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Purpose: Behavioral and electrophysiological studies have shown that vision is slower under scotopic conditions (dark, activating only rods) than photopic conditions (light, activating only cones). However, slower scotopic processing cannot be solely explained by findings that rod signals are slower than cone signals, and it is unknown whether temporal processing differences persist in cortex. Flickering stimuli have previously been used in functional MRI (fMRI) studies to probe photopic cortical temporal sensitivity. This fMRI study investigates flicker sensitivity under photopic and scotopic conditions across the cortical visual hierarchy.
Methods: Fourteen participants viewed a stimulus flickering at six frequencies (2-10 Hz) under photopic and scotopic conditions during fMRI scanning. Retinotopic and high-level visual areas were delineated for each subject with population receptive field modeling (using a drifting bar) and a functional localizer (using images of objects).
Results: In most areas, higher mean activation was observed under photopic than under scotopic conditions. However, peak activation was higher only in V1 and ventral retinotopic areas. The pattern of change over frequencies differed between lighting conditions in retinotopic areas, but not in most high-level areas. Under scotopic conditions, the largest BOLD response was observed at low frequencies throughout visual cortex. Under photopic conditions, BOLD responses appeared largely unchanging across frequencies, with a trend towards preferring higher frequencies in V1.
Conclusions: Selectivity for lower frequencies under scotopic conditions was observed throughout visual cortex, in contrast to limited selectivity under photopic conditions. This low-frequency preference could allow more time for extracting information from sparse scotopic stimuli.
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http://dx.doi.org/10.1167/iovs.66.12.12 | DOI Listing |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12416517 | PMC |
Invest Ophthalmol Vis Sci
September 2025
Department of Ophthalmology, Edward S. Harkness Eye Institute, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, Columbia University, New York, New York, United States.
Purpose: To characterize a no b-wave (nob) mouse model of congenital stationary night blindness (CSNB) caused by a Grm6 variant that disrupts photoreceptor-to-bipolar cell signaling. Additionally, we aim to evaluate the efficacy of gene therapy in restoring visual function.
Methods: The nob mouse was generated through selective breeding to regenerate the nob phenotype.
Invest Ophthalmol Vis Sci
September 2025
fMRI unit, Department of Neurology, Hadassah Medical Organization and Faculty of Medicine, The Hebrew University of Jerusalem, Ein Karem, Jerusalem, Israel.
Purpose: Behavioral and electrophysiological studies have shown that vision is slower under scotopic conditions (dark, activating only rods) than photopic conditions (light, activating only cones). However, slower scotopic processing cannot be solely explained by findings that rod signals are slower than cone signals, and it is unknown whether temporal processing differences persist in cortex. Flickering stimuli have previously been used in functional MRI (fMRI) studies to probe photopic cortical temporal sensitivity.
View Article and Find Full Text PDFAm J Ophthalmol
August 2025
Department of Ophthalmology and Visual Sciences, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL; Department of Ophthalmology, University Hospital Bonn, Bonn, Germany.
Purpose: To investigate the presence of hypertransmission (HT) in normal aging, early (e)AMD, and intermediate (i)AMD, changes over 3 years, and the impact of HTs ≥ 250 µm (LHyperTD) on seven tests of scotopic, mesopic, and photopic vision.
Design: Prospective cohort study.
Subjects: Participants of the Alabama Study on Early Age-Related Macular Degeneration 2.
Diabetologia
August 2025
Wellcome-Wolfson Institute for Experimental Medicine, Queen's University, Belfast, UK.
Aims/hypothesis: Diabetic retinal disease (DRD) is characterised by progressive neurovascular unit (NVU) dysfunction, often occurring before visible microvascular damage. Our previous studies suggested that the accumulation of acrolein (ACR)-derived protein adducts on retinal Müller cells and neuronal proteins may contribute to NVU dysfunction in diabetes, although this has yet to be directly tested. In this study, we evaluated the effects of the novel ACR-scavenging drug 2-hydrazino-4,6-dimethylpyrimidine (2-HDP) on retinal NVU dysfunction in experimental diabetes and explored its potential for systemic delivery in humans.
View Article and Find Full Text PDFJ Biol Chem
August 2025
Department of Ophthalmology, Duke University School of Medicine, Durham, North Carolina, USA. Electronic address:
Mutations in the mitochondrial respiratory complex I accessory subunit NADH:ubiquinone oxidoreductase subunit S4 (ndufs4) can cause the mitochondrial disease Leigh syndrome, which may be associated with vision loss. We previously demonstrated that mice with global deletion of ndufs4 exhibited impaired in vivo photoreceptor light responses prior to the early death of the mice around postnatal day 50. However, ex vivo electrophysiology recordings performed on retinas from ndufs4 mice were normal, suggesting that the in vivo phenotype may reflect altered homeostasis of the extracellular environment of photoreceptors rather than their intrinsic metabolic dysfunction.
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