HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Role of 15-deoxy delta(12,14) prostaglandin J2 and Nrf2 pathways in protection against acute lung injury.

AbstractRATIONALE:
Acute lung injury (ALI) is a disease process that is characterized by diffuse inflammation in the lung parenchyma. Recent studies demonstrated that cyclooxygenase-2 (COX-2) induced at the late phase of inflammation aids in the resolution of inflammation by generating 15-deoxy-delta(12,14)-prostaglandin J2 (15d-PGJ2). Transcription factor Nrf2 is activated by electrophiles and exerts antiinflammatory effects by inducing the gene expression of antioxidant and detoxification enzymes.
OBJECTIVES:
Because 15d-PGJ2 is an endogenous electrophile, we hypothesized that it protects against ALI by activating Nrf2.
METHODS:
To test this hypothesis, we generated a reversible ALI model by intratracheal injection of carrageenin, an inducer of acute inflammation, whose stimulation has been known to induce COX-2.
MAIN RESULTS:
We found that ALI induced by carrageenin was markedly exacerbated in Nrf2-knockout mice, compared with wild-type mice. Analysis of bronchoalveolar lavage fluids also revealed that the magnitude and the duration of acute inflammation, indicated by albumin concentration and the number of neutrophils, were significantly enhanced in Nrf2-knockout mice. Treatment of wild-type mice with NS-398, a selective COX-2 inhibitor, significantly exacerbated ALI to the level of Nrf2-knockout mice. In the lungs of NS-398-treated wild-type mice, both the accumulation of 15d-PGJ2 and the induction of Nrf2 target antioxidant genes were significantly attenuated. Exogenous administration of 15d-PGJ2 reversed the exacerbating effects of NS-398 with the induction of antioxidant genes.
CONCLUSIONS:
These results demonstrated in vivo that 15d-PGJ2 plays a protective role against ALI by exploiting the Nrf2-mediated transcriptional pathway.
AuthorsMie Mochizuki, Yukio Ishii, Ken Itoh, Takashi Iizuka, Yuko Morishima, Toru Kimura, Takumi Kiwamoto, Yosuke Matsuno, Ahamed E Hegab, Akihiro Nomura, Tohru Sakamoto, Koji Uchida, Masayuki Yamamoto, Kiyohisa Sekizawa
JournalAmerican journal of respiratory and critical care medicine (Am J Respir Crit Care Med) Vol. 171 Issue 11 Pg. 1260-6 (Jun 01 2005) ISSN: 1073-449X [Print] United States
PMID15750045 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • 15-deoxy-delta(12,14)-prostaglandin J2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • DNA-Binding Proteins
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Nitrobenzenes
  • Sulfonamides
  • Trans-Activators
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide
  • Carrageenan
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Prostaglandin D2
Topics
  • Animals
  • Carrageenan
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors (therapeutic use)
  • DNA-Binding Proteins (metabolism)
  • Disease Models, Animal
  • Macrophages (metabolism)
  • Mice
  • Mice, Inbred BALB C
  • NF-E2-Related Factor 2
  • Nitrobenzenes (therapeutic use)
  • Pneumonia (drug therapy, etiology, metabolism)
  • Prostaglandin D2 (analogs & derivatives, metabolism)
  • Prostaglandin-Endoperoxide Synthases (metabolism)
  • Respiratory Distress Syndrome (chemically induced, complications, drug therapy, immunology, metabolism)
  • Sulfonamides (therapeutic use)
  • Trans-Activators (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: