Bright flash response recovery of mammalian rods in vivo is rate limited by RGS9.

The temporal resolution of scotopic vision is thought to be constrained by the signaling kinetics of retinal rods, which use a highly amplified G-protein cascade to transduce absorbed photons into changes in membrane potential. Much is known about the biochemical mechanisms that determine the kinetics of rod responses ex vivo, but the rate-limiting mechanisms in vivo are unknown. Using paired flash electroretinograms with improved signal-to-noise, we have recorded the amplitude and kinetics of rod responses to a wide range of flash strengths from living mice.

The scotopic electroretinogram of the sugar glider related to histological features of its retina.

The flash electroretinogram (ERG) was used to characterize the scotopic retinal function in a marsupial. Key parameter values of the a- and b-waves of adult male sugar gliders, Petaurus breviceps breviceps, elicited with ganzfeld flashes were determined under dark- and light-adapted conditions. Using standard histological methods, the thicknesses of the major layers of the retina were assessed to provide insight into the nature of the ERG responses.

Dark light, rod saturation, and the absolute and incremental sensitivity of mouse cone vision.

Visual thresholds of mice for the detection of small, brief targets were measured with a novel behavioral methodology in the dark and in the presence of adapting lights spanning ∼8 log(10) units of intensity. To help dissect the contributions of rod and cone pathways, both wild-type mice and mice lacking rod (Gnat1(-/-)) or cone (Gnat2(cpfl3)) function were studied. Overall, the visual sensitivity of mice was found to be remarkably similar to that of the human peripheral retina.

The sensitivity and spectral identity of the cones driving the b-wave of the rat electroretinogram.

In the retina of rat, cones make up approximately 0.85% of the photoreceptor population: 93% of these cones contain a midwave-sensitive pigment, the rest expresses a short-wave-sensitive pigment (Szel & Rohlich, 1992). We used normal adult Long Evans rats to determine the spectral sensitivity of the cone-driven electroretinogram (ERG) b-wave and its absolute sensitivity at lambda(max) of the cone pigments.

Absolute and relative sensitivity of the scotopic system of rat: electroretinography and behavior.

The goal of the present study was to relate the dark and light-adapted flash sensitivity of the scotopic threshold response (STR) and rod b-wave of the electroretinogram (ERG) to behaviorally measured rod increment threshold responses. Small amplitudes of the dark-adapted STR and b-wave, the latter after application of NMDA, were found to increase in proportion to flash intensity. The value obtained for the sensitivity of the b-wave would be expected if signals from rods were summed linearly by the rod bipolar cell.

RGS9-1 is required for normal inactivation of mouse cone phototransduction.

Purpose: To test the hypothesis that Regulator of G-protein Signaling 9 (RGS9-1) is necessary for the normal inactivation of retinal cones.

Methods: Mice having the gene RGS9-1 inactivated in both alleles (RGS9-1 -/-) were tested between the ages 8-10 weeks with electroretinographic (ERG) protocols that isolate cone-driven responses. Immunohistochemistry was performed with a primary antibody against RGS9-1 (anti-RGS9-1c), with the secondary conjugated to fluorescein isothiocyanate, and with rhodamine-conjugated peanut agglutinin.

The d-wave of the rod electroretinogram of rat originates in the cone pathway.

We studied the off-response of the rat ERG evoked with long duration, mesopic stimuli during light and dark adaptation, and after intravitreal injection of aspartate and (+/-)-cis-piperidine-2,3-dicarboxylic acid (PDA). At stimulus offset, the dark-adapted ERG always showed a rapid negative deflection followed by a positive deflection after which the potential returned to baseline. When the stimulus was turned off in the presence of a background of scotopic intensity, the positive deflection consisted of two components.

Summation of rod and S cone signals at threshold in human observers.

We examined whether signals from rods and S cones can combine to produce a threshold response. Test flashes of specific wavelengths superposed on a long wavelength adapting field were used to isolate threshold responses from the two receptor systems, simultaneously and at the same retinal location. Dark adaptation experiments and spectral sensitivity determinations indicated that, in the adaptational range from about 1.

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.

A human rhodopsin mutation, Gly-90-->Asp (Gly90Asp), cosegregated with an unusual trait of congenital nightblindness in 22 at-risk members of a large autosomal dominant kindred. Although rhodopsin mutations typically are associated with retinal degeneration, Gly90Asp-affected subjects up to age 33 did not show clinical retinal changes. Absolute threshold for visual perception was elevated nearly 3 logarithmic units in 7 individuals tested (ages 11-64), indicating greatly compromised rod threshold signaling.

Push-pull model of the primate photopic electroretinogram: a role for hyperpolarizing neurons in shaping the b-wave.

Existing models of the primate photopic electroretinogram (ERG) attribute the light-adapted b-wave to activity of depolarizing bipolar cells (DBCs), mediated through a release of potassium that is monitored by Müller cells. However, possible ERG contributions from OFF-bipolar cells (HBCs) and horizontal cells (HzCs) have not been explored. We examined the contribution of these hyperpolarizing second-order retinal cells to the photopic ERG of monkey by applying glutamate analogs to suppress photoreceptor transmission selectively to HBC/HzCs vs.

Dopaminergic modulation of rod pathway signals does not affect the scotopic ERG of cat at dark-adapted threshold.

1. Two rod-driven electroretinogram (ERG) components were recorded to monitor scotopic retinal signals during experimental manipulation of dopamine and gamma-aminobutyric acid (GABA) in normal cat eyes and in eyes pretreated with 6-hydroxydopamine (6-OHDA). The scotopic threshold response (STR) was elicited near absolute threshold to monitor signals traversing the rod pathway near quantal threshold; scotopic PII, which normally begins approximately 2 log units higher, was also monitored.

The scotopic threshold response of the cat ERG is suppressed selectively by GABA and glycine.

Corneal electroretinograms (ERGs) were recorded from anesthetized cats under scotopic conditions. We examined whether the scotopic threshold response (STR) of the ERG could be functionally distinguished from scotopic PII and a-wave using intravitreal application of neuroactive agents. We found that neurotransmitters with active sites on third order neurons had several different effects.

The influence of short-term adaptation of human rods and cones on cone-mediated grating visibility.

1. The influences of short-term visual adaptation of either rods or cones upon cone-mediated grating visibility were compared with their influences upon detection threshold in both the fovea and parafoveal retina. Short-term visual adaptation was induced by 20 deg diameter adapting fields (AFs) generally of 500 ms duration.

Rod light and dark adaptation influence cone-mediated spatial acuity.

The influence of rod light and dark adaptation upon cone mediated spatial acuity was studied in the near parafoveal retina of normal human observers. The luminance just necessary to detect squarewave test gratings of variable frequency provided an index of spatial acuity. Such thresholds were determined in the presence of background fields which were varied in luminance, shape, and size, or throughout the time period of dark adaptation.

The influence of cone adaptation upon rod mediated flicker.

The influence of annular fields on sensitivity to sinusoidal flicker was assessed in the dark adapted parafoveal retina. Test stimuli were 2 degrees 20' in diameter; annuli had a 2 degrees 20' inner and 7 degrees 30' outer diameter. Rod flicker was studied with a "green" stimulus too dim to influence cones.