Dark-adaptation processes in the rhodopsin rods of the frog's retina

1967 ◽  
Vol 7 (1-2) ◽  
pp. 17-41 ◽  
Author(s):  
K.O. Donner ◽  
Tom Reuter
1972 ◽  
Vol 56 (1) ◽  
pp. 119-128
Author(s):  
U. YINON

The electroretinogram pattern in the compound eye of T. molitor and the appearance of irregular small potentials and spikes superimposed on the ERG are influenced during dark and light adaptation procedures. The amplitude of the principal negative potential reflects bleaching and recovery of the photochemical process. This is not true for the latency values. The delay of the electrical response increases in the dark and decreases in the light adapted eye. These changes were influenced by the intensity of the adapting light. Mutant eyes only lack screening pigment and have normal visual neural pathways. The absence of this pigment lowered the threshold sensitivity of the unscreened eye in dark adaptation. The difference between the adaptation processes in mutants and normal animals has been suggested as a criterion for measuring the net effect of the screening pigment in the compound eye.


1972 ◽  
Author(s):  
David J. Florip ◽  
Robert W. Bayer
Keyword(s):  

1966 ◽  
Author(s):  
Gosta Ekman ◽  
Jan Hosman ◽  
Ulf Berglund
Keyword(s):  

1989 ◽  
Author(s):  
Shihong Gao ◽  
Jialong Wu ◽  
Dongxian Hao ◽  
Changming Kang

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bethany E. Higgins ◽  
Giovanni Montesano ◽  
Alison M. Binns ◽  
David P. Crabb

AbstractIn age-related macular degeneration (AMD) research, dark adaptation has been found to be a promising functional measurement. In more severe cases of AMD, dark adaptation cannot always be recorded within a maximum allowed time for the test (~ 20–30 min). These data are recorded either as censored data-points (data capped at the maximum test time) or as an estimated recovery time based on the trend observed from the data recorded within the maximum recording time. Therefore, dark adaptation data can have unusual attributes that may not be handled by standard statistical techniques. Here we show time-to-event analysis is a more powerful method for analysis of rod-intercept time data in measuring dark adaptation. For example, at 80% power (at α = 0.05) sample sizes were estimated to be 20 and 61 with uncapped (uncensored) and capped (censored) data using a standard t-test; these values improved to 12 and 38 when using the proposed time-to-event analysis. Our method can accommodate both skewed data and censored data points and offers the advantage of significantly reducing sample sizes when planning studies where this functional test is an outcome measure. The latter is important because designing trials and studies more efficiently equates to newer treatments likely being examined more efficiently.


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