Abstract
The migration of the screening pigment was investigated in the retina of the intact squid. The action spectrum of pigment migration corresponds to the action spectrum of the visual pigment, rhodopsin, rather than to the absorption spectrum of the screening pigment. The total number of quanta required for a fixed criterion of pigment migration is the same, when the quanta are delivered over any period of time from 6 s to an hour or more. When less than 3–10% of the rhodopsin is isomerized, the screening pigment migrates out to the tips of the receptors with a time-course of 5–15 min, and back again over the same period of time. When rather more than 10% is isomerized, the outward migration takes 5–15 min, but the screening pigment does not migrate inwards, even after several hours in the dark. Indirect evidence suggests that the band of screening pigment, when it reaches the tips of the receptors, is approximately equivalent to a filter of 0.6 log units. The spectral sensitivity of the optic nerve response was measured, and was found to be broader than the absorption spectrum of squid rhodopsin in vitro; the broadness could be explained by self-screening, assuming a density of rhodopsin of 0.6 log units at 500 nm.
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Selected References
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- BOYCOTT B. B., LETTVIN J. Y., MATURANA H. R., WALL P. D. OCTOPUS OPTIC RESPONSES. Exp Neurol. 1965 Jul;12:247–256. doi: 10.1016/0014-4886(65)90070-1. [DOI] [PubMed] [Google Scholar]
- BYZOV A. L., ORLOV O. Iu, UTINA Ia. [Investigations on the adaptation on the eye of Cephalopoda]. Biofizika. 1962;7:318–327. [PubMed] [Google Scholar]
- Cohen A. I. An ultrastructural analysis of the photoreceptors of the squid and their synaptic connections. I. Photoreceptive and non-synaptic regions of the retina. J Comp Neurol. 1973 Feb 1;147(3):351–378. doi: 10.1002/cne.901470304. [DOI] [PubMed] [Google Scholar]
- HUBBARD R., ST GEORGE R. C. The rhodopsin system of the squid. J Gen Physiol. 1958 Jan 20;41(3):501–528. doi: 10.1085/jgp.41.3.501. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagins F. M. Purification and partial characterization of the protein component of squid rhodopsin. J Biol Chem. 1973 May 10;248(9):3298–3304. [PubMed] [Google Scholar]
- Hagins W. A. Electrical signs of information flow in photoreceptors. Cold Spring Harb Symp Quant Biol. 1965;30:403–418. doi: 10.1101/sqb.1965.030.01.040. [DOI] [PubMed] [Google Scholar]
- Hagins W. A., Penn R. D., Yoshikami S. Dark current and photocurrent in retinal rods. Biophys J. 1970 May;10(5):380–412. doi: 10.1016/S0006-3495(70)86308-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liebman P. A., Carroll S., Laties A. Spectral sensitivity of retinal screening pigment migration in the frog. Vision Res. 1969 Mar;9(3):377–384. doi: 10.1016/0042-6989(69)90084-4. [DOI] [PubMed] [Google Scholar]
- Tsukahara Y., Tasaki K. Dark recovery of ERP in isolated octopus retina. Tohoku J Exp Med. 1972 Sep;108(1):97–98. doi: 10.1620/tjem.108.97. [DOI] [PubMed] [Google Scholar]
- Wolbarsht M. L., Macnichol E. F., Jr, Wagner H. G. Glass Insulated Platinum Microelectrode. Science. 1960 Nov 4;132(3436):1309–1310. doi: 10.1126/science.132.3436.1309. [DOI] [PubMed] [Google Scholar]
