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March 12, 2026eLife0 citationsOpen Access

Descending locus coeruleus noradrenergic signaling to spinal astrocyte subset is required for stress-induced mechanical pain hypersensitivity

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RKRiku Kawanabe-KobayashiSUSawako UchiyamaKYKohei Yoshihara

Key Points

  • The research aims to understand how stress alters pain sensitivity through specific neuronal circuits.
  • Identified locus coeruleus neurons that project to spinal dorsal horn astrocytes in mice.
  • Examined the role of α 1A -adrenergic receptors in astrocytes and their effect on inhibitory neurons during stress.
  • Utilized genetic knockdown techniques to investigate the role of adenosine receptors in pain pathways.
  • Activation of locus coeruleus descending neurons was linked to increased mechanical pain sensitivity during stress.
  • α 1A -adrenergic receptors in Hes5 positive astrocytes were confirmed as key mediators of stress-induced pain.
  • Adenosine receptor knockdown in spinal inhibitory neurons attenuated stress-related pain hypersensitivity.

Abstract

It is known that stress powerfully alters pain, but its underlying mechanisms remain elusive. Here, we identified a circuit, locus coeruleus descending noradrenergic neurons projecting to the spinal dorsal horn (LC →SDH -NA neurons), that is activated by acute exposure to restraint stress and is required for stress-induced mechanical pain hypersensitivity in mice. Interestingly, the primary target of spinal NA released from descending LC →SDH -NAergic terminals causing the stress-induced pain hypersensitivity was α 1A -adrenaline receptors (α 1A Rs) in Hes5 -positive ( Hes5 + ) astrocytes located in the SDH, an astrocyte subset that has an ability to induce pain sensitization. Furthermore, activation of Hes5 + astrocytes reduced activity of SDH-inhibitory neurons (SDH-INs) that have an inhibitory role in pain processing. This astrocytic reduction of IN activity was canceled by an A 1 -adenosine receptor (A 1 R)-knockdown in SDH-INs, and the A 1 R-knockdown suppressed pain hypersensitivity caused by acute restraint stress. Therefore, our findings suggest that LC →SDH -NA neuronal signaling to Hes5 + SDH astrocytes and subsequent astrocytic reduction of SDH-IN activity are essential for mechanical pain facilitation caused by stress.

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Cite This Study

Kawanabe-Kobayashi et al. (2026) studied this question.

synapsesocial.com/papers/69b258a396eeacc4fcec8896https://doi.org/10.7554/elife.104453.3
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