Locus coeruleus noradrenaline elicits response profiles distinct from natural arousal in hippocampal neurons and astrocytes

Abstract

The locus coeruleus (LC)-noradrenaline (NA) system is a central component of the brains response to arousal and stress. Yet how LC activity contributes to the cellular response profiles observed during natural arousal remains unclear. Here, we directly compared natural arousal with selective LC activation in mouse CA1, using physiologically titrated optogenetics, fiber photometry of NA and calcium signals, chronic two-photon imaging, and behavioral monitoring. While natural arousal robustly activated astrocytes, pyramidal cells, and interneurons, direct LC stimulation revealed a striking divergence in cellular response polarity and sensitivity. At levels of LC activation that correspond to arousal and moderate stress, we observed strong and reliable calcium responses in astrocytes, whereas pyramidal neurons and interneurons remained largely unaffected. Only at high-intensity LC stimulation did neurons exhibit a response, characterized by broad population-level inhibition of both pyramidal cells and interneurons, alongside the transient activation of an interneuron subpopulation that occupied distinct laminar positions in CA1. Thus, LC-driven NA release produces cell-specific effects in hippocampal CA1 that are distinct from and, at the population level for neurons even opposite to, cellular dynamics during natural arousal. Together, our results reveal a divergence in how astrocytes and neurons respond to LC-driven NA release and suggest that noradrenergic effects in the hippocampus at moderate levels of arousal and stress are predominantly mediated by astrocytes.