Pain,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 8, 2024
Abstract
Repetitive
ischemia
with
reperfusion
(I/R)
injury
is
a
common
cause
of
myalgia.
Ischemia
injuries
occur
in
many
conditions
that
differentially
affect
males
and
females
including
complex
regional
pain
syndrome
fibromyalgia.
Our
preclinical
studies
have
indicated
primary
afferent
sensitization
behavioral
hypersensitivity
caused
by
I/R
may
be
due
to
sex-specific
gene
expression
the
dorsal
root
ganglia
(DRG)
distinct
upregulation
growth
factors
cytokines
affected
muscles.
To
determine
how
these
unique
programs
established
sex-dependent
manner
model
more
closely
mimics
clinical
scenarios,
we
used
developed
prolonged
ischemic
myalgia
mice
whereby
animals
experience
repeated
compared
results
unbiased
targeted
screening
strategies
male
female
DRG.
Several
proteins
were
found
expressed
DRG,
phosphorylated
AU-rich
element
RNA-binding
protein
(pAUF1),
which
known
regulate
expression.
Nerve-specific
siRNA-mediated
knockdown
AUF1
inhibited
only,
whereas
overexpression
DRG
neurons
increased
pain-like
responses.
was
able
specifically
inhibit
I/R-induced
potentially
downstream
prolactin
receptor
signaling.
Data
suggest
such
as
pAUF1
underlie
effects
on
modulates
after
through
This
study
aid
finding
differences
related
evolution
acute
chronic
muscle
development
between
sexes.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: June 9, 2023
Repetitive
ischemia
with
reperfusion
(I/R)
injury
is
a
common
cause
of
myalgia.
I/R
injuries
occur
in
many
conditions
that
differentially
affect
males
and
females
including
complex
regional
pain
syndrome
fibromyalgia.
Our
preclinical
studies
have
indicated
primary
afferent
sensitization
behavioral
hypersensitivity
due
to
may
be
sex
specific
gene
expression
the
DRGs
distinct
upregulation
growth
factors
cytokines
affected
muscles.
In
order
determine
how
these
unique
programs
established
dependent
manner
model
more
closely
mimics
clinical
scenarios,
we
utilized
newly
developed
prolonged
ischemic
myalgia
mice
whereby
animals
experience
repeated
forelimb
compared
results
unbiased
targeted
screening
strategies
male
female
DRGs.
Several
proteins
were
found
expressed
DRGs,
AU-rich
element
RNA
binding
protein
(AUF1),
which
known
regulate
expression.
Nerve
siRNA-mediated
knockdown
AUF1
inhibited
only,
while
overexpression
DRG
neurons
increased
some
pain-like
responses.
Further,
was
able
specifically
inhibit
induced
but
not
males.
Data
suggests
like
underlie
effects
on
modulate
after
injury.
This
study
aid
finding
receptor
differences
related
evolution
acute
chronic
muscle
development
between
sexes.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 14, 2024
Physical
activity
is
commonly
used
for
both
measuring
and
treating
dysfunction.
While
preclinical
work
has
been
historically
biased
towards
males,
the
use
of
male
female
animals
gaining
popularity
after
multiple
NIH
initiatives.
With
increasing
inclusion
sexes,
it
become
imperative
to
determine
sex
differences
in
common
behavioral
assays.
The
purpose
this
study
was
baseline
3
assays:
voluntary
wheel
running,
forced
treadmill
open
field
testing.
Pain,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 8, 2024
Abstract
Repetitive
ischemia
with
reperfusion
(I/R)
injury
is
a
common
cause
of
myalgia.
Ischemia
injuries
occur
in
many
conditions
that
differentially
affect
males
and
females
including
complex
regional
pain
syndrome
fibromyalgia.
Our
preclinical
studies
have
indicated
primary
afferent
sensitization
behavioral
hypersensitivity
caused
by
I/R
may
be
due
to
sex-specific
gene
expression
the
dorsal
root
ganglia
(DRG)
distinct
upregulation
growth
factors
cytokines
affected
muscles.
To
determine
how
these
unique
programs
established
sex-dependent
manner
model
more
closely
mimics
clinical
scenarios,
we
used
developed
prolonged
ischemic
myalgia
mice
whereby
animals
experience
repeated
compared
results
unbiased
targeted
screening
strategies
male
female
DRG.
Several
proteins
were
found
expressed
DRG,
phosphorylated
AU-rich
element
RNA-binding
protein
(pAUF1),
which
known
regulate
expression.
Nerve-specific
siRNA-mediated
knockdown
AUF1
inhibited
only,
whereas
overexpression
DRG
neurons
increased
pain-like
responses.
was
able
specifically
inhibit
I/R-induced
potentially
downstream
prolactin
receptor
signaling.
Data
suggest
such
as
pAUF1
underlie
effects
on
modulates
after
through
This
study
aid
finding
differences
related
evolution
acute
chronic
muscle
development
between
sexes.