PURPOSE. The purpose of this study is to determine the topography of bleaching in rods, middle/long-wavelength (M/ L) and short-wavelength (S) cones in the macaque retina by using a modified retinal densitometry technique.
METHODS.A modified commercial digital fundus camera system was used to measure continuously the intensity of the light reflectance during bleaching with band pass lights in the ocular fundus of three adult Rhesus monkeys (Macaca mulatta) under general anesthesia. The topography of bleaching in rods, M/L-, and S-cones was obtained separately by considering the characteristic time course of the reflectance changes, depending on the wavelengths of light and retinal locations.
RESULTS.The distribution of M/L-cones response had a steep peak at the foveal center and was elongated horizontally. The distribution of rod responses was minimum at the foveal center and maximum along a circular region at the eccentricity of the optic disc. The distribution of S-cone responses was highest at the fovea and was excavated centrally. There was a circular region with the maximal responses at 0.38 to 1.0 degrees from the foveal center. T he human visual system is a duplex system, consisting of a rod system for scotopic conditions and a cone system for photopic conditions. Three types of cones mediate color vision; long (L), middle (M), and short (S) wavelength-sensitive cones. The distribution of the photoreceptors has been well investigated on postmortem eyes of humans and macaques. [1][2][3][4][5][6][7][8][9] These studies reported the anatomical densities of the different types of photoreceptors, but the results did not necessarily reflect their functional properties. Psychophysical experiments also have been used to assess photoreceptor function. [10][11][12][13][14][15] However, the results reflect not only the retinal function, but the visual function from the photoreceptors to the visual cortex.Approximately 50 years ago, the time course of the bleaching of photopigments was determined quantitatively by measuring the reflectance changes during bleaching and regeneration of the visual pigments in human retinas. [16][17][18][19][20][21][22] This method, retinal densitometry, was used to determine the in vivo kinetics of the photopigments of cones and rods quite accurately. The spatial distribution of the reflectance changes was determined later by examining images obtained by either a fundus camera or a scanning laser ophthalmoscope (SLO), that is, imaging fundus reflectometry. [23][24][25][26][27][28][29][30][31][32][33] With these techniques, the distribution of photoreceptors was mapped objectively and non-invasively as bleach-derived light reflectance changes in normal and diseased eyes. However, the responses of the different types of photoreceptors, especially rods and S-cones, could not be segregated accurately because the response time courses were not monitored accurately.We developed a new retinal densitometry system that can measure the retinal reflectance changes continuously after bleaching with...