Award details

Non-canonical binocular pathways in human vision

Reference	BB/V007580/1
Principal Investigator / Supervisor	Dr Daniel Baker
Co-Investigators / Co-Supervisors	Professor Alex Wade
Institution	University of York
Department	Psychology
Funding type	Research
Value (£)	595,896
Status	Current
Type	Research Grant
Start date	01/09/2021
End date	31/08/2024
Duration	36 months

Abstract

Binocular combination occurs in primary visual cortex (V1), and results in a cyclopean percept of the external world. But the brain also combines information across the eyes in other anatomically distinct pathways that bypass the canonical V1 route, and which govern other functions including pupil diameter, and responses to rapid motion. Although the anatomical connections are known, the functional properties of these non-canonical binocular pathways have not been well established. This project will use an interdisciplinary, multimodal approach to investigate the computational algorithms involved non-canonical binocular signal combination. We will use fMRI and MEG to compare monocular and binocular responses across the whole brain. In V1, gain control processes balance excitation and inhibition, and binocular and monocular responses are equal. But in the non-canonical pathways, we anticipate much greater binocular responses, in some areas more than twice the monocular response. Next we will use a combination of pupillometry and steady-state EEG to measure the functional properties of the subcortical pathway that governs pupil diameter, and compare this to cortical responses. By targeting specific photoreceptor classes (e.g. melatonin, S-cones) we can investigate binocular interactions within and between pathways. We will also explore the contributions of different chromatic pathways to reflexive eye movements, because there is a direct (koniocellular) pathway that projects directly to MT and is not constrained by the combination rules of V1. Finally, we will test individuals with amblyopia on a subset of experimental paradigms to determine if binocular combination remains intact in non-canonical binocular pathways; this may be key to developing effective treatments for this condition. All experiments will be informed by the use of contemporary computational models of binocular vision, which provide a single point of comparison across distinct anatomical pathways.

Summary

The human brain combines information from many sources, including across our two forward-facing eyes with overlapping visual fields. This results in a single image of the external world, and provides us with stereo (3D) vision. But the brain also combines information across the eyes for several other reasons. One example is the response of our pupils to changes in light levels - the brain must use light levels from both eyes to decide how much to dilate or constrict the pupils. This happens in a completely different network of brain regions to those involved in perception. Separately, studies in animals have found a direct pathway to motion-sensitive regions of the brain, that may govern automatic eye movements to fast moving objects. Although we know about the anatomy of these other binocular pathways, we understand much less about precisely what they are doing. This project aims to understand the computations involved, and to compare them to those in the perceptual pathway, which are better understood, and for which mathematical models already exist. To achieve this, we will perform experiments in human volunteers. Our first study will focus on the pathway that governs pupil diameter. We can measure how the pupils constrict and dilate in response to flickering lights by using an eye-tracker. These responses can be compared to the responses of the perceptual parts of the brain, which we measure at the same time using EEG (a technique that records electrical brain activity at the scalp). Our visual system involves multiple 'colour channels', that are fed by cells in the eye that respond to different wavelengths of light. Some of these appear to be more important than others for deciding the pupil response, so we will compare the characteristics of binocular combination across the different channels. We will also look at whether the channels interact across the eyes, e.g. if we show light of different wavelengths to the left and right eyes, how does activity in thedifferent colour channels interact? Next, we will investigate the operation of the pathway that governs automatic eye movements to moving objects. The anatomical pathways involved may be directly activated by specific wavelengths of light (blue coloured light, that activates the S-cone pathway). By measuring eye movements in response to fast moving stimuli presented to one or both eyes, targeted towards a particular colour pathway, we can directly assess the contribution of different channels in this calculation. We will also measure brain activity directly, again using EEG, to help us understand the timecourse of the neural operations that govern binocular eye movement planning. We will also repeat some of the above experiments in patients with amblyopia, a disorder of binocular vision in which one eye contributes much less to vision than the other. Although we know much about the consequences of amblyopia for perception, it may be that other binocular pathways remain unaffected. Understanding this will aid the development of treatments for this condition in the future. A final study will use state-of-the art brain scanners (MRI and MEG) to measure the response of the brain to images shown to either one or two eyes, using a 3D projector. In the perceptual regions of the brain, the increased response when both eyes are open is balanced by a process of suppression between the eyes. This means that the brain activity is about the same whether one or both eyes see the stimulus, consistent with our everyday observation that the world does not change in appearance when two eyes are open compared to one. But we suspect that in the other binocular pathways, there might be a much bigger increase when both eyes are stimulated. So, we will look for brain regions that give a larger response to binocular stimulation than to monocular stimulation. We will do this for a range of different stimuli that are designed to target specific pathways (e.g. the motion pathway).

Committee	Research Committee A (Animal disease, health and welfare)
Research Topics	Neuroscience and Behaviour, Systems Biology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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