Molecular Pharmacology,
Год журнала:
2024,
Номер
105(3), С. 250 - 259
Опубликована: Янв. 5, 2024
Opioid
analgesics
are
frequently
associated
with
gastrointestinal
side
effects,
including
constipation,
nausea,
dysphagia,
and
reduced
gastric
motility.
Though
it
has
been
shown
that
stimulation
of
opioid
receptors
expressed
in
enteric
motor
neurons
contributes
to
opioid-induced
remains
unclear
whether
activation
gastric-projecting
nodose
ganglia
the
reduction
motility
emptying
use.
In
present
study,
whole-cell
patch-clamp
recordings
were
performed
determine
mechanism
underlying
receptor–mediated
modulation
Ca2+
currents
acutely
isolated
vagal
afferent
neurons.
Our
results
demonstrate
CaV2.2
channels
provide
majority
(71%
±
16%)
Furthermore,
we
found
application
oxycodone,
U-50488,
or
deltorphin
II
on
inhibited
through
a
voltage-dependent
by
coupling
Gαi/o
family
heterotrimeric
G-proteins.
Because
previous
studies
have
demonstrated
expresses
low
levels
δ-opioid
receptors,
also
determined
concentration-response
relationship
assessed
deltorphin-mediated
current
inhibition
following
exposure
receptor
antagonist
ICI
174,864
(0.3
µM).
The
peak
mean
was
47%
24%
(EC50
=
302.6
nM),
blocked
II–mediated
(4%
4%
versus
37%
20%).
Together,
our
suggest
targeting
any
subtype
can
modulate
circuits.
SIGNIFICANCE
STATEMENT
This
study
neurons,
agonists
all
three
classical
subtypes
(μ,
δ,
κ)
inhibit
voltage-gated
Gαi/o.
These
findings
would
circuits
responsible
for
regulating
reflexes.
The Annual Review of Pharmacology and Toxicology,
Год журнала:
2022,
Номер
63(1), С. 491 - 515
Опубликована: Сен. 28, 2022
In
ligand
bias
different
agonist
drugs
are
thought
to
produce
distinct
signaling
outputs
when
activating
the
same
receptor.
If
these
mediate
therapeutic
versus
adverse
drug
effects,
then
agonists
that
selectively
activate
pathway
would
be
extremely
beneficial.
It
has
long
been
μ-opioid
receptor
G
protein–
over
β-arrestin-dependent
pathways
effective
analgesia
without
effects
such
as
respiratory
depression.
However,
more
recent
data
indicate
most
of
and
agonist-induced
activation
actually
mediated
by
protein–dependent
pathway,
a
number
described
protein
biased
in
fact
may
not
biased,
but
instead
low-intrinsic-efficacy
agonists.
this
review
we
discuss
current
state
field
at
other
opioid
subtypes.
Nature Neuroscience,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 5, 2024
Abstract
Breathing
is
vital
and
must
be
concurrently
robust
flexible.
This
rhythmic
behavior
generated
maintained
within
a
rostrocaudally
aligned
set
of
medullary
nuclei
called
the
ventral
respiratory
column
(VRC).
The
properties
individual
VRC
are
well
known,
yet
technical
challenges
have
limited
interrogation
entire
population
simultaneously.
Here
we
characterize
over
15,000
units
using
high-density
electrophysiology,
opto-tagging
histological
reconstruction.
Population
dynamics
analysis
reveals
consistent
rotational
trajectories
through
low-dimensional
neural
manifold.
These
rotations
even
during
opioid-induced
depression.
During
severe
hypoxia-induced
gasping,
reconfigure
from
to
all-or-none,
ballistic
efforts.
Thus,
latent
provide
unifying
lens
onto
activities
large,
heterogeneous
populations
neurons
involved
in
simple,
vital,
breathing,
describe
how
these
respond
variety
perturbations.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Фев. 21, 2023
Abstract
Breathing
is
regulated
automatically
by
neural
circuits
in
the
medulla
to
maintain
homeostasis,
but
breathing
also
modified
behavior
and
emotion.
Mice
have
rapid
patterns
that
are
unique
awake
state
distinct
from
those
driven
automatic
reflexes.
Activation
of
medullary
neurons
control
does
not
reproduce
these
patterns.
By
manipulating
transcriptionally
defined
parabrachial
nucleus,
we
identify
a
subset
express
Tac1
,
Calca
gene
exerts
potent
precise
conditional
awake,
anesthetized,
via
projections
ventral
intermediate
reticular
zone
medulla.
Activating
drives
frequencies
match
physiological
maximum
through
mechanisms
differ
underlie
breathing.
We
postulate
this
circuit
important
for
integration
with
state-dependent
behaviors
emotions.
Opioids
depress
breathing
by
inhibition
of
interconnected
respiratory
nuclei
in
the
pons
and
medulla.
Mu
opioid
receptor
(MOR)
agonists
directly
hyperpolarize
a
population
neurons
dorsolateral
pons,
particularly
Kölliker-Fuse
(KF)
nucleus,
that
are
key
mediators
opioid-induced
depression.
However,
projection
target
synaptic
connections
MOR-expressing
KF
unknown.
Here,
we
used
retrograde
labeling
brain
slice
electrophysiology
to
determine
project
ventrolateral
medulla,
including
preBötzinger
complex
(preBötC)
rostral
ventral
group
(rVRG).
These
medullary-projecting,
pontine
express
FoxP2
distinct
from
calcitonin
gene-related
peptide-expressing
lateral
parabrachial
neurons.
Furthermore,
release
glutamate
onto
excitatory
preBötC
rVRG
via
monosynaptic
projections,
which
is
inhibited
presynaptic
receptors.
Surprisingly,
majority
receiving
MOR-sensitive
glutamatergic
input
themselves
hyperpolarized
opioids,
suggesting
selective
opioid-sensitive
circuit
inhibit
this
pontomedullary
three
mechanisms-somatodendritic
MORs
on
medullary
neuron
terminals
medulla-all
could
contribute
Journal of Neurophysiology,
Год журнала:
2024,
Номер
132(1), С. 108 - 129
Опубликована: Май 15, 2024
Opioid
drugs
can
cause
serious
respiratory
side-effects
by
binding
to
µ-opioid
receptors
(MORs)
in
brainstem
regions
that
control
breathing.
To
better
understand
the
and
their
cellular
subpopulations
may
be
vulnerable
modulation
opioids,
we
provide
a
comprehensive
map
of
Oprm1
(gene
encoding
MORs)
mRNA
expression
throughout
modulate
Notably,
identify
glutamatergic
neurokinin-1
receptor-expressing
cells
as
potentially
opioid
worthy
further
investigation
using
targeted
approaches.
Frontiers in Pharmacology,
Год журнала:
2022,
Номер
13
Опубликована: Май 26, 2022
Endogenous
and
exogenously
administered
S-nitrosothiols
modulate
the
activities
of
central
peripheral
systems
that
control
breathing.
We
have
unpublished
data
showing
deleterious
effects
morphine
on
arterial
blood-gas
chemistry
(i.e.,
pH,
pCO2,
pO2,
sO2)
Alveolar-arterial
gradient
index
gas
exchange)
were
markedly
diminished
in
anesthetized
Sprague
Dawley
rats
received
a
continuous
intravenous
infusion
endogenous
S-nitrosothiol,
S-nitroso-L-cysteine.
The
present
study
extends
these
findings
by
unanesthetized
adult
male
receiving
an
S-nitroso-L-cysteine
(100
or
200
nmol/kg/min)
ability
injections
potent
synthetic
opioid,
fentanyl
(10,
25,
50
μg/kg),
to
depress
frequency
breathing,
tidal
volume,
minute
ventilation.
Our
also
found
intravenously
injected
μg/kg)
disturb
eupneic
which
was
measured
as
marked
increase
non-eupneic
breathing
index,
substantially
reduced
infusions
nmol/kg/min).
In
contrast,
ventilation
fully
expressed
(200
parent
amino
acid,
L-cysteine,
D-isomer,
namely,
S-nitroso-D-cysteine.
addition,
antinociceptive
actions
above
doses
monitored
tail-flick
latency
assay,
enhanced
S-nitroso-L-cysteine,
but
not
L-cysteine
Taken
together,
add
existing
knowledge
stereoselectively
modulates
detrimental
opioids
opens
door
for
mechanistic
studies
designed
establish
whether
pharmacological
involve
signaling
processes
include
1)
activation
plasma
membrane
ion
channels
receptors,
2)
selective
intracellular
entry
and/or
3)
S-nitrosylation
events.
Whether
alterations
bioavailability
bioactivity
is
key
factor
determining
potency/efficacy
intriguing
question.
Journal of Applied Physiology,
Год журнала:
2024,
Номер
136(4), С. 821 - 843
Опубликована: Фев. 22, 2024
Opioids
are
well-known
to
cause
respiratory
depression,
but
despite
clinical
evidence
of
dysphagia,
the
effects
opioids
on
swallow
excitability
and
motor
pattern
unknown.
We
tested
clinically
relevant
opioid
buprenorphine
pharyngeal
drive
in
male
female
rats.
also
evaluated
utility
5-HT