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1.
J Neuroophthalmol ; 2024 Jul 05.
Article in English | MEDLINE | ID: mdl-38965655

ABSTRACT

BACKGROUND: Neuro-ophthalmology frequently requires a complex and multi-faceted clinical assessment supported by sophisticated imaging techniques in order to assess disease status. The current approach to diagnosis requires substantial expertise and time. The emergence of AI has brought forth innovative solutions to streamline and enhance this diagnostic process, which is especially valuable given the shortage of neuro-ophthalmologists. Machine learning algorithms, in particular, have demonstrated significant potential in interpreting imaging data, identifying subtle patterns, and aiding clinicians in making more accurate and timely diagnosis while also supplementing nonspecialist evaluations of neuro-ophthalmic disease. EVIDENCE ACQUISITION: Electronic searches of published literature were conducted using PubMed and Google Scholar. A comprehensive search of the following terms was conducted within the Journal of Neuro-Ophthalmology: AI, artificial intelligence, machine learning, deep learning, natural language processing, computer vision, large language models, and generative AI. RESULTS: This review aims to provide a comprehensive overview of the evolving landscape of AI applications in neuro-ophthalmology. It will delve into the diverse applications of AI, optical coherence tomography (OCT), and fundus photography to the development of predictive models for disease progression. Additionally, the review will explore the integration of generative AI into neuro-ophthalmic education and clinical practice. CONCLUSIONS: We review the current state of AI in neuro-ophthalmology and its potentially transformative impact. The inclusion of AI in neuro-ophthalmic practice and research not only holds promise for improving diagnostic accuracy but also opens avenues for novel therapeutic interventions. We emphasize its potential to improve access to scarce subspecialty resources while examining the current challenges associated with the integration of AI into clinical practice and research.

2.
J Neurosci ; 34(48): 16103-16, 2014 Nov 26.
Article in English | MEDLINE | ID: mdl-25429151

ABSTRACT

Animals must distinguish behaviorally relevant patterns of sensory stimulation from those that are attributable to their own movements. In principle, this distinction could be made based on internal signals related to motor commands, known as corollary discharge (CD), sensory feedback, or some combination of both. Here we use an advantageous model system--the electrosensory lobe (ELL) of weakly electric mormyrid fish--to directly examine how CD and proprioceptive feedback signals are transformed into negative images of the predictable electrosensory consequences of the fish's motor commands and/or movements. In vivo recordings from ELL neurons and theoretical modeling suggest that negative images are formed via anti-Hebbian plasticity acting on random, nonlinear mixtures of CD and proprioception. In support of this, we find that CD and proprioception are randomly mixed in spinal mossy fibers and that properties of granule cells are consistent with a nonlinear recoding of these signals. The mechanistic account provided here may be relevant to understanding how internal models of movement consequences are implemented in other systems in which similar components (e.g., mixed sensory and motor signals and synaptic plasticity) are found.


Subject(s)
Feedback, Physiological/physiology , Movement/physiology , Proprioception/physiology , Sensory Receptor Cells/physiology , Signal Transduction/physiology , Animals , Electric Fish , Female , Forecasting , Male , Random Allocation
3.
Neuron ; 82(4): 896-907, 2014 May 21.
Article in English | MEDLINE | ID: mdl-24853945

ABSTRACT

The capacity to predict the sensory consequences of movements is critical for sensory, motor, and cognitive function. Though it is hypothesized that internal signals related to motor commands, known as corollary discharge, serve to generate such predictions, this process remains poorly understood at the neural circuit level. Here we demonstrate that neurons in the electrosensory lobe (ELL) of weakly electric mormyrid fish generate negative images of the sensory consequences of the fish's own movements based on ascending spinal corollary discharge signals. These results generalize previous findings describing mechanisms for generating negative images of the effects of the fish's specialized electric organ discharge (EOD) and suggest that a cerebellum-like circuit endowed with associative synaptic plasticity acting on corollary discharge can solve the complex and ubiquitous problem of predicting sensory consequences of movements.


Subject(s)
Cerebellum/cytology , Electric Organ/physiology , Movement/physiology , Nerve Net/physiology , Neuronal Plasticity/physiology , Neurons/physiology , Animals , Biophysics , Calbindins/metabolism , Cerebellum/physiology , Dendrites/physiology , Electric Fish , Electric Stimulation , Functional Laterality , Nerve Fibers/physiology , Neurons/cytology , Patch-Clamp Techniques
4.
Sci Am ; 305(2): 18, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21827112
5.
Curr Opin Neurobiol ; 21(4): 602-8, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21704507

ABSTRACT

This review focuses on recent progress in understanding mechanisms for filtering self-generated sensory signals in cerebellum-like circuits in fish and mammals. Recent in vitro studies in weakly electric gymnotid fish have explored the interplay among anti-Hebbian plasticity, synaptic dynamics, and feedforward inhibition in canceling self-generated electrosensory inputs. Studies of the mammalian dorsal cochlear nucleus have revealed multimodal integration and anti-Hebbian plasticity, suggesting that this circuit may adaptively filter incoming auditory information. In vivo studies in weakly electric mormryid fish suggest a key role for granule cell coding in sensory filtering. The clear links between synaptic plasticity and systems level sensory filtering in cerebellum-like circuits may provide insights into hypothesized adaptive filtering functions of the cerebellum itself.


Subject(s)
Cerebellum/cytology , Cerebellum/physiology , Nerve Net/physiology , Neurons/physiology , Sensory Gating/physiology , Animals , Electric Fish/physiology , Electric Organ/cytology , Neuronal Plasticity
7.
Sci Am ; 305(6): 21, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22214121
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