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February 12, 2026The Journal of Physiology0 citations

The pyrogenic mediator prostaglandin E 2 elicits warmth seeking via EP3 receptor‐expressing parabrachial neurons: a potential mechanism of chills

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TYTakaki YahiroYNYoichi NakamuraKNK. Nakamura

Key Points

  • This research aims to explore the central mechanisms behind warmth-seeking behavior during infection, focusing on the role of prostaglandin E2.
  • Conducted thermal preference tests in rats
  • Utilized in vivo physiological recordings
  • Performed functional neuronal tracing and immunostaining for Fos
  • PGE2 acting on EP3 receptors in the LPB increases warmth-seeking behavior in rats
  • PGE2 does not trigger brown adipose tissue thermogenesis
  • LPB EP3R neurons significantly project to the CeA, not to the POA
  • LPB EP3R neurons enhance cold sensory signal transmission to the CeA

Abstract

Abstract Seeking warmth during infection is a sickness behaviour that contributes to the development of fever and is often accompanied by chills. However, the central mechanism underlying this behaviour remains unknown. We recently reported two ascending thermosensory neuronal pathways from the lateral parabrachial nucleus (LPB) of the pons that drive thermoregulatory behaviours in hot and cold environments: one pathway to the preoptic area (POA), a thermoregulatory centre, mediates heat avoidance, whereas the other to the central amygdaloid nucleus (CeA), a limbic emotion centre, mediates cold avoidance. Here we investigated the role of prostaglandin E 2 (PGE 2 ), a pyrogenic mediator produced during infection, in the LPB‐mediated mechanism of thermoregulatory behaviour in rats. Thermal preference tests and in vivo physiological recordings revealed that PGE 2 acting on the prostaglandin EP3 receptor (EP3R) in the LPB elicits behaviour that prefers warmth to a thermoneutral temperature, thereby contributing to an increase in body core temperature. However, it does not elicit brown adipose tissue thermogenesis, an autonomic febrile response. Notably, we discovered that EP3R‐expressing LPB neurons (LPB EP3R neurons) project numerous axons to the CeA, but few to the POA. Functional neuronal tracing combined with immunostaining of Fos, a marker for neuronal activation, revealed that LPB EP3R →CeA neurons are activated by cold ambient temperature and constitute the majority of the cold‐transmitting LPB→CeA neuronal population mediating cold avoidance. These results indicate that PGE 2 action on LPB EP3R neurons during infection elicits warmth‐seeking behaviour by augmenting their cold sensory transmission to the CeA, which potentially produces the unpleasant cold sensation of chills. image Key points Seeking warmth during infection is a commonly observed sickness behaviour that contributes to the development of fever, often accompanied by chills. Prostaglandin E 2 (PGE 2 ), a pyrogenic mediator, elicits warmth‐seeking behaviour in rats by acting on prostaglandin EP3 receptor (EP3R)‐expressing neurons in the lateral parabrachial nucleus (LPB) of the pons (LPB EP3R neurons). This PGE 2 action does not elicit thermogenesis in brown adipose tissue, an autonomic febrile response. LPB EP3R neurons transmit cutaneous cold sensory signals to the limbic emotion centre, central amygdaloid nucleus (CeA), but scarcely innervate the thermoregulatory centre, preoptic area. These results indicate that PGE 2 acting on LPB EP3R neurons during infection elicits warmth‐seeking behaviour by augmenting cold sensory transmission to the CeA, which is a potential mechanism of chills.

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Cite This Study

Yahiro et al. (2026) studied this question.

synapsesocial.com/papers/698d6e5a5be6419ac0d540d9https://doi.org/10.1113/jp289466
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