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Biology subjects

Hille, L.

Publications and source records attributed to Hille, L..

2 recordsLinked to original sources

Resolving temporal threat uncertainty by observational learning involves the amygdala, hippocampus and anterior insula

By observing others experiences, humans learn about threats while avoiding firsthand dangers. Yet, previous neuroscience research has focused on observational threats that are predictable. In firsthand learning, temporally predictable and unpredictable threats can be mechanistically discerned. In this study, we developed a novel observational paradigm in which participants learned from predictable and unpredictable observational threats, as well as a no-threat condition. Participants encountered the same conditions during an expression phase to investigate how the brain encodes predictive and unpredictive threat cues observed in others. Participants in Experiment 1 (n = 20, 14 female, 6 male) and Experiment 2 (n = 23, 9 female, 1 non-binary, 13 male) successfully learned threat contingencies, showing heightened threat expectations for predictive cues and unpredictable condition-onsets. Behavioral findings converged with neural (fMRI, Experiment 2) responses in the anterior insula during the expression phase. Reflecting the dynamic process of learning, amygdala activation in response to predictive threat cues displayed a linear decrease across trials. Interestingly, BOLD responses to others pain that was predictable, were enhanced within the amygdala, insula and hippocampus, compared to unpredictable conditions. Our findings suggest that humans can learn to resolve temporal threat uncertainty, through the observation of others. The present work thereby contributes to understanding the social aspects of fear and anxiety disorders.

neuroscience↗

An intrinsic neuronal manifold underlies brain-wide hierarchical organization of behavior in C. elegans

Large-scale neuronal recordings in various species have revealed behavior-related activity patterns. Surprisingly, these activities are distributed across brain regions, including sensory areas. However, their origins and functions are incompletely understood. Using whole-brain imaging in freely behaving C. elegans, we discover that such distributed brain activity is dominated by a low dimensional manifold, corresponding to the major action sequence of C. elegans. The manifold originates largely from intrinsic dynamics, with minor contributions from movement-induced sensations. We discover a new function of the manifold: to gate the activity of a large number of neuron classes. This gating constrains them to selectively encode faster time-scale motor patterns during specific brain states. We therefore propose that one principle function of brain-wide dynamics is to enable hierarchical organization of behavior: information about major actions is broadcast via a distributed manifold, to enable nesting of granular motor patterns within those major actions.

neuroscience↗