesize
neural
noradrenergic
serotonergic
circuits
modulating
synergistic-dependent
manner,
this
endeavor
will
culminate
significant
breakthrough
elucidating
precise
In
study,
use
chemogenetics,
optogenetics,
calcium
signal
recording,
bidirectional
tracing
explore
internal
DR-LC
occurrence
by
specifically
injecting
5-HT2AR
antagonist
Ketanserin
(KET)
and/or
NEα-1R
Prazosin
into
pre-Bötzinger
complex
(PBC),
was
finally
elucidate
DR-LC-PBC
network
can
effectively
reduce
incidence
SIRA.
We
firstly
proposed
powerful
target
for
exploring
reduction
which
great
clinical
translation
potential.
Developmental
and
epileptic
encephalopathies
(DEEs),
a
class
of
devastating
neurological
disorders
characterized
by
recurrent
seizures
exacerbated
disruptions
to
excitatory/inhibitory
balance
in
the
brain,
are
commonly
caused
mutations
ion
channels.
Disruption
of,
or
variants
in,
FGF13
were
implicated
as
causal
for
set
DEEs,
but
underlying
mechanisms
clouded
because
is
expressed
both
excitatory
inhibitory
neurons,
undergoes
extensive
alternative
splicing
producing
multiple
isoforms
with
distinct
functions,
overall
roles
neurons
incompletely
cataloged.
To
overcome
these
challenges,
we
generated
novel
cell-type-specific
conditional
knockout
mice.
Interneuron-targeted
deletion
Fgf13
led
perinatal
mortality
associated
impaired
hippocampal
inhibitory/excitatory
while
neuron-targeted
no
detectable
survival
deficits.
While
best
studied
voltage-gated
sodium
channel
(Na
v
)
regulator,
observed
effect
ablation
interneurons
on
Na
s
rather
marked
reduction
K
+
currents.
Re-expressing
different
splice
could
partially
rescue
deficits
interneuron
excitability
restore
current
amplitude.
These
results
enhance
our
understanding
molecular
that
drive
pathogenesis
Fgf13-
related
expand
functions
neuron
subsets.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(4), С. 1598 - 1598
Опубликована: Фев. 13, 2025
Sudden
unexpected
death
in
epilepsy
(SUDEP)
is
a
critical
concern
for
individuals
suffering
from
epilepsy,
with
respiratory
dysfunction
playing
significant
role
its
pathology.
Fatal
seizures
are
often
characterized
by
central
apnea
and
hypercapnia
(elevated
CO2
levels),
indicating
failure
ventilatory
control.
Research
has
shown
that
both
human
patients
animal
models
exhibit
reduced
hypercapnic
response
the
interictal
(non-seizure)
period,
suggesting
an
impaired
ability
to
regulate
breathing
high
levels.
This
review
examines
of
chemoreceptors-specifically
retrotrapezoid
nucleus,
raphe
nuclei,
nucleus
tractus
solitarius,
locus
coeruleus,
hypothalamus
this
These
structures
sensing
maintaining
homeostasis.
Emerging
evidence
also
implicates
neuropeptidergic
pathways
within
these
chemoreceptive
regions
SUDEP.
Neuropeptides
like
galanin,
pituitary
adenylate
cyclase-activating
peptide
(PACAP),
orexin,
somatostatin,
bombesin-like
peptides
may
modulate
chemosensitivity
function,
potentially
exacerbating
during
seizures.
Understanding
mechanisms
linking
chemoreception,
control,
signaling
essential
developing
targeted
interventions
reduce
risk
SUDEP
patients.
Annals of Neurology,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 30, 2024
Objectives
The
effects
of
seizure
control
on
outcomes
in
persons
with
dementia
(PWD)
remain
unclear.
Our
study
aimed
to
investigate
the
impact
mortality,
function,
cognition,
and
mood
among
PWD.
Methods
This
longitudinal,
multicenter
is
based
39
Alzheimer's
disease
centers
(ADCs)
United
States
from
September
2005
December
2021.
PWD
were
grouped
by
status
into
recurrent
(seizures
past
year),
remote
(prior
seizures
but
none
no
(controls).
primary
outcome
was
all‐cause
mortality
groups.
We
used
Weibull
survival
analysis
assess
risks
after
adjusting
for
age,
sex,
education,
race,
ethnicity,
hypertension,
diabetes,
hyperlipidemia,
degree
cognitive
impairment,
dominant
(AD)
mutation,
brain
trauma,
stroke,
Parkinson's
disease,
alcohol
abuse,
depression.
Cognition
(Clinical
Dementia
Rating),
function
(physical
dependence
nursing
home
residence),
day‐to‐day
activities
(Functional
Assessment
Scores),
(Geriatric
Depression
Scale)
compared
groups
duration
age.
Results
Among
26,501
participants,
374
(1.4%)
had
510
(1.9%)
seizures.
In
multivariable
analysis,
associated
a
higher
risk
than
(adjusted
hazard
ratio
[aHR],
95%
confidence
interval
[95%
CI];
aHR
=
1.79,
CI
1.51
2.12;
1.17,
0.98
1.38).
Median
time‐to‐death
recurrent,
remote,
2.4,
4.0,
4.7
years,
respectively.
People
worse
physical
those
controls.
Interpretation
poorly
controlled
have
functional,
These
findings
underscore
need
timely
identification
management
ongoing
ANN
NEUROL
2024
Epilepsia,
Год журнала:
2024,
Номер
65(9), С. 2812 - 2826
Опубликована: Июль 9, 2024
Abstract
Objective
Sudden
unexpected
death
in
epilepsy
(SUDEP)
results
more
years
of
potential
life
lost
than
any
neurological
condition
with
the
exception
stroke.
It
is
generally
agreed
that
SUDEP
happens
due
to
some
form
respiratory,
cardiac,
and
electrocerebral
dysfunction
following
a
seizure;
however,
mechanistic
cause
these
perturbations
unclear.
One
possible
explanation
lies
adenosinergic
signaling.
Extracellular
levels
inhibitory
neuromodulator
adenosine
rapidly
rise
during
seizures,
countermeasure
necessary
for
seizure
termination.
Previous
evidence
has
suggested
excessive
inhibition
could
increase
risk
by
silencing
brain
areas
life,
such
as
respiratory
nuclei
brainstem.
The
goal
this
investigation
was
further
clarify
role
seizure‐induced
dysfunction.
Methods
To
determine
postictal
physiological
dysregulation,
we
pharmacologically
manipulated
signaling
prior
amygdala‐kindled
seizures
mice
while
recording
electroencephalogram
(EEG),
electromyogram,
breathing
using
whole
body
plethysmography.
drugs
used
study
included
selective
nonselective
receptor
antagonists
inhibitors
metabolism.
Results
We
found
high
doses
caused
result
death;
counterintuitively,
animals
conditions
did
not
experience
had
little
or
no
generalized
EEG
suppression.
Inhibitors
metabolism
effect
on
but
worsen
outcomes.
Significance
observed
may
be
severity,
vasoconstriction,
phosphodiesterase
at
doses.
These
findings
have
implications
consumption
caffeine
patients
prevention
SUDEP.
Epilepsia,
Год журнала:
2024,
Номер
65(6), С. 1791 - 1800
Опубликована: Апрель 9, 2024
Abstract
Objective
Sudden
unexpected
death
in
epilepsy
(SUDEP)
is
an
underestimated
complication
of
epilepsy.
Previous
studies
have
demonstrated
that
enhancement
serotonergic
neurotransmission
suppresses
seizure‐induced
sudden
evoked
seizure
models.
However,
it
unclear
whether
elevated
serotonin
(5‐HT)
function
will
prevent
spontaneous
mortality
(SSIM),
which
characteristic
human
SUDEP.
We
examined
the
effects
5‐HT‐enhancing
agents
act
by
three
different
pharmacological
mechanisms
on
SSIM
Dravet
mice,
exhibit
a
high
incidence
SUDEP,
modeling
syndrome.
Methods
mice
both
sexes
were
evaluated
for
characterization
and
changes
induced
enhance
5‐HT‐mediated
neurotransmission.
Fluoxetine
(a
selective
5‐HT
reuptake
inhibitor),
fenfluramine
releaser
agonist),
SR
57227
specific
3
receptor
or
saline
(vehicle)
was
intraperitoneally
administered
over
8‐day
period
effect
these
treatments
examined.
Results
Spontaneous
seizures
generally
progressed
from
wild
running
to
tonic
with
without
SSIM.
at
30
mg/kg,
but
not
20
5
significantly
reduced
compared
vehicle
control.
Fenfluramine
1–10
.2
fully
protected
SSIM,
all
surviving.
Compared
control,
10
lowered
The
drugs
independent
sex.
Significance
Our
data
demonstrate
elevating
fluoxetine,
fenfluramine,
reduces
eliminates
sex‐independent
manner.
These
findings
suggest
deficits
likely
play
important
role
pathogenesis
fluoxetine
are
US
Food
Drug
Administration‐approved
medications,
may
potentially
SUDEP
at‐risk
patients.
Neurobiology of Disease,
Год журнала:
2024,
Номер
199, С. 106592 - 106592
Опубликована: Июль 4, 2024
Failure
to
recover
from
repeated
hypercapnia
and
hypoxemia
(HH)
challenges
caused
by
severe
GCS
postictal
apneas
may
contribute
sudden
unexpected
death
in
epilepsy
(SUDEP).
Our
previous
studies
found
orexinergic
dysfunction
contributes
respiratory
abnormalities
a
preclinical
model
of
SUDEP,
Kcna1−/−
mice.
Here,
we
developed
two
gas
consisting
HH
exposures
used
whole
body
plethysmography
determine
whether
mice
have
detrimental
ventilatory
responses.
exhibited
an
elevated
response
mild
hypercapnia-hypoxia
challenge
compared
WT.
Moreover,
71%
failed
survive
challenge,
whereas
all
WT
recovered.
We
next
determined
orexin
was
involved
these
differences.
Pretreating
with
dual
receptor
antagonist
rescued
the
during
subjects
survived
challenge.
In
ex
vivo
extracellular
recordings
lateral
hypothalamus
coronal
brain
slices,
reducing
pH
either
inhibits
or
stimulates
putative
neurons
similar
other
chemosensitive
neurons;
however,
significantly
greater
percentage
Kcna1−/−mice
were
stimulated
magnitude
stimulation
increased
resulting
augmentation
calculated
chemosensitivity
index
relative
Collectively,
our
data
suggest
that
activity
be
pathologic
mouse
those
at
high
risk
for
SUDEP
more
sensitive
challenges,
induced
seizures
means;
depth
length
exposure
could
dictate
probability
survival.
Orphanet Journal of Rare Diseases,
Год журнала:
2025,
Номер
20(1)
Опубликована: Апрель 8, 2025
Abstract
Background
Angelman
syndrome
(AS)
is
a
rare
genetic
neurodevelopmental
disorder
caused
by
the
absence
of
functional
UBE3A
gene,
leading
to
developmental,
behavioral,
and
medical
challenges.
Sleep
disturbances,
including
sleep-disordered
breathing,
are
common
in
AS.
This
study,
for
first
time,
investigates
nocturnal
respiration
individuals
with
AS
healthy
controls
at
home
long
term
setting.
Methods
A
non-invasive
ballistocardiography-based
(BCG)
sleep
monitoring
device
(“sleep
mat”)
placed
under
participants’
mattresses,
was
used
remotely
monitor
children
aged
1
12
years
(6.0
±
3.2
years,
n
=
40)
age-matched
typically
developing
(TDC)
(6.2
3.5
20)
approximately
months.
The
mat
recorded
physiological
signals
during
times
bed.
We
applied
fast-Fourier
transformation
(FFT)
exclude
segments
without
clear
respiratory
signal,
thereby
minimizing
impact
large
body
movements,
wakefulness,
or
seizure
activity.
Moreover,
polysomnography
(PSG)
collected
up
three
nights
each
participant
their
home.
Clinical
characteristics,
genotype,
Bayley
Scales
Infant
Toddler
Development
®
(Bayley-III)
were
also
analyzed.
Results
average
median
BCG-derived
rate
over
entire
study
duration
significantly
lower
compared
TDCs
(Cohen’s
d
1.31).
PSG-derived
data
corroborated
breathing
0.77)
revealed
strong
correlation
between
BCG
PSG
derived
(
r
0.85)
thus
convergent
validity
against
“gold
standard”
measures.
Next,
we
defined
two
groups
based
on
rates:
normal
group
rates
above
minimum
TDC,
low
below
TDC
group’s
minimum.
higher
prevalence
abnormalities
observed
deletion
carriers
(55.2%)
versus
non-deletion
(9.1%).
Pulse
oximetry
indicated
oxygen
saturation
levels
1.60).
Bayley-III
scores
group,
suggesting
link
dysfunction
outcomes
Medication
use,
particularly
antiepileptic
drugs,
found
suppress
rates,
highlighting
complex
interplay
concomitant
medication
Conclusion
Our
provides
long-term
observational
evidence
persistent
bradypnea-like
phenotype
AS,
which
may
have
significant
implications
clinical
management.
successful
use
as
ambulatory
tool
demonstrates
its
potential
digital
health
technology
detecting
pediatric
disorders.
These
findings
should
be
further
assessed
biomarker
utility
relation
management
cognitive
development.