Investigative Ophthalmology & Visual Science,
Journal Year:
2015,
Volume and Issue:
56(11), P. 6906 - 6906
Published: Oct. 27, 2015
Purpose:
To
determine
whether
melanopsin-expressing
intrinsically
photosensitive
retinal
ganglion
cell
(ipRGC)
inputs
to
the
pupil
light
reflex
(PLR)
are
affected
in
early
age-related
macular
degeneration
(AMD).
Methods:
The
PLR
was
measured
40
participants
(20
AMD
and
20
age-matched
controls)
using
a
custom-built
Maxwellian
view
pupillometer.
Sinusoidal
stimuli
(0.5
Hz,
11.9
seconds
duration,
35.6°
diameter)
were
presented
study
eye
consensual
response
lights
with
high
melanopsin
excitation
(464
nm
[blue])
low
(638
[red])
that
biased
activation
outer
retina.
Two
metrics
quantified:
phase
amplitude
percentage
(PAP)
during
sinusoidal
stimulus
presentation
post-illumination
(PIPR).
analyzed
latency
constriction,
transient
maximum
constriction
metrics.
Diagnostic
accuracy
evaluated
receiver
operating
characteristic
(ROC)
curves.
Results:
blue
PIPR
significantly
less
sustained
group
(P
<
0.001).
red
not
different
between
groups
>
0.05).
PAP
lower
There
no
significant
difference
or
for
both
ROC
analysis
showed
excellent
diagnostic
(area
under
curve
0.9).
Conclusions:
This
is
initial
report
melanopsin-controlled
dysfunctional
AMD.
noninvasive,
objective
measurement
of
ipRGC
controlled
has
Royal Society Open Science,
Journal Year:
2024,
Volume and Issue:
11(6)
Published: June 1, 2024
Vision
is
mediated
by
light
passing
through
the
pupil,
which
changes
in
diameter
from
approximately
2
to
8
mm
between
bright
and
dark
illumination.
With
age,
mean
pupil
size
declines.
In
laboratory
experiments,
factors
affecting
can
be
experimentally
controlled.
How
reflects
change
retinal
input
visual
environment
under
natural
viewing
conditions
unclear.
We
address
this
question
a
field
experiment
(
N
=
83,
43
female,
18–87
years)
using
custom-made
wearable
video-based
eye
tracker
with
spectroradiometer
measuring
near-corneal
spectral
irradiance.
Participants
moved
indoor
outdoor
environments
varying
spectrum
engaged
range
of
everyday
tasks.
Our
data
confirm
that
light-adapted
determined
level,
better
model
fit
melanopic
over
photopic
units,
it
decreased
increasing
yielding
steeper
slopes
at
lower
levels.
found
no
indication
sex,
iris
colour
or
reported
caffeine
consumption
affects
size.
exploratory
results
point
role
photoreceptor
integration
controlling
steady-state
The
provide
evidence
for
considering
age
personalized
lighting
solutions
against
use
illuminance
alone
assess
impact
real-world
conditions.
iScience,
Journal Year:
2025,
Volume and Issue:
28(2), P. 111609 - 111609
Published: Jan. 5, 2025
Our
visual
system
uses
contextual
cues
to
estimate
the
brightness
of
surfaces:
can
shift
toward
(assimilation)
or
away
from
(contrast)
surroundings.
We
investigated
induction
at
different
light
levels
and
found
a
potential
influence
rod
photoreceptors
on
induction.
then
used
novel
tetrachromatic
display
generate
stimuli
differentially
exciting
rods
cones
fixed
adaptation
level.
Under
vision,
assimilation
was
enhanced
while
contrast
not
altered
in
comparison
cone
vision.
ruled
out
that
this
effect
mediated
by
low
resolution
night
findings
suggest
vision
affects
high-level
interpretation
scenes
results
differences
but
contrast.
imply
employs
more
perceptual
inferences
under
than
solve
ambiguities
complex
spatial
displays.
Scientific Reports,
Journal Year:
2016,
Volume and Issue:
6(1)
Published: Sept. 13, 2016
Abstract
It
is
difficult
to
detect
visual
function
deficits
in
patients
at
risk
for
glaucoma
(glaucoma
suspects)
and
early
disease
stages
with
conventional
ophthalmic
tests
such
as
perimetry.
To
this
end,
we
introduce
a
novel
quadrant
field
measure
of
the
melanopsin
retinal
ganglion
cell
mediated
pupil
light
response
corresponding
typical
glaucomatous
arcuate
defects.
The
melanopsin-mediated
post-illumination
(PIPR)
was
measured
46
different
including
suspects
compared
healthy
group
21
participants
no
disease.
We
demonstrate
that
superonasal
PIPR
differentiated
from
controls
fair
(AUC
=
0.74)
excellent
0.94)
diagnostic
accuracy,
respectively.
provides
linear
functional
correlate
structural
nerve
fibre
thinning
patients.
This
first
report
stimulation
detects
dysfunction
pre-perimetric
may
have
future
implications
treatment
decisions
suspects.
Frontiers in Neurology,
Journal Year:
2018,
Volume and Issue:
9
Published: Nov. 27, 2018
The
human
pupillary
light
response
is
driven
by
all
classes
of
photoreceptors
in
the
eye-the
three
cones,
rods,
and
intrinsically
photosensitive
retinal
ganglion
cells
(ipRGCs)
expressing
photopigment
melanopsin.
These
photoreceptor
have
distinct
but
overlapping
spectral
tuning,
even
a
monochromatic
with
wavelength
matched
to
peak
sensitivity
given
will
stimulate
photoreceptors.
method
silent
substitution
uses
pairs
lights
("metamers")
selectively
class
while
keeping
activation
others
constant.
In
this
primer,
we
describe
provide
an
overview
studies
that
used
it
examine
inputs
response.
PLoS ONE,
Journal Year:
2016,
Volume and Issue:
11(8), P. e0161175 - e0161175
Published: Aug. 22, 2016
Melanopsin
expressing
intrinsically
photosensitive
Retinal
Ganglion
Cells
(ipRGCs)
entirely
control
the
post-illumination
pupil
response
(PIPR)
from
6
s
post-stimulus
to
plateau
during
redilation
after
light
offset.
However,
photoreceptor
contributions
early
phase
of
PIPR
(<
post-stimulus)
have
not
been
reported.
Here,
we
evaluated
(0.6
5.0
s)
by
measuring
spectral
sensitivity
criterion
amplitude
in
1
pulses
at
five
narrowband
stimulus
wavelengths
(409,
464,
508,
531
and
592
nm).
The
retinal
irradiance
producing
a
was
normalised
peak
fitted
either
single
photopigment
nomogram
or
combined
melanopsin
rhodopsin
nomograms
with
+L+M
cone
photopic
luminous
efficiency
(Vλ)
function.
We
show
that
times
≥
1.7
offset
is
best
described
nomogram.
At
<
s,
shifts
longer
(range:
482
498
nm)
nomogram,
major
rhodopsin.
This
first
report
line
electrophysiological
findings
ipRGC
rod
signalling
cessation
stimuli
provides
cut-off
time
for
isolating
specific
function
healthy
diseased
eyes.
Journal of Vision,
Journal Year:
2019,
Volume and Issue:
19(9), P. 5 - 5
Published: Aug. 15, 2019
The
size
of
the
pupil
depends
on
light
level.
Watson
and
Yellott
(2012)
developed
a
unified
formula
to
predict
from
luminance,
field
diameter,
age,
number
eyes.
Luminance
reflects
input
L
M
cones
in
retina
but
ignores
contribution
intrinsically
photosensitive
retinal
ganglion
cells
(ipRGCs)
expressing
photopigment
melanopsin,
which
are
known
control
pupil.
We
discuss
role
melanopsin
controlling
by
reanalyzing
an
extant
data
set
(Bouma,
1962).
confirm
that
melanopsin-weighted
quantities,
conjunction
with
Yellott's
formula,
adequately
model
intensity-dependent
size.
contributions
other
photoreceptors
into
control.
Journal of Vision,
Journal Year:
2016,
Volume and Issue:
16(11), P. 29 - 29
Published: Sept. 30, 2016
Intrinsically
photosensitive
retinal
ganglion
cells
(ipRGCs)
express
the
photopigment
melanopsin.
These
receive
afferent
inputs
from
rods
and
cones,
which
provide
to
postreceptoral
visual
pathways.
It
is
unknown,
however,
how
melanopsin
activation
integrated
with
signals
control
pupillary
light
reflex.
This
study
reports
human
flicker
responses
measured
using
stimuli
generated
a
five-primary
photostimulator
that
selectively
modulated
melanopsin,
rod,
S-,
M-,
L-cone
excitations
in
isolation,
or
combination
produce
signals.
We
first
analyzed
adaptation
behavior
of
rod
cones
Second,
we
determined
by
testing
cone
luminance,
chromatic
blue-yellow,
red-green
were
processed
magnocellular
(MC),
koniocellular
(KC),
parvocellular
(PC)
pathways,
respectively.
A
combined
response
was
also
measured.
The
relative
phase
varied
respect
phase.
results
showed
for
all
conditions
weaker
than
typical
Weber
adaptation.
Melanopsin
linearly
S-cone,
inputs,
suggesting
locus
integration
MC
KC
retinal.
contribution
phasic
pupil
lower
luminance
contributions,
but
much
higher
S-cone
contributions.
Chromatic
modulation
interacted
nonlinearly
as
described
"winner-takes-all"
process,
PC
might
be
mediated
postretinal
site.
Frontiers in Neurology,
Journal Year:
2019,
Volume and Issue:
10
Published: Feb. 12, 2019
The
pupillary
light
reflex
is
mediated
by
melanopsin-containing
intrinsically-photosensitive
retinal
ganglion
cells
(ipRGCs),
which
also
receive
input
from
rods
and
cones.
Melanopsin-dependent
responses
are
short-wavelength
sensitive,
have
a
higher
threshold
of
activation,
much
slower
to
activate
de-activate
compared
with
rod/cone-mediated
responses.
Given
that
rod/cone
photoreceptors
melanopsin
differ
in
their
response
properties,
stimuli
can
be
designed
stimulate
preferentially
each
the
different
photoreceptor
types,
providing
read-out
function.
This
has
given
rise
chromatic
pupillometry
methods
aim
assess
health
outer
ipRGCs
measuring
blue
or
red
stimuli.
Here,
we
review
types
protocols
been
tested
patients
optic
nerve
disease,
including
approaches
use
short-duration
exposures
continuous
exposure
light.
Across
protocols,
disease
(e.g.,
retinitis
pigmentosa
Leber
congenital
amaurosis)
show
reduced
absent
dim
blue-light
used
rod
function,
moderately-bright
red-light
cone
By
comparison,
glaucoma
ischemic
neuropathy,
but
not
mitochondrial
disease)
impaired
during
bright
stimuli,
post-illumination
after
offset,
These
proof-of-concept
studies
demonstrate
damage
ipRGCs.
In
future
studies,
it
will
important
determine
whether
for
screening
early
detection
diseases.
Such
may
prove
useful
objectively
evaluating
degree
recovery
ipRGC
function
blind
who
undergo
gene
therapy
other
treatments
restore
vision.
Ophthalmic and Physiological Optics,
Journal Year:
2017,
Volume and Issue:
37(4), P. 440 - 450
Published: June 27, 2017
Abstract
Purpose
Exposure
to
increasing
amounts
of
artificial
light
during
the
night
may
contribute
high
prevalence
reported
sleep
dysfunction.
Release
hormone
melatonin
is
mediated
by
intrinsically
photosensitive
retinal
ganglion
cells
(ip
RGC
s).
This
study
sought
investigate
whether
level
and
quality
can
be
modulated
decreasing
night‐time
input
ip
s.
Methods
Subjects
(ages
17–42,
n
=
21)
wore
short
wavelength‐blocking
glasses
prior
bedtime
for
2
weeks.
The
‐mediated
post
illumination
pupil
response
was
measured
before
after
experimental
period.
Stimulation
presented
with
a
ganzfeld
stimulator,
including
one‐second
five‐seconds
long
wavelength
light,
imaged
an
infrared
camera.
Pupil
diameter
before,
60
s
following
stimulation,
six‐second
30
area
under
curve
offset
were
determined.
actigraph
device
objective
measurements
activity,
exposure,
sleep.
Saliva
samples
collected
assess
content.
Pittsburgh
Sleep
Quality
Index
(
PSQI
)
administered
subjective
quality.
Results
blue‐blocking
3:57
±
1:03
h
each
night.
After
period,
showed
slower
redilation
phase,
resulting
in
significantly
increased
decreased
one
five‐second
when
at
same
time
day
as
baseline.
Night
from
16.1
7.5
pg
mL
−1
25.5
10.7
P
<
0.01).
Objectively
duration
24
min,
408.7
44.9
431.5
42.9
min
0.001).
Mean
score
improved
5.6
2.9
3.0
2.2.
Conclusions
use
subjectively
objectively
levels
duration,
presumably
result
stimulation
Alterations
‐driven
suggest
shift
circadian
phase.
that
minimising
sunset
help
regulating
patterns.
The Journal of Comparative Neurology,
Journal Year:
2020,
Volume and Issue:
528(12), P. 2044 - 2067
Published: Jan. 31, 2020
Melanopsin
ganglion
cells
have
defied
convention
since
their
discovery
almost
20
years
ago.
In
the
following,
many
types
of
these
intrinsically
photosensitive
retinal
(ipRGCs)
emerged.
mouse
retina,
there
are
currently
six
known
(M1-M6)
melanopsin
cells,
each
with
unique
morphology,
mosaics,
connections,
physiology,
projections,
and
functions.
While
melanopsin-expressing
usually
associated
behaviors
like
circadian
photoentrainment
pupillary
light
reflex,
characterization
multiple
has
demonstrated
a
reach
that
may
extend
far
beyond
non-image-forming
vision.
fact,
studies
shown
individual
potential
to
impact
image-forming
functions
contrast
sensitivity
color
opponency.
Thus,
goal
this
review
is
summarize
morphological
functional
aspects
in
retina
highlight
respective
roles
Although
cell
do
project
brain
targets,
it
important
note
only
first
step
determining
influence
on
Even
so,
visual
system
canonically
been
divided
into
two
realms
begun
challenge
boundary
between
them,
providing
an
overlap
information
complementary
rather
than
redundant.
Further
photoreceptors
will
no
doubt
continue
illustrate
ever-expanding
role
for