Leading edge of the a-wave of the electroretinogram and sodium iodate-induced age-related macular degeneration: A model.

Autor: Pattanaik DK; Siksha 'O' Anusandhan University, Bhubaneswar, OR, 751030, India. Electronic address: pattanaikdeepak85@gmail.com., Lakshminarayanan V; School of Optometry and Vision Science and Departments of Physics, Electrical and Computer Engineering and System Design Engineering, University of Waterloo, Waterloo, Canada. Electronic address: Vengu@uwaterloo.ca., Sharma NK; Siksha 'O' Anusandhan University, Bhubaneswar, OR, 751030, India. Electronic address: nachiketasharma@soa.ac.in., Sahu AP; Centurion University of Technology and Management, Bhubaneswar, OR, India. Electronic address: amirprasadsahoo@gmail.com.
Jazyk: angličtina
Zdroj: Journal of theoretical biology [J Theor Biol] 2024 Sep 07; Vol. 592, pp. 111879. Date of Electronic Publication: 2024 Jun 21.
DOI: 10.1016/j.jtbi.2024.111879
Abstrakt: Background: Iron-induced oxidative stress was thought to be the reason why the a-wave amplitude of the electroretinogram (ERG) dropped when iron ions were present. It is assumed that reactive oxygen species (ROS) are generated in the presence of iron ions, and this leads to a decrease in hyperpolarization of the photoreceptor. It is known that in age-related macular degeneration (AMD), sodium iodate can induce oxidative stress, apoptosis, and retinal damage, which mimic the effects of clinical AMD. Here, the reduction of the a-wave amplitude in mice with sodium iodate-induced age-related macular degeneration is explained.
Methods: The leading edge of the a-wave is divided into voltages developed by cones and rods. The same oxidative stress model is applied here since sodium iodate causes the creation of ROS in a manner similar to that caused by iron ions, with the exception that the retina is treated as a circuit of various resistances when computing the photoresponse. Moreover, sodium iodate also leads to apoptosis and, hence, may cause misalignment in cones (not in rods) during the initial stage of apoptosis in AMD. To include the effects of apoptosis and shortening in cones and rods, we have used a factor representing the fraction of total cones and rods that are alive. To include the effect of misalignment of cones on the reduction of the a-wave amplitude, we have used the Stiles-Crawford function to calculate the number of photoisomerizations occurring in a photoreceptor misaligned at an angle θ. The results are compared with experimental data.
Results: In sodium iodate-treated eyes, the ROS produced can attract calcium ions in the photoreceptor, which increases the calcium influx. In the case of the cones, the inclusion of the misalignment angle in the phototransduction process helps in determining the voltage and slope of the voltage vs. time graph.The smaller the fraction of active photoreceptors, the smaller the amplitude of the a-wave. The calcium influx, misaligned photoreceptors, and total photoreceptor loss all cause the amplitude of the a-wave to decrease, and at any time from the beginning of phototransduction cascade, the calcium influx causes the slope of the a-wave to increase.
Conclusion: The reduction in the a-wave amplitude in the eyes of sodium iodate-treated mice is attributed to oxidative stress in both cones and rods and cone misalignment, which ultimately lead to apoptosis and vision loss in AMD.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2024 Elsevier Ltd. All rights reserved.)
Databáze: MEDLINE
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