C E Riva1, B Falsini, E Logean. 1. Institut de Recherche en Ophtalmologie, 64 Av. Grand Champsec, 1950 Sion, Switzerland. charles.riva@iro.vsnet.ch
Abstract
PURPOSE: To determine the response of human optic nerve head blood flow (R:F(onh)) to heterochromatic equiluminant flicker modulation and compare it to the response induced by pure luminance flicker. METHODS: In five normal volunteers, F(onh) measured at the neuroretinal rim was monitored continuously by laser Doppler flowmetry. Stimuli were generated by green and red light emitting diodes and delivered to the fundus in Maxwellian view (field of 25(o)). Both green (G:) and red (R:) illuminances were square-wave modulated, 180(o) out of phase, with a maximum value of 10.4 for G: and 2.64 lux for R: Flicker frequency was varied from 2 Hz to 40 Hz. R:F(onh) was defined as the change in F(onh) during stimulation relative to the prestimulus F(onh). RESULTS: Defining the color ratio r as R:/(R: + G:), the R:F(onh), measured for a 15-Hz flicker, was largest at pure luminance (r = 0 and 1), declined at mixed luminance and chromatic modulations, and reached a secondary maximum at r = 0.45, the value of psychophysical equiluminance. R:F(onh) versus flicker frequency displayed the characteristics of a low-pass function for the equiluminance flicker stimulus and of a band-pass function, with a maximum at intermediate frequencies, for the luminance flicker stimulus. CONCLUSIONS: R:F(onh) in humans can be evoked by heterochromatic flicker, modulated either in luminance or chromatic equiluminant conditions. R:F(onh) may be specific for luminance and chromatic modulations, similar to neural responses dominated by the magno- and parvocellular activity, respectively. These findings offer a new approach to study the neurovascular coupling at the optic nerve head in both physiological and diseased conditions involving predominantly or selectively the magno- and parvocellular pathways.
PURPOSE: To determine the response of human optic nerve head blood flow (R:F(onh)) to heterochromatic equiluminant flicker modulation and compare it to the response induced by pure luminance flicker. METHODS: In five normal volunteers, F(onh) measured at the neuroretinal rim was monitored continuously by laser Doppler flowmetry. Stimuli were generated by green and red light emitting diodes and delivered to the fundus in Maxwellian view (field of 25(o)). Both green (G:) and red (R:) illuminances were square-wave modulated, 180(o) out of phase, with a maximum value of 10.4 for G: and 2.64 lux for R: Flicker frequency was varied from 2 Hz to 40 Hz. R:F(onh) was defined as the change in F(onh) during stimulation relative to the prestimulus F(onh). RESULTS: Defining the color ratio r as R:/(R: + G:), the R:F(onh), measured for a 15-Hz flicker, was largest at pure luminance (r = 0 and 1), declined at mixed luminance and chromatic modulations, and reached a secondary maximum at r = 0.45, the value of psychophysical equiluminance. R:F(onh) versus flicker frequency displayed the characteristics of a low-pass function for the equiluminance flicker stimulus and of a band-pass function, with a maximum at intermediate frequencies, for the luminance flicker stimulus. CONCLUSIONS: R:F(onh) in humans can be evoked by heterochromatic flicker, modulated either in luminance or chromatic equiluminant conditions. R:F(onh) may be specific for luminance and chromatic modulations, similar to neural responses dominated by the magno- and parvocellular activity, respectively. These findings offer a new approach to study the neurovascular coupling at the optic nerve head in both physiological and diseased conditions involving predominantly or selectively the magno- and parvocellular pathways.
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