Peroxisome proliferator-activated receptor agonists inhibit inflammatory edema and hyperalgesia

Bradley K. Taylor, Niren Dadia, Carolyn B. Yang, Sendhil Krishnan, Mostafa Badr

Research output: Contribution to journalArticlepeer-review

44 Scopus citations


Previous studies have produced conflicting data on the contribution of the peroxisome proliferator-activated receptors (PPARs) to the inflammatory process. This study investigated the effects of several PPARα and PPARγ subtype-specific agonists on the inflammation and hyperalgesia produced by intraplantar carrageenan injection in unanesthetized male Sprague-Dawley rats. Intraperitoneal administration of PPARα agonists reduced edema in parallel to their potencies determined in vitro. Perfluorooctanoic acid (PFOA) inhibited carrageenan-induced edema in a dose-dependent manner, and also reduced thermal hypersensitivity. Furthermore, PFOA produced much more robust effects when administered 0.5-24 hrs before carrageenan, as compared to when it was administered 1.5 hrs after carrageenan. Intraperitoneal administration of similar doses of the PPARγ agonist rosiglitazone, but not the less potent agonist, troglitazone, reduced edema when administered before but not after carrageenan. We conclude that systemic administration of potent PPARα and PPARγ agonists exert anti-hyperalgesic and/or antiinflammatory actions in vivo, possibly by interfering with the initiation of inflammation.

Original languageEnglish (US)
Pages (from-to)121-127
Number of pages7
Issue number3
StatePublished - 2002

Bibliographical note

Funding Information:
Acknowledgments—This work was supported by Grants DA-10356 to BKT and AG18479 to MB. We would like to thank Eli Lilly, Parke-Davis and GlaxoSmithKline for their gifts of LY-171833, Troglitazone, and Rosiglitazone, respectively.

Copyright 2008 Elsevier B.V., All rights reserved.


  • Carrageenan
  • Nuclear hormone receptors
  • Pain
  • Perfluorooctanoic acid
  • Rosiglitazone

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