The
function
of
the
smooth
muscle
cells
lining
walls
systemic
arteries
and
arterioles
is
to
regulate
diameter
vessels
control
blood
flow
pressure.
Here,
we
describe
an
in-silico
model,
which
call
"Hernandez-Hernandez
model",
electrical
Ca2+
signaling
in
arterial
myocytes
based
on
new
experimental
data
indicating
sex-specific
differences
male
female
from
resistance
arteries.
model
suggests
fundamental
ionic
mechanisms
underlying
membrane
potential
intracellular
during
development
myogenic
tone
vessels.
Although
suggest
that
KV1.5
channel
currents
have
similar
amplitudes,
kinetics,
voltage
dependencies
myocytes,
simulations
current
dominant
regulating
myocytes.
In
cells,
larger
KV2.1
expression
longer
time
constants
for
activation
than
predictions
simulated
plays
a
primary
role
potential.
Over
physiological
range
potentials,
gating
small
number
voltage-gated
K+
channels
L-type
are
predicted
drive
excitability.
We
also
show
idealized
computational
vessel,
exhibits
heightened
sensitivity
commonly
used
blockers
compared
male.
summary,
present
framework
investigate
impact
anti-hypertensive
drugs.
The
function
of
the
smooth
muscle
cells
lining
walls
systemic
arteries
and
arterioles
is
to
regulate
diameter
vessels
control
blood
flow
pressure.
Here,
we
describe
an
in
silico
model,
which
call
“Hernandez-Hernandez
model”,
electrical
Ca2+
signaling
arterial
myocytes
based
on
new
experimental
data
indicating
sex-specific
differences
male
female
from
resistance
arteries.
model
suggests
fundamental
ionic
mechanisms
underlying
membrane
potential
intracellular
during
development
myogenic
tone
vessels.
Although
suggest
that
KV1.5
channel
currents
have
similar
amplitudes,
kinetics,
voltage
dependencies
myocytes,
simulations
current
dominant
regulating
myocytes.
In
cells,
larger
KV2.1
expression
longer
time
constants
for
activation
than
predictions
simulated
plays
a
primary
role
potential.
Over
physiological
range
potentials,
gating
small
number
voltage-gated
K+
channels
L-type
are
predicted
drive
excitability.
We
also
show
idealized
computational
vessel,
exhibits
heightened
sensitivity
commonly
used
blockers
compared
male.
summary,
present
framework
investigate
impact
anti-hypertensive
drugs.
The
function
of
the
smooth
muscle
cells
lining
walls
systemic
arteries
and
arterioles
is
to
regulate
diameter
vessels
control
blood
flow
pressure.
Here,
we
describe
an
in
silico
model,
which
call
“Hernandez-Hernandez
model”,
electrical
Ca
2+
signaling
arterial
myocytes
based
on
new
experimental
data
indicating
sex-specific
differences
male
female
from
resistance
arteries.
model
suggests
fundamental
ionic
mechanisms
underlying
membrane
potential
intracellular
during
development
myogenic
tone
vessels.
Although
suggest
that
K
V
1.5
channel
currents
have
similar
amplitudes,
kinetics,
voltage
dependencies
myocytes,
simulations
current
dominant
regulating
myocytes.
In
cells,
larger
2.1
expression
longer
time
constants
for
activation
than
predictions
simulated
plays
a
primary
role
potential.
Over
physiological
range
potentials,
gating
small
number
voltage-gated
+
channels
L-type
are
predicted
drive
excitability.
We
also
show
idealized
computational
vessel,
exhibits
heightened
sensitivity
commonly
used
blockers
compared
male.
summary,
present
framework
investigate
impact
anti-hypertensive
drugs.
The
function
of
the
smooth
muscle
cells
lining
walls
systemic
arteries
and
arterioles
is
to
regulate
diameter
vessels
control
blood
flow
pressure.
Here,
we
describe
an
in-silico
model,
which
call
“Hernandez-Hernandez
model”,
electrical
Ca
2+
signaling
in
arterial
myocytes
based
on
new
experimental
data
indicating
sex-specific
differences
male
female
from
resistance
arteries.
model
suggests
fundamental
ionic
mechanisms
underlying
membrane
potential
intracellular
during
development
myogenic
tone
vessels.
Although
suggest
that
K
V
1.5
channel
currents
have
similar
amplitudes,
kinetics,
voltage
dependencies
myocytes,
simulations
current
dominant
regulating
myocytes.
In
cells,
larger
2.1
expression
longer
time
constants
for
activation
than
predictions
simulated
plays
a
primary
role
potential.
Over
physiological
range
potentials,
gating
small
number
voltage-gated
+
channels
L-type
are
predicted
drive
excitability.
We
also
show
idealized
computational
vessel,
exhibits
heightened
sensitivity
commonly
used
blockers
compared
male.
summary,
present
framework
investigate
impact
anti-hypertensive
drugs.
The
function
of
the
smooth
muscle
cells
lining
walls
systemic
arteries
and
arterioles
is
to
regulate
diameter
vessels
control
blood
flow
pressure.
Here,
we
describe
an
in-silico
model,
which
call
"Hernandez-Hernandez
model",
electrical
Ca2+
signaling
in
arterial
myocytes
based
on
new
experimental
data
indicating
sex-specific
differences
male
female
from
resistance
arteries.
model
suggests
fundamental
ionic
mechanisms
underlying
membrane
potential
intracellular
during
development
myogenic
tone
vessels.
Although
suggest
that
KV1.5
channel
currents
have
similar
amplitudes,
kinetics,
voltage
dependencies
myocytes,
simulations
current
dominant
regulating
myocytes.
In
cells,
larger
KV2.1
expression
longer
time
constants
for
activation
than
predictions
simulated
plays
a
primary
role
potential.
Over
physiological
range
potentials,
gating
small
number
voltage-gated
K+
channels
L-type
are
predicted
drive
excitability.
We
also
show
idealized
computational
vessel,
exhibits
heightened
sensitivity
commonly
used
blockers
compared
male.
summary,
present
framework
investigate
impact
anti-hypertensive
drugs.
The
function
of
the
smooth
muscle
cells
lining
walls
systemic
arteries
and
arterioles
is
to
regulate
diameter
vessels
control
blood
flow
pressure.
Here,
we
describe
an
in-silico
model,
which
call
"Hernandez-Hernandez
model",
electrical
Ca2+
signaling
in
arterial
myocytes
based
on
new
experimental
data
indicating
sex-specific
differences
male
female
from
resistance
arteries.
model
suggests
fundamental
ionic
mechanisms
underlying
membrane
potential
intracellular
during
development
myogenic
tone
vessels.
Although
suggest
that
KV1.5
channel
currents
have
similar
amplitudes,
kinetics,
voltage
dependencies
myocytes,
simulations
current
dominant
regulating
myocytes.
In
cells,
larger
KV2.1
expression
longer
time
constants
for
activation
than
predictions
simulated
plays
a
primary
role
potential.
Over
physiological
range
potentials,
gating
small
number
voltage-gated
K+
channels
L-type
are
predicted
drive
excitability.
We
also
show
idealized
computational
vessel,
exhibits
heightened
sensitivity
commonly
used
blockers
compared
male.
summary,
present
framework
investigate
impact
anti-hypertensive
drugs.