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Hofstetter, C.

Publications and source records attributed to Hofstetter, C..

3 recordsLinked to original sources

Emotional modulation of visual cortical reactivation during true and false memories

Previous research revealed that memory retrieval is associated with a reactivation of sensory cortices reflecting the content of the memory. Further, such reactivation is stronger when retrieval is cued with emotional information as compared with neutral information. However, past studies focused on correct retrieval, and it remains unknown whether a similar reactivation occurs during memory errors, and whether this is enhanced in emotional contexts. Here, we hypothesized that emotion may influence memory errors due to an increase of sensory cortical reactivation at the cost of recovering episodic details (i.e. leading to incorrect retrieval of non-specific associations shared with other cues). We compared brain activations during successful memory retrieval and memory errors in 18 healthy participants who encoded unique negative or neutral scenes paired with one of four associated faces, shared with other trials. Participants were tested the next day with a scene-cued associative retrieval test, while undergoing functional magnetic resonance imaging (fMRI). Results from a face-responsive region of interest in fusiform cortex (unlike a control place-responsive region in parahippocampal cortex) showed stronger activation for both Hits ("Old" | Target) and False Alarms ("Old" | Foil), as compared with Misses ("New" | Target) and Correct Rejections ("New" | Foil). The emotional content of scene cues did not modulate activation patterns during correct retrieval but produced specific effects on Misattribution errors (incorrect "Old" | Target, i.e., retrieval of an incorrect face cued by a previously seen scene). Specifically, Misattributions were accompanied by increased fusiform activation comparable to Hits when cued by negative scenes, but low fusiform activation similar to Misses when cued by neutral scenes. Unlike Misattributions, however, Hits cued by emotional information recruited a distinctive network previously linked to personal episodic memories, including medial prefrontal, cingulate, and hippocampal regions, together with enhanced functional coupling between the latter and fusiform cortex. No implicit effect of previous face exposure was observed in the fusiform during Misses, regardless of emotion context. Our results suggest that the reactivation of sensory areas follows subjective memory experience during retrieval, and that emotion can enhance such mechanism when the cue is recognized but detailed episodic memory mediated by fronto-hippocampal circuits is absent, leading to the retrieval of inappropriate associations and false memories.

neuroscience↗

A Reference Atlas of the Human Dorsal Root Ganglion

Somatosensory perception largely emerges from diverse peripheral sensory neurons whose cell bodies reside in dorsal root ganglia (DRG). Damage or dysfunction of DRG neurons is a major cause of chronic pain and sensory loss. In mice, deep single-cell transcriptomic profiling and genetically defined models have offered important clues into DRG function, but in humans, the cellular and molecular landscape of DRG neurons remains less understood. Here, we constructed a reference cell atlas of the human DRG by profiling transcriptomes of cells and nuclei from 126 donors sampled across cervical, thoracic, and lumbar DRGs. This atlas resolves 22 neuronal subtypes, including known and previously unrecognized subtypes linked to nociception, mechanosensation, thermosensation, and proprioception, as well as 10 types of non-neuronal cells. Cross-species integration, spatial transcriptomics, and microneurography enabled cell-type-specific comparisons of soma size and conduction velocity between species. Human DRG somata are larger across all cell types than their mouse counterparts, and the conduction velocities of human hair follicle innervating A-fibers are faster than in mice, suggesting a functional shift in rapid mechanical detection in humans. This integrated human DRG reference cell atlas provides a resource for exploring new molecular and physiological features of human DRG, which could help identify new strategies for treating chronic pain and other diseases of the peripheral nervous system.

neuroscience↗

Healthcare experience disrupts representational similarity between one's and others' pain in anterior insula

Medical students and professional healthcare providers often underestimate patients pain, together with decreased neural responses to pain information in the anterior insula (AI), a brain region implicated in self-pain processing and negative affect. However, the functional significance and specificity of these neural changes remains debated. Across two experiments, we recruited university medical students and emergency nurses to test the role of healthcare experience on the brain reactivity to others pain, emotions, and beliefs, using both pictorial and verbal cues. Brain responses to self-pain was also assessed and compared with those to observed pain. Our results confirmed that healthcare experience decreased the activity in AI in response to others suffering. This effect was independent from stimulus modality (pictures or texts), but specific for pain, as it did not generalize to inferences about other mental or affective states. Furthermore, representational similarity and multivariate pattern analysis revealed that healthcare experience impacted specifically a component of the neural representation of others pain that is shared with that of first-hand nociception, and related more to AI than to other pain-responsive regions. Taken together, our study suggests a decreased propensity to appraise others suffering as ones own, associated with a reduced recruitment of pain-specific information in AI. These findings provide new insights into neural mechanisms leading to pain underestimation by caregivers in clinical settings.

neuroscience↗