Neural Activity: All eyes on attention
You are a football player, running at full speed. The ball is at your feet, your gaze and ‘overt’ attention fixed on it. Suddenly, in the corner of your eye, a player from the opposing team appears. You do not move your eyes away from the ball, but your attention shifts to monitoring your surroundings and ensuring the opponent does not get in your way. This ‘covert’ attention allows the brain to keep track of the player without looking at them (Figure 1A).
According to the premotor theory of attention, when you were covertly monitoring the player, your brain was getting ready for (but not necessarily executing) eye movements towards that spot: this motor preparation would be both necessary and sufficient for attention to shift towards the new spatial location. In other words, spatial attention and motor preparation would share the same neural underpinnings. And indeed, the neural mechanisms and brain areas involved in the control of the fast eye movements (or saccades) needed to explore a scene are similar to those related to shifts in attention (Goldberg and Wurtz, 1972). In fact, activity in these areas is causally linked with how well individuals perform during attentional tasks (Cavanaugh and Wurtz, 2004).
Yet, recently, several studies have seriously challenged the assumptions that underlie the premotor theory of attention (see Smith and Schenk, 2012, for a review). In particular, they have demonstrated that attention can be shifted to different sites without preparing eye movements directed at those locations (Juan et al., 2004). In addition, different neural mechanisms mediate (or ‘modulate’) the changes in neural activity that are linked to covert spatial attention and the preparation for a shift in gaze (Li et al., 2021).
Still, new evidence has revived the idea that spatial attention may be intrinsically linked to eye movements. Even as you were keeping your gaze on the ball, your eyes were never stationary: they constantly moved due to tiny movements, or microsaccades, which shift the center of the gaze around the fixated location (for a review of this topic, see Rucci and Poletti, 2015).
Most likely, these microsaccades were directed towards the player coming your way – indeed, we tend to perform microsaccades towards covertly attended locations as we fixate on a different object. If these small eye movements are absent or directed away from the location which requires covert attention, neural and behavioral changes associated with attention disappear or decrease (Hafed and Clark, 2002; Lowet et al., 2018). This poses a serious problem to scientists. If generating microsaccades causes modulation of neuronal activity, the very idea of covert attention – where attention shifts without moving the eyes – may no longer be valid. Put differently, if small eye movements are causally linked to a change in attention, is there still room for the very concept of covert attention in our neuroscience handbooks?
Now, in eLife, Gongchen Yu, Richard Krauzlis and colleagues at the National Eye Institute, Bethesda and the University of Pittsburgh report cleverly designed experiments that help to address this crucial question (Yu et al., 2022). In particular, they managed to disentangle confounding factors which limited previous investigations into this topic (Meyberg et al., 2017).
The team recorded eye movement and activity in the superior colliculus (a brain area which integrates visual and motor information to initiate eye movements) in two monkeys trained to perform a covert spatial attention task (Figure 1B). The animals were required to fixate on a dot displayed on a monitor while holding a joystick. A brief visual cue was then flashed on the left or the right, automatically attracting the (covert) attention of the monkeys. Soon after, two visual stimuli appeared over the cued and un-cued location. One of these signals would then change color, and the monkeys were trained to release the joystick only if this switch took place at the cued location.
The results replicated well-known neural and behavioral attention-related effects: activity in the superior colliculus was enhanced when the visual stimulation occurred at the cued location (Figure 1C), and this increase correlated with monkeys being less likely to make mistakes during the task. Yu et al. then compared how neural activity modulation linked to attention differed when microsaccades were absent, directed towards the cued location, or away from it. Dissecting the relative contributions of microsaccades and spatial attention in this way revealed that neural modulation was present irrespective of microsaccades. In fact, it followed a very similar pattern of activity when microsaccades were absent or directed towards the cue (Figure 1C). Taken together, these findings demonstrate that microsaccades are not necessary for attention-related modulation in the superior colliculus.
The results provided by Yu et al. nicely complement previous behavioral studies which suggest that spatial attention can occur in the absence of microsaccades (Li et al., 2021; Meyberg et al., 2017; Poletti et al., 2017). Yet, outside of the lab, we rarely stare at dots on a screen the way test subjects are asked to do. In fact, in ‘real life’, microsaccades are often leveraged to precisely enhance fine spatial vision, and to explore the rich visual details which form the stimuli we hold at the center of our gaze, such as a fast-moving ball (Intoy and Rucci, 2020). Would the neural modulations associated with microsaccades reported by Yu et al. still occur in these more ecological settings? Only further research will be able to tell. In the meantime, this work makes a case for covert attention to remain in our neuroscience handbooks – for now.
References
-
Subcortical modulation of attention counters change blindnessThe Journal of Neuroscience 24:11236–11243.https://doi.org/10.1523/JNEUROSCI.3724-04.2004
-
Activity of superior colliculus in behaving monkey. II. Effect of attention on neuronal responsesJournal of Neurophysiology 35:560–574.https://doi.org/10.1152/jn.1972.35.4.560
-
Microsaccades as an overt measure of covert attention shiftsVision Research 42:2533–2545.https://doi.org/10.1016/s0042-6989(02)00263-8
-
Finely tuned eye movements enhance visual acuityNature Communications 11:795.https://doi.org/10.1038/s41467-020-14616-2
-
Different computations underlie overt presaccadic and covert spatial attentionNature Human Behaviour 5:1418–1431.https://doi.org/10.1038/s41562-021-01099-4
-
Selective attention within the foveolaNature Neuroscience 20:1413–1417.https://doi.org/10.1038/nn.4622
-
Control and functions of fixational eye movementsAnnual Review of Vision Science 1:499–518.https://doi.org/10.1146/annurev-vision-082114-035742
-
The premotor theory of attention: time to move onNeuropsychologia 50:1104–1114.https://doi.org/10.1016/j.neuropsychologia.2012.01.025
Article and author information
Author details
Publication history
Copyright
© 2022, Benedetto and Poletti
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
Metrics
-
- 1,122
- views
-
- 131
- downloads
-
- 1
- citations
Views, downloads and citations are aggregated across all versions of this paper published by eLife.
Download links
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Further reading
-
- Neuroscience
The concept that dimeric protein complexes in synapses can sequentially replace their subunits has been a cornerstone of Francis Crick’s 1984 hypothesis, explaining how long-term memories could be maintained in the face of short protein lifetimes. However, it is unknown whether the subunits of protein complexes that mediate memory are sequentially replaced in the brain and if this process is linked to protein lifetime. We address these issues by focusing on supercomplexes assembled by the abundant postsynaptic scaffolding protein PSD95, which plays a crucial role in memory. We used single-molecule detection, super-resolution microscopy and MINFLUX to probe the molecular composition of PSD95 supercomplexes in mice carrying genetically encoded HaloTags, eGFP, and mEoS2. We found a population of PSD95-containing supercomplexes comprised of two copies of PSD95, with a dominant 12.7 nm separation. Time-stamping of PSD95 subunits in vivo revealed that each PSD95 subunit was sequentially replaced over days and weeks. Comparison of brain regions showed subunit replacement was slowest in the cortex, where PSD95 protein lifetime is longest. Our findings reveal that protein supercomplexes within the postsynaptic density can be maintained by gradual replacement of individual subunits providing a mechanism for stable maintenance of their organization. Moreover, we extend Crick’s model by suggesting that synapses with slow subunit replacement of protein supercomplexes and long-protein lifetimes are specialized for long-term memory storage and that these synapses are highly enriched in superficial layers of the cortex where long-term memories are stored.
-
- Neuroscience
Motivation depends on dopamine, but might be modulated by acetylcholine which influences dopamine release in the striatum, and amplifies motivation in animal studies. A corresponding effect in humans would be important clinically, since anticholinergic drugs are frequently used in Parkinson’s disease, a condition that can also disrupt motivation. Reward and dopamine make us more ready to respond, as indexed by reaction times (RT), and move faster, sometimes termed vigour. These effects may be controlled by preparatory processes that can be tracked using electroencephalography (EEG). We measured vigour in a placebo-controlled, double-blinded study of trihexyphenidyl (THP), a muscarinic antagonist, with an incentivised eye movement task and EEG. Participants responded faster and with greater vigour when incentives were high, but THP blunted these motivational effects, suggesting that muscarinic receptors facilitate invigoration by reward. Preparatory EEG build-up (contingent negative variation [CNV]) was strengthened by high incentives and by muscarinic blockade, although THP reduced the incentive effect. The amplitude of preparatory activity predicted both vigour and RT, although over distinct scalp regions; frontal activity predicted vigour, whereas a larger, earlier, central component predicted RT. The incentivisation of RT was partly mediated by the CNV, though vigour was not. Moreover, the CNV mediated the drug’s effect on dampening incentives, suggesting that muscarinic receptors underlie the motivational influence on this preparatory activity. Taken together, these findings show that a muscarinic blocker impairs motivated action in healthy people, and that medial frontal preparatory neural activity mediates this for RT.