Brain’s Arousal Fine-Tunes Visual Signals – Neuroscience News

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Summary: Arousal levels directly influence how the brain processes visual information. Researchers found that the firing patterns of neurons in the thalamus, a key relay station for visual signals, change in response to pupil dilation and constriction, indicators of arousal. This modulation of neural activity provides a mechanistic explanation for how our internal states shape our visual perception.

Key Facts:

  • Arousal levels influence neural activity in the visual thalamus.
  • Different firing patterns occur during phases of pupil dilation and constriction.
  • This modulation of visual signals provides insight into how our internal state shapes perception.

Source: LMU

What we see is not simply just a neural representation of the pattern of light in the eye, but an interpretation of this image, to which our needs and expectations contribute.

These factors are shaped by earlier experiences and also depend on inner states like our behavioral activity and our vigilance or attentiveness – often collectively known as “arousal.”

“Our research therefore shows that fundamental visual information is transmitted with differential encoding to ‘higher’ areas of the brain like the visual cortex in different phases of arousal,” summarizes neurobiologist Laura Busse. Credit: Neuroscience News

In a new study recently published in the journal PLoS Biology, researchers from LMU, the University of Freiburg, and the Bernstein Center for Computational Neuroscience analyzed neural activity in the visual thalamus.

This is an area of the brain that receives visual signals directly from the eye via the optic nerve before processing them and passing them on.

More specifically, they investigated the thalamic dorsal lateral geniculate nucleus (dLGN), the primary interface for visual signals from the retina to the visual cortex.

What happens in the thalamus?

“It’s long been known that the neurons of the dLGN, like the neurons in other thalamic nuclei, exhibit conspicuous patterns of activity that are related to arousal,” explains LMU Professor Laura Busse, lead investigator of the study and soon to be principal investigator in the SyNergy Cluster of Excellence.

Two state-dependent firing modes had been described in particular: burst firing, which tends to occur during states of low arousal and behavioral inactivity; and tonic firing, which is observed during states of vigilance.

“This led to the hypothesis that thalamic nuclei use burst and tonic firing modes to dynamically control or modify the information flow to and between cortical areas according to the state of arousal of the animal.”

However, this proposition has not yet been experimentally tested.

“The neural mechanisms by which arousal influences the processing of visual information remain largely unexplained.”

In the new study, Busse’s team directly compared the activity measured in the thalamus with the degree of arousal.

“Arousal is reflected in the pupil diameter of mammals, with larger pupils indicating an aroused state,” explains the neurobiologist.

In this way, we can make inferences about the state of arousal of an animal from changes in the size of their pupils. The coupled investigation of thalamic and pupil activity helped Busse’s team obtain a clear perspective on the connection between thalamic activity and degree of arousal.

Sensory impressions are modulated

“We discovered that during certain phases of pupil dilation and constriction, different patterns of neural activation occur,” says Professor Christian Leibold from the University of Freiburg and the Bernstein Center for Computational Neuroscience, one of the senior authors of the study.

“The electrical activity in the visual thalamus is coupled with the pupil dynamics over timeframes ranging from seconds to several minutes.”

This modulation of neural activity patterns during arousal was robust: It did not depend on other factors, such as what the animal saw or whether it was moving, sitting still, or moving its eyes.

“Our research therefore shows that fundamental visual information is transmitted with differential encoding to ‘higher’ areas of the brain like the visual cortex in different phases of arousal,” summarizes neurobiologist Laura Busse.

This supplies a first mechanistic explanation for how visual perception can be influenced by changes in the state of arousal.

“Our results support the hypothesis that arousal-dependent modulation is not a singular process, but probably an interplay of changes taking place over various timescales.”

About this visual neuroscience research news

Author: Constanze Drewlo
Source: LMU
Contact: Constanze Drewlo – LMU
Image: The image is credited to Neuroscience News

Original Research: Open access.
Spiking activity in the visual thalamus is coupled to pupil dynamics across temporal scales” by Laura Busse et al. PLOS Biology


Abstract

Spiking activity in the visual thalamus is coupled to pupil dynamics across temporal scales

The processing of sensory information, even at early stages, is influenced by the internal state of the animal. Internal states, such as arousal, are often characterized by relating neural activity to a single “level” of arousal, defined by a behavioral indicator such as pupil size.

In this study, we expand the understanding of arousal-related modulations in sensory systems by uncovering multiple timescales of pupil dynamics and their relationship to neural activity.

Specifically, we observed a robust coupling between spiking activity in the mouse dorsolateral geniculate nucleus (dLGN) of the thalamus and pupil dynamics across timescales spanning a few seconds to several minutes.

Throughout all these timescales, 2 distinct spiking modes—individual tonic spikes and tightly clustered bursts of spikes—preferred opposite phases of pupil dynamics.

This multi-scale coupling reveals modulations distinct from those captured by pupil size per se, locomotion, and eye movements.

Furthermore, coupling persisted even during viewing of a naturalistic movie, where it contributed to differences in the encoding of visual information.

We conclude that dLGN spiking activity is under the simultaneous influence of multiple arousal-related processes associated with pupil dynamics occurring over a broad range of timescales.

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