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Havenith, M.

Publications and source records attributed to Havenith, M..

2 recordsLinked to original sources

Eyes on the prize: Mice deploy task-driven saccades during naturalistic foraging

Active sensing allows organisms to shape incoming sensory information through self-generated actions, and saccadic eye movements provide a key readout of this process in vision. In primates, saccades are strongly modulated by cognitive variables such as uncertainty, value, and behavioural goals, particularly in complex, naturalistic settings. In rodents, by contrast, saccades have largely been interpreted as reflexive or compensatory, and evidence that they are modulated by cognitive state, such as trial outcome, expectation, or task demands, has remained sparse. Here, we examined how mice use saccades during a vision-dependent foraging task in a traversable immersive virtual environment with naturalistic stimuli. We correlated their saccade dynamics with behavioural strategies observed within the virtual environment. Target-directed saccades emerged specifically when informative sensory evidence was available, but also occurred anticipatorily when animals could rely on previously learned spatial contingencies, indicating that saccades were guided not only by immediate visual input but also by internal representations. Strikingly, the temporal structure of inter-saccade intervals resembled signatures previously reported in primates and lengthened with increased processing demand following changes in task contingencies. Together, these findings show that mouse saccades are not merely reflexive gaze corrections, but form part of a cognitively modulated active sampling strategy. More broadly, they suggest that key principles of active visual sensing may be conserved across species and establish mouse oculomotor behaviour as a tractable readout of internal cognitive state.

neuroscience↗

Central infusion of prostaglandin E2 reveals a unified representation of sickness in the mouse insular cortex

During infections, vertebrates develop stereotypic symptoms such as elevated body temperature, reduced appetite, and lethargy. These changes, collectively known as sickness syndrome, are orchestrated by the brain in response to immune mediators released during systemic inflammation. While the roles of subcortical regions, including the hypothalamus and brainstem nuclei, in regulating sickness symptoms are well established, the contribution of the neocortex to the encoding and modulation of the sick state remains less well understood. We examined the neuronal correlates of sickness in the neocortex of awake mice following a single intracerebroventricular (i.c.v.) injection of prostaglandin E2 (PGE2), a well-characterized mediator of sickness. Behavioral analysis revealed that PGE2 elicited a rapid and robust sickness response, characterized by fever, slower locomotion, quiescence, anorexia, and eye squinting. Whole-brain Fos mapping showed that PGE2 generates a distinct neural activation pattern encompassing much of the interoceptive network. Electrophysiological recordings using Neuropixel probes in awake mice together with dimensionality reduction and decoding analysis revealed that neuronal population dynamics in the insular cortex (IC) and the primary somatosensory cortex (SSp), two regions involved in body state representation, encode sickness-related information, such as body temperature, walking velocity, grooming, and eye squinting. However, unlike SSp, ongoing neuronal activity in IC exhibited a better decoding performance for an integrated measure of sickness rather than individual symptoms. Together, these results suggest that PGE2 induces a coordinated physiological and behavioral response akin to a sick state, which is preferentially encoded in the IC.

neuroscience↗