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    • Oxytocin in the amygdala links social and reward signals to cataplexy in mice

      Loss of orexin neurons in narcolepsy leads to sleepiness and cataplexy episodes, which are most common in social contexts. In a mouse model, an oxytocin-sensitive circuit in the central amygdala is both necessary and sufficient for cataplexy induced by socialization and reward, which links positive emotional signals to motor suppression and highlights a potential therapeutic target.

      Research Briefing
    • Neural timescales from a computational perspective

      This review integrates computational approaches to provide a unified view on how data analysis methods, biophysical mechanistic models and machine learning approaches can help to uncover the origins and functions of neural timescales.

      • Roxana Zeraati
      • Anna Levina
      • Richard Gao
      Review Article
    • Just how goal-directed are hippocampal theta sweeps, anyway?

      Planning is a cognitive process that is thought to be grounded in hippocampal sequences, but recent studies have suggested that a simpler mechanism, fundamentally incompatible with those planning hypotheses, underlies these sequences. Two studies in this issue of Nature Neuroscience provide the first steps to resolving that controversy.

      • Brandy Schmidt
      • Celia M. Gagliardi
      • A. David Redish
      News & Views
    • Mitochondrial stress response drives microglial senescence

      The mitochondrial unfolded protein response (UPRmt) drives microglial senescence and disrupts essential glia–neuron communication. By triggering lipid droplet accumulation and dysregulating the S-adenosylmethionine–polyamine axis, UPRmt fuels the senescence-associated secretory pathway, impairs synaptic pruning and accelerates misfolded protein pathology. In this issue of Nature Neuroscience, Perez et al. identify UPRmt as a primary driver of metabolic vulnerability in human microglia.

      • Luca Peruzzotti-Jametti
      • Stefano Pluchino
      News & Views
    • DBS: from neuromodulation to neuroremodelling

      Deep-brain stimulation (DBS) treats movement and neuropsychiatric disorders through mechanisms that remain unclear. Two studies that combine longitudinal neuroimaging, stimulation experiments and tissue-level analysis show that the effects of DBS evolve in space and time, demonstrating acute effects on network activity as well as providing insights into chronic effects that reshape the networks it engages.

      • Valentina Lind
      • Ludvic Zrinzo
      • Harith Akram
      News & Views

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