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Updated: Jun 21, 2026

Injections of Lipopolysaccharide into Mice to Mimic Entrance of Microbial-derived Products After Intestinal Barrier Breach
Published on: May 2, 2018
Prostaglandin D2 produced by hematopoietic prostaglandin D synthase contributes to LPS-induced fever
1Pharmazentrum Frankfurt/ZAFES, Institut für Klinische Pharmakologie, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.
Abstract:
A large body of evidence has implicated prostaglandin E(2) (PGE(2)) in fever production. However, the role of PGD(2) in this context is only poorly understood. We therefore determined by LC-MS/MS analyses the content of PGD(2) and PGE(2) in cerebrospinal fluid (CSF), plasma and lungs of rats over 5 hours after fever induction by intraperitoneal injection of lipopolysaccharide (LPS, 50 microg/kg). Both PGD(2) and PGE(2) were detected in CSF, plasma and lungs of saline-treated control animals. The injection of LPS evoked fever and an increase of PGE(2) in the CSF, while the CSF content of PGD(2) was not significantly altered. However, both PGE(2) and PGD(2) levels were elevated in plasma and lungs after LPS injection. Interestingly, pretreatment with a novel selective inhibitor of hematopoietic prostaglandin D synthase (H-PGDS), EDJ300520 (10-40 mg/kg p.o.), selectively and dose-dependently prevented the LPS-induced increase of PGD(2) in plasma and lungs but did not affect the PGE(2) content. Most remarkably, EDJ300520 pretreatment led to an hypothermic response after LPS injection during the first 3 h and prevented fever induction. These data indicate that PGD(2) produced peripherally by H-PGDS essentially contributes to LPS-induced fever.
Insights
Prostaglandin D2 (PGD2), produced peripherally by hematopoietic prostaglandin D synthase (H-PGDS), plays a crucial role in lipopolysaccharide (LPS)-induced fever. Inhibiting H-PGDS prevents fever, highlighting PGD2
Area of Science:
- Immunology
- Neuroscience
- Pharmacology
Background:
- Prostaglandin E2 (PGE2) is well-established in fever production.
- The role of Prostaglandin D2 (PGD2) in fever remains poorly understood.
- Lipopolysaccharide (LPS) is a common fever inducer.
Purpose of the Study:
- To investigate the role of PGD2 in LPS-induced fever.
- To quantify PGD2 and PGE2 levels in response to LPS.
- To evaluate the effect of a novel H-PGDS inhibitor on fever.
Main Methods:
- LC-MS/MS analysis of PGD2 and PGE2 in rat CSF, plasma, and lungs.
- Fever induction using intraperitoneal LPS injection.
- Administration of a selective H-PGDS inhibitor (EDJ300520) prior to LPS.
Main Results:
- LPS increased PGE2 in CSF and both PGD2 and PGE2 in plasma and lungs.
- CSF PGD2 levels were not significantly altered by LPS.
- H-PGDS inhibition by EDJ300520 dose-dependently reduced plasma and lung PGD2, prevented fever, and induced hypothermia.
- EDJ300520 did not affect PGE2 levels.
Conclusions:
- Peripheral PGD2 production by H-PGDS is essential for LPS-induced fever.
- Targeting H-PGDS may be a viable strategy for fever management.
- PGD2, not just PGE2, is a key mediator in the fever pathway.
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