Responses from two types of orientation-selective units of retinal origin were recorded extracellularly from their axon terminals in the medial sublaminae of tectal retinorecipient layer of immobilized cyprinid fish Carassius gibelio. Excitatory and inhibitory interactions in the receptive field were analyzed with two narrow stripes of optimal orientation flashing synchronously, one in the center and the other in different parts of the periphery. The general pattern of results was that the influence of the remote peripheral stripe was inhibitory, irrespective of the polarity of each stripe (light or dark). In this regard, the orientation-selective ganglion cells of the fish retina differ from the classical orientation-selective complex cells of the mammalian cortex, where the remote paired stripes of the opposite polarity (one light and one dark) interact in a facilitatory fashion. The consequence of these differences may be a weaker lateral inhibition in the latter case in response to stimulation by periodic gratings, which may contribute to a better spatial frequency tuning in the visual cortex.
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http://dx.doi.org/10.1142/S0219635212500124 | DOI Listing |
PLoS One
January 2025
Department of Ophthalmology, Keck School of Medicine, USC Roski Eye Institute, University of Southern California, Los Angeles, California, United States of America.
Failure of central nervous system (CNS) axons to regenerate after injury results in permanent disability. Several molecular neuro-protective and neuro-regenerative strategies have been proposed as potential treatments but do not provide the directional cues needed to direct target-specific axon regeneration. Here, we demonstrate that applying an external guidance cue in the form of electric field stimulation to adult rats after optic nerve crush injury was effective at directing long-distance, target-specific retinal ganglion cell (RGC) axon regeneration to native targets in the diencephalon.
View Article and Find Full Text PDFDrug Deliv Transl Res
January 2025
School of Pharmacy, Medical Biology Centre, Queen's University Belfast, Belfast, UK.
Glaucoma is an optic neuropathy in which progressive degeneration of retinal ganglion cells and the optic nerve leads to irreversible visual loss. Glaucoma is one of the leading causes of blindness. The pathogenesis of glaucoma is determined by different pathogenetic mechanisms, including increased intraocular pressure, mechanical stress, excitotoxicity, resistance to aqueous drainage and oxidative stress.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Background: The early detection of preclinical dementia is crucial, prompting investigations into retinal biomarkers using optical coherence tomography (OCT). Inconsistent and limited longitudinal studies have been done to clarify the association between the retinal nerve fiber layer (RNFL) and ganglion cell-inner plexiform layer (GC-IPL) thickness and cognitive function over time. This study aims to explore the association between retinal biomarkers and cognitive function over time in non-demented older adults.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
University of California, Los Angeles, Los Angeles, CA, USA.
Background: Alzheimer's Disease and other neurodegenerative diseases are characterized by abnormal tau protein accumulation in the brain. PET imaging utilizing the [F-18]flortaucipir tracer is a widely used method for visualizing such conditions, yet its effectiveness can be compromised by off-target binding. To shed light on this issue, our study focuses on how elevated cholesterol concentrations of low-density lipoproteins (LDL) and standard uptake values (SUVR) from corresponding tau-PET scans may influence the efficacy of [F-18]flortaucipir.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
University of California, Riverside, Riverside, CA, USA.
Background: Alzheimer's Disease (AD) is characterized by the accumulation of beta-amyloid plaques and tau protein tangles and neurodegeneration, with growing interest in the role of neuroinflammation. The neuroinflammatory response to an insult is modulated by microglia, which transition from a resting state marked by ramified, branching processes to an activated stated in which they proliferate, migrate, and swell (processes shorten, somas enlarge). Animal studies have shown that diffusion-weighted magnetic resonance imaging (MRI) is sensitive to these morphological differences in microglia, with higher diffusion in brain regions experiencing inflammation.
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